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  • Xiao, Meifang  (4)
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  • 1
    In: Journal of Clinical Laboratory Analysis, Wiley, Vol. 36, No. 3 ( 2022-03)
    Abstract: Hainan 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. Methods We 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. Results In 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 ‐α 3.7 /αα (19.70%), ‐α 4.2 /αα (19.39%), αα/‐‐ SEA (15.60%), α WS α/αα (9.24%), and ‐α 3.7 /‐α 4.2 (8.90%), and those of β‐thalassemia were β CD41/42(−TTCT) /β N (58.92%), β −28(A 〉 G) /β N (16.05%), β IVS−Ⅱ−654(C 〉 T) /β N (8.42%), β CD71/72(+A) /β N (6.03%), β CD17(A 〉 T) /β N (5.47%), and β CD26 (GAG 〉 AAG) /β N (2.69%). In addition, the frequencies and hematological profiles of many rare mutations of α‐ [Fusion, HKαα, αααanti 4.2 , 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. Conclusion Our 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.
    Type of Medium: Online Resource
    ISSN: 0887-8013 , 1098-2825
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 2001635-9
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  • 2
    Online Resource
    Online Resource
    Frontiers Media SA ; 2022
    In:  Frontiers in Nutrition Vol. 9 ( 2022-11-17)
    In: Frontiers in Nutrition, Frontiers Media SA, Vol. 9 ( 2022-11-17)
    Abstract: There are limited studies on iron-deficiency anemia (IDA) in carriers of various thalassemia genotypes. However, for pregnant women (PW) with high iron demand, ignoring the phenomenon of carrying the thalassemia genes combined with IDA may lead to adverse pregnancy outcomes. Methods The hematological phenotype indexes of 15,051 PW who received a prenatal diagnosis of thalassemia in our hospital were analyzed, and the plasma ferritin (PF) of 714 anemic pregnant women (APW) was determined. Results The results showed that 87.43% of APW without thalassemia suffered from IDA. Among APW with various thalassemia genotypes, we found that 40.00∼77.78% of subjects with α-thalassemia silent genotypes [α CS (or QS) α/αα (40.00%), –α 3.7(or 4.2) /αα (57.65%), and α WS α/αα (77.78%)] and 18.18∼84.21% of subjects with α-thalassemia minor genotypes [α CS (or QS) α/–α 3.7(or 4.2) (18.18%), –α 3.7(or 4.2) /–α 3.7(or 4.2) (40.00%), αα/– SEA (44.55%), and α WS α/–α 3.7(or 4.2) (84.21%)] developed IDA, while in subjects with α-thalassemia intermedia genotypes, only α WS α/– SEA was associated with IDA, with an incidence of 16.67%. However, the incidence of IDA in APW with common β-thalassemia minor genotypes (β CD17(A & gt;T) /β, β CD41/42 (–TTCT) /β, β CD71/72(+ A ) /β, β IVS– II –654(C & gt;T) /β, and β –28(A & gt;G) /β) was less than 10.85%. In addition, the APW with β-thalassemia minor had a higher PF level than the APW without thalassemia. Conclusion Our study is the first to reveal differences in the prevalence of IDA among PW with various thalassemia genotypes, indicating that the possibility of IDA should be fully considered when managing PW with α-thalassemia silent or minor genotypes in high-risk areas, and that iron supplementation should be monitored dynamically for PW with β-thalassemia minor genotypes.
    Type of Medium: Online Resource
    ISSN: 2296-861X
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2022
    detail.hit.zdb_id: 2776676-7
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  • 3
    Online Resource
    Online Resource
    Frontiers Media SA ; 2022
    In:  Frontiers in Genetics Vol. 13 ( 2022-6-13)
    In: Frontiers in Genetics, Frontiers Media SA, Vol. 13 ( 2022-6-13)
    Abstract: Background: There are limited studies on the molecular profile of thalassemia in Hainan, the free trade island in China. Our aim was to reveal the prevalence and molecular mutation spectrum of thalassemia in different ethnic groups and regions of Hainan through a large sample study for the first time. Methods: A total of 231,596 individuals from 19 cities and counties in Hainan were screened by hematological parameter analysis, and further genetic analysis was performed on individuals with MCV less than 82 fL. Results: Totally, 31,780 (13.72%) subjects were diagnosed as thalassemia carriers. The overall prevalence of α-thalassemia, β-thalassemia, and α+β-thalassemia were 11.04%, 1.48%, and 1.20%, respectively. We further analyzed the molecular profiles of thalassemia in various ethnic groups and mainly compared the difference between Han and Li. The results showed that the frequency of thalassemia in the Li population (47.03%) was much higher than that in Han (9.37%). Except for β-thalassemia (1.31% of Li vs. 1.47% of Han), the frequencies of α-thalassemia (39.59% of Li vs. 7.35% of Han) and α+β-thalassemia (6.13% of Li vs. 0.56% of Han) in the Li were obviously higher than those in Han. The high-frequent genotypes of α-thalassemia in Han were αα/-- SEA (25.55%), -α 3.7 /αα (22.17%), -α 4.2 /αα (21.59%), α WS α/αα (8.93%), and -α 3.7 /-α 4.2 (4.17%) and those of Li were -α 4.2 /αα (17.24%), -α 3.7 /αα (17.16%), -α 3.7 /-α 4.2 (15.09%), α WS α/αα (9.69%), and α WS α/-α 3.7 (8.06%), respectively. The αα/-- SEA was the highest genotype of α-thalassemia in Han but only accounted for 1.87% in Li. For β-thalassemia, the top three high-frequent genotypes in both Han and Li were β CD41/42(-TTCT) /β N , β -28(A & gt;G) /β N , and β IVS-Ⅱ-654(C & gt;T) /β N , but the frequency of β CD41/42(-TTCT) /β N in Li (90.96%) was much higher than that in Han (56.32%) and the data reported in other provinces of China. Additionally, the prevalence of thalassemia ranged from 8.16% to 34.35% in Hainan, Wuzhishan, Baoting, Qiongzhong, and Baisha have a higher prevalence than other areas. Conclusion: Our study revealed the characteristics of ethnic and regional differences in the prevalence of thalassemia in the childbearing age population of Hainan for the first time, indicating that the prevalence of thalassemia among Li nationality is the highest in China. Those findings will be useful for genetic counseling and the prevention of thalassemia.
    Type of Medium: Online Resource
    ISSN: 1664-8021
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2022
    detail.hit.zdb_id: 2606823-0
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  • 4
    In: Frontiers in Nutrition, Frontiers Media SA, Vol. 10 ( 2023-8-30)
    Type of Medium: Online Resource
    ISSN: 2296-861X
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2023
    detail.hit.zdb_id: 2776676-7
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