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Objective. To determine relative influences of intrauterine growth restriction (IUGR) and preterm birth on risks of cardiovascular, renal, or metabolic dysfunction in adolescent children. Study Design. Retrospective cohort study. 71 periadolescent children were classified into four groups: premature small for gestational age (SGA), premature appropriate for gestational age (AGA), term SGA, and term AGA. Outcome Measures. Systolic blood pressure (SBP), augmentation index (Al), glomerular filtration rate (GFR) following protein load; plasma glucose and serum insulin levels. Results. SGA had higher SBP (average 4.6mmHg) and lower GFR following protein load (average 28.5mL/min/1.73m2) than AGA. There was no effect of prematurity on SBP (P = .4) or GFR (P = .9). Both prematurity and SGA were associated with higher AI (average 9.7%) and higher serum insulin levels 2hr after glucose load (average 15.5mIU/L) than all other groups. Conclusion. IUGR is a more significant risk factor than preterm birth for later systolic hypertension and renal dysfunction. Among children born preterm, those who are also SGA are at increased risk of arterial stiffness and metabolic dysfunction.
Low birth weight (LBW) is associated with increased risk of cardiovascular disease (CVD) and the related disorders, hypertension, stroke, and type-2 diabetes, later in life [1–3]. LBW may be due to preterm birth, poor fetal growth, or a combination of both. Although their relative importance is unknown, it is thought that intrauterine growth restriction (IUGR) is more important than preterm birth per se in the development of subsequent CVD . With the increasing survival of extremely preterm infants, this may no longer be true. Early postnatal growth restriction, common in very preterm babies, may be as important in development of later organ dysfunction as IUGR at a similar gestational age (GA). Furthermore, such infants might have been exposed to glucocorticoids, either antenatally to accelerate lung maturation or postnatally to facilitate weaning from mechanical ventilation. This therapy may also result in later adverse renal or cardiovascular outcomes [5, 6].
Approximately 7% of babies are born preterm (<37 weeks gestation)  with 1% being with very LBW (<1500g) or very preterm (<29 weeks gestation) . To date, most long-term followup of very preterm infants have focused on neurodevelopmental and respiratory complications, with little attention to cardiovascular, renal, or metabolic outcomes. Suboptimal intrauterine nutrition may alter fetal programming during critical periods of growth, causing permanent changes in metabolism and cardiovascular or renal structure and function. If abnormal programming occurred postnatally in children born preterm, this would provide an opportunity for appropriate postnatal interventions.
This study was undertaken to determine the relative influence of IUGR and preterm birth on subsequent cardiovascular, renal, and metabolic dysfunction. It was designed to be clinically relevant, practical, and easily achieved in settings with limited facilities.
A retrospective cohort study was conducted at Royal North Shore Hospital (RNSH), Sydney, Australia. Children who had been born at RNSH between 1st January 1992 and 31st December 1995 with birth weight <1500g or GA ≤32 weeks were identified from the neonatal intensive care records and studied at present time (2006–2008) to assess their cardiovascular, renal, and metabolic function. Recruitment of term subjects, who were born in 1992–95 and ≥37 weeks gestation, was obtained by advertisement in local media and through word-of-mouth by study participants. Subjects were divided into the following four groups based on gender-specific, birth weight percentiles by GA, Australian national data 1991–94 : preterm and small for gestational age (Prem-SGA), preterm and appropriate for gestational age (Prem-AGA), term and SGA (Term-SGA), term and AGA (Term-AGA). Birth weights were converted to z score by the formula: (x − mean)/standard deviation.
Our sample size was calculated to detect a 10% difference in the primary outcomes with 80% power, for a two-tailed test and 5% significance level. For a 10% reduction in renal response following protein challenge in children with standard deviation of 5mL/min , 25 were required in each group. For 10% systolic blood pressure (SBP) increase in 13-14-year-old children , 22 were required. We aimed to recruit 25 children into each of the four groups.
Ethics approval was granted by the Human Research Ethics Committee, Northern Sydney Central Coast, NSW Health as Protocol 0501-028M.
The primary outcomes were as follows.
Informed consent was obtained from both mothers and children. Children performed a self-assessment of puberty stage.
Subjects fasted overnight from 9pm but were allowed plain water ad libitum. The first morning urine specimen was collected as midstream into boric acid, for urinary microscopy and measurement of protein/creatinine ratio. Upon arrival at 0850hr, weight, height, and BP were measured. Body mass index (BMI) and BSA were calculated. BP was measured by standard mercury sphygmomanometry , and the average of duplicate readings 5mins apart recorded. All clinical measurements were performed by one unblind investigator.
A second urine sample was tested for leucocytes, nitrites, protein, pH, blood, specific gravity, ketones, and glucose. Blood was collected for fasting glucose, insulin, creatinine, sodium, and potassium levels.
An oral protein load 1g/kg body weight , in the form of Aussie Bodies (Aussie Bodies Pty Ltd.)(drink: skim milk, Aussie Bodies Protein Blend [4.8%] (calcium caseinate, whey protein concentrate), fructose, skim milk powder, emulsifier (471), stabilisers (401, 407, 412), acidity regulator (331), flavours, colour (120), sweetener (955), contains milk, soy, and wheat. Bars: protein blend (31%) (isolated soy protein (tapioca starch, emulsifier (322), salt), whey protein isolate, calcium caseinate (soy lecithin)), milk chocolate compound (20%) (sugar, vegetable fat, milk solids, cocoa, cocoa mass, emulsifiers (492, 322), flavours, salt), glycerine, Aussie Bodies caramel (10%) (glucose, sweetened condensed milk, polydextrose, vegetable fat (antioxidant (307)), emulsifier (471), salt), glucose, peanuts (8%), cocoa (2%), emulsifier (322), vegetable fat, flavour) was taken over 30–45mins. Oral glucose load 1.75g/kg body weight to maximum 75g  was taken over 10mins (with Glucaid) after accounting for the glucose in Aussie Bodies. Subjects were given oral fluid loading 20mL/kg body weight with water (after accounting for the fluid from protein and glucose drinks).
Subjects reclined throughout the study period. The right radial pulse-wave characteristics were assessed by applanation tonometry (SphygmoCor, AtCor Medical, Australia) .
Urine samples were collected 1 and 2hr after protein load. Volume and time were recorded, and urinary creatinine and glucose were measured. The amount voided was replaced with water orally. Further blood sample 2hr after glucose load was collected for plasma glucose, serum insulin, and creatinine measurement.
Analyses were performed using SPSS v16 for Windows (2007 SPSS Inc., Chicago). The Kruskal-Wallis test was used to compare continuous variables across the four groups, and chi-square test for proportions. Statistical tests were two tailed and statistically significant if P < .05.
To separate the relative influences of IUGR and preterm birth on cardiovascular, renal, and metabolic functions, multiple linear regression (MLR) analyses were performed for continuous outcomes. The study factors (size at birth and preterm birth) were categorized as either SGA or AGA and preterm (≤32 weeks gestation) or term (≥37 weeks gestation), to allow easier interpretation and clinical application. They were kept in the multivariate model, regardless of statistical significance. Other variables were included in the baseline multivariate model if the univariate P < .25. Variables not known to be confounders or nonsignificant (P ≥ .05) in the multivariate model were progressively eliminated, starting with the least significant.
Effect of modification on the two study factors was examined by including an interaction term in the model. Where the interaction term was significant (P < .05), further testing was done to determine which subgroups were significantly different from each other.
Assumptions of MLR in the final model were checked for normality, linearity, and homoscedasticity by examining residuals and normal probability plots. Collinearity problems were checked by stability of baseline models, parameter estimates, and standard errors.
A total of 71 periadolescent children were studied: 14 Prem-SGA (group 1), 25 Prem-AGA (group 2), 7 Term-SGA (group 3), and 25 Term-AGA (group 4).
Table 1 summarizes the clinical characteristics and measurements, at birth and at the time of study. There were expected differences in GA, birth weight, and birth weight z-score amongst the four groups (P < .001). There were no significant differences in gender, age, weight, BMI, SBP, and DBP at time of study. The Prem-AGA group was taller than the other 3 groups at the time of study (P = .009), with an associated increased BSA.
Maternal characteristics of the children, at birth and time of study, are summarized (Table 2). The highest level of maternal educational attainment at the time of study is recorded; all mothers had at least secondary education. Of the Prem-SGA, 86% gave a history of preeclampsia during pregnancy compared with 16% Term-AGA (P < .001).
SBP and DBP measurements are summarized in Figure 1. By χ2 analysis, there were no significant differences in SBP or DBP across the 4 groups. However, in the multivariate analysis of SBP, SGA was a significant risk for increased SBP (P = .002), but preterm was not (P = .4) after adjusting for current BMI and DBP (Table 3). The model remained stable, without collinear problems, and interaction between the study factors was not significant (P = .53). SGA children had an average SBP 4.6 mmHg higher (95% CI: 1.8–7.3mmHg) than those born AGA (Table 3).
Arterial stiffness findings (AI at 75) are summarized in Figure 2. There were significant differences across the four groups (χ2 = 12.21 with 3df, P = .007). In the multivariate analysis of AI at 75, BSA remained the only significant non-study variable in the model. There was a significant interaction between preterm and size for GA (P = .01). AI at 75 was significantly higher (average: 9.7%, 95% CI: 2.3–17.1%) in the subgroup Prem-SGA compared with all other groups (Table 4).
Results for GFR (measured as true endogenous creatinine clearance) corrected for BSA, before and after protein load are summarized in Figure 3. There were no differences across the groups in GFR prior to protein load (χ2 = 7.17 with 3df, P = .07), but results after protein loading showed a reduction in functional renal reserve in SGA children (χ2 = 8.27 with 3df, P = .04).
In the multivariate analysis of GFR after protein load, the only non-study factor variable remaining was GFR pre-protein (Table 5). Interaction between the study factors was not significant (P = .8). The GFR following protein load was significantly lower in SGA children (P = .01), while there was no difference in preterm children (P = .9). For a SGA child, the average GFR following protein load was 28.5mL/min/1.73m2 lower than that of an AGA child (95% CI: −50.1 to −6.8mL/min/1.73m2) (Table 5).
There was no significant difference across the four groups for HOMA-IR (χ2 = 2.58 with 3df, P = .5), glucose level either at fasting (χ2 = 2.81 with 3df, P = .4) or after glucose load (χ2 = 5.72 with 3df, P = .13), and insulin level either at fasting (χ2 = 2.36 with 3df, P = .5) or after glucose load (χ2 = 1.77 with 3df, P = .6).
In the multivariate analysis, neither being preterm (P = .4) nor SGA (P = .6) was significant for HOMA-IR. For 2-hr glucose level following glucose load, preterm birth was significant (P = .03) while being SGA was not (P = .9). In preterm children, the mean 2-hr glucose level (3.9mmol/L) following glucose load was 0.25mmol/L lower (95% CI: −0.48 to −0.02mmol/L) than that of term children, a statistically but not clinically significant difference. However, being both preterm and SGA was significantly associated with increased 2-hr insulin level following glucose load; the average level (35.6mIU/L) was 15.5mIU/L higher (95% CI: 5.6–25.5mIU/L, P = .003) compared with all other groups (Table 6).
In this cohort of periadolescent children, we have shown subtle but definite and different long-term effects of both IUGR and preterm. These effects were evident in cardiovascular, renal, and metabolic function.
Our result on the risk of increased SBP in children born with IUGR is consistent with some [3, 17, 18] but not all [19–21] previous studies. In some of the latter publications, it is not possible to separate the effects of preterm and IUGR, because of noncomparability of their study groups [19, 20]. Johansson et al.  reported an increased risk of high SBP in SGA born preterm amongst young adult men. These results are compatible with ours. BP is “tracked” across age , and any effect of low birth weight on BP will be magnified in an older cohort study . In addition, young adult men are generally at greater risk of cardiovascular disease than young women . Changes could be more subtle in our subjects because they are younger. Huxley et al.  suggested that the inverse relationship between birth weight and SBP may be spurious, because of adjustment for current weight by investigators. However, a more recent meta-analysis by Gamborg et al.  concluded that the relationship was present regardless of current BMI—this is consistent with our results. Although the average difference in SBP between SGA and AGA groups (3.7mmHg) was reduced without adjustment for current BMI (4.6mmHg), it was still significant (P = .02).
The subjects were 12–15 years old when this study was conducted. Adolescents experience complex physiological changes which may confound/mask an association between birth weight and SBP . Despite this, we found an inverse association between birth weight and SBP, consistent with other studies [27, 28].
Our finding of increased arterial stiffness in children born both preterm and SGA is consistent with the findings of Cheung et al.  and Singhal et al. . Several studies have failed to distinguish between low birth weight related to preterm and that due specifically to IUGR [31–33]. This makes comparisons to our findings impossible. A recent systematic review  concluded that poor fetal growth and preterm birth produce different patterns of altered vascular system development, with different implications for cardiovascular health in adult life.
The mechanism whereby discordance between birth weight and GA leads to an increase in arterial stiffness in preterm children remains unclear. The reported impairment of endothelial function in preterm and SGA individuals  suggests functional alteration of arterial tone contributing to the increase in systemic arterial stiffness. While the underlying cause is yet to be revealed, whether epigenetic modification , accelerated telomere ablation , or other mechanisms, it appears that altered vascular physiology associated with LBW is largely irreversible. Children born SGA and/or very preterm should therefore be followed up for future cardiovascular risk.
As we did not expect major overt renal functional impairment, GFR under protein-loaded conditions was measured to detect subtle changes in RFR. It is clear from our results that IUGR was associated with reduced RFR (P = .01) while preterm per se was not (P = .9). This may lead to earlier appearance of the reduced GFR encountered in disorders such as hypertension, type-2 diabetes, and the metabolic syndrome. These findings are consistent with previous studies describing associations of LBW with severity of expression and progression of kidney disease from various causes [37–39] and indicate real value for early screening in these individuals.
Long-term data on renal function in subjects born very preterm are few. Two studies compared renal function in preterm subjects or those with IUGR with full-term subjects [40, 41]. In the first, reduced creatinine clearances were found in 40 school-age children born preterm compared with 43 controls of similar age (but no differences were detected when Preterm-SGA and AGA groups were compared with each other) . In the second, examining young adult women, the Term-SGA and preterm groups showed a nonsignificant reduction in GFR, but no Preterm-SGA subjects were included . Neither study measured the effect of protein loading on renal function and therefore did not assess RFR.
A recent study  investigating 23 Preterm-SGA, 29 Preterm-AGA (<32 weeks), and 30 Term-AGA controls, at a mean age of 20.7 years showed that Preterm-SGA subjects had a lower baseline GFR (using inulin clearance) than either Preterm-AGA or control. Unfortunately, there was no Term-SGA group included, making it difficult to separate the effects of IUGR and preterm. Stimulation by high-protein meals increased GFR in all three groups. Surprisingly (given that baseline GFR was lower in the Preterm-SGA group), following adjustment for current BSA, stimulated GFR was not significantly different among the groups.
Brenner and colleagues [43, 44] hypothesized that IUGR may cause a low nephron number, thus predisposing to later hypertension and renal disease. Subsequent studies showed that LBW and IUGR were associated with mild to moderate elevations of BP , reduced numbers of compensatory hypertrophied glomeruli [46–48], lower GFR, and higher urine albumin-to-creatinine ratio [37, 49]. Preterm infants have fewer glomeruli than infants born at term . Therefore, both IUGR and preterm may lead to reduced number of nephrons.
Although preterm birth was not found to be an independent risk factor for renal dysfunction in our study, larger studies should be undertaken and adults with preterm births followed-up as renal function decreases with age.
Using HOMA-IR  as an outcome measure of insulin resistance, neither being born preterm (P = .4) nor SGA (P = .6) was significant risk factor. Similarly, fasting glucose and fasting insulin levels were not significantly different across the four groups.
With glucose levels 2hr after glucose load as outcome measure, being preterm was significant (P = .03) while being SGA was not (P = .9). In preterm children, the mean 2-hr glucose level was 0.25mmol/L lower (95% CI −0.48 to −.02mmol/L) than that in term children. Although statistically significant, such a difference is not clinically significant. This is in contrast to Hovi et al.  who reported significantly higher 2hr glucose concentrations in preterm LBW young adults compared with term controls. The difference in findings could be due to an older age group studied (range: 18–27 years), in contrast to our study mean age of 13.8 years (range: 11.3–15.6 years). Similar to our study, the differences between SGA and AGA in the preterm groups were not significant.
In children born both preterm and SGA, the average 2-hr insulin level following glucose load was 15.5mIU/L higher (95% CI: 5.6–25.5mIU/L) than in all other groups. This suggests that poor fetal growth and preterm birth are both significant risk factors for diabetes in later life. The results support the previously reported inverse association between birth weight and later development of diabetes [2, 54–58] and provide evidence for an interaction between preterm and poor fetal growth. Hofman et al.  found that children born preterm, whether AGA or SGA, had reduced insulin sensitivity similar to that seen in term-SGA. Hovi et al.  also reported that young adults born preterm with very LBW (<1500g) had higher 2hr glucose concentration and more insulin resistance than those born at term. A recent study has suggested that the association between LBW and risk for diabetes is mediated through poor fetal growth and preterm birth . Another study has shown an inverse relationship between birth weight and fasting plasma glucose, following glucose load and hemoglobin A1C , but information regarding GA and preterm birth was not given. A recent systematic review concluded that birth weight was inversely related to a risk of type-2 diabetes .
The findings presented here support the hypothesis that children born with IUGR are at risk of later systolic hypertension, cardiovascular, renal, and metabolic dysfunction. Among children born preterm, only those with IUGR appear to be at increased risk of arterial stiffness and metabolic dysfunction. It has been recognised for over 30 years that maternal undernutrition during pregnancy results in infants of LBW and that these infants exhibit in late adult life an increased risk of cardiovascular morbidity, renal disease and type II diabetes mellitus , all associated with an increased rate of preterm death. More recent publications have shown that the increase in these disorders is already present in young adults and is found to be not only consequent on maternal under-nutrition but also more specifically on fetal growth restriction from a variety of causes [64, 65]. In the current study, evidence is presented that subtle but significant differences in cardiovascular function, renal function, and glucose metabolism are detectable in LBW infants even before adult life. In addition, it appears that preterm birth and IUGR expose infants to separate and probably additive risks of these adverse outcomes.
The limitations of this study must be acknowledged. The main problem encountered was recruiting children for a study involving venepuncture. Recruitment of children is more difficult and challenging compared with adults [66, 67]. The period of recruitment was limited, to reduce the potential confounding impact of developments in neonatal care. Some of the nonsignificant results may be due to the sample size being too small to detect differences. Pre-eclampsia is frequently associated with IUGR. It is also a significant risk factor for renal dysfunction and associated with metabolic syndrome—larger numbers may expose a relationship. Nevertheless, several significant results despite the sample size suggest that the differences are relatively large.
As puberty affects cardiovascular, renal, and metabolic functions, another limitation of the study is that pubertal stage was not formally assessed. As there were no significant age differences across the groups, and age was further tested as a potential confounder in regression analyses, one would expect the effects of puberty to be equal across all groups despite the variable onset of puberty. Ideally, children would be followed after puberty, as young adults.
The findings of this study indicate pressing reasons for supervision of the health and nutrition of all LBW infants—at least into adult life—regardless of the cause of their LBW. Since the advent of specialised neonatal intensive care, the survival of extremely preterm and/or growth-restricted babies has increased significantly. Efforts to identify individuals at increased disease risk well before any clinical manifestation provide a window of time that may allow delay or prevention of overt disease. Clearly, screening of this population for abnormalities will be most achievable if the measurements are clinically and technically simple, relatively noninvasive, and inexpensive. All of the measurements made in this study meet these criteria. They can be performed in a community setting and require only basic diagnostic laboratory facilities.
That such significant findings were evident in a relatively small cohort study provides strong support for a larger community-based examination of blood pressure, arterial stiffness, renal functional reserve, and glucose tolerance. The relevant preventive measures and interventions which can be achieved postnatally will need to be assessed and evaluated in further well-designed studies.