Literature DB >> 16874769

Abnormalities of cholesterol metabolism in autism spectrum disorders.

Elaine Tierney1, Irena Bukelis, Richard E Thompson, Khalid Ahmed, Alka Aneja, Lisa Kratz, Richard I Kelley.   

Abstract

Although Smith-Lemli-Opitz Syndrome (SLOS), a genetic condition of impaired cholesterol biosynthesis, is associated with autism [Tierney et al., 2001; Am J Med Genet 98:191-200.], the incidence of SLOS and other sterol disorders among individuals with autism spectrum disorders (ASD) is unknown. This study investigated (1) the incidence of biochemically diagnosed SLOS in blood samples from a cohort of subjects with ASD from families in which more than one individual had ASD and (2) the type and incidence of other sterol disorders in the same group. Using gas chromatography/mass spectrometry, cholesterol, and its precursor sterols were quantified in 100 samples from subjects with ASD obtained from the Autism Genetic Resource Exchange (AGRE) specimen repository. Although no sample had sterol levels consistent with SLOS, 19 samples had total cholesterol levels lower than 100 mg/dl, which is below the 5th centile for children over age 2 years. These findings suggest that, in addition to SLOS, there may be other disorders of sterol metabolism or homeostasis associated with ASD.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16874769      PMCID: PMC2553243          DOI: 10.1002/ajmg.b.30368

Source DB:  PubMed          Journal:  Am J Med Genet B Neuropsychiatr Genet        ISSN: 1552-4841            Impact factor:   3.568


  8 in total

Review 1.  Inborn errors of sterol biosynthesis.

Authors:  R I Kelley; G E Herman
Journal:  Annu Rev Genomics Hum Genet       Date:  2001       Impact factor: 8.929

2.  Borderline normal intelligence in the Smith-Lemli-Opitz (RSH) syndrome.

Authors:  R B Lowry; S L Yong
Journal:  Am J Med Genet       Date:  1980

3.  Behavior phenotype in the RSH/Smith-Lemli-Opitz syndrome.

Authors:  E Tierney; N A Nwokoro; F D Porter; L S Freund; J K Ghuman; R I Kelley
Journal:  Am J Med Genet       Date:  2001-01-15

Review 4.  Etiology of autism: genetic influences.

Authors:  S E Folstein; J Piven
Journal:  Pediatrics       Date:  1991-05       Impact factor: 7.124

5.  Defective cholesterol biosynthesis associated with the Smith-Lemli-Opitz syndrome.

Authors:  G S Tint; M Irons; E R Elias; A K Batta; R Frieden; T S Chen; G Salen
Journal:  N Engl J Med       Date:  1994-01-13       Impact factor: 91.245

6.  Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders.

Authors:  C Lord; M Rutter; A Le Couteur
Journal:  J Autism Dev Disord       Date:  1994-10

7.  Diagnosis of Smith-Lemli-Opitz syndrome by gas chromatography/mass spectrometry of 7-dehydrocholesterol in plasma, amniotic fluid and cultured skin fibroblasts.

Authors:  R I Kelley
Journal:  Clin Chim Acta       Date:  1995-04-30       Impact factor: 3.786

8.  Determination of serum levels of unesterified lathosterol by isotope dilution-mass spectrometry.

Authors:  E Lund; L Sisfontes; E Reihner; I Bjorkhem
Journal:  Scand J Clin Lab Invest       Date:  1989-04       Impact factor: 1.713

  8 in total
  45 in total

1.  Desmosterolosis and desmosterol homeostasis in the developing mouse brain.

Authors:  Luke B Allen; Thiago C Genaro-Mattos; Ned A Porter; Károly Mirnics; Zeljka Korade
Journal:  J Inherit Metab Dis       Date:  2019-04-08       Impact factor: 4.982

Review 2.  Why are astrocytes important?

Authors:  Alexei Verkhratsky; Maiken Nedergaard; Leif Hertz
Journal:  Neurochem Res       Date:  2014-08-12       Impact factor: 3.996

Review 3.  The Role of Lipidomics in Autism Spectrum Disorder.

Authors:  Afaf El-Ansary; Salvatore Chirumbolo; Ramesa Shafi Bhat; Maryam Dadar; Eiman M Ibrahim; Geir Bjørklund
Journal:  Mol Diagn Ther       Date:  2020-02       Impact factor: 4.074

4.  Maternal Dyslipidemia, Plasma Branched-Chain Amino Acids, and the Risk of Child Autism Spectrum Disorder: Evidence of Sex Difference.

Authors:  Anita A Panjwani; Yuelong Ji; Jed W Fahey; Amanda Palmer; Guoying Wang; Xiumei Hong; Barry Zuckerman; Xiaobin Wang
Journal:  J Autism Dev Disord       Date:  2020-02

5.  Corpus callosum measurements correlate with developmental delay in Smith-Lemli-Opitz syndrome.

Authors:  Ryan W Y Lee; Shoko Yoshida; Eun Sol Jung; Susumu Mori; Eva H Baker; Forbes D Porter
Journal:  Pediatr Neurol       Date:  2013-08       Impact factor: 3.372

6.  Mutation of 3-hydroxy-3-methylglutaryl CoA synthase I reveals requirements for isoprenoid and cholesterol synthesis in oligodendrocyte migration arrest, axon wrapping, and myelin gene expression.

Authors:  Emily S Mathews; David J Mawdsley; Macie Walker; Jacob H Hines; Marina Pozzoli; Bruce Appel
Journal:  J Neurosci       Date:  2014-02-26       Impact factor: 6.167

7.  Exploiting aberrant mRNA expression in autism for gene discovery and diagnosis.

Authors:  Jinting Guan; Ence Yang; Jizhou Yang; Yong Zeng; Guoli Ji; James J Cai
Journal:  Hum Genet       Date:  2016-04-30       Impact factor: 4.132

Review 8.  Neurometabolic disorders and dysfunction in autism spectrum disorders.

Authors:  Nassim Zecavati; Sarah J Spence
Journal:  Curr Neurol Neurosci Rep       Date:  2009-03       Impact factor: 5.081

Review 9.  Advances in autism genetics: on the threshold of a new neurobiology.

Authors:  Brett S Abrahams; Daniel H Geschwind
Journal:  Nat Rev Genet       Date:  2008-05       Impact factor: 53.242

10.  Antioxidant supplementation ameliorates molecular deficits in Smith-Lemli-Opitz syndrome.

Authors:  Zeljka Korade; Libin Xu; Fiona E Harrison; Refayat Ahsen; Sarah E Hart; Oakleigh M Folkes; Károly Mirnics; Ned A Porter
Journal:  Biol Psychiatry       Date:  2013-07-26       Impact factor: 13.382

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.