Abstract

Treatment options for several chronic infectious and inflammatory conditions have expanded in recent years. This may have implications for evolving competing risks for chronic inflammation-associated comorbidities, including cardiovascular diseases (CVDs). Yet sparse data exist on patterns over time in cardiovascular mortality for chronic infectious and inflammatory conditions. We used data from the Centers for Disease Control and Prevention 1999–2018 Multiple Causes of Death database to investigate patterns in CVD mortality from January 1, 1999 to December 31, 2018 in several infectious and inflammatory conditions. Specifically, we determined age-adjusted proportionate CVD mortality separately for patients with the following conditions (as well as the general population): hepatitis C virus (HCV), human immunodeficiency virus (HIV), inflammatory bowel diseases (IBD), psoriasis (PSO), rheumatoid arthritis (RA), and systemic lupus erythematosus (SLE). Proportionate CVD mortality differed significantly in 1999 and 2018 for each condition compared with the general population (p < 0.0001). Proportionate CVD mortality decreased steadily in the general population (40.9 to 30.6%) but increased for patients with HCV (7.0 to 10.2%) and HIV (1.9 to 6.7%). For IBD, PSO, RA, and SLE, proportionate CVD mortality initially decreased followed by plateauing or increasing rates. Underlying disease-specific pathophysiologies, changes in natural history, and competing risks of chronic end-organ diseases contributing to these differences merit further study.

Highlights

  • Treatment options for several chronic infectious and inflammatory conditions have expanded in recent years

  • Patterns in proportionate cardiovascular diseases (CVDs) mortality for the general population compared with chronic infectious and inflammatory diseases (CID)

  • Whereas patterns of proportionate cardiovascular mortality (PCVM) declined for rheumatoid arthritis (RA), inflammatory bowel diseases (IBD), and PSO largely in parallel to the general population from 1999 to 2018, PCVM increased significantly for human immunodeficiency virus (HIV) and hepatitis C virus (HCV) over the same time period and remained largely stable for systemic lupus erythematosus (SLE)

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Summary

Introduction

Treatment options for several chronic infectious and inflammatory conditions have expanded in recent years. We determined age-adjusted proportionate CVD mortality separately for patients with the following conditions (as well as the general population): hepatitis C virus (HCV), human immunodeficiency virus (HIV), inflammatory bowel diseases (IBD), psoriasis (PSO), rheumatoid arthritis (RA), and systemic lupus erythematosus (SLE). Recent decades have seen an increasing body of evidence for the contribution of inflammation to cardiovascular disease (CVD) in both the general population and sub-populations with chronic infectious and inflammatory c­ onditions[3,4,5,6,7] We hypothesized that these changes in treatment of chronic infectious and inflammatory conditions may have implications on evolving risks for cardiovascular disease (CVD) and all-cause mortality. Relatively little is known regarding the overall burden of CVD mortality associated with these conditions, especially given their evolving natural histories (e.g., decreased HCV-related hepatocellular carcinoma/death or improved disease control with biologic therapies for inflammatory diseases) and related changes in competing causes of death

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