Key result
Pneumoconiosis-associated IHD mortality declines ~61% among older US adults over two decades.
Why the study?
Pneumoconiosis may promote cardiovascular injury via chronic inflammation and hypoxemia, but national trends in IHD mortality when pneumoconiosis is co-mentioned remain poorly described.
Observational
Effect estimate: AAPC -5.66%/yr (95% CI -6.06 to -5.25)
Ischemic heart disease mortality with co-existing pneumoconiosis declined significantly in the US from 1999 to 2020, though disparities persist in rural areas and a slight uptick was observed in 2020.
IHD mortality trends with co-mentioned pneumoconiosis remain hypothesis-generating; leaves open whether inflammation or hypoxemia drives excess cardiovascular risk.
Rationale Pneumoconiosis—coal workers’ pneumoconiosis (CWP), asbestosis, silicosis—may promote cardiovascular injury via chronic inflammation and hypoxemia. National trends in Ischemic Heart Disease (IHD) mortality when pneumoconiosis is co-mentioned remain poorly described. Methods Using CDC Wide-ranging Online Data for Epidemiologic Research (CDC WONDER) Multiple Cause of Death (MCOD), we identified U.S. decedents aged ≥55 years (1999-2020) with IHD AND pneumoconiosis listed on the death certificate (ICD-10 underlying or contributing codes). We obtained CDC WONDER-reported age-adjusted mortality rates (AAMR) per 100,000 (2000 U.S. standard) overall and by sex, race/ethnicity, 2013 National Center for Health Statistics (NCHS) urbanization, and pneumoconiosis subtype. We use Crude Mortality Rate (CMR) for 10-year agre groups. Joinpoint log-linear models estimated annual percent change (APC) and average APC (AAPC). NS = nonsignificant. Results AAMR declined from 1.25 in 1999 to 0.49 in 2020 (nadir 0.40 in 2019); APC/AAPC −5.66%/yr (95% CI − 6.06 to − 5.25).Sex: Men accounted for most of the deaths; male AAMR 3.20→1.09, with a 2018 joinpoint (1999-2018 −6.54%/yr; 2018-2020 +3.24%/yr, NS). Female series were frequently suppressed.Age: All bands declined with 2020 upticks—AAPC −7.48%/yr (65-74 y), −6.01%/yr (75-84 y), −4.09%/yr (≥85 y). CMR remained highest in ≥ 85 y.Race/ethnicity: Only White adults supported annual modeling (AAMR 1.27→0.56; 2017 joinpoint: −5.85%/yr then +2.92%/yr, NS; AAPC −4.65%/yr). Counts for Black, Hispanic, American Indian/Alaska Native, and Asian/Pacific Islander adults were often <20/year with suppression, limiting inference.Urbanization: All six 2013 NCHS strata declined (0 joinpoints); AAPC ranged −6.74%/yr (micropolitan) to −3.55%/yr (noncore rural). In 2020, AAMR was highest in noncore rural (1.07) and lowest in large central metro (0.21).Subtype: CWP showed two joinpoints with sustained declines (1999-2005 −8.89%/yr; 2005-2013 −14.33%/yr; 2013-2020 −6.36%/yr; AAPC −10.18%/yr). Asbestosis declined (AAPC −3.80%/yr) but rose in 2020 (0.35 vs 0.29 in 2019). Silicosis counts were sparse/unreliable annually. Conclusions From 1999-2020, IHD mortality with pneumoconiosis co-mention fell markedly, driven by sharp reductions in CWP, and improvements among men and younger-old adults. However, there is persistent rural excess and a 2020 uptick after a 2019 nadir. The predominance of White decedents likely reflects historical exposure patterns and may also indicate under-ascertainment/under-reporting of pneumoconiosis in other groups. In addition, asbestosis now accounts for the largest subtype share. Targeted prevention in high-risk rural/occupational cohorts, improved death-certificate coding and surveillance across races, and systematic cardiovascular risk management in patients with occupational lung disease are warranted. This abstract is funded by: None
No takes yet. Share an insight, caveat, or question.
Afzaal et al. (2026) conducted an observational in Ischemic Heart Disease and Pneumoconiosis. Ischemic heart disease mortality with pneumoconiosis co-mention among US adults ≥55 years declined from 1.25 to 0.49 per 100,000 between 1999 and 2020 (AAPC -5.66%/yr; 95% CI -6.06 to -5.25).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: