Evidence map›Paper›PMID 42008351›Full record

ArticleBlood transfusion = Trasfusione del sangue

Serology and molecular genetic analysis of weakened expression of ABO blood group antigens in Chinese pediatric population.

Qian Ren, Jinfeng Li, Chunmiao Li, Xingli Liu, Xiaolin Ma

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Article in Blood transfusion = Trasfusione del sangue. 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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5 · Who and what money

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5 authors.

Qian RenDepartment of Blood Transfusion, Jinan Children's Hospital, Jinan, Shandong Province, China.
Jinfeng LiClinical Laboroatory, People's Hospital of Zhoucun District Zibo, Zibo, Shandong Province, China.
Chunmiao LiDepartment of Blood Transfusion, Jinan Children's Hospital, Jinan, Shandong Province, China.
Xingli LiuDepartment of Blood Transfusion, Jinan Children's Hospital, Jinan, Shandong Province, China.
Xiaolin MaDepartment of Blood Transfusion, Jinan Children's Hospital, Jinan, Shandong Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe ABO blood group system is vital for red blood cell antigens. Weakened expression of ABO antigens often leads to misidentification of blood types, challenging transfusion safety. MATERIALS AND

methodsBlood samples from 44 cases underwent serological analysis using microcolumn agglutination and tube tests. To investigate genetic variations, we sequenced the promoter region and exons 1-7 of the ABO gene. We also examined the relationship between ABO haplotypes and the presence of rare alleles. We used PolyPhen-2 to predict the structure and function of glycosyltransferase B (GTB) and classify missense variants. We also conducted pedigree analysis on 4 selected cases to further understand the inheritance patterns.

resultsWe detected 18 different ABO subgroup alleles in 44 cases of weakened ABO antigen expression. We found 7 subtype A (predominantly A2), 7 subtype B (which included Bw and B3), one cisAB, and 3 group B(A). The complete phenotypes we observed included A2, Bw, B3, A2B, ABw, AB3, cisAB, and B(A). Notably, we discovered a rare B allele characterized by the c.538C>T variant, which alters residue 180 to p.Arg180Cys. This variant received a PolyPhen-2 score of 1.00, suggesting a high likelihood of damaging effects. Furthermore, pedigree analysis supported an autosomal inheritance pattern for this allele. DISCUSSION: The weakened expression of ABO antigens in young children may result from their immature immune systems or subtyping. ABO genotyping is essential to accurately identify blood groups and ensure transfusion safety.

Indexed as

ABO Blood-Group SystemAllelesBlood Grouping and CrossmatchingChildChild, PreschoolChinaEast Asian PeopleExonsFemaleHaplotypesHumansInfantMaleMutation, MissensePedigreePromoter Regions, GeneticABO Blood-Group System

Identifiers

PMID42008351
PMCPMC13368444

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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.