Human platelet antigen polymorphisms (HPA-1, -2, -3, -4, -5 and -15) in major ethnic groups of Pakistan
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Published on: September 6, 2017
1PNS Shifa Hospital, Karachi, Pakistan. farhatab@hotmail.com
Insights
This study determined human platelet antigen (HPA) gene frequencies in Pakistan, revealing variations that impact platelet transfusion and neonatal alloimmune thrombocytopenia risks. Establishing HPA-typed donor registries is recommended.
Area of Science:
- Immunogenetics
- Population genetics
- Transfusion medicine
Background:
- Human platelet antigen (HPA) gene frequencies are crucial for understanding and managing platelet immunological disorders.
- The HPA profile of the Pakistani population was previously unknown, limiting targeted transfusion strategies and disorder management.
Purpose of the Study:
- To determine the gene frequencies of key human platelet antigens (HPA-1 to -5 and -15) across major ethnic groups and castes in Pakistan.
- To assess the implications of these frequencies for platelet transfusion compatibility and the incidence of related immunological disorders.
Main Methods:
- HPA genotyping was performed on 593 individuals from diverse Pakistani ethnic backgrounds.
- The polymerase chain reaction-sequence specific primers (PCR-SSP) method was employed for genotyping, with results detected using polyacrylamide gel electrophoresis.
Main Results:
- Gene frequencies for HPA-1 to -5 and -15 alleles were established for the Pakistani population, with notable variations in HPA-3 between Pathans and Sindhis.
- Estimated mismatch probabilities for platelet transfusions range from 14-37%, indicating potential for alloimmunization.
- The expected incidence of neonatal alloimmune thrombocytopenia (NAIT) due to anti-HPA-1a is less than 1 in 1000 pregnancies, and due to anti-HPA-5b is 8-12 in 1000.
Conclusions:
- The established HPA gene frequencies provide essential data for transfusion services in Pakistan.
- There is a critical need to develop and implement HPA-typed donor registries within national transfusion centers to improve patient outcomes.
Objectives:
Gene frequencies of human platelet antigens (HPA) determine the magnitude of platelet immunological disorders like neonatal alloimmune thrombocytopenia, platelet refractoriness and ease of availability of particular HPA-typed platelet donors in a given community.
Background:
However, the pattern of HPA in Pakistani population is not known.
Aim:
The aim of present study was to determine the gene frequencies of HPA (HPA-1 to -5 and -15) in individuals belonging to major ethnic groups and castes of Pakistani population.
Materials And Methods:
HPA genotyping was done in 593 individuals belonging to all ethnic groups of Pakistan, by polymerase chain reaction-sequence specific primers with detection on polyacrylamide electrophoresis.
Results:
The gene frequencies of the 'a' and 'b' alleles of HPA-1 to -5 and -15 in Pakistanis were as follows: HPA-1a/b, 0.885/0.115; HPA-2a/b, 0.92/0.08; HPA-3a/b, 0.69/0.31; HPA-4a/b, 1/0; HPA-5a/b, 0.9/0.1; HPA-15a/b, 0.59/0.41. Except for significant difference regarding gene frequency of HPA-3 between Pathans and Sindhis, there was no significant difference of HPA-1 to -5 and -15 between major ethnic groups of Pakistan. The estimated mismatch probability regarding platelet antigens 1-5 and 15 in Pakistanis, after transfusion of random donor platelets, is from 14 to 37%. The expected incidence of neonatal alloimmune thrombocytopenia due to anti-HPA-1a in Pakistani pregnant females is < 1 of 1000 pregnancies and 8-12 of 1000 in case of anti-HPA-5b. Homozygosity of HPA-1b, -2b and -5b genotypes ranged from 1 to 2% in the Pakistani population, whereas homozygosity of HPA-3b and -15b was 11 and 18%.
Conclusions:
There is a need to establish donor registries typed for HPA in the transfusion centres of the country.
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