Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia

被引:0
|
作者
Alexandros Rammos
George Kirov
Leon Hubbard
James T. R. Walters
Peter Holmans
Michael J. Owen
Michael C. O’Donovan
Elliott Rees
机构
[1] Cardiff University,Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences
来源
Molecular Psychiatry | 2023年 / 28卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Impaired cognition in schizophrenia is associated with worse functional outcomes. While genetic factors are known to contribute to variation in cognition in schizophrenia, few rare coding variants with strong effects have been identified, and the relative effects from de novo, inherited and non-transmitted alleles are unknown. We used array and exome sequencing data from 656 proband-parent trios to examine the contribution of common and rare variants to school performance, and by implication cognitive function, in schizophrenia. Parental transmission of common alleles contributing to higher educational attainment (p value = 0.00015; OR = 2.63) and intelligence (p value = 0.00009; OR = 2.80), but not to schizophrenia, were associated with higher proband school performance. No significant effects were seen for non-transmitted parental common alleles. Probands with lower school performance were enriched for damaging de novo coding variants in genes associated with developmental disorders (DD) (p value = 0.00026; OR = 11.6). Damaging, ultra-rare coding variants in DD genes that were transmitted or non-transmitted from parents, had no effects on school performance. Among probands with lower school performance, those with damaging de novo coding variants in DD genes had a higher rate of comorbid mild intellectual disability (p value = 0.0002; OR = 15.6). Overall, we provide evidence for rare and common genetic contributions to school performance in schizophrenia. The strong effects for damaging de novo coding variants in DD genes provide further evidence that cognitive impairment in schizophrenia has a shared aetiology with developmental disorders. Furthermore, we report no evidence in this sample that non-transmitted parental common alleles for cognitive traits contributed to school performance in schizophrenia via indirect effects on the environment.
引用
收藏
页码:2081 / 2087
页数:6
相关论文
共 50 条
  • [1] Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia
    Rammos, Alexandros
    Kirov, George
    Hubbard, Leon
    Walters, James T. R.
    Holmans, Peter
    Owen, Michael J.
    O'Donovan, Michael C.
    Rees, Elliott
    MOLECULAR PSYCHIATRY, 2023, 28 (05) : 2081 - 2087
  • [2] Analysis of Rare Genetic Variants in Family-based Sequence Data
    Sung, Yun Ju
    Wang, Lihua
    Rao, D. C.
    GENETIC EPIDEMIOLOGY, 2012, 36 (02) : 129 - 129
  • [3] Family-based genetic analysis in schizophrenia by whole-exome sequence to identify rare pathogenic variants
    Shang, Binli
    Yang, Runxu
    Lian, Kun
    Dong, Lei
    Liu, Hongbing
    Wang, Tianlan
    Yang, Guangya
    Xi, Kang
    Xu, Xiufeng
    Cheng, Yuqi
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2024, 195 (05)
  • [4] A SEARCH FOR RARE GENETIC VARIANTS IN A FAMILY-BASED STUDY OF AUTISM
    Ghralaigh, Fiana Ni
    Kenny, Elaine
    Gallagher, Louise
    Lopez, Lorna
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2019, 29 : 1278 - 1278
  • [5] Different approaches for dealing with rare variants in family-based genetic studies: application of a Genetic Analysis Workshop 17 problem
    Marcio Augusto Alfonso de Almeida
    Andrea Roseli Vançan Russo Horimoto
    Paulo Sérgio Lopes de Oliveira
    José Eduardo Krieger
    Alexandre da Costa Pereira
    BMC Proceedings, 5 (Suppl 9)
  • [6] The relative contribution of common and rare genetic variants to ADHD
    J Martin
    M C O'Donovan
    A Thapar
    K Langley
    N Williams
    Translational Psychiatry, 2015, 5 : e506 - e506
  • [7] The relative contribution of common and rare genetic variants to ADHD
    Martin, J.
    O'Donovan, M. C.
    Thapar, A.
    Langley, K.
    Williams, N.
    TRANSLATIONAL PSYCHIATRY, 2015, 5 : e506 - e506
  • [8] Common and Rare DUOX Variants in Patients With Congenital Hypothyroidism: Case-control Study and Family-based Analysis
    Jia, Yaning
    Wang, Xiaoyu
    Zhang, Liqin
    Duan, Yanan
    Zou, Hui
    Wang, Fengqi
    Liu, Xiangju
    Li, Miaomiao
    Liu, Shiguo
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2025,
  • [9] Rare variants are common in schizophrenia
    Jacob Gratten
    Nature Neuroscience, 2016, 19 : 1426 - 1428
  • [10] Rare variants are common in schizophrenia
    Gratten, Jacob
    NATURE NEUROSCIENCE, 2016, 19 (11) : 1426 - 1428