Gene expression profiling and racial disparities in outcomes after heart transplantation

被引:21
|
作者
Moayedi, Yasbanoo [1 ,2 ,3 ]
Fan, Chun-Po S. [3 ]
Miller, Robert J. H. [1 ,2 ]
Tremblay-Gravel, Maxime [1 ,2 ]
Posada, Juan G. Duero [3 ]
Manlhiot, Cedric [1 ,2 ]
Hiller, David [4 ]
Yee, James [4 ]
Woodward, Robert [4 ]
McCaughan, Jennifer A. [5 ]
Shullo, Michael A. [6 ]
Hall, Shelley A. [7 ]
Pinney, Sean [8 ]
Khush, Kiran K. [1 ,2 ]
Ross, Heather J. [3 ]
Teuteberg, Jeffrey J. [1 ,2 ]
机构
[1] Stanford Univ, Sect Heart Failure Cardiac Transplant & Mech Circ, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Med, Stanford, CA 94305 USA
[3] Univ Hlth Network, Ted Rogers Ctr Excellence Heart Res, Peter Munk Cardiac Ctr, Toronto, ON, Canada
[4] CareDx, Brisbane, Qld, Australia
[5] Belfast City Hosp, Div Nephrol, Belfast, Antrim, North Ireland
[6] West Virginia Univ, Morgantown, WV 26506 USA
[7] Baylor Univ, Med Ctr, Ctr Adv Heart & Lung Dis, Dallas, TX USA
[8] Mt Sinai Hosp, New York, NY 10029 USA
来源
关键词
gene expression profiling; race/ethnicity; heart transplantation; survival; graft failure; REJECTION; RISK; IMPACT; RACE; ANTIBODIES; SURVIVAL;
D O I
10.1016/j.healun.2019.05.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: African Americans (AAs) have lower survival rates after heart transplantation (HTx) than Caucasians. The aim of this analysis was to evaluate racial differences in gene expression and their associations with survival and the composite outcome of death, retransplant, rejection with hemodynamic compromise, and graft dysfunction in the Outcomes AlloMap Registry. METHODS: Registry participants included low-risk Caucasian and AA heart transplant recipients with a baseline and at least 1 follow-up gene expression test (AlloMap(C)) within the first year after HTx. The Kaplan-Meier method with delayed entry was used to describe differences in outcomes. Multivariable Cox hazard regression was used to evaluate the associations of overall gene expression profiling score, MARCH8 and FLT3 expression, and tacrolimus levels with each outcome, and stratified Cox models were developed to quantify race-specific associations. RESULTS: Among 933 eligible recipients, 737 (79%) were Caucasian and 196 (21%) were AA. Compared with Caucasians, AAs were significantly younger (55 vs 59 years, p < 0.001), with higher rates of non-ischemic cardiomyopathy (68% vs 50%, p < 0.001), sensitization (> 10% panel reactive antibody, 16% vs 9.1%, p = 0.009), and human leukocyte antigen mismatches (7 vs 7, p = 0.01), but less frequent primary cytomegalovirus serostatus mismatch (14.31% vs 27.3%, p < 0.001). Overall, AAs had an increased adjusted mortality risk (hazard ratio [HR] 4.13, p = 0.007). Higher tacrolimus levels were associated with decreased mortality in AAs (HR 0.62, p = 0.009). Overall gene expression profiling score was associated with increased mortality among Caucasians (HR 1.21, p = 0.048). In Caucasians, but not AAs, overexpression of MARCH8 was associated with increased mortality (HR 2.90, p = 0.001). FLT3 upregulation was associated with increased mortality (HR 2.42, p = 0.033) in AAs. There was an inverse relationship between FLT3 expression and tacrolimus levels (-0.029 and -0.176, respectively) in Caucasians and AAs. CONCLUSIONS: AAs have a significantly higher mortality risk after HTx than Caucasians, even in the low-risk Outcomes AlloMap Registry population. AAs and Caucasians had differential outcomes based upon the varying expression of MARCH8 and FLT3 genes following HTx. (C) 2019 International Society for Heart and Lung Transplantation. All rights reserved.
引用
收藏
页码:820 / 829
页数:10
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