Hoffenberg Edward J, MacKenzie Todd, Barriga Katherine J, Eisenbarth George S, Bao Fei, Haas Joel E, Erlich Henry, Bugawan Tl T l, Sokol Ronald J, Taki Iman, Norris Jill M, Rewers Marian
Department of Pediatrics, Barbara Davis Center for Childhood Diabetes, University of Colorado, Denver, USA.
J Pediatr. 2003 Sep;143(3):308-14. doi: 10.1067/s0022-3476(03)00282-8.
To estimate the frequency of celiac disease (CD) in children in the general population of Denver, Colorado.
From 22,346 newborns characterized as expressing 0, 1, or 2 HLA-DR3(DQB1*0201) alleles, 987 were selected for a prospective stratified cohort study. Participants were followed for as long as 7 years with serial testing for serum IgA anti-transglutaminase antibodies and for evidence of CD (intestinal mucosal changes or persistent seropositivity).
Of 40 children with at least one positive serologic test, 19 had evidence of CD (10 by biopsy, 9 by persistent seropositivity). Those expressing 0, 1, or 2 HLA-DR3 alleles had, respectively, 0.3% (95% CI, 0.0-2.7), 3.4% (3.0-11.7), and 3.2% (1.0-11.0) risk for evidence of CD by age 5 years. The adjusted risk estimate for evidence of CD by age 5 years for the Denver general population was 0.9% (0.4-2.0), or 1 in 104 (1:49-221). After adjusting for number of HLA-DR3 alleles expressed, risk was higher in females: RR=3.34 (1.00-10.9, P=.048). Evidence of CD was not observed before age 2.6 years.
Celiac disease may affect 0.9% of Denver children by 5 years of age. Children positive for the HLA-DR3 allele and females appear to be at increased risk.
评估科罗拉多州丹佛市普通人群中儿童乳糜泻(CD)的发病率。
从22346名携带0、1或2个HLA - DR3(DQB1*0201)等位基因的新生儿中,选取987名进行前瞻性分层队列研究。对参与者进行长达7年的随访,定期检测血清抗组织转谷氨酰胺酶IgA抗体以及乳糜泻证据(肠道黏膜变化或持续血清学阳性)。
40名至少有一次血清学检测呈阳性的儿童中,19名有乳糜泻证据(10名经活检确诊,9名因持续血清学阳性确诊)。携带0、1或2个HLA - DR3等位基因的儿童在5岁时出现乳糜泻证据的风险分别为0.3%(95%CI,0.0 - 2.7)、3.4%(3.0 - 11.7)和3.2%(1.0 - 11.0)。丹佛普通人群中5岁儿童出现乳糜泻证据的校正风险估计为0.9%(0.4 - 2.0),即1/104(1:49 - 221)。在调整所表达的HLA - DR3等位基因数量后,女性风险更高:RR = 3.34(1.00 - 10.9,P = 0.048)。2.6岁之前未观察到乳糜泻证据。
到5岁时,乳糜泻可能影响0.9%的丹佛儿童。HLA - DR3等位基因呈阳性的儿童和女性似乎风险更高。