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1.
Mol Psychiatry ; 10(6): 563-71, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15558079

ABSTRACT

Several genome-wide screens have indicated the presence of an autism susceptibility locus within the distal long arm of chromosome 7 (7q). Mapping at 7q22 within this region is the candidate gene reelin (RELN). RELN encodes a signaling protein that plays a pivotal role in the migration of several neuronal cell types and in the development of neural connections. Given these neurodevelopmental functions, recent reports that RELN influences genetic risk for autism are of significant interest. The total data set consists of 218 Caucasian families collected by our group, 85 Caucasian families collected by AGRE, and 68 Caucasian families collected at Tufts University were tested for genetic association of RELN variants to autism. Markers included five single-nucleotide polymorphisms (SNPs) and a repeat in the 5'-untranslated region (5'-UTR). Tests for association in Duke and AGRE families were also performed on four additional SNPs in the genes PSMC2 and ORC5L, which flank RELN. Family-based association analyses (PDT, Geno-PDT, and FBAT) were used to test for association of single-locus markers and multilocus haplotypes with autism. The most significant association identified from this combined data set was for the 5'-UTR repeat (PDT P-value=0.002). These analyses show the potential of RELN as an important contributor to genetic risk in autism.


Subject(s)
5' Untranslated Regions/genetics , Autistic Disorder/genetics , Cell Adhesion Molecules, Neuronal/genetics , Chromosomes, Human, Pair 7/genetics , Extracellular Matrix Proteins/genetics , Genetic Predisposition to Disease/genetics , Nerve Tissue Proteins/genetics , Serine Endopeptidases/genetics , Female , Genotype , Humans , Infant , Linkage Disequilibrium , Male , Pedigree , Polymorphism, Single Nucleotide/genetics , Reelin Protein , White People/genetics
2.
Am J Med Genet B Neuropsychiatr Genet ; 127B(1): 104-12, 2004 May 15.
Article in English | MEDLINE | ID: mdl-15108191

ABSTRACT

Autism is a complex genetic neurodevelopmental disorder in which affected individuals display deficits in language, social relationships, and patterns of compulsive and stereotyped behaviors and rigidity. Linkage analysis in our dataset of 57 New England and 80 AGRE multiplex autism families reveals a multipoint heterogeneity LOD (HLOD) score of 2.74 at D17S1871 in 17q11.2. Analysis of phenotypic subsets shows an increased HLOD of 3.62 in families with compulsive behaviors and rigidity. The serotonin transporter locus (SLC6A4) maps nearby and is considered a functional candidate gene in autism and obsessive-compulsive disorder. We genotyped an insertion/deletion polymorphism in the promoter (5-HTTLPR), and seven single nucleotide polymorphisms (SNPs) across the 38-kb transcriptional unit. Transmission disequilibrium (TD) analysis reveals nominal association at a SNP in intron 5 (P = 0.02) as well as 5-HTTLPR (P = 0.01), corresponding to over-transmission of the short allele. TD analysis in the rigid-compulsive subset shows no evidence for association. Intermarker linkage disequilibrium was determined. All SNPs define a single haplotype block, while 5-HTTLPR lies 5' to this block. Three SNPs are sufficient to detect all common alleles (> or =5%) in this > 26-kb block. Analysis of haplotypes for these markers demonstrates no evidence for association to autism. These data indicate that a common allele within the coding region of SLC6A4 is not responsible for the observed linkage. However, the presence of heterogeneous disease variants within the block or the existence of a common disease-associated allele either upstream or downstream of this block is possible. In fact, such variants may well account for linkage to 17q11.2 in our families.


Subject(s)
Autistic Disorder/genetics , Carrier Proteins/genetics , Membrane Glycoproteins/genetics , Membrane Transport Proteins , Nerve Tissue Proteins/genetics , Autistic Disorder/classification , Chromosome Mapping , Chromosomes, Human, Pair 17/genetics , DNA/chemistry , DNA/genetics , DNA Mutational Analysis , Family Health , Gene Frequency , Genetic Linkage , Genotype , Haplotypes , Humans , Linkage Disequilibrium , Microsatellite Repeats , Polymorphism, Single Nucleotide , Serotonin Plasma Membrane Transport Proteins
3.
Mol Psychiatry ; 9(10): 968-72, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15098001

ABSTRACT

Impaired reciprocal social interaction is one of the core features of autism. While its determinants are complex, one biomolecular pathway that clearly influences social behavior is the arginine-vasopressin (AVP) system. The behavioral effects of AVP are mediated through the AVP receptor 1a (AVPR1a), making the AVPR1a gene a reasonable candidate for autism susceptibility. We tested the gene's contribution to autism by screening its exons in 125 independent autistic probands and genotyping two promoter polymorphisms in 65 autism affected sibling pair (ASP) families. While we found no nonconservative coding sequence changes, we did identify evidence of linkage and of linkage disequilibrium. These results were most pronounced in a subset of the ASP families with relatively less severe impairment of language. Thus, though we did not demonstrate a disease-causing variant in the coding sequence, numerous nontraditional disease-causing genetic abnormalities are known to exist that would escape detection by traditional gene screening methods. Given the emerging biological, animal model, and now genetic data, AVPR1a and genes in the AVP system remain strong candidates for involvement in autism susceptibility and deserve continued scrutiny.


Subject(s)
Autistic Disorder/genetics , Receptors, Vasopressin/genetics , Autistic Disorder/epidemiology , Codon/genetics , DNA Mutational Analysis , Exons/genetics , Family Health , Genetic Linkage , Genetic Predisposition to Disease , Genetic Testing , Genotype , Humans , Language Disorders/epidemiology , Language Disorders/genetics , Linkage Disequilibrium , Lod Score , Polymorphism, Genetic , Promoter Regions, Genetic/genetics , Siblings , United States
4.
Mol Psychiatry ; 8(6): 624-34, 570, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12851639

ABSTRACT

Autism [MIM 209850] is a neurodevelopmental disorder exhibiting a complex genetic etiology with clinical and locus heterogeneity. Chromosome 15q11-q13 has been proposed to harbor a gene for autism susceptibility based on (1) maternal-specific chromosomal duplications seen in autism and (2) positive evidence for linkage disequilibrium (LD) at 15q markers in chromosomally normal autism families. To investigate and localize a potential susceptibility variant, we developed a dense single nucleotide polymorphism (SNP) map of the maternal expression domain in proximal 15q. We analyzed 29 SNPs spanning the two known imprinted, maternally expressed genes in the interval (UBE3A and ATP10C) and putative imprinting control regions. With a marker coverage of 1/10 kb in coding regions and 1/15 kb in large 5' introns, this map was employed to thoroughly dissect LD in autism families. Two SNPs within ATP10C demonstrated evidence for preferential allelic transmission to affected offspring. The signal detected at these SNPs was stronger in singleton families, and an adjacent SNP demonstrated transmission distortion in this subset. All SNPs showing allelic association lie within islands of sequence homology between human and mouse genomes that may be part of an ancestral haplotype containing a functional susceptibility allele. The region was further explored for recombination hot spots and haplotype blocks to evaluate haplotype transmission. Five haplotype blocks were defined within this region. One haplotype within ATP10C displayed suggestive evidence for preferential transmission. Interpretation of these data will require replication across data sets, evaluation of potential functional effects of associated alleles, and a thorough assessment of haplotype transmission within ATP10C and neighboring genes. Nevertheless, these findings are consistent with the presence of an autism susceptibility locus in 15q11-q13.


Subject(s)
Autistic Disorder/genetics , Chromosomes, Human, Pair 15 , Linkage Disequilibrium , Genetic Markers , Genetic Predisposition to Disease , Haplotypes , Humans , Polymorphism, Single Nucleotide
5.
Mol Psychiatry ; 8(3): 288-98, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12660801

ABSTRACT

The purpose of this study was to assess 65 pedigrees ascertained through a Bipolar I (BPI) proband for evidence of linkage, using nonparametric methods in a genome-wide scan and for possible parent of origin effect using several analytical methods. We identified 15 loci with nominally significant evidence for increased allele sharing among affected relative pairs. Eight of these regions, at 8q24, 18q22, 4q32, 13q12, 4q35, 10q26, 2p12, and 12q24, directly overlap with previously reported evidence of linkage to bipolar disorder. Five regions at 20p13, 2p22, 14q23, 9p13, and 1q41 are within several Mb of previously reported regions. We report our findings in rank order and the top five markers had an NPL>2.5. The peak finding in these regions were D8S256 at 8q24, NPL 3.13; D18S878 at 18q22, NPL 2.90; D4S1629 at 4q32, NPL 2.80; D2S99 at 2p12, NPL 2.54; and D13S1493 at 13q12, NPL 2.53. No locus produced statistically significant evidence for linkage at the genome-wide level. The parent of origin effect was studied and consistent with our previous findings, evidence for a locus on 18q22 was predominantly from families wherein the father or paternal lineage was affected. There was evidence consistent with paternal imprinting at the loci on 13q12 and 1q41.


Subject(s)
Bipolar Disorder/genetics , Chromosomes, Human , Genetic Linkage , Genome, Human , Adolescent , Adult , Chromosomes, Human, Pair 13 , Chromosomes, Human, Pair 18 , Chromosomes, Human, Pair 2 , Chromosomes, Human, Pair 4 , Chromosomes, Human, Pair 8 , Family Health , Genomic Imprinting , Genotype , Humans , Parents , Pedigree
6.
Am J Med Genet B Neuropsychiatr Genet ; 117B(1): 90-6, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12555242

ABSTRACT

Previous genetic and cytogenetic studies provide evidence that points to one or more autism susceptibility genes residing on chromosome 7q (AUTS1, 115-149 cM on the Marshfield map). However, further localization using linkage analysis has proven difficult. To overcome this problem, we examined the Collaborative Linkage Study of Autism (CLSA) data-set to identify only the families potentially linked to chromosome 7. Out of 94, 47 families were identified and 17 markers were used to generate chromosomal haplotypes. We performed recombination breakpoint analysis to determine if any portion of the chromosome was predominately shared across families. The most commonly shared region spanned a 6 cM interval between D7S501 and D7S2847. Additional markers at 1 cM intervals within this region were genotyped and association and recombination breakpoint analysis was again performed. Although no significant allelic association was found, the recombination breakpoint data points to a shared region between D7S496-D7S2418 (120-123 cM) encompassing about 4.5 Mb of genomic DNA containing over 50 genes.


Subject(s)
Autistic Disorder/genetics , Chromosome Mapping , Chromosomes, Human, Pair 7 , Family Health , Genetic Linkage , Genetic Markers , Genetic Predisposition to Disease , Genotype , Haplotypes , Humans , Recombination, Genetic
7.
Nat Rev Genet ; 2(12): 943-55, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11733747

ABSTRACT

Since autism was first recognized as a disorder in 1943, speculation about its aetiology has ranged from biological to psychological and back again. After twin studies during the 1970s and 1980s yielded unequivocal evidence for a genetic component, aetiological research in autism began to focus primarily on uncovering the genetic mechanisms involved. The identification of chromosomal abnormalities and Mendelian syndromes among individuals with autism, in conjunction with data from genome screens and candidate-gene studies, has helped to refine the view of the complex genetics that underlies autism spectrum conditions.


Subject(s)
Autistic Disorder/genetics , Autistic Disorder/etiology , Chromosome Mapping , Female , Genetic Counseling , Genome, Human , Humans , Male , Phenotype
8.
Genomics ; 77(1-2): 105-13, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11543639

ABSTRACT

Autistic disorder is a neurodevelopmental disorder with a complex genetic etiology. Observations of maternal duplications affecting chromosome 15q11-q13 in patients with autism and evidence for linkage and linkage disequilibrium to markers in this region in chromosomally normal autism families indicate the existence of a susceptibility locus. We have screened the families of the Collaborative Linkage Study of Autism for several markers spanning a candidate region covering approximately 2 Mb and including the Angelman syndrome gene (UBE3A) and a cluster of gamma-aminobutyric acid (GABA(A)) receptor subunit genes (GABRB3, GABRA5, and GABRG3). We found significant evidence for linkage disequilibrium at marker D15S122, located at the 5' end of UBE3A. This is the first report, to our knowledge, of linkage disequilibrium at UBE3A in autism families. Characterization of null alleles detected at D15S822 in the course of genetic studies of this region showed a small (approximately 5-kb) genomic deletion, which was present at somewhat higher frequencies in autism families than in controls.


Subject(s)
Angelman Syndrome/genetics , Autistic Disorder/genetics , Ligases/genetics , Linkage Disequilibrium , Alleles , Base Sequence , Chromosome Deletion , Chromosomes, Human, Pair 15/genetics , DNA/chemistry , DNA/genetics , DNA Mutational Analysis , Family Health , Female , Gene Frequency , Genotype , Humans , Male , Microsatellite Repeats , Molecular Sequence Data , Polymorphism, Single Nucleotide , Protein Subunits , Receptors, GABA-A/genetics , Sequence Deletion , Ubiquitin-Protein Ligases
9.
Am J Med Genet ; 105(5): 406-13, 2001 Jul 08.
Article in English | MEDLINE | ID: mdl-11449391

ABSTRACT

We examined WNT2 as a candidate disease gene for autism for the following reasons. First, the WNT family of genes influences the development of numerous organs and systems, including the central nervous system. Second, WNT2 is located in the region of chromosome 7q31-33 linked to autism and is adjacent to a chromosomal breakpoint in an individual with autism. Third, a mouse knockout of Dvl1, a member of a gene family essential for the function of the WNT pathway, exhibits a behavioral phenotype characterized primarily by diminished social interaction. We screened the WNT2 coding sequence for mutations in a large number of autistic probands and found two families containing nonconservative coding sequence variants that segregated with autism in those families. We also identified linkage disequilibrium (LD) between a WNT2 3'UTR SNP and our sample of autism-affected sibling pair (ASP) families and trios. The LD arose almost exclusively from a subgroup of our ASP families defined by the presence of severe language abnormalities and was also found to be associated with the evidence for linkage to 7q from our previously published genomewide linkage screen. Furthermore, expression analysis demonstrated WNT2 expression in the human thalamus. Based on these findings, we hypothesize that rare mutations occur in the WNT2 gene that significantly increase susceptibility to autism even when present in single copies, while a more common WNT2 allele (or alleles) not yet identified may exist that contributes to the disorder to a lesser degree.


Subject(s)
Autistic Disorder/genetics , Proto-Oncogene Proteins/genetics , Amino Acid Sequence , Amino Acid Substitution , Autistic Disorder/pathology , Base Sequence , Blotting, Northern , Brain/metabolism , DNA/chemistry , DNA/genetics , DNA Mutational Analysis , Family Health , Female , Gene Expression , Humans , Linkage Disequilibrium , Male , Pedigree , Point Mutation , Polymorphism, Single Nucleotide , Polymorphism, Single-Stranded Conformational , RNA, Messenger/genetics , Sequence Homology, Amino Acid , Wnt2 Protein
11.
Am J Med Genet ; 88(6): 609-15, 1999 Dec 15.
Article in English | MEDLINE | ID: mdl-10581478

ABSTRACT

Autism is a severe neurodevelopmental disorder defined by social and communication deficits and ritualistic-repetitive behaviors that are detectable in early childhood. The etiology of idiopathic autism is strongly genetic, and oligogenic transmission is likely. The first stage of a two-stage genomic screen for autism was carried out by the Collaborative Linkage Study of Autism on individuals affected with autism from 75 families ascertained through an affected sib-pair. The strongest multipoint results were for regions on chromosomes 13 and 7. The highest maximum multipoint heterogeneity LOD (MMLS/het) score is 3.0 at D13S800 (approximately 55 cM from the telomere) under the recessive model, with an estimated 35% of families linked to this locus. The next highest peak is an MMLS/het score of 2.3 at 19 cM, between D13S217 and D13S1229. Our third highest MMLS/het score of 2.2 is on chromosome 7 and is consistent with the International Molecular Genetic Study of Autism Consortium report of a possible susceptibility locus somewhere within 7q31-33. These regions and others will be followed up in the second stage of our study by typing additional markers in both the original and a second set of identically ascertained autism families, which are currently being collected. By comparing results across a number of studies, we expect to be able to narrow our search for autism susceptibility genes to a small number of genomic regions. Am. J. Med. Genet. (Neuropsychiatr. Genet.) 88:609-615, 1999.


Subject(s)
Autistic Disorder/genetics , Chromosome Mapping , Genetic Linkage/genetics , Genetic Predisposition to Disease/genetics , Genetic Testing , Adolescent , Adult , Autistic Disorder/etiology , Child , Child, Preschool , Chromosomes, Human, Pair 13/genetics , Chromosomes, Human, Pair 7/genetics , Family Health , Female , Gene Frequency , Genes, Recessive/genetics , Humans , Intelligence Tests , Male , Models, Genetic
12.
J Child Psychol Psychiatry ; 40(7): 1117-28, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10576540

ABSTRACT

In a case-control study of cognitive performance, tests of intelligence, reading, spelling, and pragmatic language were administered to the parents and siblings of 90 community-ascertained probands with autism (AU group) and to the parents and siblings of 40 similarly ascertained probands with trisomy 21 Down syndrome (DS group). The two samples were comparable for age and parents' education; both groups were well-educated and had above-average intelligence. AU parents scored slightly but significantly lower on the WAIS-R Full Scale and Performance IQ, on two subtests (Picture Arrangement and Picture Completion), and on the Word Attack Test (reading nonsense words) from the Woodcock-Johnson battery. There were no differences between AU and DS siblings. As in earlier studies, AU parents, more often than DS parents, reported a history of early language-related cognitive difficulties; we were not able to replicate this in siblings. AU parents who reported such difficulties scored significantly lower on Verbal IQ, spelling, and the nonsense reading test. AU parents without a history of early language-related cognitive difficulties often had a Verbal IQ that exceeded Performance IQ by more than one standard deviation. AU siblings with early language-related difficulties had similar findings: lower Verbal IQ, poorer spelling, and poorer reading scores, compared to AU siblings without such a history. Parents with a positive history also scored worse on a measure of pragmatic language,the Pragmatic Rating Scale, but not on measures of social-related components of the broader autism phenotype. We propose that cognitive differences in a subset of autism family members are manifestations of the language-related component of the broader autism phenotype, and separate from the social-related component. This is consistent with the hypothesis that there are several genes that may interact to cause autism which segregate independently and have distinguishable manifestations in family members. The hypothesis would be further supported by finding different patterns of genetic loci linked to autism in families where one or both parents has language difficulties.


Subject(s)
Autistic Disorder/genetics , Cognition Disorders/genetics , Down Syndrome/genetics , Adolescent , Autistic Disorder/psychology , Case-Control Studies , Child , Child, Preschool , Cognition Disorders/psychology , Down Syndrome/psychology , Dyslexia/etiology , Dyslexia/genetics , Family Health , Female , Humans , Language Disorders/genetics , Language Disorders/psychology , Male
13.
J Autism Dev Disord ; 28(5): 439-45, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9813779

ABSTRACT

Although autism is clearly inherited, it may be challenging to find the genes involved: The mechanism of inheritance is unknown, families with an autistic child are usually small, parent-child pairs are rare, and a fairly large number of genes may be involved, some or all of which may have a small effect on the phenotype. We discuss several strategies for finding genes, all of which may be used in combination to find the relevant genes.


Subject(s)
Autistic Disorder/genetics , Genetic Markers , Family , Genetic Linkage , Humans , Phenotype , Research Design
14.
J Am Acad Child Adolesc Psychiatry ; 36(2): 282-90, 1997 Feb.
Article in English | MEDLINE | ID: mdl-9031582

ABSTRACT

OBJECTIVE: To explore the frequency and onset of macrocephaly in autism and its relationship to clinical features. METHOD: Head circumferences at birth, during early childhood, and at the time of examination were studied in a community-based sample of autistic children and adults. The authors investigated whether head circumference at the time of examination was associated with clinical features. RESULTS: Fourteen percent of the autistic subjects had macrocephaly: 11% of males and 24% of females. In most, the macrocephaly was not present at birth; in some it became apparent in early and middle childhood as a result of increased rate of head growth. A small relationship was noted between head circumference percentile and less severe core features of autism. Neither macrocephaly nor head circumference percentile was associated with nonverbal IQ, verbal status, seizure disorder, neurological soft signs or minor physical anomalies in the autistic subjects. CONCLUSION: Macrocephaly is common in autism and usually is not present at birth. Rates of head growth may be abnormal in early and middle childhood in some (37%) children with autism. Macrocephaly does not define a homogeneous subgroup of autistic individuals according to clinical features.


Subject(s)
Autistic Disorder/complications , Autistic Disorder/physiopathology , Craniofacial Abnormalities/complications , Craniofacial Abnormalities/physiopathology , Head/abnormalities , Adolescent , Adult , Chi-Square Distribution , Child , Child, Preschool , Cross-Sectional Studies , Female , Humans , Male , Retrospective Studies , Sampling Studies
15.
Mov Disord ; 11(5): 549-54, 1996 Sep.
Article in English | MEDLINE | ID: mdl-8866496

ABSTRACT

One hundred patients with clinically diagnosed Huntington's disease (HD) were randomized to either idebenone, an antioxidant and enhancer of oxidative metabolism, or placebo, in a 1-year, double-blind, parallel-group study aimed at slowing the rate of progression of the disease. Ninety-one patients completed the study. There were no significant differences between groups on the primary outcome measures of the Huntington's Disease Activities of Daily Living Scale (ADL-an index of functional status) and the Quantified Neurologic Examination (QNE). Sample size calculations based on progression of the ADL and QNE in this study group revealed that a larger study group is necessary to detect any differences less than an almost complete halting of the disease. This argues for multicenter efforts for future therapeutic trials in HD.


Subject(s)
Antioxidants/pharmacology , Antioxidants/therapeutic use , Benzoquinones/pharmacology , Benzoquinones/therapeutic use , Huntington Disease/drug therapy , Activities of Daily Living , Adult , Double-Blind Method , Female , Humans , Longitudinal Studies , Male , Middle Aged , Placebos , Receptors, Glutamate/drug effects , Treatment Outcome , Ubiquinone/analogs & derivatives
16.
Arch Neurol ; 53(4): 316-24, 1996 Apr.
Article in English | MEDLINE | ID: mdl-8929153

ABSTRACT

OBJECTIVE: To examine basal ganglia dysfunction and atrophy in patients with mild to moderate Huntington's disease, with correlation of imaging measures with clinical and neuropsychological measures. DESIGN: Survey study in patients with Huntington's disease and matched controls, with imaging measures being evaluated by investigators unaware of the diagnosis. SETTING: Baltimore Huntington's Disease Project, The Johns Hopkins Hospital, Baltimore, Md. PATIENTS AND OTHER PARTICIPANTS: Subjects included 10 patients with mild to moderate Huntington's disease and nine healthy age-matched control subjects. MAIN OUTCOME MEASURES: Imaging measures included single photon emission computed tomographic regional cerebral blood flow in caudate, putamen, and thalamus, and magnetic resonance imaging measures of caudate and putamen volumes and bicaudate ratios. Patients underwent neurologic and mental status examinations and neuropsychological tests. RESULTS: The measure with the greatest difference between patients and control subjects was mean putamen volume, reduced 54.3% in patients, with no overlap between groups (P<.001). Of the cerebral blood flow measures, caudate showed the greatest difference (21.5% decrease; P<.001). Quantitative neurologic indexes of disease severity correlated with both putamen measures (P<.03), while Mini-Mental State Examination scores correlated with caudate volume (P<.02). Bicaudate ratio correlated with both clinical measures and was the best index of neurologic deterioration (r=.95; P<.001), while global atrophy (measured by cerebrospinal fluid percentage) was the best correlate of several neuropsychological tests, such as the Trail Making Test (r=93; P<.001). CONCLUSIONS: Volumetric measurement of putamen best discriminated patients with Huntington's disease from healthy subjects. Measures of caudate atrophy or single photon emission computed tomographic measures performed less well. Neurologic decline correlated best with subcortical atrophy measured by the bicaudate ratio, but neuropsychological performance best corresponded to cerebrospinal fluid percentage, a measure of global atrophy.


Subject(s)
Basal Ganglia/blood supply , Basal Ganglia/diagnostic imaging , Cerebrovascular Circulation , Huntington Disease/diagnosis , Adult , Aged , Basal Ganglia/pathology , Female , Humans , Huntington Disease/diagnostic imaging , Huntington Disease/psychology , Magnetic Resonance Imaging , Male , Middle Aged , Neuropsychological Tests , Reference Values , Tomography, Emission-Computed, Single-Photon
17.
Am J Psychiatry ; 152(12): 1771-5, 1995 Dec.
Article in English | MEDLINE | ID: mdl-8526244

ABSTRACT

OBJECTIVE: Evidence suggests that the neuropathology of Huntington's disease, a neuropsychiatric disorder due to a mutation on chromosome 4, results from excessive activation of glutamate-gated ion channels, which kills neurons by oxidative stress. Therefore, the authors hypothesized that alpha-tocopherol, which reduces oxyradical damage to cell membranes, might slow the course of Huntington's disease. METHOD: A prospective, double-blind; placebo-controlled study of high-dose d-alpha-tocopherol treatment was carried out with a cohort of 73 patients with Huntington's disease who were randomly assigned to either d-alpha-tocopherol or placebo. Patients were monitored for changes in neurologic and neuropsychologic symptoms. RESULTS: Treatment with d-alpha-tocopherol had no effect on neurologic and neuropsychiatric symptoms in the treatment group overall. However, post hoc analysis revealed a significant selective therapeutic effect on neurologic symptoms for patients early in the course of the disorder. CONCLUSIONS: Antioxidant therapy may slow the rate of motor decline early in the course of Huntington's disease.


Subject(s)
Antioxidants/therapeutic use , Huntington Disease/drug therapy , Vitamin E/therapeutic use , Chromosomes, Human, Pair 4/genetics , Double-Blind Method , Humans , Huntington Disease/genetics , Isomerism , Oxidative Stress/drug effects , Placebos , Prospective Studies , Treatment Outcome , Vitamin E/pharmacology
18.
Mov Disord ; 10(6): 778-87, 1995 Nov.
Article in English | MEDLINE | ID: mdl-8749997

ABSTRACT

We assessed the influence of the neurological and cognitive impairments of Huntington's disease (HD) on automobile driving. In a group of 73 HD outpatients, 53 (72%) continued to drive after illness onset. Those no longer driving had more severe symptoms than those still driving. Twenty-nine HD patients who were still driving and 16 healthy control subjects underwent a clinical examination, a cognitive examination, a driving-simulator assessment, and completed questionnaires about driving history and habits. HD patients performed significantly worse than control subjects on the driving-simulator tasks and were more likely to have been involved in a collision in the preceding 2 years (58% of HD vs. 11% of control subjects). Patients with collisions were less functionally impaired but had slower simple reaction time scores than did those without collisions. HD patients are at increased risk for accidents, but patients who have accidents are not easily distinguished from those who do not.


Subject(s)
Automobile Driving/psychology , Disability Evaluation , Huntington Disease/diagnosis , Neurologic Examination , Neuropsychological Tests , Psychomotor Performance/physiology , Accidents, Traffic/prevention & control , Accidents, Traffic/psychology , Adult , Computer Simulation , Female , Humans , Huntington Disease/genetics , Huntington Disease/psychology , Male , Mental Status Schedule , Middle Aged , Risk Factors
19.
J Neuropathol Exp Neurol ; 54(1): 105-20, 1995 Jan.
Article in English | MEDLINE | ID: mdl-7815073

ABSTRACT

During the first years of symptomatic Huntington's disease (HD), no readily apparent pathology is seen in the neostriatum at autopsy. To investigate the pathological correlates of chorea and other early clinical signs, we examined the evolution of neuronal loss and accompanying astrocytosis in neostriatal tissue from autopsy cases of early HD. We found scattered islands of astrocytosis and neuronal loss that were present before the previously described ventrally progressive wave of generalized neuronal loss. Histological demonstration of these islands, which are apparently specific to HD, is very helpful in the pathological differential diagnosis of this disease. Immunocytochemical stains for glial fibrillary acidic protein and for markers of the neostriatal striosome-matrix system showed that these islands correspond to the striosome compartment. Striosomal neuronal loss was present throughout the dorsoventral extent of the caudate nucleus and putamen during the early phase of symptomatic disease, and this loss extended to the most ventral region of the nucleus accumbens in later stages. Analysis of the functional circuitry of the basal ganglia suggests that early degeneration of striosomal neurons may produce hyperactivity of the nigrostriatal dopaminergic pathway, causing chorea and other early clinical manifestations of HD.


Subject(s)
Corpus Striatum/pathology , Huntington Disease/pathology , Neurons/pathology , Astrocytes/pathology , Cadaver , Cell Death , Corpus Striatum/metabolism , Glial Fibrillary Acidic Protein/metabolism , Humans , Huntington Disease/metabolism , Immunohistochemistry , Time Factors
20.
J Autism Dev Disord ; 24(5): 587-601, 1994 Oct.
Article in English | MEDLINE | ID: mdl-7814308

ABSTRACT

The presentation of affective disorders in people with autism and autistic-like disorders is discussed based upon a review of 17 published cases. Half of the patients were female and almost all of the patients had IQs in the mentally retarded range. 35% of the patients had the onset of affective disorder in childhood. Of the cases mentioning family history, 50% had a family history of affective disorder or suicide. Changes in mood, self-attitude, and vital sense were rarely reported by the patients. A change in mood, attitude toward self and others, and vegetative changes were inferred based on the observations of others. Difficulties in diagnosing affective disorders in autistic people are presented and suggestions are made for diagnosis, treatment, and research.


Subject(s)
Autistic Disorder/diagnosis , Mood Disorders/diagnosis , Adolescent , Adult , Autistic Disorder/psychology , Child , Child, Preschool , Comorbidity , Down Syndrome/diagnosis , Down Syndrome/psychology , Female , Humans , Intellectual Disability/diagnosis , Intellectual Disability/psychology , Intelligence , Male , Mood Disorders/psychology
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