4.3 Article

The Association Between Psychiatric Disorders and Telomere Length: A Meta-Analysis Involving 14,827 Persons

Journal

PSYCHOSOMATIC MEDICINE
Volume 78, Issue 7, Pages 776-787

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/PSY.0000000000000356

Keywords

telomere length; depressive disorders; anxiety disorders; psychosis; posttraumatic stress disorder; bipolar disorders

Funding

  1. National Institutes of Health [R01 MH096767]
  2. NWO-VICI [91811602]
  3. Swedish Society of Medicine [SLS-244821]
  4. Swedish Research Council [2015-00387]
  5. Marie Sklodowska Curie Actions, Cofund [INCA 600398]
  6. Sjobring Foundation
  7. OM Persson Foundation
  8. province of Scania (Sweden) state grants
  9. NIMH [R01 MH083784]
  10. DOD [W81XWH-10-1-0021]
  11. O'Shaughnessy Foundation
  12. Tinberg Family

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Objective This study examined the relationship between leukocyte telomere length (LTL), a marker of cell aging, and psychiatric disorders in adults compared with controls using meta-analytic methods. Methods Data were abstracted from studies examining the relationship between LTL and adult psychiatric disorders. In addition to an overall estimate of effect size, subgroup analyses and meta-regression were performed to examine whether covariates (including psychiatric diagnoses) moderated the estimate. Results A significant overall effect size showing LTL shortening was found across all psychiatric disorders (Hedge g = -0.50, p < .001). Subgroup analyses did not demonstrate significant differences in effect size based on individual covariates (psychiatric disorder, sex, age, or assay method). The meta-regression indicated that although type of disorder and, likely, age moderate the overall effect size, the heterogeneity between studies could not be explained by a model that included these variables as well as sex and assay method. Although not significantly different, posttraumatic stress disorder, anxiety disorders, and depressive disorders had comparatively larger effect sizes (-1.27, -0.53, and -0.55), and psychotic and bipolar disorders had comparatively smaller ones (-0.23 and -0.26). Conclusions We observed a robust effect size of LTL shortening for psychiatric disorders as a whole compared with controls. The results were less straightforward regarding relative differences in the strength of this association by specific disorder. Future studies should focus on mechanisms explaining accelerated cell aging with psychiatric illness, defining directions (if any) of causality and elucidating possible differences in this association between disorders.

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