Journal Home
Search for

Volume 120, Issue 1, Pages 108-112 (July 2010)


View previous. 17 of 39 View next.

Consanguinity and increased risk for schizophrenia in Egypt

Hader Mansourab, Warda Fathib, Lambertus Kleia, Joel Wooda, Kodavali Chowdaria, Annie Watsona, Ahmed Eissab, Mai Elassyb, Ibtihal Alib, Hala Salahb, Amal Yassinb, Salwa Tobarb, Hala El-Boraieb, Hanan Gaafarb, Nahed E. Ibrahima, Kareem Kandila, Wafaa El-Bahaeib, Osama El-Boraieb, Mohamed Alatrounyb, Farha El-Chennawic, Bernie Devlinad, Vishwajit L. NimgaonkaradCorresponding Author Informationemail address

Received 4 January 2010; accepted 22 March 2010. published online 03 May 2010.

Abstract 

Background

Consanguinity has been suggested as a risk factor for psychoses in some Middle Eastern countries, but adequate control data are unavailable. Our recent studies in Egypt have shown elevated parental consanguinity rates among patients with bipolar I disorder (BP1), compared with controls. We have now extended our analyses to schizophrenia (SZ) in the same population.

Methods

A case–control study was conducted at Mansoura University Hospital, Mansoura, Egypt (SZ, n=75; controls, n=126, and their available parents). The prevalence of consanguinity was estimated from family history data (‘self report’), followed by DNA analysis using short tandem repeat polymorphisms (STRPs, n=63) (‘DNA-based’ rates).

Results

Self-reported consanguinity was significantly elevated among the patients (SZ: 46.6%, controls: 19.8%, OR 3.53, 95% CI 1.88, 6.64; p=0.000058, 1 d.f.). These differences were confirmed using DNA-based estimates for coefficients of inbreeding (inbreeding coefficients as means±standard error, cases: 0.058±0.007, controls: 0.022±0.003).

Conclusions

Consanguinity rates are signifcantly elevated among Egyptian SZ patients in the Nile delta region. The associations are similar to those observed with BP1 in our earlier study. If replicated, the substantial risk associated with consanguinity raises public health concerns. They may also pave the way for gene mapping studies.

a Department of Psychiatry, University of Pittsburgh School of Medicine, Western Psychiatric Institute and Clinic, Pittsburgh, PA, United States

b Department of Psychiatry, Mansoura University School of Medicine, Mansoura, Egypt

c Department of Clinical Pathology, Mansoura University School of Medicine, Mansoura, Egypt

d Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States

Corresponding Author InformationCorresponding author. WPIC, Room. 441, 3811 O'Hara Street, Pittsburgh, PA 15213, United States. Tel.: +1 412 246 6353; fax: +1 412 246 6350.

PII: S0920-9964(10)01197-7

doi:10.1016/j.schres.2010.03.026


View previous. 17 of 39 View next.