Zulkeflee, Razan Hayati and Ramli, Marini and Abdul Halim, Sarah and Adzahar, Sumaiyah and Syukri, Faris Danish and Zulkafli, Zefarina and Bahar, Rosnah and suhaimi, Zharif
(2026)
A systematic review of the prevalence and phenotypic characteristics of hemoglobin Malay in Southeast Asia.
Iraqi Journal of Haematology, 15 (1).
pp. 8-15.
ISSN 2072-8069
E-ISSN 2543-2702
Abstract
BACKGROUND:
Hemoglobin (Hb) Malay is a β-globin variant associated with a β⁺⁺-thalassemia phenotype, resulting from a point mutation at codon 19 of the β-globin gene. Data on its prevalence and phenotypic characteristics remain fragmented.
AIMS:
This study aimed to determine the prevalence of Hb Malay and describe its phenotypic spectrum across different regions.
METHODS:
A systematic literature search was conducted using Medline (PubMed), CINAHL (EBSCOhost), and ScienceDirect. Relevant studies published from database inception to 2024 were screened according to predefined eligibility criteria. Meta-analysis was performed using Review Manager (RevMan) version 5.4. Pooled prevalence estimates were calculated, and outcomes were reported with corresponding 95% confidence intervals.
RESULTS:
Twenty-two studies involving 19,956 participants were included. Due to substantial heterogeneity among studies (I2 = 86%, P < 0.001), a random-effects model was applied. The overall pooled prevalence of Hb Malay was 3.53%. The highest prevalence was observed in Indonesia (12.18%), followed by Thailand (3.43%), Malaysia (3.02%), and Singapore (0.75%).
CONCLUSION:
This study represents the first comprehensive meta-analysis of Hb Malay prevalence and phenotypic characteristics over 30 years (1990–2024). Although Hb Malay is a relatively rare Hb variant largely confined to Southeast Asia, its clinical relevance is significant, particularly when coinherited with other β-thalassemia mutations, which may modify disease severity and increase transfusion requirements. These findings provide valuable evidence to inform regional thalassemia screening strategies and support targeted genetic counselling programmes
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