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Familial hypercholesterolaemia (FH), defined as the heritable occurrence of severe hypercholesterolaemia with cholesterol deposits in tendons and premature heart disease, is caused by at least four genes in sterol and lipoprotein pathways and displays varying gene-dose effects. The genes are the low-density lipoprotein (LDL) receptor, apolipoprotein (apo) B, proprotein convertase subtilisin/kexin 9, and the autosomal recessive hypercholesterolaemia (ARH) adaptor protein. All of these disorders have in common defective clearance of LDL within a complex system of lipid and lipoprotein metabolism and regulation. Normal cellular cholesterol and lipoprotein metabolism is reviewed before describing the disorders, their metabolic derangements and their clinical effects. FH is classified as two simplified phenotypes of disease according to the severity of the metabolic derangement. The dominantly inherited heterozygous phenotype comprises defects in the LDL receptor, apoB100, and neural apoptosis regulatory cleavage protein. The homozygous phenotype is co-dominant in defects of the LDL receptor, and occurs also as the ARH of adapter protein mutations. Defective binding of apoB100 does not result in a significant gene dose effect, but enhances the severity of heterozygotes for LDL receptor mutations. The genetic diagnosis of FH has provided greater accuracy in definition and detection of disease and exposes information about migration of populations. All of these disorders pose a high risk of atherosclerosis, especially in the homozygous phenotype. Studies of influences on the phenotype and responses to treatment are also discussed in the context of the metabolic derangements.
FH is an interesting disease to which attention was drawn by a pathologist, Harbitz, by virtue of the coincidence of lipid deposits (xanthomata) in tendons and sudden death, before being described by Muller as a clinical entity in the first half of the previous century.1 Studies in patients and cultured cells revealed a defect in the receptor for LDL and culminated in the Nobel prize for Brown and Goldstein who also investigated the regulation of the cholesterol synthetic pathway.2,3 The world-wide prevalence of FH is about 1 in 500 people. This prevalence is sufficiently high to warrant the diagnosis and treatment of FH at primary health care level by the World Health Organisation.4 More recently, FH has been shown to be due to other molecular mechanisms in lipoprotein metabolism.5
In the past decade alone, there have been more than 2000 publications on FH. This article will provide a brief review of cholesterol metabolism in cells and circulatory lipoproteins to provide the context in which FH occurs. The genetic disorders are discussed, with an emphasis on the more common disorders. Recent investigations that give insight into the pathophysiology of disease and factors modulating the phenotype are discussed and referenced. Although this review focuses on the role of the LDL receptor in cholesterol metabolism, other roles for this receptor and related receptors are emerging in endocytosis and signalling.6
FH is best defined as an entity in clinical practice that is recognisable from features in the patient’s family and personal history and physical examination, as well as readily available chemical analysis of the blood. The diagnosis of FH is important not only for the prognosis of the patient, but also has implications for the family members who may have inherited the same disorder. The clinical pattern is also an important starting point of research for the biochemist, clinical pathologist, epidemiologist, geneticist or healthcare provider.
FH may be defined as an heritable disorder, involving a single gene, that produces a clinically recognisable pattern (in the majority of subjects) that consists of severe hypercholesterolaemia due to the accumulation of LDL in the plasma, cholesterol deposition in tendons and occasionally in skin, and a high risk of atherosclerosis manifesting almost exclusively as coronary artery disease (CAD). These disorders all share the mechanism of decreased clearance of LDL, but their inheritance may be autosomal dominant or recessive and not all dominant disorders have a gene-dose effect.
FH may be loosely classified into an “heterozygous” and an “homozygous” clinical phenotype (Table 1). The heterozygous phenotype is inherited in an autosomal dominant manner and has a LDL-cholesterol concentration between 5 and 12 mmol/L, tendon xanthomata are common and CAD before 55 years of age is also common. The leading cause of the heterozygous phenotype is a mutation in the LDL receptor. Occasionally a mutation disrupting the binding of apoB to the LDL receptor is encountered. Recently a newly discovered protein, neural apoptosis regulated convertase 1 (NARC1), the product of the gene proprotein convertase subtilisin/kexin type 9 (PCSK9) has been referred to as autosomal dominant FH 3.
The homozygous phenotype has more severe LDL hypercholesterolaemia (>12 mmol/L) and typically there are also xanthomata in the skin and tendons. On westernised diets, the LDL-cholesterol concentration usually exceeds 15 mmol/L. Included in this phenotype of cutaneous and tendinous xanthomata are other sterol disorders that do not result in the same degree of hypercholesterolaemia: phytosterolaemia and cerebrotendinous xanthomatosis (CTX). The genetic causes of the homozygous phenotype include the concurrence of two LDL receptor defects, but the same phenotype is not seen with concurrence of binding defective apoB for reasons that will be discussed below. The homozygous phenotype is recessively inherited when mutations disrupt the function of an adaptor protein, now known by its property to confer ARH. Phytosterolaemia is inherited in an autosomal recessive manner as a result of mutations in adenosine binding cassette transporter proteins G5 and G8. Whilst phytosterolaemia can have significant hypercholesterolaemia, it seldom exceeds the heterozygous FH range. CTX, also autosomal recessively inherited, is due to mutations in 27-hydroxylase (CYP27). CTX is not associated severe hypercholesterolaemia.
The term FH is thus restricted to specific disorders and does not simply mean a heritable hypercholesterolaemia. Whilst some lipidologists may still retain the term FH specifically for LDL receptor defects, the heterozygous phenotype was and still is used to identify subjects who were inferred to have LDL receptor defects but who may well have had some of the other defects outlined in this review. It is conceivable that more defects for these phenotypes will still be discovered. In this review, FH will refer to the broader context outlined in Table 1 and will generally refer to the heterozygous pattern.
In this section cholesterol synthesis in the cell and its regulation will be discussed. The course of cholesterol can be traced within the cell, to its incorporation into lipoproteins and delivery to cells, recycling, conversion to bile acids and excretion. Figure 1 summarises cholesterol metabolism in the hepatocyte, the most active cell in cholesterol metabolism and homeostasis of the human body. Figure 2 depicts the general scheme of lipoprotein metabolism.
Cholesterol is an essential component of cell membranes but is also used by hepatocytes and enterocytes for the production of lipoproteins. The hepatocyte also secretes bile that contains cholesterol and bile acids that are derived from cholesterol. Adrenal and gonadal cells synthesise corticosteroid hormones from cholesterol. All nucleated cells can synthesise the enzymes to produce cholesterol. This synthetic pathway produces cholesterol as well as other isoprene products involved in the prenylation of proteins and the synthesis of ubiquinone. The rate-limiting enzyme in this pathway is 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase. The product of HMG-CoA reductase, mevalonic acid, appears in plasma and urine and may be used as a guide to cholesterol synthetic acitivity. The plasma mevalonate concentration varies in a diurnal rhythm with the highest synthetic rate in the early hours of the morning.
There is a demand for cholesterol during cell growth and in cells that use cholesterol for specialised purposes. To meet such demands, the cell can synthesise cholesterol de novo, can import it through specialised receptors such as the LDL and related receptors, and can use cholesterol after cleavage of stored cholesterol ester (CE) by the action of neutral cholesterol ester hydrolase (NCEH). The regulation of both cholesterol synthesis and importation by LDL receptors occurs by sensing the amount of cholesterol in the membranes. A depletion of membrane cholesterol will up-regulate transcription of both HMG-CoA reductase and the LDL receptor through a complex mechanism.7
The upregulation of cholesterol synthesis and importation in the time of need is made possible by an interaction of a regulatory protein with the promoters of the genes for the LDL receptor, HMG-CoA reductase and HMG-CoA synthase. The LDL receptor promoter has three imperfect repeats. Repeat 2, consisting of 16 base pairs, forms a sterol regulatory element (SRE) that interacts with the SRE binding protein (SREBP) under cholesterol deprivation. SREBP has three isoforms in humans, each comprising approximately 1150 amino acids. SREBP has three domains: the amino-terminal domain contains a basic helix-loop-helix leucine zipper region that enables it to bind to DNA, a carboxy-terminal domain binding to sterol cleavage activating protein (SCAP) at the cell membrane, and an intermediate domain that contains two transmembrane portions linked by a loop of about 30 amino acids into the lumen of the endoplasmic reticulum (ER). SCAP is associated with SREBP in the membrane where the complex is stationary until cholesterol depletion permits its migration to the Golgi apparatus. In the Golgi apparatus two membrane-bound proteases process the SREBP:SCAP complex to create a cleavage product that migrates to the nucleus. Site 1 protease is a serine protease that cleaves the loop in the central domain of SREBP. Site 2 protease is a metalloprotease that cleaves the amino-terminal portion of SREBP that translocates to the nucleus. Additional complexity is introduced into the regulation of lipid metabolism by the three isoforms of SREBP. Alternative transcription start sites on chromosome 17 create differences in exon 1 of SREBP to produce SREBP1a and SREBP1c. SREBP2 is coded on chromosome 22. Whilst SREBP1a has broad specificity for all genes with SREBP response elements, SREBP1c favours promoters of genes for fatty acid synthesis and SREBP2 enhances cholesterol synthesis and importation into the cell.
Cholesterol importation into cells typically involves a high affinity, saturable process by means of the LDL receptor and a low affinity process of passive association with the cell membrane and internalisation. Additional receptors, such as the LDL receptor-related protein (LRP), may import lipoproteins in certain cells.8 Whilst the low affinity process accounts for very little uptake at low concentrations of LDL, higher concentrations of LDL may result in the internalisation of sufficient cholesterol to result in storage of cholesterol as its ester, to regulate cholesterol synthesis and possibly also LDL receptor expression. At least some contribution to low affinity clearance may be attributable to an interaction of fatty acids with cell membranes at physiologically appropriate concentration9 and some clearance may also take place by means of the scavenger receptor B1 (SRB1) even though this receptor has conventionally been viewed as a receptor for other lipoproteins.10
The LDL receptor is a well-characterised transmembrane protein encoded on chromosome 19 and comprises 18 exons in 48 kb.2 The 843 amino acids can be placed in the following domains: ligand-binding domain (about 292 amino acids, exons 2 to 6), epidermal growth factor precursor homologous domain (about 400 amino acids, exons 7 to 14), a carbohydrate-rich domain (about 58 amino acids, exon 15), a transmembrane domain (about 22 amino acids, exon 16) and a cytoplasmic tail (about 50 amino acids). The protein is translated to form a 120 kDa precursor that matures in the Golgi apparatus to 160 kDa before being transported to the cell surface. On the cell surface it finds its way to the clathrin-coated pits.
The amino-terminus of the LDL receptor is situated extracellularly and has 7 repeats of about 40 amino acids in the binding domain. Cysteine is prominent in these “LDL-A” modules that mediate binding to lipoproteins.11 Binding requires calcium and involves interaction with negatively charged amino acids. The fifth repeat is essential for binding apoE whilst repeats 2 to 7 are necessary to bind the larger ligand, apoB. After synthesis and maturation, the LDL receptor is sorted and trafficks to the basolateral surface of the cell. The bound complex of lipoprotein and receptor is internalised through the clathrin-coated pit with assistance by adapter proteins. The cytoplasmic tail has an important function in signalling internalisation. Once in the endosomal trafficking system, the LDL receptor dissociates from the lipoprotein during acidification; the epidermal growth factor-like domain is critical for this function. The epidermal growth factor-like domain has repeats A and B, a β-propeller structure and a repeat C. The β-propeller region competes for binding to the LDL-A repeats 4 and 5 and the lipoprotein leaves the LDL receptor in the endosome.12 Hereafter, the lipoprotein proceeds to the lysosome for enzymic degradation into its constituent cholesterol, fatty acids and amino acids. The receptor recycles approximately 150 times.
Since excess cholesterol in cell membranes imparts unfavourable properties, excess cholesterol is metabolised within cells to CE by the action of acylcoenzyme A:cholesterol acyltransferase (ACAT). This enzyme is embedded in the membrane and is allosterically activated by cholesterol. ACAT1 is a transmembrane protein with its catalytic site orientated towards the cytosol which houses the cholesterol ester formed under overloading conditions. Under conditions of cholesterol overload, HMG-CoA reductase is subject to instant control through phosphorylation. Furthermore, excess cholesterol will also result in down-regulation of HMG-CoA reductase and LDL receptors by limiting the migration of the SREBP-SCAP complex. Cellular cholesterol balance has been reviewed in detail recently.13 Adenosine binding cassette (ABC) protein A1 facilitates transfer of intracellular cholesterol to apoprotein or lipoprotein acceptors to rid cells of excess free cholesterol.14
Lipoproteins, composed of lipid and apolipoproteins, are a means of transporting insoluble lipids, chiefly triacylglycerol (TG), CE and cholesterol. Different mechanisms exist to target TG and cholesterol within lipoproteins to cells that require fatty acids and/or cholesterol. Lipoproteins generally have a spherical shape but vary significantly in size, density, and constituent lipids and apoproteins. Greater lipid content makes for larger diameters and lower density, chiefly by TG content. The shell contains phospholipid (PL), cholesterol and apoproteins while the core contains TG and CE.
The enterocyte and hepatocyte are the sites of assembly for TG-rich lipoproteins, using apoB for assembly of the lipoproteins. The TG-rich lipoproteins secreted by the enterocyte are termed chylomicrons (CM) and those secreted by the hepatocytes are termed very low-density lipoproteins (VLDL). The enterocyte uses an edited mRNA of apoB100 to synthesise apoB48.15 CMs contain one copy of apoB48 and VLDL contains one copy of apoB100.
Almost half of the cholesterol in the gut is absorbed but this efficiency varies amongst individuals. Enterocytes, like hepatocytes, express ACAT2 that produces CE but in contrast to ACAT1, its catalytic site is on the lumenal aspect of the ER. The CE globules as well as those of TG in the lumen of the ER, are used in lipoprotein assembly. Both enterocytes and hepatocytes initiate lipoprotein assembly by adding a critical initial amount of neutral lipid to apoB so that this constitutively expressed protein is protected from ubiquitinylation and degradation. The critical protein responsible for this is microsomal TG transfer protein (MTP). Further remodelling of the lipoprotein takes place in the Golgi region before secretion.
As may be expected, there is in reality a range in size and content of lipoproteins secreted by lipoprotein-producing cells, especially by hepatocytes. These include: TG-rich VLDL with flotation rates of Sf 60–400 termed VLDL1, smaller CE-rich VLDL (Sf 20–60) termed VLDL2, intermediate-density lipoproteins (IDL, Sf 12–20) and LDL (Sf 0–12).
A general scheme of lipoprotein metabolism is presented in Figure 2. CMs enter the venous circulation from the thoracic duct and lipoproteins made by the liver enter the hepatic venous system. Redistribution of apoproteins from especially high-density lipoprotein (HDL) supplies the bulk of the apoproteins on these TG-rich lipoproteins.
The circulating TG-rich lipoproteins attach briefly to proteoglycans in the vascular beds of muscle and adipose tissue. Lipoprotein lipase (LPL) also resident on the proteoglycans, is activated by apoC-II and inhibited by apoC-III. TG is hydrolysed by activated LPL to release fatty acids that will diffuse into the tissue or be sequestered on albumin. The lipolytic process results in a smaller core and the redundant shell around the core buds off with apoA-I to form HDL.
The remnants of CM and VLDL return to the liver, being cleared by virtue of apoE that serves as the ligand for the LDL receptor, as well as the LRP. VLDL remnants, entering the IDL flotation range, are further hydrolysed by hepatic lipase (HL) to produce LDL. ApoB is the only apoprotein on LDL. Only on LDL will apoB serve as the ligand for the LDL receptor.
Whilst it is known that the liver can secrete a range of apoB-containing lipoproteins, the classical pathway is the production of mainly VLDL1 with subsequent conversion of this lipoprotein through VLDL2 to IDL before being removed into the liver from the circulation; but some IDL is metabolised to LDL. The half-lives of the lipoproteins increase down the lipolytic cascade, with LDL being the longest resident in plasma.
The larger lipoproteins are remodelled in the circulation by LPL as mentioned above. Smaller lipoproteins like IDL, LDL and HDL are modified by HL. An additional complexity is brought about by CE transfer protein (CETP) which exchanges neutral lipids between lipoproteins; TG being moved towards cholesterol-rich LDL and HDL, and CE being moved from these lipoproteins to CM and VLDL. The latter two apoB-containing lipoproteins can thus participate in the reverse cholesterol transport (RCT) of cholesterol from HDL to the liver. TG-rich LDL and HDL are substrates for HL, the action of which will decrease their size by hydrolysis of TG.
The lipoproteins that lack apoB constitute mainly HDL. This class of lipoproteins is important for RCT. The other functions of HDL include being a reservoir for apopoproteins A, C and E, CETP and lecithin:cholesterol acyltransferase (LCAT), the provision of anti-oxidant activity by paraoxonase, and modulation of endothelial function and immunity. Having accepted cholesterol from a cell, a small HDL particle will enlarge as a result of esterification of cholesterol by LCAT as CE migrates to the core and additional cholesterol that is now accommodated in the shell, also becomes esterified. Not only can HDL transfer CE to the TG-rich lipoproteins, but it can deliver it directly to the liver through SRB1.
In clinical practice, the heterozygous FH phenotype (see Table 1) is encountered most often whilst the rarely encountered homozygous phenotype has much worse sequelae. Patients with FH typically presented with premature CAD in the past but today with greater awareness, simpler chemical assays that are widely available, the diagnosis is made earlier. FH management with modern drug treatment has improved the prognosis.16
The family history of premature ischaemic heart disease is very helpful to identify an autosomal dominant mode of inheritance and the patient’s ancestry may suggest the molecular defect if there is a link to a population with a founder effect. Despite the high risk of heart disease in heterozygous FH, the risk is significantly modified by other genes and environmental factors, so that the family history may occasionally be misleadingly benign. In such a setting, a recessive disorder should be considered, or a new mutation giving rise to a dominantly inherited pattern should be considered.17,18
Physical signs due to lipid deposition in the eye, the skin, and the tendons are valuable, but not invariant clues. The physical signs are depicted in Figure 3. The heterozygous phenotype generally has tendinous manifestations alone and the homozygous phenotype tends to have both tendinous and cutaneous manifestations. In the heterozygous phenotype the manifestations are usually not readily apparent until about the age of 25 to 30 years, whereas in the homozygous phenotype they are usually evident before the age of 10 years.
The palpation of the Achilles tendon requires some experience, but is the best clinical sign for diagnosing FH. Ultrasound examination can establish more accurate dimensions. Thickening of the tendons by cholesterol deposition may lead to inflammation and pain and eventually the deposition of lipid leads to an irregular surface with nodules and sometimes visibly enlarged tendons. The high tension transmitted through the relatively avascular tendon to its septae containing the blood vessels is presumed to cause exudation or bleeds into the tissue. The connective tissue appears to bind lipoproteins and cholesterol accumulates. RCT is not effective as the high plasma LDL concentration and the relatively poor blood supply favour the accumulation of tissue lipid. Uncommonly, xanthomata also form in the extensor tendons to the fingers and rarely elsewhere in the body. The detection of xanthomata at clinical examination not only has diagnostic implications, but may also indicate risk, as FH subjects with xanthomata were found to have more heart disease.19
Deposition of lipid on the cornea of the eye results in a crescentic white line referred to as an arcus cornealis. The deposition of lipid in the eyelids as flat yellow plaques, referred to as xanthelasma, is not specific for FH and may even be observed in individuals without significant disturbances of the plasma lipoproteins.
Subclinical atherosclerosis is evident in young persons with FH when sought by vascular imaging techniques. In homozygous FH patients, aortic stenosis is a well-established complication as a result of lipid deposition in the aortic valve and root. Other vessels may also have turbulent flow in homozygous FH, especially the femoral arteries.
Atherosclerosis is imperfectly understood, but is clearly a multifactorial disease in which especially in FH, LDL hypercholesterolaemia plays a strong role. In FH, the disease is more severe and results in clinical complications earlier. High concentrations of LDL, resident in the circulation for prolonged periods, permit more oxidative modification in the circulation and tissues. These oxidised lipoproteins influence vascular endothelium adversely, promoting the attraction of monocytes that penetrate into or remain in the sub-endothelial space, where an indolent form of chronic inflammation takes place.20 Monocytes mature into macrophages that take up the lipid to become foam cells when ACAT1 esterifies cholesterol. Whilst the proportion of apoB that is glycated is normal in FH, the absolute concentration is increased.21 This may contribute to atherosclerosis by the adverse effects of advanced glycation endproducts. Under relatively low rates of entrance of post-prandial and endogenous lipoproteins into the arterial wall and low oxidative stress on these lipoproteins, RCT may counter atherogenesis and its complications that include inflammation, plaque rupture and thrombosis. The pathological outcome in a high risk condition such as FH, may thus still be modulated by many additional factors to apoB-containing lipoproteins, including RCT and factors governing tissue responses suggested above.
FH can thus serve as a model for investigating the utility of other strategies for prevention of atherosclerosis, even if the contribution from other risk factors may be greater in less severe dyslipidaemia. Modern non-invasive vascular imaging with ultrasound has also shown that the intima-media thickness of the carotid increases more rapidly in adolescents with FH, when compared with their peers.22 Vascular endothelial function is impaired in children with FH.23 Aggressive lipid-lowering therapy can improve the vascular abnormality in FH.24
The genetic reasons for the heterozygous phenotype are mutations in the LDL receptor, apoB100 and NARC1. All 3 are characterised by an increase in LDL-cholesterol and normal VLDL concentrations. There is controversy about the metabolism of remnants of TG-rich lipoproteins, especially with LDL receptor defects. Differences in biochemical derangement and atherogenic impact LDL receptor and apoB defects are also controversial, along with responses to treatment.
The discovery of the LDL receptor and its defective function led to a great advance in the understanding of the pathophysiology of FH.2 Although importation rates of cholesterol into growing cells would theoretically be impaired and plasma concentration approximately doubled in heterozygous FH, cells can compensate by synthesising more cholesterol and can also obtain more cholesterol by low affinity processes as a result of a higher concentration in their surrounds. Assuming for the moment that hepatocytes export lipoproteins at a normal rate in FH, hyperlipidaemia will result from reduced clearance of IDL and LDL. A reduction in the clearance of IDL would promote conversion of IDL to LDL, compounding the increase in LDL already induced by the decreased clearance of LDL. The clinical homozygous FH phenotype may be due to a true genetic homozygote which has the same mutation on both alleles, or may be due to a genetically compound heterozygote in which a different mutation is found at each allele. The impact on LDL hypercholesterolaemia is much more severe, with more striking clinical features and vascular disease.
The hepatocyte has significant demands for cholesterol. De novo synthesis of cholesterol and some input from LDL receptor activity may be regulatable, but the higher plasma LDL-cholesterol concentration results in greater uptake of cholesterol and storage as CE. An increase in CE may be postulated to cause greater lipoprotein production that compounds the LDL hypercholesterolaemia. When both genes for the LDL receptor are dysfunctional, the impact would be worse because clearance of LDL is negligible or absent. Depending on the dietary cholesterol intake and absorption, biliary secretion and bile acids synthesis and losses, de novo synthesis of cholesterol will vary in the maintenance of the steady state conditions in FH.
Initially, LDL receptor activity was studied in the homozygous phenotype. The LDL receptor activity was declared “defective” if LDL handling by the cultured fibroblasts was low (<30%), and “negative” if the handling was <2% when compared with normal fibroblasts. Typically radio-iodinated LDL and a monoclonal antibody, IgGC7 are used to describe LDL handling in fibroblasts which have undergone incubation in a lipoprotein deficient medium to maximally upregulate LDL receptors. At 4°C, LDL receptor trafficking is disrupted and binding to the cell surface can be studied, the number of receptors can be determined using the antibody and their binding activity by using LDL. Immunoprecipitation of radio-isotopically labelled LDL receptors can be used to examine their expression and maturation in cells.
Defects in the LDL receptor are functionally divided into six classes depending on the impact of the mutation on the presence of mRNA, receptor maturation in cells, disparity between LDL and immunoglobulin binding on the cell surface, LDL receptor degradation and trafficking. Class 1 defects, mainly due to promoter mutations, leave no detectable mRNA and no detectable LDL receptor. Class 2 defects are due to mutations that retard the maturation of the LDL receptor by glycosylation, from 120 to 160 kDa; either in a limited fashion (class 2B) or completely (class 2A). Mutations such as D206E in exon 4 and involving binding modules, have persistent folding defects demonstrable on nuclear magnetic resonance spectroscopy that will influence maturation.25 In Class 3 the defective LDL receptors mature normally but have defects in binding the ligand. In Class 4, mutated LDL receptors mature normally to occupy the cell membrane but are not internalised, typically due to mutations in the cytoplasmic tail. Class 5 mutations relate to LDL receptor degradation that prevents receptors from reaching the cell surface and from recycling to the cell surface. Class 6 mutations are due to a failure of directing LDL receptors to the basolateral surface of polarised cells.26
The determination of the amino acid sequence of the LDL receptor and the impressive developments in molecular biology over the past two decades have permitted the characterisation of related receptors to the LDL receptor.27 Numerous defects in the LDL receptor have been catalogued and gave an understanding into their functional impact.28 A register of LDL receptor mutations is available at a website (http//:www.ucl.uk/fh).29
In contrast to the numerous mutations in the LDL receptor disrupting the binding of apoE and apoB, very few mutations have been reported in apoB100 that will disrupt binding to the LDL receptor.
ApoB100, a large protein of 550 kDa, is encoded on chromosome 2 and has 26 exons. The binding region is rich in positively charged amino aids and interacts with the binding domains of the LDL receptor when the conformation is appropriate on LDL. As a result of impaired clearance relative to normal apoB, the defective apoB100 becomes enriched in LDL. In contrast to subjects with LDL receptor mutations in whom IDL clearance will be impaired, apoE remains a normally functioning ligand on these particles in familial binding defective apoB100 (FDB). The functional LDL receptor in these subjects will permit normal entry of cholesterol into the liver from remnants of CM and VLDL. This was confirmed by a study in which there was decreased production of LDL.30 A compensatory upregulation of LDL receptors can be expected to ameliorate the biochemical abnormality in heterozygotes for FDB and especially in homozygotes.
The clinical phenotypes of LDL receptor mutations and FDB are very similar, but FDB does seem to be biochemically less severe in children.31 Increased LDL receptor activity during growth may be responsible for this finding. In a comparison of the impacts of LDL receptor and apoB mutations on atherosclerosis, it was found that LDL receptor mutations rendered the plasma lipoprotein concentration higher and was associated with higher incidences of coronary artery complications, as well as carotid plaques.32 There is evidence that there is a more benign phenotype for FDB when compared with LDL receptor defects in adults,33 but the clinical features and complications are so similar for the heterozygous phenotype that they could be viewed as identical.34–37
In homozygous FDB, there appears to be no significant gene dose effect.38 Two homozygotes for FDB were reported to have cholesterol concentrations in the range for heterozygotes for LDL receptor mutations.39 The binding affinity for LDL receptors of VLDL was shown to be normal in these subjects whilst LDL affinity was 10% of normal. In homozygous FDB, the longer plasma residence time of the LDL particle renders it smaller, presumably from modulation by CETP and HL.40 FDB has been attributed to recurrent mutations. A Chinese subject was shown to have the R3500Q mutation on a different haplotype of apoB100 to Caucasian subjects with the same condition.41 There appears to be a higher prevalence of FDB in subjects of Celtic origin and even a founder effect in central Europe for FDB that is very rare in some populations, including Finland.42,43
The homozygous FH phenotype in subjects whose parents had normal plasma lipoprotein concentrations was found to relate to a problem of LDL receptor internalisation.44 Endocytosis was disrupted less in up-regulated cultured fibroblasts than in lymphoblasts. The disorder is due to mutations in the adaptor protein for endocytosis of the LDL receptor.45 A very specific interaction between the cytoplasmic tail of the LDL receptor (NPVY) with the phosphotyrosine binding domain of ARH is defective, failing to link the LDL receptor to clathrin and the adapter protein 2.46 The impact on the clearance of LDL into the liver is such that a homozygous FH phenotype results. This disorder seems to be more prevalent in Sardinia.47
Autosomal dominant FH3 refers to a heterozygous FH phenotype due to mutations in NARC1, a protein of 692 amino acids coded for by the gene PCSK9 on chromosome 1p32.48 This protein is part of the subtilase family of proteases that includes subtilisin kexin iso-enzyme 1/site-1-protease that has an important role in sterol regulatory element binding protein metabolism.
Phytosterolaemia is due to an overabsorption of plant sterols from enterocytes, as well as an underexcretion from hepatocytes into the bile as a result of disruptions of ABC transporters G5 and G8 and has variable LDL hypercholes-terolaemia and high plasma plant sterol concentrations. CTX is due to mutations in cholesterol 27 hydroxylase, an essential step in cholesterol oxidation for bile acid synthesis.49 Although LDL-cholesterol is not raised, the xanthomata resemble the homozygous FH phenotype, but in addition the nervous system and lenses of the eye are affected.
A detailed description of serum apoproteins in FH found apoB concentration to be 2.5 times normal, consistent with the elevation in LDL-cholesterol.50 ApoC-I, C-II and E were significantly increased whilst apoA-I and apoA-II concentrations were not significantly different.
Turnover studies done with radio-iodinated ultracentrifugally isolated apoB-containing lipoproteins were traditionally employed to study lipoprotein metabolism, but currently synthetic rates and clearance rates for apoB-containing lipoproteins can be worked out more directly with stable isotope studies.51 Non-steady state kinetic analyses may also be done, but are subject to several assumptions, the most important of which are the occurrences of compensatory changes in production or clearance as a result of interventions (plasmapheresis). A direct comparison of steady state kinetics with radio-iodine studies and plasma exchange was done by Eriksson et al. who found that radioiodination studies yielded higher synthetic rates in normal and heterozygous FH states.52 Maugeais et al. also found no statistically significant differences between modelling with stable isotopes and non-steady state kinetics after apheresis in heterozygous FH, although there was a trend for increasing the clearance of LDL that may be attributable to an upregulation of LDL receptors.53 In homozygous FH, non-steady state turnover data may be more reliable because of the very low LDL receptor activity.
The traditional view that a defect in the LDL receptor brings about an increase of LDL only as a result of decreased clearance, explains most, but not all of the dyslipoproteinaemia in FH. The overproduction of apoB-containing lipoproteins, the suppression of HMG-CoA reductase and the increased hepatic content of cholesterol in FH were indicators of a need to review the classic paradigm.54 Barrett and Watts more recently reviewed the possibility of increased production of apoB-containing lipoproteins and concluded that there is increased production of apoB-containing lipoproteins in FH.55
A comparison of the turnover of apoB-containing lipoproteins in normal and FH subjects, revealed that in normal subjects almost all the LDL is formed from VLDL while in FH almost a third of LDL is formed by the secretion of IDL-LDL particles.56 Additionally, there was almost complete conversion of VLDL to LDL in FH, whereas in normal subjects there is considerable efflux of TG-rich lipoprotein remnants. Investigations of heterozygous FH and normal subjects found increased LDL production in heterozygous FH as well as a reduced fractional catabolic rate.52 A study undertaken by Zulewski et al. found increased production of apoB containing lipoproteins in subjects with heterozygous FH phenotype, including FDB.57 A study examined the impact of high carbohydrate low fat diets that are generally accepted as lowering plasma cholesterol in normal subjects and FH.58 As expected for such diets, plasma TG was raised. Kinetic modelling of apoB revealed increased production of more TG-rich VLDL and a greater delay in its release. Only normal subjects showed increased clearance of the precursors for LDL. Both normal and heterozygous FH subjects had increased clearance of LDL. It can be deduced that dietary cholesterol restriction increased LDL receptor expression but not cholesterol synthesis as faecal sterol balance studies showed a decrease in cholesterol synthesis.
There is no final explanation for the overproduction (over-secretion) of smaller, cholesterol-rich lipoproteins in FH. It is possible that the higher influx of cholesterol through low-affinity processes, compounded by a lack of a mechanism to regulate this influx, leads to increased cholesterol esterification, at least in part by ACAT2, and becomes available in the lumen of the ER where this neutral lipid can promote the commitment of apoB to synthesis of smaller cholesterol-rich lipoproteins. Another attractive hypothesis is that functional LDL receptors could retain newly synthesised lipoproteins and possibly target them for degradation during vesicular trafficking in the cell. Evidence for this came from the observation that a LDL receptor mutation construct that retains the receptors in the ER, practically abolished the secretion of apoB-containing lipoproteins.59 This effect was examined quantitatively in cell culture experiments: LDL receptor-negative cells degraded less than 20% of apoB whereas wildtype cells degraded about 55%.60 LDL receptors may thus modulate pre-secretory degradation of apoB and/or mediate immediate re-uptake and degradation of secreted lipoproteins. The overproduction of apoB-containing lipoproteins in FDB could be as a result of the same phenomenon when this ligand does not bind the LDL receptor.57
A turnover study of apoB in normal, LDL receptor deficient and FDB subjects revealed similarly decreased FCR for LDL in the LDL receptor deficient and FDB subjects but striking differences in the conversion of VLDL to LDL: this step was 44% less in FDB when compared to the other two states.61
HDL metabolism is also of interest in FH. Whilst the contention that HDL cholesterol is generally low in FH may be true, in clinical practice there is significant variation. A preponderance of smaller HDL species was linked to increased HL activity in FH.62 A detailed study found that HDL cholesterol, but not apoA-I concentration, was lower in FH when compared to normal subjects.63 This was also found previously.50 The production and clearance rates of apoA-I were both increased. To establish whether LDL concentration influences HDL metabolism directly, subjects with FH who had undergone plasmapheresis to reduce LDL concentration, were studied.64 The HDL measurements were stable. The calculated fractional catabolic rate for apoA-I was not statistically significantly higher, but the production rate increased.
Biliary cholesterol excretion may be increased in FH. A decrease in the cholesterol saturation index of fasting gall bladder bile was noted during treatment with pravastatin,65 and another study confirmed supersaturation of bile with cholesterol.66
Lipoprotein(a) [Lp(a)] is formed by the linking of a LDL-like lipoprotein by a disulphide bridge to apo(a). The apo(a) consists of kringle-like repeats probably duplicated from plasminogen and apo(a) also has an inactive protease domain of plasminogen. The number of kringle repeats determines the molecular mass of apo(a). The plasma concentration of Lp(a) is determined by the molecular mass of apo(a), in an inverse fashion. It appears that the production rate of Lp(a) is the main determinant of its concentration,67 and its clearance is little affected by homozygous FH.68 Nevertheless, heterozygous FH is associated with a higher plasma concentration of Lp(a) and this appears to affect prognosis.69
Repeated elevations of serum creatine kinase of skeletal muscle origin in about 40% of heterozygous FH subjects who were untreated and in whom exercise was not contributing to such elevations, suggests that there may be secondary abnormalities in muscle function.70 Heterozygous FH subjects had greater exercise-related release of creatine kinase and myoglobin, but was not aggravated by simvastatin.71
The heterozygous and homozygous FH phenotypes are subject to considerable variation in their degree of metabolic derangement, as well as clinical and therapeutic outcome. Modulation of the phenotype may not only relate to the gene responsible for the disease, but also may relate to the impact of the mutation on this molecule. Additionally, other proteins that modulate lipoprotein assembly, metabolism and clearance can influence the phenotype.
Residual LDL receptor activity influences LDL concentration in heterozygous FH. A LDL receptor mutation that confers a very mild phenotype lacks exon 15 which is thought to act only as a stalk for the receptor.72 A comparison of plasma LDL concentration in Afrikaners with a defective mutation (D206E) and a negative mutation (V408M) in the LDL receptor demonstrated significant differences in LDL-cholesterol concentration.73 Amongst French Canadian heterozygous FH subjects, receptor-negative patients had worse hypercholesterolaemia and more vascular disease.74 In the homozygous phenotype, LDL receptor activity also influenced the LDL-cholesterol concentration, with almost no overlap between negative and defective LDL receptor status in French Canadians.75
Since remnants of the TG-rich lipoproteins are cleared by the binding of apoE to the LDL receptor and LRP, it is of interest to examine the clearance of remnants in FH. CM can be labelled with orally administered retinyl esters and the plasma excursion of retinyl palmitate can be followed in whole plasma or in different density fractions for analysis. An alternative strategy to examine CM clearance is to measure plasma apoB48 concentration. Cabezas et al. examined retinyl palmitate clearance in untreated heterozygous FH and normal subjects.76 Whilst TG clearance (lipolysis) displayed no difference, retinyl palmitate clearance was delayed significantly in FH. ApoB48 concentration in heterozygous FH was more than double that of normal persons.77,78 This abnormality was also reported in homozygous FH.79 Retinyl palmitate clearance was not abnormal in the early part of an oral fat loading test in homozygous FH.80 The findings by Watts et al. in a novel breath test that examined oxidation of C13-labelled acyl-cholesterol in subjects with proven LDL receptor defects in the homozygous phenotype, also suggested that remnant-like particle clearance is not impaired.81 Since apoB48 is a specific and sensitive marker for chylomicron remnant clearance and increased CM production is unlikely in FH, its elevation should be taken as proof of impaired clearance of remnants of TG-rich lipoproteins.
ApoE influences the LDL-cholesterol concentration: the E2 isoform binds poorly to the LDL receptor and results in delayed clearance of remnants and consequently in increased clearance of LDL after up-regulation of the LDL receptor. In the setting of normal production rates of VLDL and limited dietary fat intake, apoE2 homozygosity is thus associated with a lower LDL concentration, whilst apoE concentration is increased. ApoE4 homozygosity is associated with higher LDL-cholesterol concentration, that is attributable to increased absorption. The impact of apoE on the FH phenotype has not been consistent. ApoE isoforms were not found to influence LDL concentration in several studies.82–84
Cholesterol esterase is an enzyme of pancreatic origin that requires bile acids for full activation. Unexpectedly, it appears to influence plasma LDL concentration significantly in normal individuals and to promote the formation of smaller LDL particles. In FH, serum cholesterol esterase activity is not increased, but its impact on LDL concentration is not known.85
The possible influence of the TaqIB polymorphism in CETP on the heterozygous FH phenotype was examined by Carmena-Ramon et al.86 The B2 allele was associated with higher HDL-cholesterol as well as apoA-I concentrations and lower LDL-cholesterol. This seemed to translate to a more benign clinical phenotype.
ApoH, modulating lipolysis, was found to influence the TG concentration by the V247L mutation.87 A functional polymorphism of MTP was found to influence the lipoprotein phenotype of FH differently to normal subjects.88 The -439G/G status in the promoter for MTP was responsible for practically a doubling of serum TG concentration when compared with the T/T status. In contrast to healthy individuals, there appeared to be no effect on LDL concentration in FH. This supports the notion that lipoprotein clearance and not production, is the major problem in FH.
The ApoA-I promoter polymorphism (-75 A/G) that may influence metabolism of HDL and indirectly also LDL, had an impact on LDL and apoB concentrations with G/A subjects having lower values.89 A normal variant of apoA-IV that may influence fat absorption, apoA-IV-2, was responsible for a mild lowering effect on LDL cholesterol in heterozygous FH, but less dietary responsiveness of LDL cholesterol concentration.90
A curious variant form of FH has corneal opacification, and polyneuropathy, as well as stroke due to carotid disease.91 The index patient had a mosaicism of 46XX/45XO, defective monocyte function and elevations of serum lipid hydroperoxides. This is presumed to be due to additional genetic abnormalities to the causes of FH.
A genetic disorder, unrelated to lipoprotein metabolism, may affect the phenotype of FH as well. In Sardinia, subjects with proven mutations of the LDL receptor had an average lowering of LDL cholesterol by 2.49 mmol/L when the subject also inherited β-thalassaemia.92 The mechanism may relate to consumption of LDL by erythroid hyperplasia.
LDL particle size and density vary according to the properties of the secreted form of the lipoprotein and the modulation of LDL particle size by hypertriglyceridaemia, CETP and HL. The metabolic syndrome (atherogenic lipoprotein phenotype) in subjects with insulin resistance is characterised by mild hypertriglyceridaemia, low HDL-cholesterol and small LDL particles. This lipoprotein phenotype is due to environmental and likely multiple genetic factors. In diabetes, the lack of suppression of hormone-sensitive lipase in adipocytes leads to increased release of fatty acids. After re-assembly of fatty acids into TG in the liver, the increased secretion of VLDL, as well as a modest reduction in the expression of LPL in the diabetic state, leads to hypertriglyceridaemia, low HDL-cholesterol concentrations and small dense LDL, as well as increased glycation of plasma proteins. To date, there has been little information on the interaction of diabetes and FH, although it is known that remnants are increased even further in diabetics or in subjects who have impaired glucose tolerance.93 LDL particle size was described as being large in 16 of 26 FH subjects and was influenced by TG concentration.94 More studies are required to establish whether LDL in FH has the same sensitivity to modulation and whether small LDL has a significant impact on the pathogenesis of atherosclerosis.
The co-existence of FH and FDB has been described.95–97 The clinical features of the complex heterozygote for LDL receptor and apoB mutations was no different to heterozygous FH in one case, and intermediate between heterozygous and homozygous FH in the other 2 cases.95
Until there is a specific marker for familial combined hyperlipidaemia (FCH), its co-existence with FH cannot be studied properly. Since FCH is believed to be due to an overproduction of VLDL, it is possible that it may account for hypertriglyceridaemia occasionally seen in FH. More severe hypertriglyceridaemia may also be seen with concurrent dysbetalipoproteinaemia and FH.
ApoE plays an important role in the clearance of apoB-containing lipoproteins larger than LDL. The apoE2 isoform is homozygous in approximately 1% of the population. Under conditions that increase lipoprotein production and/or decrease clearance, remnants of TG-rich lipoproteins accumulate to produce a mixed hyperlipidaemia (dysbetal-ipoproteinaemia). The phenotype in FH subjects also homozygous for apoE2 could be similarly affected to normal subjects. An initial amelioration in childhood could reverse after changes in metabolism with age and disease to produce significant hypertriglyceridaemia and cutaneous xanthomata. The presence of significant concentrations of LDL in subjects with dysbetalipoproteinaemia should suggest the co-existence of FH. A study of a relatively small cohort of co-existent dysbetalipoproteinaemia and FH revealed no aggravation of the atherosclerosis complications.98 Cutaneous xanthomata, rare in heterozygous FH may be prominent in coexisting dysbetalipoproteinaemia and FH.99
FH subjects with LPL deficiency have no LDL.100 The co-inheritance of hypobetalipoproteinaemia and a heterozygous FH condition would render the LDL cholesterol low.
The initial clinical observations led to biochemical investigations that provided insight into the causes and pathophysiology of FH. The advances in biochemistry and genetics now allow better research into and understanding of observations of clinical phenotypes and therapeutic manipulation and its variability.
A thorough clinical assessment and the results from routine chemical assays deriving LDL-cholesterol concentration by the Friedewald calculation [LDL-cholesterol = total cholesterol − HDL-cholesterol − (TG/2.2) in mmol/L] or directly, can identify the heterozygous phenotype, and could even discriminate the rare sterol defects within the homozygous phenotype.
The clinical diagnosis of the heterozygous FH phenotype is adequate for risk stratification and appropriate pharmaceutical management by general practitioners and specialists. Precision in the diagnosis of FH could be of value for discriminating between polygenic or secondary dyslipidaemias and FH in family studies. Genetic counselling is similar as all three disorders are inherited in an autosomal dominant fashion, but for affected couples accurate diagnosis may be of value in counselling about disease in offspring. When both parents are heterozygous for LDL receptor defects, there is a 25% chance of producing a homozygote. However, in counselling the inheritance of dyslipidaemia in couples who have different genes for the heterozygous phenotype, it is known that co-inheritance of LDL receptor mutation and FDB results in an intermediate phenotype. The co-inheritance of LDL receptor defects and NARC1 has not yet been reported, but is likely similar to FDB and LDL receptor co-inheritance.
Although investigations with radio-iodinated LDL can demonstrate deficient clearance of normal LDL in FH subjects with LDL receptor defects, and abnormal clearance of binding defective LDL in normal subjects, these procedures are labour intensive, expensive and not used in practice. Analysis of peripheral blood mononuclear cells101 or cultured cells after up-regulation of LDL receptors with lipoprotein deficient media by means of radio-iodinated or fluorescent LDL or by fluorescently-tagged antibodies in flow cytometry may discriminate normal from heterozygous FH subjects, but remains experimental.
The genetic diagnosis by polymerase chain reaction for LDL and apoB defects is now available in many laboratories. Only a few mutations are known in apoB, but there are more than 750 LDL receptor mutations. In populations with founder effects, genetic diagnosis is easier. In other populations, where research centres can sequence the genes in affected families, molecular diagnosis can be made in family members. In the future, micro-array chips may provide simultaneous evaluation for many mutations.
Patients with a homozygous FH phenotype should be referred to specialised centres for diagnostic work-up and management. Cell culture is more reliable to identify LDL receptor defects. In fibroblast cultures, LDL receptor mutations will result in low binding, whereas adaptor protein mutations will not. It is worth considering measurement of plasma phytosterols for phytosterolaemia and cholestanol for CTX and investigating the genes influencing the concentration of these products.
The frequency of FH has been established at approximately 0.002 in the general population at large. There is a very low mutation rate in genes that result in FH and heterozygous FH seldom if ever results in death before reproduction, so that the mutated genes are retained. A variety of mutations in the LDL receptor can be demonstrated in populations that have been isolated for long periods of time and have grown to large numbers.
The founder effect refers to the occurrence of FH at a higher frequency than 0.002 and/or the predominance of one or a few mutations in a population. This phenomenon is typically found in more recently established populations that have migrated in small groups and expanded into a geographically and/or culturally isolated setting. Examples are the Afrikaners in South Africa, French Canadians, Christian Lebanese and the Finns. Such a founder effect may undergo genetic drift according to selection or may become diluted by admixture.
South Africa is well known for its high prevalence of FH in Afrikaners, due to three founder mutations.102 The prevalence of FH was estimated at 1 in 83 in a rural community.103 Although it is generally true that three founder mutations explain 95% of FH,104 the extent to which these three founder mutations account for FH in the Afrikaner varies. A lower proportion of FH is attributable to the founder mutations in the Cape, the portal of entry into South Africa.105 The V408M mutation that ranks second in frequency in the Afrikaner has been described from the Netherlands and there was evidence that it came from northern Germany.106 Ancestral linkage of these populations was indicated by the presence of a specific haplotype, which included the Dutch immigrants to Canada. A recurrent mutation of V408M has been reported in a different population group in South Africa and Cuba.107,108 The prevalence of FH is estimated to be high in the South African Jews, with the common mutation being the deletion of codon 197 that is believed to be from Lithuania and also accounts for about a third of FH in St Petersburg and appears limited to Jews in this region.109 The occurrence of the same haplotype on samples from Jews with FH in many countries also indicated an ancestral link.110 In South Africa, FH in the Jewish community is also accounted for by local mutations.111
In French Canadians, 11 mutations in the LDL receptor describe approximately 90% of subjects with FH,112 and regional variation in the prevalence of different mutations is striking.113 A recently identified founder effect has been described from Tunisia which, at 1 in 165, is less common than in French Canada.114 In most countries, a wider range of mutations has been reported in the LDL receptor. In the Danish population about 5 of the 29 documented mutations occurred in 50% of the population.115 Germany also lacks a founder effect: 37 mutations have been described in 56 individuals with FH.116 At least 29 mutations have been identified in the Chinese, with no apparent founder effect.117
Modern pharmacotherapy can achieve desirable concentrations of LDL in heterozygotes, but treatment for homozygotes remains problematic. Heterozygous FH responds like normal subjects to lipid-modifying treatment, as there is a functional LDL receptor that will clear LDL from plasma. Dietary cholesterol and saturated fat restriction will have a modest LDL-lowering effect owing to an up-regulation of LDL receptors when the liver receives less cholesterol through CM remnants. The reduction achieved in plasma LDL-cholesterol is approximately 10%, but is variable. A low-fat and low-cholesterol diet may not only up-regulate LDL receptor activity, but may also decrease the endogenous synthesis of cholesterol as suggested by decreased lathosterol concentration in a study of high- and low- fat diets together with statin treatment.118
Bile acid sequestrants that waste more bile acids for the patient result in a reduction of the cholesterol pool in cells, and there is a consequent increase in de novo cholesterol synthesis, as well as in LDL receptor synthesis. LDL-cholesterol concentration decreases by 25% at maximal doses. Cholesterol absorption is reduced by phytosterols and phytostanols. LDL concentrations decrease by about 6 to 10%.
The most powerful cholesterol-lowering agents for FH are the statins. By inhibiting de novo cholesterol synthesis at HMG-CoA reductase, compensatory upregulation of LDL receptors lowers plasma LDL concentration. FH subjects who achieved steady states of sterol and lipoprotein metabolism with higher de novo cholesterol synthetic rates have higher fasting early morning plasma mevalonic acid concentration and respond better to statins than those with lower plasma mevalonic acid concentration.119
There is no clarity about residual activity of LDL receptors and response to treatment in heterozygous FH. A greater percentage decrease of LDL-cholesterol was reported in receptor-negative subjects.120,121 One study that examined LDL responses in heterozygous FH subjects treated with pravastatin, found some correlation (r = 0.68) between maximal fibroblast LDL receptor activity and LDL reduction that ranged from 30 to 70%.122 A comparison of responses of cohorts with different mutations revealed that the LDL receptor mutation explained 41% of the response in LDL-cholesterol to fluvastatin.123 Two mutations with detectable differences in their phenotype responded similarly to statins.124 FDB responds well to statins125 as the LDL receptor up-regulation increases the clearance of both remnants and LDL. It is also likely that statins reduce the production of lipoproteins.
If up-regulation of LDL receptors were the only mechanism by which statins lowered LDL, subjects with homozygous FH due to complete absence of LDL receptor activity will not respond. A decreased production rate of LDL was described in a small cohort of homozygous FH subjects on statins whose rebounds in plasma LDL were analysed.126 Clearance constants for LDL did not change significantly. One subject had receptor-negative status. These findings indicated that lipoprotein production must be limited, but it is not clear how this happens. De novo synthesised cholesterol or a regulatory response to cholesterol depletion may play an important role in lipoprotein assembly and secretion. It appeared unlikely that delivery of lipoproteins to the liver plays a strong modulatory role in production and clearance rates for apoB-containing lipoproteins in the plasma as regular apheresis resulted in no change of these parameters.127
Ezetimibe, a recently developed drug that limits cholesterol absorption, lowers LDL cholesterol by about 15%. Interestingly, the impact is similar in heterozygous and homozygous FH.128 The mechanism of its action is presumably by limiting lipoprotein production through a poorly understood disruption of cholesterol supply to the liver by lipoprotein remnants.
The inhibition of MTP disrupts lipoprotein assembly and is highly successful at controlling hypercholesterolaemia in the Watanabe rabbit, an animal model of homozygous FH.129 However, the accumulation of fat in the liver as a result of decreased export may be detrimental.
Plasmapheresis is a well-established procedure that, together with statin and ezetimibe therapy is the treatment of choice for homozygous FH. The original procedure of plasma exchange in which albumin in sterile physiologic saline is used, has been replaced by more specific adsorption of lipoproteins onto dextran sulphate or anti-apoB immunoglobulin columns, extracorporeal precipitation with heparin, or double filtration. Liver transplantation, by correcting the function of the most important organ in cholesterol homeostasis, is probably reserved for subjects requiring heart transplant. Gene therapy will hopefully permit effective treatment of this severe disorder in the future.
FH is a serious and common disorder that results in premature atherosclerosis, but recently, with the advent of statin treatment, has become amenable to treatment. This review has assigned a broad definition to FH and has categorised the disorder as it may present to medical practitioners as a heterozygous, homozygous and intermediate phenotype. Molecular and metabolic differences in disorders producing the phenotypes have been outlined. The LDL receptor has been characterised in detail and the abundance of mutations in this receptor has given insight into the cell biology of receptor maturation, localisation, endocytosis and recycling. Genetic tests offer specific aetiologic diagnosis, but are currently not practicable in countries which do not have founder effects. FDB is amenable to genetic diagnosis by screening for a few mutations. The prevalence and metabolic implications of the more recently discovered disorders still need more study. Other monogenic disorders causing hypercholesterolaemia may still be uncovered in the future.
The complexity of lipoprotein metabolism has been described to provide insight into the multiple genes that may affect the clinical and biochemical manifestations of the disease. These genes may account for variability in the biochemical phenotype, atherosclerosis and factors that influence drug response but probably act in concert, rather than singly, to modify the high risk of atherosclerosis in FH.
The author expresses his gratitude to the staff in Lipidology in the Cape Heart Centre, especially Dr D J Blom and Mrs S Jones, for their assistance and support in making this review possible.