1. Age dependent association of inbreeding with risk for schizophrenia in Egypt
- Author
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Salwa Tobar, Ahmed Eissa, Nahed E. Ibrahim, Shawn Wood, Serkan Erdin, Bernie Devlin, Wafaa El-Bahaei, Ahmed R. Ali, Warda Fathi, Hala El-Boraie, Amal Yassein, Ibtihal Ibrahim, Lambertus Klei, Eman Elsheshtawy, Vishwajit L. Nimgaonkar, Alina Maysterchuk, Hanan El Sayed, Lora McClain, Hala Salah, Farha A El-Chennawi, Chowdari Kodavali, Joel Wood, Hader Mansour, and Michael E. Talkowski
- Subjects
Adult ,Microcephaly ,Consanguinity ,Biology ,Polymorphism, Single Nucleotide ,Article ,03 medical and health sciences ,0302 clinical medicine ,medicine ,Humans ,Inbreeding ,Risk factor ,Genotyping ,Biological Psychiatry ,Exome sequencing ,Genetics ,Homozygote ,medicine.disease ,030227 psychiatry ,Psychiatry and Mental health ,Schizophrenia ,Statistical genetics ,Egypt ,030217 neurology & neurosurgery - Abstract
Background Self-reported consanguinity is associated with risk for schizophrenia (SZ) in several inbred populations, but estimates using DNA-based coefficients of inbreeding are unavailable. Further, it is not known whether recessively inherited risk mutations can be identified through homozygosity by descent (HBD) mapping. Methods We studied self-reported and DNA-based estimates of inbreeding among Egyptian patients with SZ (n = 421, DSM IV criteria) and adult controls without psychosis (n = 301), who were evaluated using semi-structured diagnostic interview schedules and genotyped using the Illumina Infinium PsychArray. Following quality control checks, coefficients of inbreeding (F) and regions of homozygosity (ROH) were estimated using PLINK software for HBD analysis. Exome sequencing was conducted in selected cases. Results Inbreeding was associated with schizophrenia based on self-reported consanguinity (χ2 = 4.506, 1 df, p = 0.034) and DNA-based estimates for inbreeding (F); the latter with a significant F × age interaction (β = 32.34, p = 0.0047). The association was most notable among patients older than age 40 years. Eleven ROH were over-represented in cases on chromosomes 1, 3, 6, 11, and 14; all but one region is novel for schizophrenia risk. Exome sequencing identified six recessively-acting genes in ROH with loss-of-function variants; one of which causes primary hereditary microcephaly. Conclusions We propose consanguinity as an age-dependent risk factor for SZ in Egypt. HBD mapping is feasible for SZ in adequately powered samples.
- Published
- 2020
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