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DOI 10.1093/hmg/ddu480

Медицинская библиотека · Human molecular genetics · 2014

New susceptibility variants to narcolepsy identified in HLA class II region.

Miyagawa Taku, Toyoda Hiromi, Hirataka Akane, Kanbayashi Takashi, Imanishi Aya, Sagawa Yohei, Kotorii Nozomu, Kotorii Tatayu, Hashizume Yuji, Ogi Kimihiro, Hiejima Hiroshi, Kamei Yuichi, Hida Akiko, Miyamoto Masayuki, Imai Makoto, Fujimura Yota, Tamura Yoshiyuki, Ikegami Azusa, Wada Yamato, Moriya Shunpei, Furuya Hirokazu, Kato Mitsuhiro, Omata Naoto, Kojima Hiroto, Kashiwase Koichi, Saji Hiroh, Khor Seik-Soon, Yamasaki Maria, Wada Yuji, Ishigooka Jun, Kuroda Kenji, Kume Kazuhiko, Chiba Shigeru, Yamada Naoto, Okawa Masako, Hirata Koichi, Uchimura Naohisa, Shimizu Tetsuo, Inoue Yuichi, Honda Yutaka, Mishima Kazuo, Honda Makoto, Tokunaga Katsushi

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Narcolepsy, a sleep disorder characterized by excessive daytime sleepiness, cataplexy and rapid eye movement sleep abnormalities, is tightly associated with human leukocyte antigen HLA-DQB1*06:02. DQB1*06:02 is common in the general population (10-30%); therefore, additional genetic factors are needed for the development of narcolepsy. In the present study, HLA-DQB1 in 664 Japanese narcoleptic subjects and 3131 Japanese control subjects was examined to determine whether HLA-DQB1 alleles located in trans of DQB1*06:02 are associated with narcolepsy. The strongest association was with DQB1*06:01 (P = 1.4 × 10(-10), odds ratio, OR = 0.39), as reported in previous studies. Additional predisposing effects of DQB1*03:02 were also found (P = 2.5 × 10(-9), OR = 1.97). A comparison between DQB1*06:02 heterozygous cases and controls revealed dominant protective effects of DQB1*06:01 and DQB1*05:01. In addition, a single-nucleotide polymorphism-based conditional analysis controlling for the effect of HLA-DQB1 was performed to determine whether there were other independent HLA associations outside of HLA-DQB1. This analysis revealed associations at HLA-DPB1 in the HLA class II region (rs3117242, P = 4.1 × 10(-5), OR = 2.45; DPB1*05:01, P = 8.1 × 10(-3), OR = 1.39). These results indicate that complex HLA class II associations contribute to the genetic predisposition to narcolepsy.

Для цитирования: Miyagawa Taku, Toyoda Hiromi, Hirataka Akane, Kanbayashi Takashi, Imanishi Aya, Sagawa Yohei, Kotorii Nozomu, Kotorii Tatayu, Hashizume Yuji, Ogi Kimihiro, Hiejima Hiroshi, Kamei Yuichi, Hida Akiko, Miyamoto Masayuki, Imai Makoto, Fujimura Yota, Tamura Yoshiyuki, Ikegami Azusa, Wada Yamato, Moriya Shunpei, Furuya Hirokazu, Kato Mitsuhiro, Omata Naoto, Kojima Hiroto, Kashiwase Koichi, Saji Hiroh, Khor Seik-Soon, Yamasaki Maria, Wada Yuji, Ishigooka Jun, Kuroda Kenji, Kume Kazuhiko, Chiba Shigeru, Yamada Naoto, Okawa Masako, Hirata Koichi, Uchimura Naohisa, Shimizu Tetsuo, Inoue Yuichi, Honda Yutaka, Mishima Kazuo, Honda Makoto, Tokunaga Katsushi. New susceptibility variants to narcolepsy identified in HLA class II region.. Human molecular genetics. 2014. DOI: 10.1093/hmg/ddu480.

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