Abstract

BackgroundHainan has one of the high incidences of thalassemia in China, but the epidemiological data in the whole province has not been reported yet. The objective of our study was to reveal the true prevalence and molecular mutation spectrum of thalassemia in the population of Hainan who are of childbearing age.MethodsWe screened 166,936 individuals from 19 cities and counties in Hainan by hematological parameters analysis, and further conducted genetic analysis for individuals whose MCV was less than 82fL.ResultsIn total, 21,619 (12.95%) subjects were diagnosed as thalassemia carriers or patients. The overall prevalence of α‐thalassemia, β‐thalassemia, and α+β‐thalassemia were 10.39%, 1.38%, and 1.18%, respectively. Eleven α‐thalassemia mutations and sixteen β‐thalassemia mutations were identified. The high‐frequent genotypes of α‐thalassemia were ‐α3.7/αα (19.70%), ‐α4.2/αα (19.39%), αα/‐‐SEA (15.60%), αWSα/αα (9.24%), and ‐α3.7/‐α4.2 (8.90%), and those of β‐thalassemia were βCD41/42(−TTCT)/βN (58.92%), β−28(A>G)/βN (16.05%), βIVS−Ⅱ−654(C>T)/βN (8.42%), βCD71/72(+A)/βN (6.03%), βCD17(A>T)/βN (5.47%), and βCD26 (GAG>AAG)/βN (2.69%). In addition, the frequencies and hematological profiles of many rare mutations of α‐ [Fusion, HKαα, αααanti4.2, IVS‐II‐55 (T>G), IVS‐II‐119 (−G,+CTCGGCCC)] and β‐globin genes [−50 (G>A), IVS‐Ⅱ‐81 (C>T)] in Hainan were reported for the first time.ConclusionOur study revealed the high prevalence and extensive molecular spectrum of thalassemia in childbearing age population of Hainan, suggesting thalassemia in Hainan ranks second in prevalence among all regions in China. The findings will be useful for genetic counseling and prevention of thalassemia.

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