Childhood hospitalisation with infection and cardiovascular disease in early-mid adulthood: a longitudinal population-based study

PLoS One. 2015 May 4;10(5):e0125342. doi: 10.1371/journal.pone.0125342. eCollection 2015.

Abstract

Background: Pathogen-specific and overall infection burden may contribute to atherosclerosis and cardiovascular disease (CVD), but the effect of infection severity and timing is unknown. We investigated whether childhood infection-related hospitalisation (IRH, a marker of severity) was associated with subsequent adult CVD hospitalisation.

Methods: Using longitudinal population-based statutorily-collected administrative health data from Western Australia (1970-2009), we identified adults hospitalised with CVD (ischaemic heart disease, ischaemic stroke, and peripheral vascular disease) and matched them (10:1) to population controls. We used Cox regression to assess relationships between number and type of childhood IRH and adulthood CVD hospitalisation, adjusting for sex, age, Indigenous status, socioeconomic status, and birth weight.

Results: 631 subjects with CVD-related hospitalisation in adulthood (≥ 18 years) were matched with 6310 controls. One or more childhood (< 18 years) IRH was predictive of adult CVD-related hospitalisation (adjusted hazard ratio, 1.3; 95% CI 1.1-1.6; P < 0.001). The association showed a dose-response; ≥ 3 childhood IRH was associated with a 2.2 times increased risk of CVD-related hospitalisation in adulthood (adjusted hazard ratio, 2.2; 95% CI 1.7-2.9; P < 0.001). The association was observed across all clinical diagnostic groups of infection (upper respiratory tract infection, lower respiratory tract infection, infectious gastroenteritis, urinary tract infection, skin and soft tissue infection, and other viral infection), and individually with CVD diagnostic categories (ischaemic heart disease, ischaemic stroke and peripheral vascular disease).

Conclusions: Severe childhood infection is associated with CVD hospitalisations in adulthood in a dose-dependent manner, independent of population-level risk factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cardiovascular Diseases / epidemiology*
  • Cardiovascular Diseases / mortality
  • Child
  • Child, Preschool
  • Communicable Diseases / epidemiology*
  • Female
  • Hospitalization / statistics & numerical data*
  • Humans
  • Kaplan-Meier Estimate
  • Longitudinal Studies
  • Male
  • Risk Factors

Grants and funding

The research was supported by the Victorian Government's Operational Infrastructure Support Program and a University of Western Australia Research Development Award. DPB is supported by a Senior Research Fellowship from the National Health and Medical Research Council (APP1064629), Australia and by an honorary Future Leader Fellowship from the National Heart Foundation (100026), Australia. HCM is supported by an Early Career Fellowship from the National Health and Medical Research Council, Australia. KWC is supported by the McCusker Charitable Foundation Bioinformatics Centre. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.