Mat Ghani Siti Nor Assyuhada , Che Ghazali Norul Hajar , Siti-Azhani Amran , Zefarina Zulkafli , Nilie Syamila Mohammad Isa , Nur Saiyidah Hanisah Ali , Siti Aisyah Mohamad , Fika Tri Anggraini , Geoffrey Keith Chambers , Hisham Atan Edinur
{"title":"婆罗洲四个人群中人类血小板抗原编码基因的等位基因变异","authors":"Mat Ghani Siti Nor Assyuhada , Che Ghazali Norul Hajar , Siti-Azhani Amran , Zefarina Zulkafli , Nilie Syamila Mohammad Isa , Nur Saiyidah Hanisah Ali , Siti Aisyah Mohamad , Fika Tri Anggraini , Geoffrey Keith Chambers , Hisham Atan Edinur","doi":"10.1016/j.transci.2025.104158","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Human platelet antigens (HPAs) are clinically significant markers in immune-mediated disorders. Comprehensive understanding of HPA genetic profiles at population level is essential for the prevention and management of these medical conditions. Such data for HPA allele frequencies have been collected for many ethnic groups in Peninsular Malaysia, but none from Sabah and Sarawak of Borneo. This study aims to determine the frequencies of HPA alleles in Bajau, Kadazan-Dusun, Murut and Melanau populations of Borneo.</div></div><div><h3>Methodology</h3><div>Seven HPA loci (HPA-1 to −6 and −15) were genotyped using the polymerase chain reaction assay with sequence specific primers for 457 DNA samples representing four Borneo indigenous groups.</div></div><div><h3>Results</h3><div>Significant departures from Hardy-Weinberg equilibrium (HWE) were observed for HPA-3 in Bajau, Kadazan-Dusun, Murut and Melanau groups and for HPA-15 in Bajau and Murut. High frequencies of HPA-1a, −2a, −4a, −5a, and −6a alleles were observed across all four populations. Exact tests showed significant differentiation between Borneo and Peninsular Malaysia populations, particularly for HPA-3 and −15. Principal component (PCA) analysis showed that the Borneo indigenous groups clustered closely with other Austronesian populations, consistent with the idea that they share genetic ancestry.</div></div><div><h3>Conclusion</h3><div>Observed HPA allele frequency spectra are uniquely distributed in Bajau, Kadazan-Dusun, Murut and Melanau population groups. The HPA population datasets generated from this study can be used as guidelines for health policy decision making and as reference sources for studying diseases associated with HPAs.</div></div>","PeriodicalId":49422,"journal":{"name":"Transfusion and Apheresis Science","volume":"64 3","pages":"Article 104158"},"PeriodicalIF":1.4000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Allelic variations in the genes coding for human platelet antigens in four population groups in Borneo\",\"authors\":\"Mat Ghani Siti Nor Assyuhada , Che Ghazali Norul Hajar , Siti-Azhani Amran , Zefarina Zulkafli , Nilie Syamila Mohammad Isa , Nur Saiyidah Hanisah Ali , Siti Aisyah Mohamad , Fika Tri Anggraini , Geoffrey Keith Chambers , Hisham Atan Edinur\",\"doi\":\"10.1016/j.transci.2025.104158\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><div>Human platelet antigens (HPAs) are clinically significant markers in immune-mediated disorders. Comprehensive understanding of HPA genetic profiles at population level is essential for the prevention and management of these medical conditions. Such data for HPA allele frequencies have been collected for many ethnic groups in Peninsular Malaysia, but none from Sabah and Sarawak of Borneo. This study aims to determine the frequencies of HPA alleles in Bajau, Kadazan-Dusun, Murut and Melanau populations of Borneo.</div></div><div><h3>Methodology</h3><div>Seven HPA loci (HPA-1 to −6 and −15) were genotyped using the polymerase chain reaction assay with sequence specific primers for 457 DNA samples representing four Borneo indigenous groups.</div></div><div><h3>Results</h3><div>Significant departures from Hardy-Weinberg equilibrium (HWE) were observed for HPA-3 in Bajau, Kadazan-Dusun, Murut and Melanau groups and for HPA-15 in Bajau and Murut. High frequencies of HPA-1a, −2a, −4a, −5a, and −6a alleles were observed across all four populations. Exact tests showed significant differentiation between Borneo and Peninsular Malaysia populations, particularly for HPA-3 and −15. Principal component (PCA) analysis showed that the Borneo indigenous groups clustered closely with other Austronesian populations, consistent with the idea that they share genetic ancestry.</div></div><div><h3>Conclusion</h3><div>Observed HPA allele frequency spectra are uniquely distributed in Bajau, Kadazan-Dusun, Murut and Melanau population groups. The HPA population datasets generated from this study can be used as guidelines for health policy decision making and as reference sources for studying diseases associated with HPAs.</div></div>\",\"PeriodicalId\":49422,\"journal\":{\"name\":\"Transfusion and Apheresis Science\",\"volume\":\"64 3\",\"pages\":\"Article 104158\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2025-05-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Transfusion and Apheresis Science\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1473050225000953\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transfusion and Apheresis Science","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1473050225000953","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"HEMATOLOGY","Score":null,"Total":0}
Allelic variations in the genes coding for human platelet antigens in four population groups in Borneo
Introduction
Human platelet antigens (HPAs) are clinically significant markers in immune-mediated disorders. Comprehensive understanding of HPA genetic profiles at population level is essential for the prevention and management of these medical conditions. Such data for HPA allele frequencies have been collected for many ethnic groups in Peninsular Malaysia, but none from Sabah and Sarawak of Borneo. This study aims to determine the frequencies of HPA alleles in Bajau, Kadazan-Dusun, Murut and Melanau populations of Borneo.
Methodology
Seven HPA loci (HPA-1 to −6 and −15) were genotyped using the polymerase chain reaction assay with sequence specific primers for 457 DNA samples representing four Borneo indigenous groups.
Results
Significant departures from Hardy-Weinberg equilibrium (HWE) were observed for HPA-3 in Bajau, Kadazan-Dusun, Murut and Melanau groups and for HPA-15 in Bajau and Murut. High frequencies of HPA-1a, −2a, −4a, −5a, and −6a alleles were observed across all four populations. Exact tests showed significant differentiation between Borneo and Peninsular Malaysia populations, particularly for HPA-3 and −15. Principal component (PCA) analysis showed that the Borneo indigenous groups clustered closely with other Austronesian populations, consistent with the idea that they share genetic ancestry.
Conclusion
Observed HPA allele frequency spectra are uniquely distributed in Bajau, Kadazan-Dusun, Murut and Melanau population groups. The HPA population datasets generated from this study can be used as guidelines for health policy decision making and as reference sources for studying diseases associated with HPAs.
期刊介绍:
Transfusion and Apheresis Science brings comprehensive and up-to-date information to physicians and health care professionals involved in the rapidly changing fields of transfusion medicine, hemostasis and apheresis. The journal presents original articles relating to scientific and clinical studies in the areas of immunohematology, transfusion practice, bleeding and thrombotic disorders and both therapeutic and donor apheresis including hematopoietic stem cells. Topics covered include the collection and processing of blood, compatibility testing and guidelines for the use of blood products, as well as screening for and transmission of blood-borne diseases. All areas of apheresis - therapeutic and collection - are also addressed. We would like to specifically encourage allied health professionals in this area to submit manuscripts that relate to improved patient and donor care, technical aspects and educational issues.
Transfusion and Apheresis Science features a "Theme" section which includes, in each issue, a group of papers designed to review a specific topic of current importance in transfusion and hemostasis for the discussion of topical issues specific to apheresis and focuses on the operators'' viewpoint. Another section is "What''s Happening" which provides informal reporting of activities in the field. In addition, brief case reports and Letters to the Editor, as well as reviews of meetings and events of general interest, and a listing of recent patents make the journal a complete source of information for practitioners of transfusion, hemostasis and apheresis science. Immediate dissemination of important information is ensured by the commitment of Transfusion and Apheresis Science to rapid publication of both symposia and submitted papers.