Literature DB >> 2035720

Psychiatric disorders in 36 families with Wolfram syndrome.

R G Swift1, D O Perkins, C L Chase, D B Sadler, M Swift.   

Abstract

OBJECTIVE: The purpose of this study was to test the hypothesis that heterozygous carriers of the gene for the Wolfram syndrome, who constitute about 1% of the population, are predisposed to significant psychiatric illness. The Wolfram syndrome is an autosomal recessive neurodegenerative syndrome in which 25% of the individuals who are homozygous for the condition have severe psychiatric symptoms that lead to suicide attempts or psychiatric hospitalizations.
METHOD: The authors collected questionnaires, death certificates, and hospital records for blood relatives and their spouses in 36 families of individuals with the Wolfram syndrome and compared the proportion of blood relatives who had had psychiatric hospitalizations, had committed suicide, or had self-reported mental illness to the proportion of spouses with the same manifestations.
RESULTS: The proportion of blood relatives who had had psychiatric hospitalizations, had committed suicide, or had self-reported mental illness significantly exceeded the proportion of spouses with the same manifestations.
CONCLUSIONS: Since heterozygous carriers of the gene for the Wolfram syndrome are 50-fold more common among the blood relatives than among the spouses, the larger proportion among blood relatives is evidence that heterozygous carriers of the gene for the Wolfram syndrome are predisposed to significant psychiatric illness.

Entities:  

Mesh:

Year:  1991        PMID: 2035720     DOI: 10.1176/ajp.148.6.775

Source DB:  PubMed          Journal:  Am J Psychiatry        ISSN: 0002-953X            Impact factor:   18.112


  20 in total

1.  Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

Authors:  I N Bespalova; G Van Camp; S J Bom; D J Brown; K Cryns; A T DeWan; A E Erson; K Flothmann; H P Kunst; P Kurnool; T A Sivakumaran; C W Cremers; S M Leal; M Burmeister; M M Lesperance
Journal:  Hum Mol Genet       Date:  2001-10-15       Impact factor: 6.150

2.  A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome.

Authors:  A Barrientos; V Volpini; J Casademont; D Genís; J M Manzanares; I Ferrer; J Corral; F Cardellach; A Urbano-Márquez; X Estivill; V Nunes
Journal:  J Clin Invest       Date:  1996-04-01       Impact factor: 14.808

3.  Wfs1 mutation makes mice sensitive to insulin-like effect of acute valproic acid and resistant to streptozocin.

Authors:  Anton Terasmaa; Ursel Soomets; Julia Oflijan; Marite Punapart; Mats Hansen; Vallo Matto; Kersti Ehrlich; Anne Must; Sulev Kõks; Eero Vasar
Journal:  J Physiol Biochem       Date:  2011-04-02       Impact factor: 4.158

4.  Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.

Authors:  D A Collier; T G Barrett; D Curtis; A Macleod; M J Arranz; J A Maassen; S Bundey
Journal:  Am J Hum Genet       Date:  1996-10       Impact factor: 11.025

5.  Significant expressivity of Wolfram syndrome: phenotypic assessment of two known and one novel mutation in the WFS1 gene in three Iranian families.

Authors:  Maryam Sobhani; Mohammad Amin Tabatabaiefar; Asadollah Rajab; Abdol-Mohammad Kajbafzadeh; Mohammad Reza Noori-Daloii
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6.  Autoimmune disease in a DFNA6/14/38 family carrying a novel missense mutation in WFS1.

Authors:  Michael S Hildebrand; Jessica L Sorensen; Maren Jensen; William J Kimberling; Richard J H Smith
Journal:  Am J Med Genet A       Date:  2008-09-01       Impact factor: 2.802

Review 7.  Neurodegenerative disorders associated with diabetes mellitus.

Authors:  Michael Ristow
Journal:  J Mol Med (Berl)       Date:  2004-06-03       Impact factor: 4.599

8.  Wolframin gene H611R polymorphism: no direct association with suicidal behavior but possible link to mood disorders.

Authors:  Gil Zalsman; Mark J Mann; Yung-Yu Huang; Maria A Oquendo; David A Brent; Ainsley K Burke; Steven P Ellis; J John Mann
Journal:  Prog Neuropsychopharmacol Biol Psychiatry       Date:  2009-03-26       Impact factor: 5.067

9.  The novel compound heterozygous mutations, V434del and W666X, in WFS1 gene causing the Wolfram syndrome in a Chinese family.

Authors:  Jie Hong; Yu-Wen Zhang; Hui-Jie Zhang; Hui-Ying Jia; Yu Zhang; Xiao-Yi Ding; Dan-Yang Zhou; Hui-Ping Chen; Xiao-Hua Jiang; Bin Cui; Xiao-Ying Li; Guang Ning
Journal:  Endocrine       Date:  2009-01-22       Impact factor: 3.633

10.  Early presentation of gait impairment in Wolfram Syndrome.

Authors:  Kristen A Pickett; Ryan P Duncan; James Hoekel; Bess Marshall; Tamara Hershey; Gammon M Earhart
Journal:  Orphanet J Rare Dis       Date:  2012-12-08       Impact factor: 4.123

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