Evidence map›Paper›PMID 7626550›Full record

ArticleThe Korean journal of internal medicine1995

Relationships among 64k autoantibodies, pancreatic beta-cell function, HLA-DR antigens and HLA-DQ genes in patients with insulin-dependent diabetes mellitus in Korea.

H C Lee, B S Cha, M S Nam, Y D Song, S K Lim, D H Kim, K B Huh, Y Koh

Open access · goldAbstract readComparative Study
In one paragraph

Article in The Korean journal of internal medicine, 1995. 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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0citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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0 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

H C LeeDepartment of Internal Medicine, Pediatrics, Yonsei University, College of Medicine, Seoul, Korea.
B S Cha
M S Nam
Y D Song
S K Lim
D H Kim
K B Huh
Y Koh
Yonsei University · KRKorea Institute of Drug Safety and Risk Management · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAmong autoantibodies detected in patients with insulin-dependent diabetes mellitus (IDDM), antibodies to 64,000(Mr) islet protein(64k), now recognized as glutamic acid decarboxylase(GAD), appear to be an even more predictive marker of IDDM than islet cytoplasmic antibody (ICA) or insulin autoantibody (IAA). We examined the relationships among 64k autoantibodies, pancreatic beta-cell function, HLA-DR antigens and HLA-DQ genes in patients with IDDM in Korea.

methodsTo identify the 64k autoantibody, the immunoprecipitation method was performed for 35 patients with IDDM and 10 normal controls. In patients with IDDM, serum C-peptide levels were measured and HLA-DR typings and HLA-DQA1 and DQB1 gene typings were performed.

results12 of 35 (34%) patients with IDDM were positive for 64k autoantibody in contrast to none of 10(0%) normal controls. There were no differences in residual pancreatic beta-cell function between 64k autoantibody positive and negative groups. 64k autoantibody was detected more frequently in patients with recent (duration < 6 months, 10/25[40%]) and young -aged(aged < 15 years, 7/18[39%]) onset of IDDM. All of 3(100%) patients with HLA-DR3/DR4 heterotypes were positive in 64k autoantibody, in contrast to 1 of 7(14%) patients without HLA-DR3 nor DR4. The frequencies of HLA-DQA1*0301, HLA-DQB1*0201, DQB1* 0302 and DQB1*0303 gene types were higher in patients with 64k autoantibody (12/12 [100%]) vs. without 64k autoantibody 18/22[81%], 5/11[45%] vs. without 64k autoantibody 5/22[23%], 5/11[45%] vs. without 64k autoantibody 8/22[36%] and 6/11 [55%] vs. without 64k autoantibody 9/22[41%].

conclusionsThere results suggest that 64k autoantibodies have some relationship with HLA-DR, DQA1 and DQB1 genes, but not with residual pancreatic beta-cell function in Korean patients with IDDM.

Indexed as

AdolescentAdultAllelesAnimalsAntibody SpecificityAsian PeopleAutoantibodiesAutoantigensAutoimmune DiseasesChildChild, PreschoolC-PeptideDiabetes Mellitus, Type 1Disease SusceptibilityFemaleGenetic Predisposition to DiseaseAutoantibodiesAutoantigensC-PeptideGlutamate DecarboxylaseHLA-DQA1 antigenHLA-DQ alpha-ChainsHLA-DQ AntigensHLA-DQB1 antigenHLA-DQ beta-ChainsHLA-DR Antigens

Identifiers

PMID7626550
PMCPMC4532034
OpenAlexW1491452949

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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.