Related Experiment Video
Updated: Jul 15, 2026

Longitudinal In Vivo Imaging of the Cerebrovasculature: Relevance to CNS Diseases
Published on: December 6, 2016
Cardiovascular Mortality in Amyloidosis: Long-Term Trends, Disparities, and Projections in the United States
Zhan Chen1, Ying Tian2, Yue Zhang3
1Department of Vascular Surgery, Beijing Haidian Hospital, Beijing, People's Republic of China.
Insights
Cardiovascular mortality in U.S. adults with amyloidosis has nearly tripled since 1999, with significant increases in heart failure deaths and widening disparities. Projections show continued upward trends, highlighting a growing public health concern.
Area of Science:
- Cardiovascular epidemiology
- Public health surveillance
- Amyloidosis research
Background:
- Cardiac involvement significantly impacts prognosis in systemic amyloidosis.
- Population-level trends in cardiovascular mortality for amyloidosis patients are not well-characterized.
Purpose of the Study:
- To analyze temporal trends and disparities in cardiovascular mortality among U.S. adults with amyloidosis.
- To project future cardiovascular mortality rates through 2033.
Main Methods:
- Retrospective analysis of U.S. death certificate data (1999-2023) for adults aged ≥45 with amyloidosis.
- Identification of cardiovascular disease (CVD) deaths using ICD-10 codes.
- Calculation of age-adjusted mortality rates (AAMRs) and assessment of trends using joinpoint regression and ARIMA models.
Main Results:
- Cardiovascular mortality nearly tripled from 0.80 to 2.27 per 100,000 between 1999 and 2023.
- Heart failure was the leading cause of CVD deaths; mortality rates were higher in males, older adults, and non-Hispanic Black individuals.
- Disparities widened over time, with similar upward trends across regions and urbanization levels.
Conclusions:
- Substantial increase and recent acceleration in cardiovascular mortality among U.S. adults with amyloidosis.
- Persistent and widening population-level disparities underscore a growing public health burden.
- Findings support enhanced surveillance, earlier detection, and equitable access to specialized care.
Background:
Cardiac involvement is a major determinant of prognosis in systemic amyloidosis, but population-level trends in cardiovascular mortality remain insufficiently characterized.
Methods:
We performed a retrospective, population-based analysis of U.S. adults aged ≥45 years with amyloidosis using death certificate data from the Centers for Disease Control and Prevention Wide-ranging Online Data for Epidemiologic Research (CDC WONDER) database from 1999 through 2023. Cardiovascular disease (CVD)-related deaths were identified using ICD-10 codes and classified into heart failure (HF), atrial fibrillation/flutter (AF), ischemic heart disease (IHD), or other CVD categories. Age-adjusted mortality rates (AAMRs) were calculated using the 2000 U.S. standard population. Joinpoint regression assessed temporal trends, and autoregressive integrated moving average (ARIMA) models projected mortality through 2033.
Results:
A total of 35,222 CVD-related deaths occurred among adults with amyloidosis during the study period, yielding an overall AAMR of 1.12 per 100,000 population. Cardiovascular mortality increased nearly threefold, from 0.80 per 100,000 in 1999 to 2.27 per 100,000 in 2023, with a marked acceleration beginning in the late 2010s. HF consistently accounted for the largest proportion of CVD-related deaths. Mortality rates were higher among males, older adults, and non-Hispanic Black individuals, with demographic and geographic disparities widening over time. Similar upward trajectories were observed across U.S. Census regions and levels of urbanization. Projections indicated continued increases in cardiovascular mortality through 2033.
Conclusion:
Cardiovascular mortality among U.S. adults with amyloidosis has increased substantially over the past 25 years, with recent acceleration and persistent population-level disparities. These findings highlight a growing public health burden and support earlier detection, equitable access to specialized care, and continued national surveillance.
Related Concept Videos
Amyloid Fibrils
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining, normally used to...
Amyloid Fibrils
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining, normally used to...
Cardiomyopathy V: Interprofessional Care
Alzheimer Disease l: Introduction
Atherosclerosis III: Management
Cardiomyopathy II: Dilated Cardiomyopathy

