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中国汉族慢性阻塞性肺疾病与人类白细胞抗原相关性研究 被引量:1

Association Research of Chinese Han Chronic Obstructive Pulmonary Disease and Human Leucocyte Antigen
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摘要 目的:探索我国汉族人群人类白细胞抗原(HLA)等位基因多态性与慢性阻塞性肺疾病(COPD)的易感性。方法:对COPD组及对照组进行HLA分型和临床研究。结果:COPD组HLA-AW30/31,HLA-BW54位点抗原频率较对照组明显增高(频率41%、31%,相对危险率分别是9.09和10.91,P<0.01)。AW30/31阳性者病程长,肺功能呈混合性通气障碍,多伴呼吸衰竭。伴副鼻窦炎者23%(5/22),TBLB呈肺泡上皮增生变厚,肺泡壁纤维组织弥漫增生。BW54阳性者,病程相对短,肺功能呈重度阻塞性和轻度限制性通气障碍。伴副鼻窦炎者60%(6/10)。CD4/CD8升高,IgA增加。TBLB呈淋巴细胞和浆细胞浸润、增生,少量纤维化。结论:COPD与AW30/31,BW54位点抗原密切相关——即具有AW30/31,BW54抗原的人群易患COPD。BW54位点阳性者,可能是弥漫性泛细支气管炎。它们的确混淆在COPD之中。 Objective:Association research of Chinese Han chronic obstructive pulmonary disease (COPD) and human leucocyte antigen(HLA).Methods:We performed the HLA A B C antigen analysis of patients of COPD and the clinical research.Results:The HLA A W30/31 and HLA B W54 significantly increased (frequency 41%,31%,RR 9.09,10.91 respectively P <0.01).HLA A W30/31 had long course,disorder of mixventilation in lung function.Company with respiretary failure,had paranasal sinusitis 23%(5/22).TBLB showed alveoli epitheliosis.alveoli wall fibroid tissue hyperplasia widely.HLA B W54 had sort course,disorder of obstrutive ventilation,had paranasal sinusitis 60% (6/10).CD 4/CD 8 increased,IgA increased also.TBLB showed lymphocyte erosion,hyperplasia a little fibrosis.Conclusion:On or some of the genes controlling the susceptibility and/or immune responsiveness of COPD might be located near HLA A W30/31 and B W54 ,the patients with HLA B W54 confused among COPD might be DPB.
出处 《中国慢性病预防与控制》 CAS 1999年第4期165-167,共3页 Chinese Journal of Prevention and Control of Chronic Diseases
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  • 1Gennaro D, Marzano C, Fratello F, et al. The electroencephalographic fingerprint of sleep is genetically determined: a twin study. Ann Neurol, 2008, 64: 455-460.
  • 2Koh K, Joine WJ, Wu MN,et al. Identification of SLEEPLESS, a sleep-promoting factor. Science, 2008, 321:372-376.
  • 3Yuan L, Chen X. Diversity of potassium channels in neuronal dendrites. Prog Neurobiol,2006, 78: 374-389.
  • 4Liguori R, Vincent A, Clover L, et al. Morvan' s syndrome: peripheral and central nervous system and cardiac involvement with antibodies to voltage-gated potassium channels. Brain ,2001, 124 : 2417-2426.
  • 5Crunelli V, Cope D, Hughes S. Thalamic T-type Ca2 + channels and NREM sleep. Cell Calcium, 2006, 40: 175-190.
  • 6Archer SN, Carpen JD, Gibson M, et al. Polymorphism in the PER3 promoter associates with diurnal preference and delayed sleep phase disorder. Sleep, 2010, 33:695-701.
  • 7Chellappa SL, Viola AU, Schmidt C, et al. Human melatonin and alerting response to blue-enriched light depend on a polymorphism in the clock gene PER3. J Clin Endocrinol Metab, 2012, 97 :E433-437.
  • 8Toh K, Jones C, He Y, et al. An hPer2 phosphorylation site mutation in familial advanced sleep phase syndrome. Science,2001, 291: 1040-1043.
  • 9Xu Q, Robert E, Christopher R, et al. Functional consequences of a CKI~ mutation causing familial advanced sleep phase syndrome. Nature, 2005, 434: 640-644.
  • 10Shanware NP, Hutchinson JA, Kim SH, et al. Casein kinase 1- dependent phosphorylation of familial advanced sleep phase syndrome-associated residues controls PERIOD 2 stability. J Biol Chem, 2011, 286 : 12766-12774.

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