Abstract 4368312: Demographics and Trends in Reported Amyloidosis Mortality in the United States, 1999-2023

V Vikash Jaiswal F FNU Danisha (Dow University of Health Sciences, Karachi, Pakistan) K Kriti Kalra (Medstar, Alexandria, Virginia, United States) Y Yusra Mashkoor (Dow University of Health Sciences, Karachi, Pakistan) F Fakhar Latif Y Yusra Nasir (University of Oklahoma, Oklahoma city, Oklahoma, United States) K Kevin Alexander (Division of Cardiovascular Medicine, Department of Medicine, Stanford Center for Clinical Research, Stanford University School of Medicine, Palo Alto, California, United States) A Arman Qamar

Abstract

Background: Amyloidosis represents a heterogeneous group of disorders characterized by extracellular deposition of misfolded protein fibrils, leading to progressive organ dysfunction and death. Despite its clinical significance, there is a paucity of large-scale epidemiologic data characterizing mortality trends associated with amyloidosis in the United States. Objective: To evaluate temporal trends and demographic patterns in amyloidosis-related mortality across the US population from 1999 to 2023. Methods: This population-based, retrospective cohort study utilized publicly available mortality data from the Centers for Disease Control and Prevention (CDC) Wide-ranging Online Data for Epidemiologic Research (WONDER) database spanning from 1999 to 2023. The study included decedents of all ages in whom amyloidosis was listed as either an underlying or contributing cause of death on death certificates. The primary outcome was the age-adjusted mortality rate for amyloidosis-related deaths per 100,000 population. AAMRs were stratified by sex, race and ethnicity, US census region, state, place of death, and age group. Results: From 1999 to 2023, a total of 52,659 amyloidosis-related deaths were recorded in the US. Most deaths occurred in medical facilities and homes. The overall AAMR nearly doubled from 4.95 (95% CI: 4.68–5.21) in 1999 to 10.30 (95% CI: 9.99–10.60) in 2022. After an initial period of relative stability from 1999–2012, AAMRs significantly increased from 2012–2018 [ Annual percent changes (APC): 5.24; 95% CI: 3.87–10.36] and again from 2018–2023 [APC: 11.13; 95% CI: -48.67–17.07]. Males consistently exhibited higher mortality rates than females (8.24 vs. 4.20), and among racial/ethnic groups, NH Black individuals had the highest AAMR (11.26), while NH Asians had the lowest (3.46). Since 2014, all U.S. census regions have shown a significant rise in amyloidosis-related AAMRs, following earlier periods of stability or modest increases. States such as Massachusetts, Vermont, Minnesota, and the District of Columbia exhibited the highest mortality burdens, whereas states like Louisiana, Arkansas, and Mississippi had the lowest. Mortality rates increased with advancing age, with individuals aged ≥85 years exhibiting the highest crude mortality rate (CMR: 64.29). Conclusion: Amyloidosis-related mortality has markedly increased over the past two decades in the US, with significant disparities across sex, age, racial/ethnic, and geographic groups.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (8)

V

Vikash Jaiswal

F

FNU Danisha

Dow University of Health Sciences, Karachi, Pakistan

K

Kriti Kalra

Medstar, Alexandria, Virginia, United States

Y

Yusra Mashkoor

Dow University of Health Sciences, Karachi, Pakistan

F

Fakhar Latif

Y

Yusra Nasir

University of Oklahoma, Oklahoma city, Oklahoma, United States

K

Kevin Alexander

Division of Cardiovascular Medicine, Department of Medicine, Stanford Center for Clinical Research, Stanford University School of Medicine, Palo Alto, California, United States

A

Arman Qamar