Prevention and control of thalassemia in Guangdong Province, Southern China: insights from an 11-year retrospective study
Background Thalassemia, a prevalent monogenic inherited disorder, represents a significant public health concern in southern China. This comprehensive study retrospectively analysed prenatal diagnostic data for thalassemia over an 11-year period in Guangdong Province, a high-prevalence region in sou...
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Published in | Annals of medicine (Helsinki) Vol. 57; no. 1 |
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31.12.2025
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Abstract | Background Thalassemia, a prevalent monogenic inherited disorder, represents a significant public health concern in southern China. This comprehensive study retrospectively analysed prenatal diagnostic data for thalassemia over an 11-year period in Guangdong Province, a high-prevalence region in southern China.Methods Prenatal diagnosis (PND) of thalassemia was performed on 22,127 foetuses from at-risk pregnancies, following standardized protocols for invasive sampling, foetal sample collection and laboratory processing. Thalassemia mutations were identified using PCR-based molecular techniques.Results The analysis revealed that 16,812 cases (75.98%) were diagnosed with thalassemia, including 12,636 cases (57.11%) identified as α-thalassemia, 3961 cases (17.90%) as β-thalassemia and 215 cases (0.97%) as co-inheritance of α- and β-thalassemia. Among these, 5769 cases (26.08%) were diagnosed with intermedia or severe thalassemia genotypes, of which 2593 underwent pregnancy termination. Additionally, our study detected 275 cases of rare thalassemia variants. The retrospective analysis encompassed critical aspects including the timing of PND, genotype spectrum and rare variant identification, complemented by a synthesis of clinical practice insights.Conclusions This large-scale study provides substantial epidemiological data and clinical insights that significantly contribute to the enhancement of thalassemia prevention and control strategies in Guangdong Province. |
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AbstractList | Background Thalassemia, a prevalent monogenic inherited disorder, represents a significant public health concern in southern China. This comprehensive study retrospectively analysed prenatal diagnostic data for thalassemia over an 11-year period in Guangdong Province, a high-prevalence region in southern China.Methods Prenatal diagnosis (PND) of thalassemia was performed on 22,127 foetuses from at-risk pregnancies, following standardized protocols for invasive sampling, foetal sample collection and laboratory processing. Thalassemia mutations were identified using PCR-based molecular techniques.Results The analysis revealed that 16,812 cases (75.98%) were diagnosed with thalassemia, including 12,636 cases (57.11%) identified as α-thalassemia, 3961 cases (17.90%) as β-thalassemia and 215 cases (0.97%) as co-inheritance of α- and β-thalassemia. Among these, 5769 cases (26.08%) were diagnosed with intermedia or severe thalassemia genotypes, of which 2593 underwent pregnancy termination. Additionally, our study detected 275 cases of rare thalassemia variants. The retrospective analysis encompassed critical aspects including the timing of PND, genotype spectrum and rare variant identification, complemented by a synthesis of clinical practice insights.Conclusions This large-scale study provides substantial epidemiological data and clinical insights that significantly contribute to the enhancement of thalassemia prevention and control strategies in Guangdong Province. |
Author | Wu, Jing Luo, Mingyong Qin, Danqing Liang, Jie Yao, Cuize Liang, Kailing Wang, Yixia He, Wei Bao, Xiuqin Du, Li Wang, Jicheng Zhu, Juan |
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Cites_doi | 10.1016/j.bpobgyn.2016.10.013 10.1080/16078454.2023.2184118 10.1016/j.bpobgyn.2006.11.009 10.1016/j.clinbiochem.2019.11.003 10.1016/j.ogc.2017.02.004 10.1016/j.blre.2023.101074 10.1177/10760296221119807 10.3389/fgene.2023.1208102 10.1177/03000605211031429 10.4103/ijpvm.IJPVM_83_16 10.1515/jpm-2015-0434 10.1002/mgg3.1699 10.1002/jcla.23982 10.1371/journal.pone.0283051 10.1007/s00404-018-4807-4 10.1111/j.1471-0528.1991.tb13511.x 10.1159/000075140 10.1186/s40246-023-00486-4 10.2147/IJWH.S89308 10.1038/s41598-017-00967-2 10.1080/03630269.2017.1378672 10.3760/cma.j.issn.1003-9406.2015.02.016 10.1371/journal.pone.0089855 10.1186/1471-2458-14-905 10.1002/pd.1079 10.1067/mob.2001.111716 10.1080/03630269.2021.2008960 |
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Notes | Li Du and Jing Wu are co-corresponding authors with equal contribution Supplemental data for this article can be accessed online at https://doi.org/10.1080/07853890.2025.2548970. |
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References | e_1_3_4_4_1 e_1_3_4_3_1 e_1_3_4_2_1 Qin DQ (e_1_3_4_6_1) 2022; 45 e_1_3_4_9_1 e_1_3_4_8_1 e_1_3_4_7_1 e_1_3_4_20_1 e_1_3_4_5_1 e_1_3_4_23_1 e_1_3_4_24_1 Qin DQ (e_1_3_4_28_1) 2020; 28 e_1_3_4_21_1 e_1_3_4_22_1 e_1_3_4_27_1 e_1_3_4_26_1 e_1_3_4_29_1 Li M (e_1_3_4_25_1) 2016; 31 e_1_3_4_31_1 e_1_3_4_30_1 e_1_3_4_12_1 e_1_3_4_13_1 e_1_3_4_10_1 e_1_3_4_11_1 e_1_3_4_16_1 e_1_3_4_17_1 e_1_3_4_14_1 e_1_3_4_15_1 e_1_3_4_18_1 e_1_3_4_19_1 |
References_xml | – ident: e_1_3_4_2_1 doi: 10.1016/j.bpobgyn.2016.10.013 – ident: e_1_3_4_8_1 doi: 10.1080/16078454.2023.2184118 – ident: e_1_3_4_20_1 doi: 10.1016/j.bpobgyn.2006.11.009 – ident: e_1_3_4_7_1 doi: 10.1016/j.clinbiochem.2019.11.003 – ident: e_1_3_4_14_1 doi: 10.1016/j.ogc.2017.02.004 – ident: e_1_3_4_3_1 doi: 10.1016/j.blre.2023.101074 – ident: e_1_3_4_23_1 doi: 10.1177/10760296221119807 – ident: e_1_3_4_26_1 doi: 10.3389/fgene.2023.1208102 – volume: 28 start-page: 577 issue: 2 year: 2020 ident: e_1_3_4_28_1 article-title: Gene diagnosis and phenotypic analysis of β-thalassemia caused from a rare synonymous mutation CD29 (C > T) publication-title: Zhongguo Shi Yan Xue Ye Xue Za Zhi – ident: e_1_3_4_30_1 doi: 10.1177/03000605211031429 – ident: e_1_3_4_16_1 doi: 10.4103/ijpvm.IJPVM_83_16 – volume: 31 start-page: 541 issue: 3 year: 2016 ident: e_1_3_4_25_1 article-title: Analysis on genotype distribution and prenatal diagnosis of thalassemia in different nationalities in Guangxi publication-title: Matern Child Health Care China – ident: e_1_3_4_15_1 doi: 10.1515/jpm-2015-0434 – volume: 45 start-page: 483 issue: 5 year: 2022 ident: e_1_3_4_6_1 article-title: A retrospective analysis of 8005 cases of prenatal genetic diagnosis of thalassemia using PCR‐flow fluorescence hybridization publication-title: Chin J Lab Med – ident: e_1_3_4_29_1 doi: 10.1002/mgg3.1699 – ident: e_1_3_4_13_1 doi: 10.1002/jcla.23982 – ident: e_1_3_4_21_1 doi: 10.1371/journal.pone.0283051 – ident: e_1_3_4_22_1 doi: 10.1007/s00404-018-4807-4 – ident: e_1_3_4_17_1 doi: 10.1111/j.1471-0528.1991.tb13511.x – ident: e_1_3_4_19_1 doi: 10.1159/000075140 – ident: e_1_3_4_27_1 doi: 10.1186/s40246-023-00486-4 – ident: e_1_3_4_5_1 doi: 10.2147/IJWH.S89308 – ident: e_1_3_4_4_1 doi: 10.1038/s41598-017-00967-2 – ident: e_1_3_4_12_1 doi: 10.1080/03630269.2017.1378672 – ident: e_1_3_4_31_1 doi: 10.3760/cma.j.issn.1003-9406.2015.02.016 – ident: e_1_3_4_9_1 doi: 10.1371/journal.pone.0089855 – ident: e_1_3_4_10_1 doi: 10.1186/1471-2458-14-905 – ident: e_1_3_4_11_1 doi: 10.1002/pd.1079 – ident: e_1_3_4_18_1 doi: 10.1067/mob.2001.111716 – ident: e_1_3_4_24_1 doi: 10.1080/03630269.2021.2008960 |
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SubjectTerms | genetic analysis Medical Genetics & Genomics prenatal diagnosis (PND) rare variant southern China Thalassemia |
Title | Prevention and control of thalassemia in Guangdong Province, Southern China: insights from an 11-year retrospective study |
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