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Genetics of type 2 diabetes (T2D) in Malaysia: a review

  • Nurul Humaira Mohd Redzuan
  • , Siti Aishah Sulaiman
  • , Nor Azian Abdul Murad
  • , Norfazilah Ahmad
  • , Chim C. Lang
  • , Rahman Jamal (Lead / Corresponding author)

Research output: Contribution to journalReview articlepeer-review

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Abstract

Type 2 diabetes (T2D) is a significant public health concern in Malaysia, with rising prevalence across its multi-ethnic population. Genetic predisposition plays a key role in the development of T2D, but studies focusing on Malaysian populations remain limited. This review summarizes existing evidence on genetic variants associated with T2D in the Malaysian population, focusing on single-nucleotide variants and ethnic-specific risk patterns. A comprehensive literature search was conducted across major databases, identifying 31 relevant studies published between 2000 and 2024. Key findings were discussed to identify commonly implicated variants and ethnic differences in the association with T2D. These findings highlight the ethnic-specific genetic risk factors within the Malaysians, confirming the need to consider ethnic diversity and inclusion in T2D genetic study design, analysis, and clinical translation. This review offers a novel insight into the ethnic-specific effects of Malaysian T2D risks, particularly the underrepresented Malay ethnic group, which is important for the future development of precision medicine strategies for T2D in Malaysia.

Original languageEnglish
Article number109
Number of pages13
JournalEgyptian Journal of Medical Human Genetics
Volume26
Issue number1
Early online date21 Jun 2025
DOIs
Publication statusPublished - Dec 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Ethnic-specific risk
  • Genetic abnormalities
  • Genetic predisposition
  • Genetic variants
  • Insulin resistance
  • Malaysia
  • Review
  • Type 2 diabetes

ASJC Scopus subject areas

  • Genetics(clinical)

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