Evidence for chronic low-grade systemic inflammation in individuals with agoraphobia from a population-based prospective study

PLoS One. 2015 Apr 13;10(4):e0123757. doi: 10.1371/journal.pone.0123757. eCollection 2015.

Abstract

Background: Anxiety disorders have been linked to an increased risk of incident coronary heart disease in which inflammation plays a key pathogenic role. To date, no studies have looked at the association between proinflammatory markers and agoraphobia.

Methods: In a random Swiss population sample of 2890 persons (35-67 years, 53% women), we diagnosed a total of 124 individuals (4.3%) with agoraphobia using a validated semi-structured psychiatric interview. We also assessed socioeconomic status, traditional cardiovascular risk factors (i.e., body mass index, hypertension, blood glucose levels, total cholesterol/high-density lipoprotein-cholesterol ratio), and health behaviors (i.e., smoking, alcohol consumption, and physical activity), and other major psychiatric diseases (other anxiety disorders, major depressive disorder, drug dependence) which were treated as covariates in linear regression models. Circulating levels of inflammatory markers, statistically controlled for the baseline demographic and health-related measures, were determined at a mean follow-up of 5.5 ± 0.4 years (range 4.7 - 8.5).

Results: Individuals with agoraphobia had significantly higher follow-up levels of C-reactive protein (p = 0.007) and tumor-necrosis-factor-α (p = 0.042) as well as lower levels of the cardioprotective marker adiponectin (p = 0.032) than their non-agoraphobic counterparts. Follow-up levels of interleukin (IL)-1β and IL-6 did not significantly differ between the two groups.

Conclusions: Our results suggest an increase in chronic low-grade inflammation in agoraphobia over time. Such a mechanism might link agoraphobia with an increased risk of atherosclerosis and coronary heart disease, and needs to be tested in longitudinal studies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Agoraphobia / complications*
  • Agoraphobia / pathology*
  • Chronic Disease
  • Female
  • Follow-Up Studies
  • Humans
  • Inflammation / complications*
  • Inflammation / pathology*
  • Male
  • Middle Aged
  • Models, Biological
  • Prospective Studies

Grants and funding

Peter Vollenweider, Gérard Waeber and Martin Preisig received two unrestricted grants from GlaxoSmithKline to build the cohort and to complete the physical and psychiatric baseline investigations. The CoLaus|PsyCoLaus study was and is supported by research grants from GlaxoSmithKline, the Faculty of Biology and Medicine of Lausanne, and the Swiss National Science Foundation (grants 3200B0-105993, 3200B0-118308, 33CSCO-122661, 33CS30-139468 and 33CS30-148401). The funders had no role in the study design, in the collection, management, analysis or interpretation of the data, in the preparation, review or approval of the manuscript, and the decision to submit the manuscript for publication.