Department of Preventive Medicine Northwestern University Feinberg School of Medicine Chicago IL.
Division of Cardiology Department of Medicine Northwestern University Feinberg School of Medicine Chicago IL.
J Am Heart Assoc. 2020 Dec;9(23):e018213. doi: 10.1161/JAHA.120.018213. Epub 2020 Nov 23.
Background Life expectancy in the United States has recently declined, in part attributable to premature cardiometabolic mortality. We characterized national trends in premature cardiometabolic mortality, overall, and by race-sex groups. Methods and Results Using death certificates from the Centers for Disease Control and Prevention's Wide-Ranging Online Data for Epidemiologic Research, we quantified premature deaths (<65 years of age) from heart disease, cerebrovascular disease, and diabetes mellitus from 1999 to 2018. We calculated age-adjusted mortality rates (AAMRs) and years of potential life lost (YPLL) from each cardiometabolic cause occurring at <65 years of age. We used Joinpoint regression to identify an inflection point in overall cardiometabolic AAMR trends. Average annual percent change in AAMRs and YPLL was quantified before and after the identified inflection point. From 1999 to 2018, annual premature deaths from heart disease (117 880 to 128 832), cerebrovascular disease (18 765 to 20 565), and diabetes mellitus (16 553 to 24 758) as an underlying cause of death increased. By 2018, 19.7% of all heart disease deaths, 13.9% of all cerebrovascular disease deaths, and 29.1% of all diabetes mellitus deaths were premature. AAMRs and YPLL from heart disease and cerebrovascular disease declined until the inflection point identified in 2011, then remained unchanged through 2018. Conversely, AAMRs and YPLL from diabetes mellitus did not change through 2011, then increased through 2018. Black men and women had higher AAMRs and greater YPLL for each cardiometabolic cause compared with White men and women, respectively. Conclusions Over one-fifth of cardiometabolic deaths occurred at <65 years of age. Recent stagnation in cardiometabolic AAMRs and YPLL are compounded by persistent racial disparities.
美国的预期寿命最近有所下降,部分原因是过早的心血管代谢性死亡。我们描述了全国范围内过早的心血管代谢性死亡的趋势,包括总体情况以及按种族和性别群体的情况。
使用疾病控制和预防中心的广泛在线流行病学研究数据中心的死亡证明,我们量化了 1999 年至 2018 年期间因心脏病、脑血管疾病和糖尿病导致的<65 岁以下的过早死亡。我们计算了每种心血管代谢性原因导致的<65 岁以下的年龄调整死亡率(AAMR)和潜在生命损失年数(YPLL)。我们使用 Joinpoint 回归来确定总体心血管代谢性 AAMR 趋势的拐点。在确定的拐点前后,我们量化了 AAMR 和 YPLL 的年平均百分比变化。从 1999 年到 2018 年,每年因心脏病(从 117880 人到 128832 人)、脑血管疾病(从 18765 人到 20565 人)和糖尿病(从 16553 人到 24758 人)作为根本死因的过早死亡人数增加。到 2018 年,所有心脏病死亡中有 19.7%、所有脑血管疾病死亡中有 13.9%、所有糖尿病死亡中有 29.1%是过早的。心脏病和脑血管疾病的 AAMR 和 YPLL 在 2011 年确定的拐点之前下降,然后在 2018 年之前保持不变。相反,糖尿病的 AAMR 和 YPLL 在 2011 年之前没有变化,然后在 2018 年增加。与白人男性和女性相比,黑人男性和女性的每种心血管代谢性病因的 AAMR 和 YPLL 更高。
超过五分之一的心血管代谢性死亡发生在<65 岁。心血管代谢性 AAMR 和 YPLL 的近期停滞,加上持续存在的种族差异,情况更加复杂。