Molecular analysis of alpha‐ and beta‐thalassemia in Meizhou region and comparison of gene mutation spectrum with different regions of southern China

Abstract

Abstract Background Thalassemia is a group of inherited autosomal recessive hemolytic anemia disease caused by reduced or absent synthesis of globin chain/chains of hemoglobin. Only few studies showed the molecular characterization of α‐ and β‐thalassemia in Meizhou city of China. Methods A total of 22,401 individuals were collected; hematological and hemoglobin electrophoresis analysis and thalassemia genetic testing were performed. Results Eleven thousand and thirty (49.24%) cases with microcytosis (mean corpuscular volume (MCV) < 82 fl), 11,074 (49.44%) cases with hypochromia (mean corpuscular Hb (MCH) < 27 pg) in 22,401 subjects, 11,085 cases with abnormal hemoglobin results were identified in subjects aged ≥6 months. 7,322 (32.69%) subjects harbored thalassemia mutations, including 4,841 (21.61%) subjects with α‐thalassemia, 2,237 (9.99%) with β‐thalassemia, and 244 (1.09%) with α‐thalassemia combined β‐thalassemia. 18 genotypes of α‐thalassemia mutations and 27 genotypes of β‐thalassemia mutations were characterized. The most frequent α gene mutation was ‐‐ SEA (64.69%), followed by ‐α 3.7 (19.93%), ‐α 4.2 (7.73%), α CS α (3.97%), and α WS α (2.83%). The six most common β‐thalassemia mutations were IVS‐II‐654 (C>T) (39.79%), CD41‐42 (‐TCTT) (33.02%), −28 (A>G) (10.38%), CD17 (A>T) (9.08%), CD27‐28 (+C) (2.14%), and CD26 (G>A) (2.02%). In addition, MCV and MCH were sensitive markers for α‐ and β‐thalassemia except for ‐α 3.7 /αα, ‐α 4.2 /αα, α CS α/αα, α WS α/αα, and β Cap+40−43 /β N . Conclusions The ‐‐ SEA , ‐α 3.7 , and ‐α 4.2 deletions were the main mutations of α‐thalassemia, while IVS‐II‐654 (C>T), CD41‐42 (‐TCTT), −28 (A>G), and CD17 (A>T) mutations of β‐thalassemia in Meizhou. There were some differences in thalassemia mutation frequencies in Meizhou city from other populations in China.

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