Submitted by ja607 on
Title | Genetics of schizophrenia in the South African Xhosa. |
Publication Type | Journal Article |
Year of Publication | 2020 |
Authors | Gulsuner, S, Stein, DJ, Susser, ES, Sibeko, G, Pretorius, A, Walsh, T, Majara, L, Mndini, MM, Mqulwana, SG, Ntola, OA, Casadei, S, Ngqengelele, LL, Korchina, V, van der Merwe, C, Malan, M, Fader, KM, Feng, M, Willoughby, E, Muzny, D, Baldinger, A, Andrews, HF, Gur, RC, Gibbs, RA, Zingela, Z, Nagdee, M, Ramesar, RS, King, M-C, McClellan, JM |
Journal | Science |
Volume | 367 |
Issue | 6477 |
Pagination | 569-573 |
Date Published | 2020 01 31 |
ISSN | 1095-9203 |
Keywords | Age Factors, Autistic Disorder, Bipolar Disorder, Dopamine, Female, gamma-Aminobutyric Acid, Genetic Variation, Glutamine, Humans, Male, Mutation, Neural Pathways, Schizophrenia, Sex Factors, South Africa, Synapses, Synaptic Transmission |
Abstract | Africa, the ancestral home of all modern humans, is the most informative continent for understanding the human genome and its contribution to complex disease. To better understand the genetics of schizophrenia, we studied the illness in the Xhosa population of South Africa, recruiting 909 cases and 917 age-, gender-, and residence-matched controls. Individuals with schizophrenia were significantly more likely than controls to harbor private, severely damaging mutations in genes that are critical to synaptic function, including neural circuitry mediated by the neurotransmitters glutamine, γ-aminobutyric acid, and dopamine. Schizophrenia is genetically highly heterogeneous, involving severe ultrarare mutations in genes that are critical to synaptic plasticity. The depth of genetic variation in Africa revealed this relationship with a moderate sample size and informed our understanding of the genetics of schizophrenia worldwide. |
DOI | 10.1126/science.aay8833 |
Alternate Journal | Science |
PubMed ID | 32001654 |
Grant List | U01 MH096756 / MH / NIMH NIH HHS / United States U01 MH096754 / MH / NIMH NIH HHS / United States U01 MH096844 / MH / NIMH NIH HHS / United States UM1 HG008898 / HG / NHGRI NIH HHS / United States |