Affiliations 

  • 1 Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong SAR, China; Asia Diabetes Foundation, Hong Kong SAR, China. Electronic address: leeling.lim@ummc.edu.my
  • 2 Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia
  • 3 Health Economics Research Centre, Nuffield Department of Public Health, University of Oxford, Oxford, United Kingdom
  • 4 Centre for Clinical Epidemiology, Institute for Clinical Research, National Institute of Health, Selangor, Malaysia
  • 5 Non-communicable Disease Section, Disease Control Division, Ministry of Health, Putrajaya, Malaysia
  • 6 Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, United Kingdom
  • 7 Health Economics Research Centre, Nuffield Department of Public Health, University of Oxford, Oxford, United Kingdom. Electronic address: philip.clarke@ndph.ox.ac.uk
Diabetes Res Clin Pract, 2023 Nov;205:110944.
PMID: 37804999 DOI: 10.1016/j.diabres.2023.110944

Abstract

AIMS: We determined 10-year all-cause mortality trends in diagnosed type 2 diabetes (T2D) population in West Malaysia, a middle-income country in the Western-Pacific region.

METHODS: One million T2D people aged 40-79 registered in the National Diabetes Registry (2009-2018) were linked to death records (censored on 31 December 2019). Standardized absolute mortality rates and standardized mortality ratios (SMRs) were estimated relative to the Malaysian general population, and standardized to the 2019 registry population with respect to sex, age group, and disease duration.

RESULTS: Overall all-cause standardized mortality rates were unchanged in both sexes. Rates increased in males aged 40-49 (annual average percent change [AAPC]: 2.46 % [95 % CI 0.42 %, 4.55 %]) and 50-59 (AAPC: 1.91 % [95 % CI 0.73 %, 3.10 %]), and females aged 40-49 (AAPC: 3.39 % [95 % CI 1.32 %, 5.50 %]). In both sexes, rates increased among those with 1) > 15 years disease duration, 2) prior cardiovascular disease, and 3) Bumiputera (Malay/native) ethnicity. The overall SMR was 1.83 (95 % CI 1.80, 1.86) for males and 1.85 (95 % CI 1.82, 1.89) for females, being higher in younger age groups and showed an increasing trend in those with either > 15 years disease duration or prior cardiovascular disease.

CONCLUSIONS: Mortality trends worsened in certain T2D population in Malaysia.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.