Temporal Trends in Mortality Associated with Comorbid Type 2 Diabetes and Schizophrenia: The Fremantle Diabetes Study.

J Clin Med

Medical School, University of Western Australia, Fremantle Hospital, P.O. Box 480, Fremantle, WA 6959, Australia.

Published: December 2022

AI Article Synopsis

  • The Fremantle Diabetes Study (FDS) aimed to determine if the mortality gap related to schizophrenia and type 2 diabetes improved from Phase I (FDS1) to Phase II (FDS2) over 15 years.
  • Participants from both phases were compared, revealing a higher mortality rate for those with both conditions, which was particularly pronounced in FDS1 and FDS2 subgroups with type 2 diabetes and schizophrenia.
  • The findings indicate that the combination of type 2 diabetes and schizophrenia continues to be linked to a significant mortality risk, highlighting an increasing concern over the years.

Article Abstract

Background: In Phase I of the community-based Fremantle Diabetes Study (FDS1), there was evidence of a deleterious interactive effect of schizophrenia and type 2 diabetes on mortality. Our aim was to investigate whether the mortality gap had improved in FDS Phase II (FDS2) conducted 15 years later.

Methods: Participants with type 2 diabetes from FDS1 (n = 1291 recruited 1993-1996) and FDS2 (n = 1509 recruited 2008-2011) were age-, sex- and postcode-matched 1:4 to people without diabetes. Schizophrenia at entry and incident deaths were ascertained from validated administrative data.

Results: Schizophrenia affected 50/11,195 (0.45%) of participants without diabetes and 17/2800 (0.61%) of those with type 2 diabetes ( = 0.284). During 142,304 person-years of follow-up, the mortality rate (95% CI) was lowest for the FDS2 subgroup without diabetes/schizophrenia (18.2 (16.9, 19.6)/1000 person-years) and highest in FDS2 and FDS1 subgroups with type 2 diabetes/schizophrenia (53.3 (14.5, 136.6) and 98.0 (31.8, 228.8)/1000 person-years, respectively). Compared to the respective FDS subgroup without diabetes/schizophrenia, the mortality rate ratio was approximately 50% higher in the type 2 diabetes subgroup, and three times higher in those with type 2 diabetes/schizophrenia. In Cox regression, unadjusted hazard ratios were highest in those with type 2 diabetes/schizophrenia in FDS1 (HR (95% CI): 3.71 (1.54, 8.93) and FDS2 (2.96 (1.11, 7.91)), increasing to 5.61 (2.33, 13.5) and 26.9 (9.94, 72.6), respectively, after adjustment for age.

Conclusions: Although limited by small numbers of schizophrenia cases, these data suggest that comorbid type 2 diabetes and schizophrenia remains associated with a substantial and possibly increasing mortality gap.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9820984PMC
http://dx.doi.org/10.3390/jcm12010300DOI Listing

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