Associations of ethnicity, skin tone, and genome-wide sequencing with bone mineral density in adolescents

被引:1
|
作者
Gordon, Catherine M. [1 ]
Fleisch, Abby F. [2 ,3 ]
Hivert, Marie-France [4 ,5 ,6 ]
Rokoff, Lisa B. [2 ]
Rifas-Shiman, Sheryl L. [5 ,6 ]
Raphael, Jean L. [7 ,8 ]
Oken, Emily [5 ,6 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Huma, Div Intramural Res, Bethesda, MD 20892 USA
[2] MaineHlth Inst Res, Ctr Interdisciplinary Populat & Hlth Res, Portland, ME USA
[3] Maine Med Ctr, Pediat Endocrinol & Diabet, Portland, ME USA
[4] Massachusetts Gen Hosp, Diabet Unit, Boston, MA USA
[5] Harvard Med Sch, Dept Populat Med, Div Chron Dis Res Lifecourse, Boston, MA USA
[6] Harvard Pilgrim Hlth Care Inst, Boston, MA USA
[7] Texas Childrens Hosp, Dept Pediat, Houston, TX USA
[8] Baylor Coll Med, Houston, TX USA
基金
美国国家卫生研究院;
关键词
GENETIC DIVERSITY; BLACK; RACE; FRACTURES; RISK; AGE; DETERMINANTS; METAANALYSIS; CHILDREN; HISTORY;
D O I
10.1038/s41390-024-03588-4
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BackgroundDual-energy x-ray absorptiometry reference data designate Black and non-Black categories, as higher BMD has been documented among Black youth. We examined associations of race, skin tone, and genetic factors with bone mineral density (BMD).Methods557 adolescents were followed longitudinally. Exposures included race, skin tone, and principal components (PC) from genome-wide arrays. Total body BMD Z-score (BMD-Z) was the primary outcome using linear regression.Results359 adolescents identified as non-Hispanic White (NHW) and 75, non-Hispanic Black (NHB). BMD-Z was higher in NHB vs. NHW (beta: 0.92 units, 95% CI: 0.64, 1.19) or those with darker skin (0.79, 95% CI: 0.49, 1.08 for brown vs. medium). The first genetic PC (PC1) correlated with identification as NHB. PC1 was associated with higher BMD-Z (0.09, 95% CI: 0.06, 0.12), even after including race (0.07, 95% CI: 0.00, 0.14) or skin tone (0.10, 95% CI: 0.05, 0.15); both race (0.26, 95% CI: -0.49, 1.01 for NHB vs. NHW) and skin tone (-0.08, 95% CI: -0.59, 0.44 for brown vs. medium) no longer predicted BMD-Z after adjustment for PC1.ConclusionGenetic similarity was robustly associated with BMD, prompting a reevaluation of adolescent BMD reference data to exclude the consideration of race.ImpactCurrent bone density reference databases include a binary assignment of patients into "Black" and "non-Black" categories, as a higher BMD has been documented among those identifying as Black compared with individuals of other racial and ethnic backgrounds.This study found genetic similarity to be more strongly associated with bone density by dual-energy x-ray absorptiometry than race or skin tone.These data emphasize a need to reevaluate how bone density measurements are interpreted, including exploring reference data that exclude the consideration of race.
引用
收藏
页数:7
相关论文
共 50 条
  • [21] Individualized evaluation of lumbar bone mineral density and bone mineral apparent density in children and adolescents
    Duran, Ibrahim
    Martakis, K.
    Rehberg, M.
    Semler, O.
    Schoenau, E.
    ARCHIVES OF OSTEOPOROSIS, 2018, 13 (01)
  • [22] A genome-wide genomic score added to standard recommended stratification tools does not improve the identification of patients with very low bone mineral density
    Therkildsen, J.
    Rohde, P. D.
    Nissen, L.
    Thygesen, J.
    Hauge, E. -m.
    Langdahl, B. L.
    Boettcher, M.
    Nyegaard, M.
    Winther, S.
    OSTEOPOROSIS INTERNATIONAL, 2023, 34 (11) : 1893 - 1906
  • [23] Identification of novel variants and candidate genes associated with porcine bone mineral density using genome-wide association study
    Nan, Jiuhong-H
    Yin, Lilin-L
    Tang, Zhenshuang-S
    Xiang, Tao
    Ma, Guanjun-J
    Li, Xinyun-Y
    Liu, Xiaolei-L
    Zhao, Shuhong-H
    Liu, Xiangdong-D
    JOURNAL OF ANIMAL SCIENCE, 2020, 98 (04)
  • [24] Genome-wide association study identifies genetic variants which predict the response of bone mineral density to teriparatide therapy
    Alonso, Nerea
    Albagha, Omar M. E.
    Azfer, Asim
    Larraz-Prieto, Beatriz
    Berg, Kathryn
    Riches, Philip L.
    Ostanek, Barbara
    Kocjan, Tomaz
    Marc, Janja
    Langdahl, Bente L.
    Ralston, Stuart H.
    ANNALS OF THE RHEUMATIC DISEASES, 2023, 82 (07) : 985 - 991
  • [25] Association of JAG1 with Bone Mineral Density and Osteoporotic Fractures: A Genome-wide Association Study and Follow-up Replication Studies
    Kung, Annie W. C.
    Xiao, Su-Mei
    Cherny, Stacey
    Li, Gloria H. Y.
    Gao, Yi
    Tso, Gloria
    Lau, Kam S.
    Luk, Keith D. K.
    Liu, Jian-min
    Cui, Bin
    Zhang, Min-Jia
    Zhang, Zhen-lin
    He, Jin-wei
    Yue, Hua
    Xia, Wia-bo
    Luo, Lian-mei
    He, Shu-li
    Kiel, Douglas P.
    Karasik, David
    Hsu, Yi-Hsiang
    Cupples, L. Adrienne
    Demissie, Serkalem
    Styrkarsdottir, Unnur
    Halldorsson, Bjarni V.
    Sigurdsson, Gunnar
    Thorsteinsdottir, Unnur
    Stefansson, Kari
    Richards, J. Brent
    Zhai, Guangju
    Soranzo, Nicole
    Valdes, Ana
    Spector, Tim D.
    Sham, Pak C.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2010, 86 (02) : 229 - 239
  • [26] Associations between a posteriori defined dietary patterns and bone mineral density in adolescents
    Monjardino, Teresa
    Lucas, Raquel
    Ramos, Elisabete
    Lopes, Carla
    Gaio, Rita
    Barros, Henrique
    EUROPEAN JOURNAL OF NUTRITION, 2015, 54 (02) : 273 - 282
  • [27] A Pilot Genome-Wide Association Study in Postmenopausal Mexican-Mestizo Women Implicates the RMND1/CCDC170 Locus Is Associated with Bone Mineral Density
    Villalobos-Comparan, Marisela
    Jimenez-Ortega, Rogelio F.
    Estrada, Karol
    Parra-Torres, Alma Y.
    Gonzalez-Mercado, Anahi
    Patino, Nelly
    Castillejos-Lopez, Manuel
    Quiterio, Manuel
    Carlos Fernandez-Lopez, Juan
    Ibarra, Bertha
    Romero-Hidalgo, Sandra
    Salmeron, Jorge
    Velazquez-Cruz, Rafael
    INTERNATIONAL JOURNAL OF GENOMICS, 2017, 2017
  • [28] Gut microbiota is associated with bone mineral density AN OBSERVATIONAL AND GENOME-wIDE ENVIRONMENTAL INTERACTION ANALYSIS IN THE UK BIOBANK COHORT
    Cheng, B.
    Wen, Y.
    Yang, X.
    Cheng, S.
    Liu, L.
    Chu, X.
    Ye, J.
    Liang, C.
    Yao, Y.
    Jia, Y.
    Zhang, F.
    BONE & JOINT RESEARCH, 2021, 10 (11): : 734 - 741
  • [29] Genome-wide associations studies for melanoma and nevi
    Yeh, Iwei
    Bastian, Boris C.
    PIGMENT CELL & MELANOMA RESEARCH, 2009, 22 (05) : 527 - 528
  • [30] Genome-wide linkage analysis combined with genome sequencing in large families with intracranial aneurysms
    Bakker, Mark K.
    Cobyte, Suze
    Hennekam, Frederic A. M.
    Rinkel, Gabriel J. E.
    Veldink, Jan H.
    Ruigrok, Ynte M.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (07) : 833 - 840