Age dependent association of inbreeding with risk for schizophrenia in Egypt
Copyright © 2019 Elsevier B.V. All rights reserved..
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.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2020 |
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| Erschienen: |
2020 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:216 |
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| Enthalten in: |
Schizophrenia research - 216(2020) vom: 09. Feb., Seite 450-459 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
McClain, Lora [VerfasserIn] |
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| Links: |
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| Themen: |
Consanguinity |
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| Anmerkungen: |
Date Completed 17.06.2021 Date Revised 17.06.2021 published: Print-Electronic Citation Status MEDLINE |
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| doi: |
10.1016/j.schres.2019.10.039 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM305275704 |
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| 245 | 1 | 0 | |a Age dependent association of inbreeding with risk for schizophrenia in Egypt |
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| 500 | |a Date Revised 17.06.2021 | ||
| 500 | |a published: Print-Electronic | ||
| 500 | |a Citation Status MEDLINE | ||
| 520 | |a Copyright © 2019 Elsevier B.V. All rights reserved. | ||
| 520 | |a 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 | ||
| 520 | |a 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 | ||
| 520 | |a 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 | ||
| 520 | |a CONCLUSIONS: We propose consanguinity as an age-dependent risk factor for SZ in Egypt. HBD mapping is feasible for SZ in adequately powered samples | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Research Support, N.I.H., Extramural | |
| 650 | 4 | |a Research Support, Non-U.S. Gov't | |
| 650 | 4 | |a Consanguinity | |
| 650 | 4 | |a Genotyping | |
| 650 | 4 | |a Psychosis | |
| 650 | 4 | |a Statistical genetics | |
| 700 | 1 | |a Mansour, Hader |e verfasserin |4 aut | |
| 700 | 1 | |a Ibrahim, Ibtihal |e verfasserin |4 aut | |
| 700 | 1 | |a Klei, Lambertus |e verfasserin |4 aut | |
| 700 | 1 | |a Fathi, Warda |e verfasserin |4 aut | |
| 700 | 1 | |a Wood, Joel |e verfasserin |4 aut | |
| 700 | 1 | |a Kodavali, Chowdari |e verfasserin |4 aut | |
| 700 | 1 | |a Maysterchuk, Alina |e verfasserin |4 aut | |
| 700 | 1 | |a Wood, Shawn |e verfasserin |4 aut | |
| 700 | 1 | |a El-Chennawi, Farha |e verfasserin |4 aut | |
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| 700 | 1 | |a Talkowski, Michael |e verfasserin |4 aut | |
| 700 | 1 | |a Nimgaonkar, Vishwajit |e verfasserin |4 aut | |
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