Assortative mating and within-spouse pair comparisons

被引:10
作者
Howe, Laurence J. [1 ,2 ]
Battram, Thomas [1 ,2 ]
Morris, Tim T. [1 ,2 ]
Hartwig, Fernando P. [1 ,3 ]
Hemani, Gibran [1 ,2 ]
Davies, Neil M. [1 ,2 ,4 ]
Smith, George Davey [1 ,2 ]
机构
[1] Univ Bristol, Med Res Council Integrat Epidemiol Unit, Populat Hlth Sci, Bristol, Avon, England
[2] Univ Bristol, Bristol Med Sch, Populat Hlth Sci, Bristol, Avon, England
[3] Univ Fed Pelotas, Postgrad Program Epidemiol, Pelotas, RS, Brazil
[4] Norwegian Univ Sci & Technol, KG Jebsen Ctr Genet Epidemiol, Dept Publ Hlth & Nursing, Trondheim, Norway
来源
PLOS GENETICS | 2021年 / 17卷 / 11期
基金
英国医学研究理事会;
关键词
GENOME-WIDE ASSOCIATION; MENDELIAN RANDOMIZATION; HEALTH; EPIDEMIOLOGY; POPULATION; VARIANTS; GENETICS; LINKAGE; DISEQUILIBRIUM; CONVERGENCE;
D O I
10.1371/journal.pgen.1009883
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Author summary There is growing evidence that genome-wide association studies capture associations relating to environmental factors, such as indirect effects from parental genotypes. Within-family models such as sibling comparisons can be used to disentangles these different sources of association but are limited by the paucity of sibling data in large biobanks. Within-spouse pair models are a potentially tractable model because spouses share environmental factors in adulthood and may also share early-life environmental factors. Here, we evaluated the application of within-spouse models in genetic association studies, specifically considering assortative mating, a phenomenon whereby individuals may select a phenotypically similar partner. We found that within-spouse pair models can detect genuine confounding in genetic association estimates but are potentially susceptible to collider bias induced by comparing assorted pairs. Within-spouse pair estimates could be useful when combining evidence from different study designs.</p> Spousal comparisons have been proposed as a design that can both reduce confounding and estimate effects of the shared adulthood environment. However, assortative mating, the process by which individuals select phenotypically (dis)similar mates, could distort associations when comparing spouses. We evaluated the use of spousal comparisons, as in the within-spouse pair (WSP) model, for aetiological research such as genetic association studies. We demonstrated that the WSP model can reduce confounding but may be susceptible to collider bias arising from conditioning on assorted spouse pairs. Analyses using UK Biobank spouse pairs found that WSP genetic association estimates were smaller than estimates from random pairs for height, educational attainment, and BMI variants. Within-sibling pair estimates, robust to demographic and parental effects, were also smaller than random pair estimates for height and educational attainment, but not for BMI. WSP models, like other within-family models, may reduce confounding from demographic factors in genetic association estimates, and so could be useful for triangulating evidence across study designs to assess the robustness of findings. However, WSP estimates should be interpreted with caution due to potential collider bias.</p>
引用
收藏
页数:18
相关论文
共 70 条
  • [1] A general test of association for quantitative traits in nuclear families
    Abecasis, GR
    Cardon, LR
    Cookson, WOC
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (01) : 279 - 292
  • [2] UK Biobank Data: Come and Get It
    Allen, Naomi E.
    Sudlow, Cathie
    Peakman, Tim
    Collins, Rory
    [J]. SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (224)
  • [3] Statistics Notes - Interaction revisited: the difference between two estimates
    Altman, DG
    Bland, JM
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 2003, 326 (7382): : 219 - 219
  • [4] A global reference for human genetic variation
    Altshuler, David M.
    Durbin, Richard M.
    Abecasis, Goncalo R.
    Bentley, David R.
    Chakravarti, Aravinda
    Clark, Andrew G.
    Donnelly, Peter
    Eichler, Evan E.
    Flicek, Paul
    Gabriel, Stacey B.
    Gibbs, Richard A.
    Green, Eric D.
    Hurles, Matthew E.
    Knoppers, Bartha M.
    Korbel, Jan O.
    Lander, Eric S.
    Lee, Charles
    Lehrach, Hans
    Mardis, Elaine R.
    Marth, Gabor T.
    McVean, Gil A.
    Nickerson, Deborah A.
    Wang, Jun
    Wilson, Richard K.
    Boerwinkle, Eric
    Doddapaneni, Harsha
    Han, Yi
    Korchina, Viktoriya
    Kovar, Christie
    Lee, Sandra
    Muzny, Donna
    Reid, Jeffrey G.
    Zhu, Yiming
    Chang, Yuqi
    Feng, Qiang
    Fang, Xiaodong
    Guo, Xiaosen
    Jian, Min
    Jiang, Hui
    Jin, Xin
    Lan, Tianming
    Li, Guoqing
    Li, Jingxiang
    Li, Yingrui
    Liu, Shengmao
    Liu, Xiao
    Lu, Yao
    Ma, Xuedi
    Tang, Meifang
    Wang, Bo
    [J]. NATURE, 2015, 526 (7571) : 68 - +
  • [5] Regional variation in health is predominantly driven by lifestyle rather than genetics
    Amador, Carmen
    Xia, Charley
    Nagy, Reka
    Campbell, Archie
    Porteous, David
    Smith, Blair H.
    Hastie, Nick
    Vitart, Veronique
    Hayward, Caroline
    Navarro, Pau
    Haley, Chris S.
    [J]. NATURE COMMUNICATIONS, 2017, 8
  • [6] Non-random Mating and Convergence Over Time for Mental Health, Life Satisfaction, and Personality: The Nord-Trondelag Health Study
    Ask, Helga
    Idstad, Mariann
    Engdahl, Bo
    Tambs, Kristian
    [J]. BEHAVIOR GENETICS, 2013, 43 (02) : 108 - 119
  • [7] Non-Random Mating and Convergence Over Time for Alcohol Consumption, Smoking, and Exercise: The Nord-Trondelag Health Study
    Ask, Helga
    Rognmo, Kamilla
    Torvik, Fartein Ask
    Roysamb, Espen
    Tambs, Kristian
    [J]. BEHAVIOR GENETICS, 2012, 42 (03) : 354 - 365
  • [8] Barbu MC, 2021, MOL PSYCHIATR, V26, P5112, DOI [10.1038/s41380-020-0808-3, 10.1051/matecconf/202030500001]
  • [9] Population Genetics: Why structure matters
    Barton, Nick
    Hermisson, Joachim
    Nordborg, Magnus
    [J]. ELIFE, 2019, 8
  • [10] Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics
    Beaumont, Robin N.
    Warrington, Nicole M.
    Cavadino, Alana
    Tyrrell, Jessica
    Nodzenski, Michael
    Horikoshi, Momoko
    Geller, Frank
    Myhre, Ronny
    Richmond, Rebecca C.
    Paternoster, Lavinia
    Bradfield, Jonathan P.
    Kreiner-Moller, Eskil
    Huikari, Ville
    Metrustry, Sarah
    Lunetta, Kathryn L.
    Painter, Jodie N.
    Hottenga, Jouke-Jan
    Allard, Catherine
    Barton, Sheila J.
    Espinosa, Ana
    Marsh, Julie A.
    Potter, Catherine
    Zhang, Ge
    Ang, Wei
    Berry, Diane J.
    Bouchard, Luigi
    Das, Shikta
    Hakonarson, Hakon
    Heikkinen, Jani
    Helgeland, Oyvind
    Hocher, Berthold
    Hofman, Albert
    Inskip, Hazel M.
    Jones, Samuel E.
    Kogevinas, Manolis
    Lind, Penelope A.
    Marullo, Letizia
    Medland, Sarah E.
    Murray, Anna
    Murray, Jeffrey C.
    Njolstad, Pal R.
    Nohr, Ellen A.
    Reichetzeder, Christoph
    Ring, Susan M.
    Ruth, Katherine S.
    Santa-Marina, Loreto
    Scholtens, Denise M.
    Sebert, Sylvain
    Sengpiel, Verena
    Tuke, Marcus A.
    [J]. HUMAN MOLECULAR GENETICS, 2018, 27 (04) : 742 - 756