Section of Heart Failure, Cardiac Transplant, and Mechanical Circulatory Support, and Department of Medicine, Stanford University, Stanford, California; Ted Rogers Centre of Excellence for Heart Research, Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada.
Ted Rogers Centre of Excellence for Heart Research, Peter Munk Cardiac Centre, University Health Network, Toronto, Ontario, Canada.
J Heart Lung Transplant. 2019 Aug;38(8):820-829. doi: 10.1016/j.healun.2019.05.008. Epub 2019 May 24.
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.
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.
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.
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.
非裔美国人(African Americans,AAs)在心脏移植(heart transplantation,HTx)后生存率低于白种人。本分析旨在评估基因表达的种族差异及其与生存率以及死亡、再次移植、伴有血流动力学障碍的排斥反应、移植物功能障碍复合结局的相关性,该研究基于 Outcomes AlloMap 注册研究。
该研究的注册参与者包括低危白种人和 AA 心脏移植受者,他们在 HTx 后 1 年内进行了基线和至少 1 次后续基因表达测试(AlloMap(C))。采用延迟进入的 Kaplan-Meier 方法描述结局差异。多变量 Cox 风险回归用于评估总基因表达谱评分、MARCH8 和 FLT3 表达以及他克莫司水平与每种结局的相关性,并建立分层 Cox 模型以量化种族特异性相关性。
在 933 名合格的受者中,737 名(79%)为白种人,196 名(21%)为 AA。与白种人相比,AA 更年轻(55 岁 vs 59 岁,p<0.001),非缺血性心肌病发生率更高(68% vs 50%,p<0.001)、致敏率(>10% 群体反应性抗体,16% vs 9.1%,p=0.009)和人类白细胞抗原错配(7 对 7,p=0.01)更高,但原发性巨细胞病毒血清学错配率较低(14.31% vs 27.3%,p<0.001)。总体而言,AA 调整后的死亡率风险更高(风险比[HR]4.13,p=0.007)。AA 中较高的他克莫司水平与死亡率降低相关(HR 0.62,p=0.009)。总基因表达谱评分与白种人死亡率增加相关(HR 1.21,p=0.048)。在白种人中,MARCH8 过表达与死亡率增加相关(HR 2.90,p=0.001)。AA 中 FLT3 上调与死亡率增加相关(HR 2.42,p=0.033)。FLT3 表达与他克莫司水平呈负相关(分别为-0.029 和-0.176),在白种人和 AA 中均如此。
即使在低危 Outcomes AlloMap 注册人群中,AA 在 HTx 后死亡率风险也显著高于白种人。AA 和白种人在 HTx 后基于 MARCH8 和 FLT3 基因的不同表达,有不同的结局。