Association of Sickle Cell Trait With Incidence of Coronary Heart Disease Among African American Individuals

被引:5
|
作者
Hyacinth, Hyacinth I. [1 ]
Franceschini, Nora [2 ]
Seals, Samantha R. [3 ]
Irvin, Marguerite R. [4 ]
Chaudhary, Ninad [4 ]
Naik, Rakhi P. [5 ]
Alonso, Alvaro [6 ]
Carty, Cara L. [7 ]
Burke, Gregory L. [8 ]
Zakai, Neil A. [9 ]
Winkler, Cheryl A. [10 ,11 ]
David, Victor A. [10 ,11 ]
Kopp, Jeffrey B. [12 ]
Judd, Suzanne E. [4 ]
Adams, Robert J. [13 ]
Gee, Beatrice E. [1 ]
Longstreth, W. T., Jr. [14 ,15 ]
Egede, Leonard [16 ]
Lackland, Daniel T. [13 ]
Greenberg, Charles S. [17 ]
Taylor, Herman [18 ]
Manson, JoAnn E. [19 ]
Key, Nigel S. [20 ]
Derebail, Vimal K. [21 ]
Kshirsagar, Abhijit V. [21 ]
Folsom, Aaron R. [22 ]
Konety, Suma H. [23 ]
Howard, Virginia [24 ]
Allison, Matthew [25 ]
Wilson, James G. [26 ]
Correa, Adolfo [27 ]
Zhi, Degui [28 ]
Arnett, Donna K. [29 ]
Howard, George [28 ]
Reiner, Alexander P. [30 ]
Cushman, Mary [9 ]
Safford, Monika M. [31 ]
机构
[1] Emory Univ, Dept Pediat, Aflac Canc & Blood Disorder Ctr, Sch Med, 2015 Uppergate Dr, Atlanta, GA 30322 USA
[2] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27515 USA
[3] Univ West Florida, Dept Math & Stat, Pensacola, FL USA
[4] Univ Alabama Birmingham, Sch Publ Hlth, Birmingham, AL 35294 USA
[5] Johns Hopkins Univ, Dept Med, Div Hematol, Baltimore, MD USA
[6] Emory Univ, Dept Epidemiol, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA
[7] Fred Hutchinson Canc Res Ctr, 1124 Columbia St, Seattle, WA 98104 USA
[8] Wake Forest Univ, Dept Publ Hlth Sci, Winston Salem, NC 27101 USA
[9] Univ Vermont, Dept Med & Pathol & Lab Med, Burlington, VT 05405 USA
[10] NCI, Basic Sci Lab, Frederick, MD 21701 USA
[11] Leidos Biomed Res, Frederick Natl Lab, Frederick, MD USA
[12] NIDDK, NIH, Bethesda, MD 20892 USA
[13] Med Univ South Carolina, Stroke Ctr, Dept Neurol, Charleston, SC 29425 USA
[14] Univ Washington, Dept Neurol, Seattle, WA 98195 USA
[15] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
[16] Med Coll Wisconsin, Div Gen Internal Med, Milwaukee, WI 53226 USA
[17] Med Univ South Carolina, Div Hematol Oncol, Charleston, SC 29425 USA
[18] Morehouse Sch Med, Cardiovasc Res Inst, Atlanta, GA 30310 USA
[19] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[20] Univ N Carolina, Div Hematol Oncol, Chapel Hill, NC 27515 USA
[21] Univ N Carolina, Kidney Ctr, Chapel Hill, NC 27515 USA
[22] Univ Minnesota, Sch Publ Hlth, Div Epidemiol & Community Hlth, Minneapolis, MN USA
[23] Univ Minnesota, Med Ctr, Div Cardiol, Minneapolis, MN 55455 USA
[24] Univ Alabama Birmingham, Sch Publ Hlth, Dept Epidemiol, Birmingham, AL 35294 USA
[25] Univ Calif San Diego, Dept Family Med & Publ Hlth, San Diego, CA 92103 USA
[26] Univ Mississippi, Dept Physiol & Biophys, Med Ctr, Jackson, MS 39216 USA
[27] Univ Mississippi, Med Ctr, Jackson Heart Study, Jackson, MS 39216 USA
[28] Univ Alabama Birmingham, Sch Publ Hlth, Dept Biostat, Birmingham, AL 35294 USA
[29] Univ Kentucky, Coll Publ Hlth, Lexington, KY 40506 USA
[30] Univ Washington, Fred Hutchinson Canc Res Ctr, Seattle, WA 98195 USA
[31] Weill Cornell Med, Div Gen Internal Med, New York, NY USA
关键词
CHRONIC KIDNEY-DISEASE; RENAL-INSUFFICIENCY COHORT; CARDIOVASCULAR-DISEASE; RISK-FACTOR; VENOUS THROMBOEMBOLISM; MEDULLARY CARCINOMA; ETHNIC-DIFFERENCES; RACIAL-DIFFERENCES; APOL1; VARIANTS; STROKE;
D O I
10.1001/jamanetworkopen.2020.30435
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCE The incidence of and mortality from coronary heart disease (CHD) are substantially higher among African American individuals compared with non-Hispanic White individuals, even after adjusting for traditional factors associated with CHD. The unexplained excess risk might be due to genetic factors related to African ancestry that are associated with a higher risk of CHD, such as the heterozygous state for the sickle cell variant or sickle cell trait (SCT). OBJECTIVE To evaluate whether there is an association between SCT and the incidence of myocardial infarction (MI) or composite CHD outcomes in African American indi viduals. DESIGN, SETTING, AND PARTICIPANTS This cohort study included 5 large, prospective, population-based cohorts of African American individuals in the Women's Health Initiative (WHI) study, the Reasons for Geographic and Racial Differences in Stroke (REGARDS) study, the Multi-Ethnic Study of Atherosclerosis (MESA), the Jackson Heart Study (JHS), and the Atherosclerosis Risk in Communities (ARIC) study. The follow-up periods included in this study were 1993 and 1998 to 2014 for the WHI study, 2003 to 2014 for the REGARDS study, 2002 to 2016 for the MESA, 2002 to 2015 for the JHS, and 1987 to 2016 for the ARIC study. Data analysis began in October 2013 and was completed in October 2020. EXPOSURES Sickle cell trait status was evaluated by either direct genotyping or high-quality imputation of rs334 (the sickle cell variant). Participants with sickle cell disease and those with a history of CHD were excluded from the analyses. MAIN OUTCOMES AND MEASURES Incident MI, defined as adjudicated nonfatal or fatal MI, and incident CHD, defined as adjudicated nonfatal MI, fatal MI, coronary revascularization procedures, or death due to CHD. Cox proportional hazards regression models were used to estimate the hazard ratio for incident MI or CHD comparing SCT carriers with noncarriers. Models were adjusted for age, sex (except for the WHI study), study site or region of residence, hypertension status or systolic blood pressure, type 1 or 2 diabetes, serum high-density lipoprotein level, total cholesterol level, and global ancestry (estimated from principal components analysis). RESULTS A total of 23 197 African American men (29.8%) and women (70.2%) were included in the combined sample, of whom 1781 had SCT (7.7% prevalence). Mean (SD) ages at baseline were 61.2 (6.9) years in the WHI study (n = 5904), 64.0 (9.3) years in the REGARDS study (n = 10 714), 62.0 (10.0) years in the MESA (n = 1556), 50.3 (12.0) years in the JHS (n = 2175), and 53.2 (5.8) years in the ARIC study (n = 2848). There were no significant differences in the distribution of traditional factors associated with cardiovascular disease by SCT status within cohorts. A combined total of 1034 participants (76 with SCT) had incident MI, and 1714 (137 with SCT) had the composite CHD outcome. The meta-analyzed crude incidence rate of MI did not differ by SCT status and was 3.8 per 1000 person-years (95% CI, 3.3-4.5 per 1000 person-years) among those with SCT and 3.6 per 1000 person-years (95% CI, 2.7-5.1 per 1000 person-years) among those without SCT. For the composite CHD outcome, these rates were 7.3 per 1000 person-years (95% CI, 5.5-9.7 per 1000 person-years) among those with SCT and 6.0 per 1000 person-years (95% CI, 4.9-7.4 per 1000 person-years) among those without SCT. Meta-analysis of the 5 study results showed that SCT status was not significantly associated with MI (hazard ratio, 1.03; 95% CI, 0.81-1.32) or the composite CHD outcome (hazard ratio, 1.16; 95% CI, 0.92-1.47). CONCLUSIONS AND RELEVANCE In this cohort study, there was not an association between SCT and increased risk of MI or CHD in African American individuals. These disorders may not be associated with sickle cell trait-related sudden death in this population. Question Is sickle cell trait associated with increased risk of myocardial infarction and coronary heart disease among African American individuals? Findings In this cohort study of 23 197 African American individuals in 5 cardiovascular epidemiologic studies, sickle cell trait was not associated with increased risk of myocardial infarction or coronary heart disease among African American individuals. Meaning In this study, sickle cell trait was not associated with increased risk of fatal and nonfatal myocardial infarction or coronary heart disease, suggesting that these disorders may not be associated with sickle cell trait-related sudden death. This cohort study evaluates whether African American individuals with sickle cell trait have a higher incidence of myocardial infarction or composite coronary heart disease outcomes compared with those without sickle cell trait.
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