Congenital Adrenal Hyperplasia and Human Leukocyte Antigen B: A Meta-Analysis

被引:0
作者
Thibaut, Dylan [1 ]
Walter, Madison R. [1 ]
McGonegal, Courtney [1 ]
Daniel, Ryan [1 ]
Goodman, Jerry [2 ]
机构
[1] Lake Erie Coll Osteopath Med, Ostepath Med, Bradenton, FL 34211 USA
[2] Lake Erie Coll Osteopath Med, Obstet & Gynecol, Bradenton, FL USA
关键词
non-classical congenital adrenal hyperplasia; congenital adrenal hyperplasia; mhc class i; hla-b; mhc; 21- hydroxylase deficiency; cah; haplotype; human leukocyte antigen; hla; COMPLEMENT C-4 GENES; STEROID; 21-HYDROXYLASE; HLA LINKAGE; LATE-ONSET; DEFICIENCY; ASSOCIATION; DIAGNOSIS; HAPLOTYPES; MUTATIONS; DELETION;
D O I
10.7759/cureus.35900
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The link between specific human leukocyte antigen (HLA)-B genes and congenital adrenal hyperplasia (CAH) has been a subject of interest. This study investigates the association between specific HLA-B haplotypes and CAH through a meta-analysis. Google Scholar was used as a database. Articles were included if the research was conducted between 1970 and 2022, was not a meta-analysis, and had odds ratios or enough data points to calculate an odds ratio. The National Institutes of Health (NIH) quality assessment tool of case-control studies was used to evaluate the risk of bias in individual studies, and MetaXL was used to generate data and create a forest plot for analysis. Twelve studies met the selection criteria and were included in the study (641 patients and 3,614 controls). Two HLA-B haplotypes showed increased odds of CAH compared to controls: B14 (OR=3.81; 95%CI=2.88, 5.05; I2=3%) and B35 (OR=1.88; 95%CI=1.22, 2.90; I2=25%). All other HLAs either showed no significant effect or had high heterogeneity. The results suggest that specific HLA-B haplotypes have increased odds of developing CAH, specifically B14 and B35. These findings may prove helpful in the pre- and post-natal diagnosis of CAH as well as the identification of carriers and prediction of patient prognosis.
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页数:9
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