From the Thurston Arthritis Research Center, and the Department of Radiology, and the Departments of Medicine and Orthopaedics, University of North Carolina, Chapel Hill, North Carolina; Departments of Medicine and Epidemiology and Public Health, University of Maryland School of Medicine; Medical Care Clinical Center, Veterans Affairs Maryland Health Care System; Geriatric Research, Education and Clinical Center, Veterans Affairs Medical Center, Baltimore, Maryland; Institute for Aging Research, Hebrew SeniorLife; Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts; Translational Genomics Research Institute, Phoenix, Arizona; Department of Internal Medicine, Ohio State University, Columbus, Ohio, USA.
Y. Liu, PhD, Thurston Arthritis Research Center, University of North Carolina; M.S. Yau, PhD, MPH, Departments of Medicine and Epidemiology and Public Health, University of Maryland School of Medicine, and the Institute for Aging Research, Hebrew SeniorLife, and the Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School; L.M. Yerges-Armstrong, PhD, Departments of Medicine and Epidemiology and Public Health, University of Maryland School of Medicine; D.J. Duggan, PhD, Translational Genomics Research Institute; J.B. Renner, MD, Thurston Arthritis Research Center, and the Department of Radiology, University of North Carolina; M.C. Hochberg, MD, MPH, Departments of Medicine and Epidemiology and Public Health, University of Maryland School of Medicine, and the Medical Care Clinical Center, Veterans Affairs Maryland Health Care System, and the Geriatric Research, Education and Clinical Center, Veterans Affairs Medical Center; B.D. Mitchell, PhD, MPH, Departments of Medicine and Epidemiology and Public Health, University of Maryland School of Medicine, and Geriatric Research, Education and Clinical Center, Veterans Affairs Medical Center; R.D. Jackson, MD, Department of Internal Medicine, Ohio State University; J.M. Jordan, MD, MPH, Thurston Arthritis Research Center, University of North Carolina, and Departments of Medicine and Orthopaedics, University of North Carolina.
J Rheumatol. 2017 Nov;44(11):1652-1658. doi: 10.3899/jrheum.161488. Epub 2017 Sep 15.
The etiology of knee osteoarthritis (OA), the most common form of arthritis, is complex and may differ by race or ethnicity. In recent years, genetic studies have identified many genetic variants associated with OA, but nearly all the studies were conducted in European whites and Asian Americans. Few studies have focused on the genetics of knee OA in African Americans.
We performed a genome-wide association study of radiographic knee OA in 1217 African Americans from 2 North American cohort studies: 590 subjects from the Johnston County Osteoarthritis Project and 627 subjects from the Osteoarthritis Initiative. Analyses were conducted in each cohort separately and combined in an inverse variance fixed effects metaanalysis, which were then included in pathway analyses. We additionally tested 12 single-nucleotide polymorphisms robustly associated with OA in European white populations for association in African Americans.
We identified a genome-wide significant variant in (minor allele frequency 12%; p = 4.11 × 10) that is less common in European white populations (minor allele frequency < 3%). Five other independent loci reached suggestive significance (p < 1 × 10). In pathway analyses, dorsal/ventral neural tube patterning and iron ion transport pathways were significantly associated with knee OA in African Americans (false discovery rate < 0.05). We found no evidence that previously reported OA susceptibility variants in European whites were associated with knee OA in African Americans.
These results highlight differences in the genetic architecture of knee OA between African American and European whites. This finding underscores the need to include more diverse populations in OA genetics studies.
膝骨关节炎(OA)是最常见的关节炎形式,其病因复杂,可能因种族或民族而异。近年来,遗传研究已经确定了许多与 OA 相关的遗传变异,但几乎所有的研究都是在欧洲白人和亚裔美国人中进行的。很少有研究关注非裔美国人的膝骨关节炎遗传。
我们对来自 2 个北美队列研究的 1217 名非裔美国人进行了全基因组关联研究:590 名来自约翰斯顿县骨关节炎项目,627 名来自骨关节炎倡议。分别在每个队列中进行分析,并在逆方差固定效应荟萃分析中进行合并,然后将其纳入途径分析。我们还测试了在欧洲白人群体中与 OA 显著相关的 12 个单核苷酸多态性在非裔美国人中的关联性。
我们在 (次要等位基因频率为 12%;p = 4.11 × 10)中发现了一个全基因组显著变异,该变异在欧洲白人群体中较少见(次要等位基因频率 < 3%)。另外 5 个独立的位点达到了提示性显著水平(p < 1 × 10)。在途径分析中,背/腹神经管模式形成和铁离子转运途径与非裔美国人的膝骨关节炎显著相关(错误发现率 < 0.05)。我们没有发现先前在欧洲白人中报道的 OA 易感性变异与非裔美国人的膝骨关节炎有关的证据。
这些结果突出了非裔美国人和欧洲白人膝骨关节炎遗传结构的差异。这一发现强调了在 OA 遗传学研究中纳入更多不同人群的必要性。