J Cardiovasc Nurs. 2021;36(2):104-115. doi: 10.1097/JCN.0000000000000718.
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disorder globally, affecting 0.2% to 0.5% of individuals. Existing clinical HCM guidelines do not address diverse populations, specifically minority groups who often experience health disparities.
The aim of this study was to describe the state of the science of HCM in black populations.
This integrated review guided by Whittemore and Knafl's methodology included literature search of multiple databases, data evaluation, and analysis. Publications between 2000 and 2020 were included if they addressed HCM cardiac anatomic manifestations, disease course, symptoms, quality of life, or outcomes in black populations.
Six articles met the inclusion criteria. Overall, blacks are underrepresented in HCM research. Certain HCM structural phenotypes are more commonly exhibited in blacks, and physiology drives HCM treatment. Sudden death events and all-cause mortality do not differ between blacks and whites with HCM. Fewer blacks with HCM undergo genetic testing than whites with HCM. The lack of diversity in general genomic databases has resulted in reclassification of several genetic variants identified as more common in blacks.
Blacks are underrepresented in HCM research, even those focused on elucidating HCM manifestations, disease course, and outcomes in black populations. This may be due in part to HCM research that is largely generated from specialty centers that can require patients to navigate complex healthcare systems to reach expert HCM care. Longitudinal studies with large samples of blacks with HCM are necessary to elucidate how HCM affects this population.
肥厚型心肌病(HCM)是全球最常见的遗传性心脏病,影响 0.2%至 0.5%的个体。现有的临床 HCM 指南并未涉及不同人群,特别是经常面临健康差距的少数群体。
本研究旨在描述黑人人群中 HCM 的科学现状。
本研究采用 Whittemore 和 Knafl 的方法进行综合综述,包括对多个数据库的文献检索、数据评估和分析。纳入的出版物发表时间在 2000 年至 2020 年之间,其内容涉及黑人人群中 HCM 的心脏解剖表现、疾病进程、症状、生活质量或结局。
共有 6 篇文章符合纳入标准。总体而言,黑人在 HCM 研究中代表性不足。某些 HCM 结构表型在黑人中更为常见,生理因素驱动 HCM 的治疗。黑人与白人 HCM 患者的猝死事件和全因死亡率无差异。接受基因检测的黑人 HCM 患者少于白人 HCM 患者。一般基因组数据库缺乏多样性,导致一些被认为在黑人中更为常见的遗传变异被重新分类。
即使是那些专注于阐明黑人人群中 HCM 表现、疾病进程和结局的 HCM 研究,黑人的代表性也不足。这部分可能是由于 HCM 研究主要来自专业中心,患者需要在复杂的医疗体系中寻找专家 HCM 治疗。需要对大量黑人 HCM 患者进行纵向研究,以阐明 HCM 如何影响这一人群。