1999-2020年美国老年人淀粉样变性心血管死亡率的显著差异

Q4 Medicine
Mustafa Shehzad, Dawood Shehzad, Logan Johnke, Dawlat Khan, Hammad Shabir Chaudhry
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引用次数: 0

摘要

淀粉样变性是一组以淀粉样原纤维积聚为特征的蛋白质折叠障碍,导致严重的器官功能障碍。本研究使用CDC WONDER数据库的数据,调查了1999年至2020年美国淀粉样变性相关心血管疾病死亡率的趋势。我们分析了不同人口、种族和地理类别的老年人(65岁以上)的年龄调整死亡率(AAMR)。研究结果表明,AAMR从1999年的1.71增加到2020年的4.23,并在2018年之后显著加速(年增长率为+ 16.30%)。男性的死亡率始终高于女性,而非西班牙裔黑人的AAMR几乎是其他种族群体的两倍。区域分析显示,东北部和西部的死亡率最高,而南部的死亡率较低,尽管该地区的黑人人口较多。这些差异突出了社会经济因素、医疗保健获取和诊断实践的潜在影响。淀粉样变相关死亡率的增加可能反映了认识的增强,而不是疾病患病率的实际上升。我们的研究结果强调,迫切需要有针对性的公共卫生干预措施来解决这些差异,并改善诊断和治疗策略。对这些趋势的潜在原因的持续调查对于提高患者预后和管理老龄化人群中淀粉样变日益增加的负担至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pronounced Disparities in Amyloidosis Cardiovascular Mortality Among Elderly Adults in the United States from 1999-2020.

Amyloidosis is a group of protein-folding disorders marked by the accumulation of amyloid fibrils, leading to significant organ dysfunction. This study investigates trends in cardiovascular mortality linked to amyloidosis in the U.S. from 1999 to 2020, using data from the CDC WONDER database. We analyzed age-adjusted mortality rates (AAMR) among older adults (older than 65 years) across various demographic, racial, and geographic categories. Findings show a concerning increase in AAMR from 1.71 in 1999 to 4.23 in 2020, with a notable acceleration after 2018 (annual percentage change of +16.30). Males consistently demonstrated higher mortality rates than females, while non-Hispanic Black individuals had nearly double the AAMR compared to other racial groups. Regional analysis revealed the highest mortality rates in the Northeast and West, contrasting with lower rates in the South despite a larger Black population in that region. These disparities highlight potential influences from socioeconomic factors, healthcare access, and diagnostic practices. The increase in amyloidosis-related mortality may reflect enhanced recognition rather than an actual rise in disease prevalence. Our results underscore the urgent need for targeted public health interventions to address these disparities and improve diagnostic and treatment strategies. Continued investigation into the underlying causes of these trends is essential for enhancing patient outcomes and managing the growing burden of amyloidosis among the aging population.

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