Genome-wide association study of abdominal MRI-measured visceral fat: The multiethnic cohort adiposity phenotype study

被引:2
作者
Streicher, Samantha A. A. [1 ]
Lim, Unhee [1 ]
Park, S. Lani [1 ]
Li, Yuqing [2 ]
Sheng, Xin [3 ]
Hom, Victor [3 ]
Xia, Lucy [3 ]
Pooler, Loreall [3 ]
Shepherd, John [1 ]
Loo, Lenora W. M. [1 ]
Ernst, Thomas [4 ]
Buchthal, Steven [1 ]
Franke, Adrian A. A. [1 ]
Tiirikainen, Maarit [1 ]
Wilkens, Lynne R. [1 ]
Haiman, Christopher A. A. [3 ]
Stram, Daniel O. O. [3 ]
Cheng, Iona [2 ]
Le Marchand, Loic [1 ]
机构
[1] Univ Hawaii Manoa, Univ Hawaii, Canc Ctr, Honolulu, HI 96822 USA
[2] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA USA
[3] Univ Southern Calif, Ctr Genet Epidemiol, Keck Sch Med, Dept Prevent Med, Los Angeles, CA USA
[4] Univ Maryland, Sch Med, Baltimore, MD USA
来源
PLOS ONE | 2023年 / 18卷 / 01期
基金
美国国家卫生研究院;
关键词
HOMEOSTASIS MODEL ASSESSMENT; CANCER; STRATIFICATION; OBESITY; PLASMA; HEALTH; LOCI;
D O I
10.1371/journal.pone.0279932
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Few studies have explored the genetic underpinnings of intra-abdominal visceral fat deposition, which varies substantially by sex and race/ethnicity. Among 1,787 participants in the Multiethnic Cohort (MEC)-Adiposity Phenotype Study (MEC-APS), we conducted a genome-wide association study (GWAS) of the percent visceral adiposity tissue (VAT) area out of the overall abdominal area, averaged across L1-L5 (%VAT), measured by abdominal magnetic resonance imaging (MRI). A genome-wide significant signal was found on chromosome 2q14.3 in the sex-combined GWAS (lead variant rs79837492: Beta per effect allele = -4.76; P = 2.62 x 10(-8)) and in the male-only GWAS (lead variant rs2968545: (Beta = -6.50; P = 1.09 x 10(-9)), and one suggestive variant was found at 13q12.11 in the female-only GWAS (rs79926925: Beta = 6.95; P = 8.15 x 10(-8)). The negatively associated variants were most common in European Americans (T allele of rs79837492; 5%) and African Americans (C allele of rs2968545; 5%) and not observed in Japanese Americans, whereas the positively associated variant was most common in Japanese Americans (C allele of rs79926925, 5%), which was all consistent with the racial/ethnic %VAT differences. In a validation step among UK Biobank participants (N = 23,699 of mainly British and Irish ancestry) with MRI-based VAT volume, both rs79837492 (Beta = -0.026, P = 0.019) and rs2968545 (Beta = -0.028, P = 0.010) were significantly associated in men only (n = 11,524). In the MEC-APS, the association between rs79926925 and plasma sex hormone binding globulin levels reached statistical significance in females, but not in males, with adjustment for total adiposity (Beta = -0.24; P = 0.028), on the log scale. Rs79837492 and rs2968545 are located in intron 5 of CNTNAP5, and rs79926925, in an intergenic region between GJB6 and CRYL1. These novel findings differing by sex and racial/ethnic group warrant replication in additional diverse studies with direct visceral fat measurements.
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共 57 条
  • [1] Health Effects of Overweight and Obesity in 195 Countries over 25 Years
    Afshin, Ashkan
    Forouzanfar, Mohammad H.
    Reitsma, Marissa B.
    Sur, Patrick
    Estep, Kara
    Lee, Alex
    Marczak, Laurie
    Mokdad, Ali H.
    Moradi-Lakeh, Maziar
    Naghavi, Mohsen
    Salama, Joseph S.
    Vos, Theo
    Abate, Kalkidan H.
    Abbafati, Cristiana
    Ahmed, Muktar B.
    Al-Aly, Ziyad
    Alkerwi, Ala'a
    Al-Raddadi, Rajaa
    Amare, Azmeraw T.
    Amberbir, Alemayehu
    Amegah, Adeladza K.
    Amini, Erfan
    Amrock, Stephen M.
    Anjana, Ranjit M.
    Arnlov, Johan
    Asayesh, Hamid
    Banerjee, Amitava
    Barac, Aleksandra
    Baye, Estifanos
    Bennett, Derrick A.
    Beyene, Addisu S.
    Biadgilign, Sibhatu
    Biryukov, Stan
    Bjertness, Espen
    Boneya, Dube J.
    Campos-Nonato, Ismael
    Carrero, Juan J.
    Cecilio, Pedro
    Cercy, Kelly
    Ciobanu, Liliana G.
    Cornaby, Leslie
    Damtew, Solomon A.
    Dandona, Lalit
    Dandona, Rakhi
    Dharmaratne, Samath D.
    Duncan, Bruce B.
    Eshrati, Babak
    Esteghamati, Alireza
    Feigin, Valery L.
    Fernandes, Joao C.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2017, 377 (01) : 13 - 27
  • [2] Autism spectrum disorder and intellectual disability in an inherited 2q14.3 micro-deletion involving CNTNAP5
    Aleo, Sebastiano
    Milani, Donatella
    Pansa, Alessandra
    Marchisio, Paola
    Guerneri, Silvana
    Silipigni, Rosamaria
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2020, 182 (12) : 3071 - 3073
  • [3] An integrated map of genetic variation from 1,092 human genomes
    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.
    Schmidt, Jeanette P.
    Sherry, Stephen T.
    Wang, Jun
    Wilson, Richard K.
    Gibbs, Richard A.
    Dinh, Huyen
    Kovar, Christie
    Lee, Sandra
    Lewis, Lora
    Muzny, Donna
    Reid, Jeff
    Wang, Min
    Wang, Jun
    Fang, Xiaodong
    Guo, Xiaosen
    Jian, Min
    Jiang, Hui
    Jin, Xin
    Li, Guoqing
    Li, Jingxiang
    Li, Yingrui
    Li, Zhuo
    Liu, Xiao
    Lu, Yao
    Ma, Xuedi
    Su, Zhe
    Tai, Shuaishuai
    Tang, Meifang
    [J]. NATURE, 2012, 491 (7422) : 56 - 65
  • [4] [Anonymous], 2006, QUANTO 1 1 COMPUTER
  • [5] [Anonymous], 2020, SCIENCE, V369, P318
  • [6] Who Are the Okinawans? Ancestry, Genome Diversity, and Implications for the Genetic Study of Human Longevity From a Geographically Isolated Population
    Bendjilali, Nasrine
    Hsueh, Wen-Chi
    He, Qimei
    Willcox, D. Craig
    Nievergelt, Caroline M.
    Donlon, Timothy A.
    Kwok, Pui-Yan
    Suzuki, Makoto
    Willcox, Bradley J.
    [J]. JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2014, 69 (12): : 1474 - 1484
  • [7] Changes in Whole Blood Gene Expression in Obese Subjects with Type 2 Diabetes Following Bariatric Surgery: a Pilot Study
    Berisha, Stela Z.
    Serre, David
    Schauer, Philip
    Kashyap, Sangeeta R.
    Smith, Jonathan D.
    [J]. PLOS ONE, 2011, 6 (03):
  • [8] Identification of metabolism genes related to hepatocarcinogenesis and progression in type 2 diabetes mellitus via co-expression networks analysis
    Bi, Yiming
    Yin, Bei
    Fan, Guanjie
    [J]. HEREDITAS, 2021, 158 (01)
  • [9] Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array
    Bien, Stephanie A.
    Wojcik, Genevieve L.
    Zubair, Niha
    Gignoux, Christopher R.
    Martin, Alicia R.
    Kocarnik, Jonathan M.
    Martin, Lisa W.
    Buyske, Steven
    Haessler, Jeffrey
    Walker, Ryan W.
    Cheng, Iona
    Graff, Mariaelisa
    Xia, Lucy
    Franceschini, Nora
    Matise, Tara
    James, Regina
    Hindorff, Lucia
    Le Marchand, Loic
    North, Kari E.
    Haiman, Christopher A.
    Peters, Ulrike
    Loos, Ruth J. F.
    Kooperberg, Charles L.
    Bustamante, Carlos D.
    Kenny, Eimear E.
    Carlson, Christopher S.
    [J]. PLOS ONE, 2016, 11 (12):
  • [10] The UK Biobank resource with deep phenotyping and genomic data
    Bycroft, Clare
    Freeman, Colin
    Petkova, Desislava
    Band, Gavin
    Elliott, Lloyd T.
    Sharp, Kevin
    Motyer, Allan
    Vukcevic, Damjan
    Delaneau, Olivier
    O'Connell, Jared
    Cortes, Adrian
    Welsh, Samantha
    Young, Alan
    Effingham, Mark
    McVean, Gil
    Leslie, Stephen
    Allen, Naomi
    Donnelly, Peter
    Marchini, Jonathan
    [J]. NATURE, 2018, 562 (7726) : 203 - +