Evidence map›Paper›PMID 41212165›Full record

ArticleHuman molecular genetics2025

Catalog of 73 novel variants in thalassemia: discoveries and insights.

Jungao Huang, Zhenchang Liu, Feng Miao, Liping Huang, Chunlong Xiao, Ping Zhang, Jiayu Huang, Yan Li, Xiaoyan Huang, Xiaoqin Xin

Abstract read
In one paragraph

Article in Human molecular genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Jungao HuangDepartment of Medical Genetic, Ganzhou Maternal and Child Health Hospital, Ganzhou, Jiangxi Province 341000, China.ORCID 0000-0002-3197-6044
Zhenchang LiuDepartment of Clinical Laboratory, Huichang County Maternal and Child Health Care Center, Ganzhou, Jiangxi Province, China.
Feng MiaoDepartment of Clinical Laboratory, Quannan County Maternal and Child Health Care Center, Ganzhou, Jiangxi Province, China.
Liping HuangDepartment of Clinical Laboratory, Xinfeng County Maternal and Child Health Care Center, Ganzhou, Jiangxi Province, China.
Chunlong XiaoDepartment of Medica, Nankang District Maternal and Child Health Care Center, Ganzhou, Jiangxi Province, China.
Ping ZhangDepartment of obstetrics and gynecology, Yudu County Maternal and Child Health Care Center, Ganzhou, Jiangxi Province, China.
Jiayu HuangDepartment of Premarital Examination, Ganxian District Maternal and Child Health Care Center, Ganzhou, Jiangxi Province, China.
Yan LiDepartment of Clinical Laboratory, Xinfeng County Maternal and Child Health Care Center, Ganzhou, Jiangxi Province, China.
Xiaoyan HuangClin Lab, BGI Genomics, Wuhan, China.
Xiaoqin XinDepartment of Clinical Laboratory, Ganzhou People's Hospital, Ganzhou, Jiangxi Province, China.

Funding

Jiangxi Provincial Natural Science Foundation 20232BAB216098
6 · The paper itself

Abstract

Thalassemia is a genetic blood disorder caused by disrupted hemoglobin synthesis, posing significant public health challenges. This study aims to expand the identification of novel thalassemia variants in a large cohort from pre-marriage screenings in Ganzhou, Southern Jiangxi, China. Data from 229 246 individuals screened through Next-Generation Sequencing (NGS) from 2019 to 2022 led to the identification of 180 participants with novel variants, marking the first large-scale documentation of such variations in the population. Among them, 51.1% were male with a mean age of 27 years, and the frequency of novel thalassemia variants was 0.079%. We uncovered 180 novel variants, including 68 α-thalassemia variants across 33 types (0.0297% frequency) and 112 β-thalassemia variants belonging to 40 unique types (0.0489% frequency). The most common α-thalassemia genotype was HBA1:c.95 + 9C > T at 17.65%, while HBB:c.-180G > C was most prevalent among β-thalassemia variants at 23.21%. Ten novel α-thalassemia variants were linked to mild α-thalassemia, and clinical phenotypes were documented for 21 complex genotypes. This study catalogues 73 novel variants and highlights the genetic diversity of thalassemia, informing future preventive strategies.

Indexed as

alpha-Thalassemiabeta-ThalassemiaGenetic VariationThalassemiaAdolescentAdultalpha-GlobinsChildChinaFemaleGenotypeHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedPhenotypealpha-Globinsgeneral populationNext-Generation Sequencing (NGS)novel variantsThalassemia

Identifiers

PMID41212165
PMCPMC12680600

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.