Analysis of HLA in Patients with Obstructive Sleep Apnea Syndrome.
10.4046/trd.2005.59.3.298
- Author:
Sang Haak LEE
1
;
Chi Hong KIM
;
Joong Hyun AHN
;
Ji Ho KANG
;
Kwan Hyoung KIM
;
Jeong Sup SONG
;
Sung Hak PARK
;
Hwa Sik MOON
;
Hee Baeg CHOI
;
Tai Gyu KIM
;
Young Mee CHOI
Author Information
1. Department of Internal Medicine, The Catholic University of Korea, College of Medicine, Seoul, Korea. hsmoon@catholic.ac.kr
- Publication Type:Original Article
- Keywords:
Obstructive sleep apnea;
HLA antigens
- MeSH:
Alleles;
Apnea;
Cytotoxicity Tests, Immunologic;
Diagnosis;
Exons;
Female;
Gene Frequency;
Genetics;
Histocompatibility Testing;
HLA Antigens;
HLA-A Antigens;
HLA-A11 Antigen;
HLA-B Antigens;
HLA-DRB1 Chains;
Humans;
Lymphocytes;
Male;
Obesity;
Polysomnography;
Risk Factors;
Sleep Apnea, Obstructive*
- From:Tuberculosis and Respiratory Diseases
2005;59(3):298-305
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: Obstructive sleep apnea syndrome (OSAS) is believed to have multifactorial causes. The major risk factors for OSAS are obesity, narrowed upper airways, and abnormal cranial-facial structures. A genetic basis for OSAS has been also suggested by reports of families with many members affected. This study analyzed the HLA typing in patients with OSAS to determine the possible role of genetics in OSAS. METHODS: Twenty-five Korean patients with OSAS (1 woman and 24 men; age range 30-66 years) were enrolled in this study. A diagnosis of OSAS was made using full-night polysomnography. The control group consisted of 200 healthy Korean people. Serologic typing of the HLA-A and B alleles was performed in all patients using a standard lymphocyte microcytotoxicity test. Analysis of the polymorphic second exons of the HLA-DRB1 gene was performed using a polymerase chain reaction-sequence specific oligonucleotide probe. RESULTS: The allele frequency of HLA-A11 was significantly lower in patients with OSAS compared with the controls (p<0.05). The HLA-B allele frequencies in the patients and controls had a similar distribution. Analysis of the HLA- DRB1 gene polymorphisms showed an increased frequency of DRB1*09 in the OSA patients compared with the controls (p<0.05). When the analysis was performed after dividing the OSAS patients according to the severity of apnea, the allele frequency of HLA-DRB1*08 was significantly higher in the severe OSA patients (apnea index>45) than in the controls (p<0.05). CONCLUSION: This study revealed an association between OSAS and the HLA-A11 and DRB1*09 alleles as well as association between the disease severity and the HLA-DRB1*08 allele in Korean patients. These results suggest that genetics plays an important role in both the development and the disease severity of OSAS.
