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Neuronal intranuclear inclusion disease (NIID) is a slowly progressive neurodegenerative disease characterized by eosinophilic hyaline intranuclear inclusions in the central and peripheral nervous system, and also in the visceral organs. NIID has been considered to be a heterogeneous disease because of the highly variable clinical manifestations, and ante-mortem diagnosis has been difficult. However, since we reported the usefulness of skin biopsy for the diagnosis of NIID, the number of NIID diagnoses has increased, in particular adult-onset NIID. In this study, we studied 57 cases of adult-onset NIID and described their clinical and pathological features. We analysed both NIID cases diagnosed by post-mortem dissection and by ante-mortem skin biopsy based on the presence of characteristic eosinophilic, hyaline and ubiquitin-positive intanuclear inclusion: 38 sporadic cases and 19 familial cases, from six families. In the sporadic NIID cases with onset age from 51 to 76, dementia was the most prominent initial symptom (94.7%) as designated ‘dementia dominant group’, followed by miosis, ataxia and unconsciousness. Muscle weakness and sensory disturbance were also observed. It was observed that, in familial NIID cases with onset age less than 40 years, muscle weakness was seen most frequently (100%), as designated ‘limb weakness group’, followed by sensory disturbance, miosis, bladder dysfunction, and dementia. In familial cases with more than 40 years of onset age, dementia was most prominent (100%). Elevated cerebrospinal fluid protein and abnormal nerve conduction were frequently observed in both sporadic and familial NIID cases. Head magnetic resonance imaging showed high intensity signal in corticomedullary junction in diffusion-weighted image in both sporadic and familial NIID cases, a strong clue to the diagnosis. All of the dementia dominant cases presented with this type of leukoencephalopathy on head magnetic resonance imaging. Both sporadic and familial NIID cases presented with a decline in Mini-Mental State Examination and Frontal Assessment Battery scores. Based on these clinicopathological features, we proposed a diagnosis flow chart of adult-onset NIID. Our study suggested that the prevalence rate of adult-onset NIID may be higher than previously thought, and that NIID may be underdiagnosed. We should take NIID into account for differential diagnosis of leukoencephalopathy and neuropathy.
Neuronal intranuclear inclusion disease (NIID), also known as neuronal intranuclear hyaline inclusion disease (NIHID) or intranuclear inclusion body disease (INIBD), is a slowly progressive neurodegenerative disease characterized by eosinophilic hyaline intranuclear inclusions in the central, peripheral and autonomic nervous system cells, and also in visceral organs cells.
The first case of NIID was reported in 1968 (Lindenberg et al., 1968). Since then, many NIID cases have been reported after post-mortem examination (Schuffler et al., 1978; Michaud and Gilbert, 1981; Patel et al., 1985; Munoz-Garcia and Ludwin, 1986; Oyer et al., 1991; Weidenheim and Dickson, 1995; Takahashi-Fujigasaki, 2003; Liu et al., 2008). The onset of disease varies from infancy to the sixties, but two-thirds of them were infantile or juvenile cases (Funata et al., 1990; Zannolli et al., 2002; Takahashi-Fujigasaki, 2003). Information on the clinical manifestations of adult-onset NIID is lacking, and there is no established clinical picture of it yet. A wide range of clinical manifestations has been reported: pyramidal and extrapyramidal symptoms, cerebellar ataxia, dementia, convulsions, neuropathy, and autonomic dysfunction. This wide range of clinical phenotypes makes ante-mortem diagnosis of NIID difficult, especially in adult-onset NIID cases. Until 2011, the number of reported NIID cases was limited to about 40 cases. One of the reasons for this is surely the small chance of diagnosis of NIID, due to it being limited to post-mortem dissection.
Some reports have described an ante-mortem diagnosis of NIID by rectal biopsy or gastrointestinal specimen removed by operation (Schuffler et al., 1978; Goutieres et al., 1990; Barnett et al., 1992; Zannolli et al., 2002; Kulikova-Schupak et al., 2004) and sural nerve biopsy (Sone et al., 2005). Both rectal and sural nerve biopsy cause significant physical stress, limiting their use. Rectal biopsy requires submucosal dissection to pick up myenteric plexus neurons, which carries a risk of perforation (Mizushima et al., 2015). Moreover, one autopsy-diagnosed NIID case reported that rectal biopsy failed to identify intranuclear inclusion ante-mortem (Wiltshire et al., 2010). Endoscopic submucosal dissection, therefore, cannot be used as a screening test for NIID, as for other neurodegenerative disease.
Recently, we reported the usefulness of skin biopsy and detection of intranuclear inclusions exactly identical, both morphologically and immunohistochemically, to those found in the central nervous tissues for the ante-mortem diagnosis of both sporadic NIID cases (Sone et al., 2014) and familial NIID cases (Sone et al., 2011). After these reports, the number of NIID cases that have been diagnosed with skin biopsy has increased (Kitagawa et al., 2014; Sasaki et al., 2015; Toyota et al., 2015). In addition, a characteristic high intensity signal in the corticomedullary junction in diffusion-weighted imaging (DWI) of head MRI has become another clue to NIID diagnosis (Sone et al., 2014), as this MRI image has been seen restricted to the cases with positive skin biopsy with intranuclear inclusions or those with post-mortem histopathological confirmation (Sone et al., 2014). In particular, diagnosis of adult-onset NIID cases with leukoencephalopathy and dementia are increasing, suggesting that the prevalence rate of the adult onset form is higher than we believed.
In this study, we analysed clinicopathological features of 57 cases of adult-onset NIID, both sporadic and familial. Most of these cases were diagnosed with skin biopsy triggered by DWI high intensity signal in corticomedullary junction on head MRI. We characterized clinical manifestations, MRI findings and pathological features of these adult-onset NIID cases, and proposed a diagnosis flow chart of adult-onset NIID.
We included the cases as NIID based on the diagnosis by post-mortem dissection, and by ante-mortem skin biopsy with the detection of characteristic intranuclear inclusions identical to those in the CNS tissues. One NIID case was first diagnosed by skin biopsy and confirmed by post-mortem dissection. We performed skin biopsy on the NIID suspected cases with DWI high intensity signal in corticomedullary junction on head MRI, and familial suspected cases with the same clinical features with histopathologically diagnosed NIID case in the same family. The DWI high intensity in the corticomedullary junction in MRI is highly restricted to the cases with intranuclear inclusions in the skin biopsy or post-mortem brain pathology. Thus, this particular DWI high intensity is the possible diagnostic marker of NIID. Intranuclear inclusions in the skin biopsy samples were confirmed on 37 sporadic NIID cases and 15 familial NIID cases from six families studied in this study, including cases we reported previously (Sone et al., 2005; Kitagawa et al., 2014; Sone et al., 2014). We also examined 52 neurologically normal control cases: 16 cases for the histopathological study (between 54 and 84 years of age, average 70.4), and 36 cases for head MRI study (between 49 to 91 years of age, average 66.6).
In this study, we defined familial NIID cases as: at least one NIID patient was diagnosed histopathologically in one family, and the other patient presented with DWI high intensity signal in corticomedullary junction in MRI findings, or medical examination of neurologist confirmed the same phenotype with histopathologically diagnosed NIID patient in the same family. We defined cases that did not meet the above familial NIID definition as sporadic NIID cases, even if the patient had a family history of dementia or neuropathy when these family members were not diagnosed by histopathological evaluation or MRI evaluation.
The detailed clinical data on the patients were obtained from each patient and patient’s families or from clinical records. Neurological examinations were performed repetitively by neurologists. Muscle strength, sensory impairment and autonomic symptoms were assessed. Presence of dementia was assessed by the interviewing of the patient or patient’s family about the presence of forgetfulness or difficulty and mistakes in daily routine tasks. Patients were also screened for executive and cognitive functions using the Mini-Mental State Examination (MMSE) and/or Frontal Assessment Battery (FAB). We used a score of 24 as the MMSE as in previous reports (Folstein et al., 1975; Diniz et al., 2007), and the published age-matched average as the cut-off score for the FAB (Dubois et al., 2000; Appollonio et al., 2005) for impaired cognitive function. Appearance of abnormal behaviour including irritability, cryptic speech, gambling addiction, behavioural apraxia, uninvited behaviour and others were assessed by examining the patient or interviewing patient’s family. Episodes of generalized convulsion, unconsciousness and the appearance of an encephalitic episode such as subacute onset of unconsciousness with fever, headache and vomiting were also assessed by examining the patient or interviewing family. Patients received head MRI, single photon emission computer tomography (SPECT), routine blood chemistry, urinalysis, CSF examination, and nerve conduction studies.
This study was performed with ethical approval of the Ethics Review Committee of Nagoya University School of Medicine. Written informed consent was obtained from all patients.
Motor and sensory conduction was measured in the median, tibial and sural nerves, using a standard method with surface electrodes for stimulation and recording (Kimura, 2001a, b). Control values of nerve conduction velocity and amplitude were obtained from our previous report (Koike et al., 2003). We defined the slowing conduction velocity when conduction velocity of each case showed below the value of control mean –2 standard deviations (SD). In the same way, we defined compound muscle action potential or sensory nerve action potential reduction as when either compound muscle or sensory nerve action potentials showed below the value of control mean −2 SD.
At autopsy, brain, spinal cord and other organs were fixed in 10% formalin solution. Samples of the main representative regions of each organ were embedded in paraffin and sectioned in 6 -μm thickness, and stained with haematoxylin and eosin and Klüver-Barrera. Skin biopsy, and following immunostaining and immunofluorescence staining were performed as described previously (Sone et al., 2011) with anti-ubiquitin antibody (Z0458, Dako) and anti-p62 antibody (sc-28359, Santa Cruz Biotechnology). For assessment of intranuclear inclusion frequency, we prepared a coronal section of cerebral hemisphere, including basal ganglia, stained with anti-p62 antibody using the LSAB Kit (Dako). We selected five random microscopic fields under a ×20 objective lens in each gyrus or basal ganglion, counted the number of neurons, astrocytes and p62-positive intranuclear inclusions and assessed the frequency of intranuclear positive neurons and astrocytes. Samples for electron microscopic study were prepared as described previously (Koike et al., 2007).
As the case with FMR1 premutation shows the symptoms and intranuclear inclusions as NIID, we performed FMR1 gene analysis. Genomic DNA was isolated from peripheral blood leucocytes using standard methods. Southern blotting was performed as described previously (Maddalena et al., 2001). We defined normal alleles as range of 5 to 44 CGG repeats, and premutation alleles as 55 to 230 CGG repeats.
We analysed 38 sporadic NIID cases, 19 familial NIID cases from six families and 16 neurologically normal controls (Fig. 1, Tables 1 and and2,2, and Supplementary Tables 1–3). Of the sporadic NIID cases, Subject S-5 was diagnosed by autopsy, Subject S-31 was diagnosed by both autopsy and skin biopsy, and the others were diagnosed by skin biopsy. Of the familial NIID cases, Family 1 and Family 2 cases were diagnosed by post-mortem dissection and skin biopsy, the other familial cases were diagnosed by skin biopsy.
Histopathological findings of autopsied NIID cases showed that eosinophilic intranuclear inclusions were widely observed in the CNS: in the cerebral cortex, basal ganglia, brainstem and spinal cord, and both in neurons and astrocytic glial cells (Table 1 and Fig. 2). Intranuclear inclusions were also observed in the peripheral nervous system cells and somatic cells of a wide variety of organs except skeletal muscle and hepatocytes (Fig. 2E, F, M, N and Table 1). These inclusions were round-shaped with a diameter of 1.5–10 μm, located in the vicinity of the nucleolus (Fig. 2A–F and I–N). The inclusions were ubiquitin-positive (Fig. 2B, C, E, F, J, M and N), p62-positive (Fig. 2K) and were composed of dense filamentous materials without membrane structure under electron microscopy (Fig. 2D and L).
Skin biopsy samples of NIID cases showed eosinophilic ubiquitin-positive and p62-positive intranuclear inclusions in adipocytes, fibroblasts and sweat gland cells (Fig. 2G and O), round-shaped with diameter of 1.5–3 μm. Electron microscopy imaging showed dense filament material without membrane (Fig. 2H and P). Light and electron microscopic features of these inclusions in the skin were almost identical to those of intranuclear inclusions in the CNS. Furthermore, the light and electron microscopic features of intranuclear inclusions on autopsy and in the skin biopsy samples mentioned above were almost identical between sporadic and familial NIID (Table 1 and Fig. 2). These identical histopathological features among the inclusion in the skin and central nervous tissues form the background of the diagnosis of NIID with skin biopsy findings.
We also investigated the frequency distribution of intranuclear inclusion-positive neurons and astrocytes in the cerebral cortex, hippocampus and basal ganglia of Subject S-5: sporadic NIID case, and Subject F1-2: familial NIID case (Fig. 3). The frequency of intranuclear inclusion in neurons was ~5–30% in the cerebral cortex and basal ganglia, with a slightly lower frequency in the hippocampus. Frequencies of astrocytes in both cases were similarly between 10% and 30%. Thus, the frequency distribution of intranuclear inclusion of neurons and astrocytes was similar among sporadic and familial NIID cases.
We also studied 16 neurologically normal control samples of the frontal lobe, cerebellum, gastro intestinal tract and kidney, and did not find any intranuclear inclusions in these normal samples.
Details of clinical manifestations of NIID cases are summarized in Table 2 and Supplementary Tables 1 and 2. The onset age of sporadic NIID cases was between 51 and 76. Disease duration ranged from 1 to 19 years. Most sporadic NIID cases presented with dementia as the initial and main clinical manifestation. Dementia was observed in almost all the cases (94.7%). Autonomic impairment of miosis and bladder dysfunction manifesting as urinary incontinence was frequently seen (Table 2 and Supplementary Table 1). Muscle weakness (27%) and sensory disturbance (28.6%) were also observed but not as frequently as in familial cases. Muscle weakness presented with mild extent in the extremities. Sensory disturbance presented with light deterioration of vibratory sense, and sometimes distal dominant numbness in the lower extremities. Tremor, rigidity and ataxia were also observed.
In 26.3% of sporadic NIID cases, patients presented with abnormal behaviour (Table 2 and Supplementary Table 2) such as irritability, cryptic speech, apraxia (e.g. trying to wear shirts as trousers), gambling addiction, disinhibition (such as smoking in non-smoking areas), and some other abnormal behaviours: putting clothes in the refrigerator and complaining ‘I cannot understand everything’, as examples.
Generalized convulsions were observed in 13.2% of sporadic cases. Disturbance of consciousness was often observed (39.5%). The duration of the disturbance varied from a few hours to several days.
In 21% of sporadic NIID cases, patients presented with characteristic symptoms of subacute onset encephalitic episodes: fever, headache, vomiting and disturbance of consciousness. These NIID cases with encephalitic episodes were admitted to the hospital via emergency visit and had a normal titre of antibody against viruses. No pleocytosis of CSF ruled out bacterial or viral meningitis and encephalitis (Table 2 and Supplementary Table 3). Some of the cases with an encephalitic episode presented with focal brain oedema with gadolinium enhancement (Fig. 4). High dose steroid administration (1000 mg prednisolone per day intravenously for 3 days) often improved encephalitic symptoms and diminished the brain oedema and gadolinium enhancement, while executive function deteriorated slowly and a state of akinetic mutism often developed in some cases.
Laboratory data are shown in Table 2 and Supplementary Table 3. Three cases (9.1%) of sporadic NIID cases showed elevated serum creatine kinase levels. Elevation of CSF protein level was frequently observed (65.5%). Approximately 20% of cases showed elevated glycated haemoglobin (HgbA1c). Almost all sporadic cases, except Subject S-16, presented abnormal findings of motor or sensory nerve conduction to a variable extent. Motor nerve conduction velocity slowing was most frequently observed in the median and tibial nerves. The distribution of peripheral nerve damage was polyneuropathy type, being distally predominant in four extremities.
Head MRI findings, showed obvious leukoencephalopathy in T2 and fluid attenuated inversion recovery (FLAIR) image (Fig. 4A–H). A high intensity area was widely observed from the corticomedullary junction to around the root of gyrus. These white matter abnormalities were confluent and bilaterally symmetrical in T2 image, but in FLAIR image, the edge of the high intensity area appeared rather dimly and generally prominent in the frontal lobe. It was also observed in the external capsule. The area that showed quite high intensity in the T2 image presented a low intensity signal in the T1 image (Fig. 4A).
On DWI, high intensity signal along the corticomedullary junction was observed in all sporadic NIID cases (Fig. 4D and G), and spread along the corticomedullary junction with advancement of the disease. At the early stage, the DWI high intensity signal was slightly observed in a small regional portion of the corticomedullary junction in the frontal lobe. As the disease worsened, the DWI high intensity signal extended only along the corticomedullary junction of the cerebrum but did not expand into deep white matter even in the extremely advanced stage of akinetic mutism showing widely expanded leukoencephalopathy in MRI T2 image (Fig. 4A–D). Such a DWI high intensity signal mentioned above was not observed in the 36 neurologically normal cases.
It is noteworthy that Subject S-25 showed focal brain oedema on head MRI simultaneously with the emergence of encephalitic symptoms (Fig. 4E–H). These brain oedemas were focal and not symmetrical in T2 and FLAIR. The oedematous portion of the brain was not high intensity on DWI (Fig. 4G), and was enhanced by gadolinium (Fig. 4H).
We analysed the CGG repeat length of the FMR1 gene of cases, with written consent, to exclude fragile X-associated tremor/ataxia syndrome (FXTAS). All cases with analysed FMR1 showed a normal range of CGG repeats (<44 repeats) (Table 2 and Supplementary Table 3).
Results of MMSE and FAB are summarized in Table 2 and Supplementary Table 2. Almost half of the cases showed decreased MMSE below cut-off score 24 (Folstein et al., 1975; Diniz et al., 2007), and >90% of cases were impaired in FAB scores of published age-matched average (Dubois et al., 2000; Appollonio et al., 2005). The decline of FAB scores was more prominent than those of MMSE scores. Subject S-9 showed marked definitive decline of both FAB and MMSE scores with extensive decline of regional cerebral blood flow in SPECT.
Subject S-7 consulted a neurologist due to forgetfulness reported by family members. She was aged 69 and had no family history or past history of neurological or psychological disease. Neurological examination revealed miosis, with a pupil size of 2 mm/2 mm and prompt light reflex. She did not present weakness on the manual muscles testing nor sensory disturbance, tremor, rigidity, ataxia or urinary incontinence. Tendon reflex showed diffuse hyporeflexia. Executive function was declined (MMSE 19/30 and FAB 6/18). Head MRI T2 image showed symmetrical, confluent and frontal dominant leukoencephalopathy. DWI showed high intensity signal along the corticomedullary junction. Skin biopsy revealed abundant intranuclear inclusions.
Subject S-9 presented with a subacute progressive encephalitic episode with fever (38°C), headache, disorientation, dyscalculia and disturbance of consciousness at age 55. He had no family history or past history of neurological or psychological disease. Head MRI showed symmetrical, confluent leukoencephalopathy and DWI showed high intensity signal along the corticomedullary junction. Repeated CSF tests showed no pleocytosis with only mild protein elevation, therefore intracranial infection was excluded. Fever and disturbance of consciousness lasted for 3 weeks and deteriorated, with no evident infectious focus in the whole body and no response to antibiotics therapy. Steroid pulse therapy (intravenous injection of methylprednisolone 1000 mg/day for 3 days) resulted in improved consciousness. MMSE score was 20 at the time of testing, but deteriorated slowly thereafter. Intranuclear inclusions were demonstrated by skin biopsy.
The onset age of Families 1–3 was between 16 and 39, and disease duration was from 3 to 44 years (Fig. 1, Table 2 and Supplementary Table 1). Main and initial clinical manifestations were limb weakness (100%), sensory disturbance and autonomic symptoms like urinary incontinence. Deterioration was slow. Over 20 years after onset, clinical symptoms became serious (Sone et al., 2005). Subject F3-1, onset age of 39, presented with dementia and leukoencephalopathy at the age of 58, but other cases did not report dementia. Diffuse limb muscle weakness was seen in all cases (Table 2), and distally dominant sensory disturbance (81.8%), autonomic symptoms of vomiting, bladder dysfunction and miosis were frequently observed. While dementia was rarely seen, ataxia, abnormal behaviour, convulsion and encephalitic episode were not seen (Table 2 and Supplementary Table 1). In laboratory data, serum creatine kinase was elevated in 87.5% of examined cases. Motor and sensory nerve conduction abnormality was present in most cases (Table 2 and Supplementary Table 2).
The onset age was between 43 and 68, and disease duration was from 1 to 15 years. The main and initial clinical manifestation was dementia (100%). Cases of these three families did not complain of weakness as the chief and initial symptom but it became evident on medical examination by the neurologist. Autonomic impairment of vomiting, bladder dysfunction and miosis were observed in similar extent to those of Families 1–3 (Table 2 and Supplementary Table 1). Tremor, rigidity, ataxia, abnormal behaviour, disturbance of consciousness and encephalitic episode (Subject F5-1) were similar to the sporadic cases (Table 2 and Supplementary Table 1). In laboratory data, serum creatine kinase elevation was only seen in one of six cases (16.6%). Motor and sensory conduction impairment was mild but present in half of the patients.
Among familial NIID cases of Families 1 and 2, head MRI showed in one case of Family 1 (Subject F1-1), with disease duration of 37 years, a mild leukoencephalopathy around the frontal and occipital horn of the lateral ventricle, and ventricular distention (Supplementary Table 2). DWI was not evaluated in Subject F1-1. Other NIID cases of Families 1 and 2 with duration of less than 30 years did not show leukoencephalopathy or ventricular distention. On SPECT finding, familial NIID Subject F2-2 showed mild decreases in regional cerebral blood flow (Fig. 4R).
Head MRI of familial NIID cases in the Families 3–6, showed obvious leukoencephalopathy in T2 and FLAIR image in all examined cases (Fig. 4I–P and Supplementary Table 2). DWI high intensity signal along the corticomedullary junction was also observed (Fig. 4L and P) in all the cases. The high intensity area of FLAIR image extended as the disease progressed (Fig. 4I–K). Subject F5-1 showed focal brain oedema on head MRI simultaneously with the emergence of encephalitic symptoms, like some sporadic NIID cases.
Familial NIID cases presented with a slight decline of MMSE scores but were above the cut-off score of 24. While FAB scores were almost equal, or slightly below the scores of published age-matched averages (Dubois et al., 2000; Appollonio et al., 2005; Diniz et al., 2007) (Supplementary Table 2), predominantly in cases with age of onset over 40 years of age.
Difficulty in jumping was the first symptom noticed by this case, at age 39. She deteriorated slowly. Her younger sister presented with distal dominant muscle weakness and hyporeflexia. At age 49, she presented with mild muscle weakness, hypotonia and hyporeflexia diffusely distributed in all four extremities. Nerve conduction studies showed slowing of motor nerve conduction velocity. At age 53, she complained of dysarthria, and head MRI showed a slight high intensity area around the anterior horn of the lateral ventricle resembling chronic ischaemic change (Fig. 4I), and at age 58, the high intensity area of head MRI extended a little (Fig. 4J). At age 60, 21 years after disease onset, walking became difficult and the patient required a wheelchair. At age 64, head MRI showed evident leukoencephalopathy (Fig. 4K) and DWI high intensity signal in the corticomedullary junction (Fig. 4L). Forgetfulness and defect of working memory while cooking became evident and MMSE was assessed. Decline in the score (25/30) was observed (Supplementary Table 2). Skin biopsy showed intranuclear inclusions.
Subject F5-2 presented with complaints of forgetfulness, dysarthria, gait disturbance and urinary incontinence at age 54. She sometimes reported dysaesthesia in the face and upper extremities. Screening head MRI showed leukoencephalopathy and NCV showed sensory-motor polyneuropathy. Her younger brother presented with irritability and leukoencephalopathy, and was diagnosed with NIID by skin biopsy. At age 59, neurological examination revealed mild dysarthria, hyporeflexia, and a mild disturbance in pain and temperature sensation in the lower extremities. She could not perform tandem walking nor stand on one leg. FAB score showed definitive decline (14/18), but MMSE score was almost normal (28/30) (Supplementary Table 2). Head MRI showed ventricular distention, leukoencephalopathy in the T2 image and high intensity signal along the corticomedullary junction in DWI (Fig. 4M–P).
As a consequence of this study, adult-onset NIID cases can be subgrouped into dementia-dominant and limb weakness-dominant phenotypes (Fig. 5).
The dementia-dominant NIID group had an onset age over 40, and in most cases, dementia was the first symptom and was the reason for consulting a neurologist. Some cases also presented with mild autonomic dysfunction, such as bladder dysfunction and miosis, ataxia, tremor and rigidity (Table 2 and Supplementary Table 1). Most of them did not complain of weakness and sensory disturbance, but subclinical neuropathy was detected by neurological examinations and nerve conduction study, we thus suppose that subclinical neuropathy related to NIID is present.
The limb weakness-dominant group was relatively young at age of onset, 16 to 39 years, and weakness of the lower limbs was the first symptom. This group consists of familial cases with the onset age less than 40 years. As the patients became older, limb weakness worsened slowly and sensory disturbances and autonomic dysfunction developed. Dementia and leukoencephalopathy was relatively mild and did not present before 20 years of disease duration. In some cases of this group, dementia did not present throughout disease duration. However, MMSE and FAB revealed mild decline of these scores, and sponsiosis of white matter was observed in autopsied cerebrum specimens (Fig. 3D). Ataxia, tremor or rigidity was not observed.
Familial NIID Subject F3-1 is of interest, because this patient presented with both clinical manifestations of the weakness-dominant and dementia-dominant phenotypes. This patient presented with limb weakness at age 39, and 20 years after disease onset, at age 58, presented with dementia and obvious leukoencephalopathy (Fig. 4I–L). This case is an example that NIID can present with both limb weakness with polyneuropathy and dementia in one patient with a variable extent of these dominancy.
The diagnosis of NIID was made histopathologically by autopsy in five cases and by skin biopsy in the other cases. Histopathological features of intranuclear inclusions of skin biopsy and post-mortem CNS tissue were very similar. The distribution of ubiquitin-positive intranuclear inclusions in all five autopsied cases was almost identical, observed in both neurons and astrocytes, and widely in CNS, peripheral nervous systems and somatic cells, including the skin. In particular, Subject S-31 was diagnosed as NIID by skin biopsy ante-mortem and then confirmed by post-mortem histopathological examination. This case (Subject S-31) is the first NIID case in which eosinophilic ubiquitin-positive intranuclear inclusion was confirmed in both skin biopsy specimen and autopsy examination and presented with leukoencephalopathy and DWI high intensity signal in the corticomedullary junction. This case again confirmed the view of diagnostic usefulness and dependability of skin biopsy (Sone et al., 2011, 2014). Based on these observations, we thought that the presence of characteristic intranuclear inclusions in the biopsied skin could be used as the major diagnostic criteria for NIID.
The light microscopic features of intranuclear inclusion of NIID somewhat resemble Marinesco bodies, which are also stained by eosin, anti-ubiquitin antibody and anti-p62 antibody (Dickson et al., 1990; Kuusisto et al., 2008; Odagiri et al., 2012; Grigoriev et al., 2015). The electron microscopic findings of Marinesco bodies, however, show aggregation of finely granular materials and a filamentous lattice-like structure (Leestma and Andrews, 1969; Okamoto and Hirai, 1981), which is different to those of NIID cases in this study and previous reports (Lindenberg et al., 1968; Takahashi-Fujigasaki, 2003). We therefore consider that the nature of Marinesco bodies differs from intranuclear inclusion of NIID as previously reported (Janota, 1979; Sung, 1980; Oyer et al., 1991).
The histopathological features of NIID partially resemble those of FXTAS. Some cases of FXTAS present with dementia and leukoencephalopathy (Kasuga et al., 2011), and eosinophilic ubiquitin-positive intranuclear inclusions are observed in FXTAS in neurons, glial cells and somatic cells, similar to NIID (Gokden et al., 2009; Hagerman, 2013; Buijsen et al., 2014). There is no literature on the skin pathological or electron microscopic findings of intranuclear inclusions in FXTAS. Therefore, at present, it is difficult to distinguish NIID from FXTAS with only the histopathological findings. Clinical features such as psychiatric problems like depression and anxiety, family history of Fragile X syndrome, and genetic evaluation of FMR1 premutation are important for the differential diagnosis of NIID and FXTAS. For this reason, we performed gene analysis for FXTAS, and confirmed that this gene mutation was not present in our case series.
Until now, NIID has been described as a heterogeneous disease entity because of the variety of clinical features and pathological findings (Munoz-Garcia and Ludwin, 1986; Takahashi-Fujigasaki, 2003) with little information about adult-onset NIID cases.
In this study, we described adult-onset NIID cases and divided them into two sub-phenotype groups of dementia-dominant and limb weakness-dominant, based on the early phase of clinical phenotypes. We consider, however, that these two NIID subgroups are not two separate disease entities, but belong to one large disease entity that presents with both dementia with leukoencephalopathy, and limb weakness with polyneuropathy. The clinical manifestations of both groups overlapped (Fig. 5), and pathological features of intranuclear inclusions such as the distribution, immunoreactivity, frequency, white matter damage in Klüver-Barrera stain and electron microscopic findings are identical.
Furthermore, we reported that, in this study, tremor, rigidity and general convulsions were rarely observed in adult-onset NIID (Table 2), and these manifestations were frequently reported in infantile and juvenile NIID cases (Sung et al., 1980; Haltia et al., 1984; Funata et al., 1990; Sloane et al., 1994; O'Sullivan et al., 2000; Paviour et al., 2005). Clinical features of infant, juvenile and adult NIID are different, but some clinical manifestations are common to them. Such a variety of NIID clinical manifestations depending on disease onset ages may resemble Alexander disease that is a white matter disease caused by GFAP (glial fibrillary acidic protein) gene mutation and clinical phenotype is different by onset age (Sawaishi, 2009; Prust et al., 2011).
We need to identify the genetic background of NIID, particularly of familial cases, to solve and confirm the clinical entity of NIID. However, in view of the above, we consider that NIID may be one large disease entity with the same histopathological background, and subdivided it into some groups by clinical phenotypes. Based on our results on adult-onset NIID, it is necessary to study the head MRI DWI and skin biopsy of infantile and juvenile NIID cases to extend our understanding of NIID.
Head MRI examination detected remarkable leukoencephalopathy and DWI high intensity signal in the corticomedullary junction in the dementia-dominant group. The DWI high intensity signal is a characteristic finding of NIID patients (Kitagawa et al., 2014; Sone et al., 2014; Sasaki et al., 2015; Toyota et al., 2015) and we could not find such findings in 36 normal controls. In this study, we found that the DWI high intensity signal extended along the corticomedullary junction, but did not expand into the deep white matter, even in the advanced stage. This finding may be a strong clue to the diagnosis of NIID, and we performed skin biopsy on the NIID-suspected patients with these DWI high intensity signals.
Nine cases of the dementia-dominant group presented with a subacute encephalitic episode and some of these cases presented with focal brain oedema simultaneously with gadolinium enhancement. However, subacute encephalitic episodes have not been reported as a NIID symptom. Martin and Banker (1969) reported a case that resembled subacute leukoencephalopathy with intranuclear inclusion. Clinical manifestations and features of intranuclear inclusions of this case were fairly similar to our NIID cases. Langford (1994) also reported on a patient, age 38, who presented with headache, progressive weakness, and two brain lesions with oedema and MRI enhancement. A brain biopsy sample revealed selective loss of myelin, reactive astrocytes and glial intranuclear inclusions looking like those of NIID under electron microscopy (Langford, 1994). The authors of both case reports discussed the similarity of clinical and histopathological features of these cases to those of NIID. There are, however, no data on DWI and ubiquitin immunohistochemistry. We consider that these two cases were NIID because of the similarity of intranuclear inclusion and distribution, and thus such an encephalitic episode is one of the NIID manifestations.
To treat these encephalitic episodes, steroid pulse therapy may be effective to some extent to reduce brain oedema and improve consciousness in the short term. Long-term efficacy of steroid pulse therapy is unknown because the number of steroid treated NIID cases is still limited.
In neurobehavioural evaluations, FAB scores more obviously declined than MMSE scores, particularly in the dementia-dominant group. MMSE is useful in the assessment of cortical function, such as language, and relatively insensitive to the executive dysfunction of white matter dementia (Filley, 2012). FAB has been found to be sensitive to white matter dysfunction (Kanno et al., 2011). White matter dementia is distinguished from cortical dementia, like Alzheimer’s disease, by relative normalcy of language function and declarative memory encoding while cognitive speed, executive function, and sustained attention are impaired (Filley, 1998; Prins et al., 2005). The FAB score decline of NIID cases may reflect the white matter damage, and this pattern of decline is similar to other neurological diseases with white matter damage, such as cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) and FXTAS (Filley et al., 1999; Schmahmann et al., 2008; Chabriat et al., 2009; Kasuga et al., 2011).
As the outcome of this study, we propose the diagnostic flow chart of adult-onset NIID (Fig. 6). In dementia-dominant patients, most of the NIID cases present with leukoencephalopathy and symptoms related to white matter damage. Therefore, the nature of dementia may be different from cortical dementia such as Alzheimer’s disease and subcortical dementia such as Huntington’s disease (Filley, 2012). Some NIID cases did not present with leukoencephalopathy in MRI T2 image in our study, and we selected the high intensity signal of corticomedullary junction in the DWI as the strongest and easiest indicator of NIID, regardless of the nature of dementia. Investigation of skin biopsy sample is recommended when DWI high signal of corticomedullary junction is observed.
In case of DWI high negative, the nerve conduction study should be assessed because over 90% of NIID cases present with subclinical neuropathy. Among cases without either DWI high or nerve conduction study abnormal results, miosis or protein elevation of CSF may suggest NIID, because over 50% of NIID cases present these findings, and skin biopsy is worth consideration.
In weakness-dominant patients, nerve conduction must be studied and motor and/or sensory nerve damage is definitive. Suspect NIID if manifestations of autonomic dysfunction, such as miosis or bladder dysfunction are observed. In case of severe sensory nerve damage applicable to sural nerve biopsy, nerve biopsy should be examined, and other neuropathies, such as Charcot-Marie-Tooth disease and familial amyloid polyneuropathy, must be ruled out. On the other hand, in case sural nerve biopsy is impracticable, proceed to the evaluation of head MRI DWI image in the dementia-dominant group flow chart and follow from there.
Skin biopsy and immunohistochemistry procedures are described previously (Sone et al., 2011). We propose that the favourable region of skin biopsy for NIID is 10 cm above lateral malleolus, because of the appropriate density of sweat glands and adipocytes, to evaluate intranuclear inclusions of adipocytes, fibroblasts and sweat gland cells in one biopsy specimen.
In cases with ubiquitin-positive intranuclear inclusions in adipocytes, fibroblasts and sweat gland cells, we suggest genetic testing for FMR1 CGG repeat expansion to rule out FXTAS. Cases without FMR1 CGG premutation are finally diagnosed NIID ante-mortem.
In this study, dementia and DWI high signal triggered skin biopsy for most of the NIID cases. However, considering the systemic-wide distribution of intranuclear inclusion and neuronal loss in reported NIID cases (Lindenberg et al., 1968; Patel et al., 1985; Funata et al., 1990; Takahashi-Fujigasaki, 2003; Woulfe, 2007; Liu et al., 2008), we should be aware of the possibility of another phenotype of NIID (neither dementia nor weakness) and accumulate histopathologically-diagnosed NIID cases to refine the whole NIID clinical picture.
Here, we report on a large number of adult-onset NIID cases and describe its clinicopathological picture for the first time. The morbidity rate of adult-onset NIID may be larger than previously thought, as many cases may remain undiagnosed. We must consider NIID as a differential diagnosis of leukoencephalopathy and neuropathy, using the NIID diagnostic flowchart to gather adult-onset NIID cases and promote research to identify a causative gene.
We thank Osamu Komure, Eriko Sugawara, Masaaki Iguchi, Kyoko Higashida, Junko Ishii, Masaya Togo, Tateo Manabe, Katsuhide Komeichi, Hisao Kitazono, Hisao Yamashiro, Mutsumi Iijima, Kouji Kitaguchi, Hiromitsu Tabata, Youichi Kanedsuka, Houdou Mori, Mika Saiki, Syougo Takamura, Takashi Tokunaga, Yasushi Kita, Tatsuhiko Yuasa and Midori Kondo for their support in assessment of each NIID case. We also thank Yuki Matsuura, Yuri Konno, Noriyo Hotta and Masamitsu Nagaoka for histopathological sample preparation.
The project was funded by the Ministry of Education, Culture, Sports, Science and Technology of Japan (grant 24591257 and 15K09312). This research is also supported by the Practical Research Project for Rare/Intractable Disease, and the Strategic Research Program for Brain Sciences from Japan Agency for Medical Research and development, AMED.
Supplementary material is available at Brain online.