Simon Francis Thomsen, Sophie van der Sluis, Kirsten Ohm Kyvik, Vibeke Backer
{"title":"同卵和异卵双胞胎的荨麻疹。","authors":"Simon Francis Thomsen, Sophie van der Sluis, Kirsten Ohm Kyvik, Vibeke Backer","doi":"10.1155/2012/125367","DOIUrl":null,"url":null,"abstract":"Aim. To identify risk factors for urticaria, to determine the relative proportion of the susceptibility to urticaria that is due to genetic factors in an adult clinical twin sample, and to further determine whether the genetic susceptibility to urticaria overlaps with the genetic susceptibility to atopic diseases. Methods. A total of 256 complete twin pairs and 63 single twins, who were selected from sibships with self-reported asthma via a questionnaire survey of 21,162 adult twins from the Danish Twin Registry, were clinically interviewed about a history of urticaria and examined for atopic diseases. Data were analysed with Cox proportional hazards regression and variance components models. Results. A total of 151 individuals (26%) had a history of urticaria, whereas 24 (4%) had had symptoms within the past year. Female sex, HR = 2.09 (1.46–2.99), P = 0.000; hay fever, HR = 1.92 (1.36–2.72), P = 0.000; and atopic dermatitis, HR = 1.44 (1.02–2.06), P = 0.041 were significant risk factors for urticaria. After adjustment for sex and age at onset of urticaria in the index twin, the risk of urticaria was increased in MZ cotwins relative to DZ cotwins, HR = 1.42 (0.63–3.18), P = 0.394. Genetic factors explained 45% (16–74%), P = 0.005, of the variation in susceptibility to urticaria. The genetic correlation between urticaria and hay fever was 0.45 (0.01–0.89), P = 0.040. Conclusions. Susceptibility to urticaria is partly determined by genetic factors. Urticaria is more common in women, and in subjects with hay fever and atopic dermatitis, and shares genetic variance with hay fever.","PeriodicalId":88910,"journal":{"name":"Journal of allergy","volume":"2012 ","pages":"125367"},"PeriodicalIF":0.0000,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2012/125367","citationCount":"2","resultStr":"{\"title\":\"Urticaria in monozygotic and dizygotic twins.\",\"authors\":\"Simon Francis Thomsen, Sophie van der Sluis, Kirsten Ohm Kyvik, Vibeke Backer\",\"doi\":\"10.1155/2012/125367\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Aim. To identify risk factors for urticaria, to determine the relative proportion of the susceptibility to urticaria that is due to genetic factors in an adult clinical twin sample, and to further determine whether the genetic susceptibility to urticaria overlaps with the genetic susceptibility to atopic diseases. Methods. A total of 256 complete twin pairs and 63 single twins, who were selected from sibships with self-reported asthma via a questionnaire survey of 21,162 adult twins from the Danish Twin Registry, were clinically interviewed about a history of urticaria and examined for atopic diseases. Data were analysed with Cox proportional hazards regression and variance components models. Results. A total of 151 individuals (26%) had a history of urticaria, whereas 24 (4%) had had symptoms within the past year. Female sex, HR = 2.09 (1.46–2.99), P = 0.000; hay fever, HR = 1.92 (1.36–2.72), P = 0.000; and atopic dermatitis, HR = 1.44 (1.02–2.06), P = 0.041 were significant risk factors for urticaria. After adjustment for sex and age at onset of urticaria in the index twin, the risk of urticaria was increased in MZ cotwins relative to DZ cotwins, HR = 1.42 (0.63–3.18), P = 0.394. Genetic factors explained 45% (16–74%), P = 0.005, of the variation in susceptibility to urticaria. The genetic correlation between urticaria and hay fever was 0.45 (0.01–0.89), P = 0.040. Conclusions. Susceptibility to urticaria is partly determined by genetic factors. Urticaria is more common in women, and in subjects with hay fever and atopic dermatitis, and shares genetic variance with hay fever.\",\"PeriodicalId\":88910,\"journal\":{\"name\":\"Journal of allergy\",\"volume\":\"2012 \",\"pages\":\"125367\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1155/2012/125367\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of allergy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1155/2012/125367\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2012/11/20 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of allergy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2012/125367","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2012/11/20 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
摘要
的目标。确定荨麻疹的危险因素,确定成人临床双胞胎样本中遗传因素对荨麻疹易感性的相对比例,并进一步确定对荨麻疹的遗传易感性是否与对特应性疾病的遗传易感性重叠。方法。通过对丹麦双胞胎登记处的21,162对成年双胞胎进行问卷调查,从自报告患有哮喘的双胞胎中选出256对完整双胞胎和63对单对双胞胎,对他们进行了荨麻疹病史的临床访谈和特应性疾病的检查。采用Cox比例风险回归和方差成分模型对数据进行分析。结果。共有151人(26%)有荨麻疹病史,24人(4%)在过去一年内出现过荨麻疹症状。女性,HR = 2.09 (1.46 ~ 2.99), P = 0.000;花粉热,HR = 1.92 (1.36-2.72), P = 0.000;异位性皮炎(HR = 1.44 (1.02 ~ 2.06), P = 0.041)是荨麻疹的显著危险因素。调整指数双胞胎的性别和发病年龄后,MZ双胞胎患荨麻疹的风险高于DZ双胞胎,HR = 1.42 (0.63-3.18), P = 0.394。遗传因素解释了45%(16-74%)的荨麻疹易感性变异,P = 0.005。荨麻疹与花粉热的遗传相关性为0.45 (0.01 ~ 0.89),P = 0.040。结论。对荨麻疹的易感性部分是由遗传因素决定的。荨麻疹在女性、花粉热和特应性皮炎患者中更为常见,并且与花粉热具有相同的遗传变异。
Aim. To identify risk factors for urticaria, to determine the relative proportion of the susceptibility to urticaria that is due to genetic factors in an adult clinical twin sample, and to further determine whether the genetic susceptibility to urticaria overlaps with the genetic susceptibility to atopic diseases. Methods. A total of 256 complete twin pairs and 63 single twins, who were selected from sibships with self-reported asthma via a questionnaire survey of 21,162 adult twins from the Danish Twin Registry, were clinically interviewed about a history of urticaria and examined for atopic diseases. Data were analysed with Cox proportional hazards regression and variance components models. Results. A total of 151 individuals (26%) had a history of urticaria, whereas 24 (4%) had had symptoms within the past year. Female sex, HR = 2.09 (1.46–2.99), P = 0.000; hay fever, HR = 1.92 (1.36–2.72), P = 0.000; and atopic dermatitis, HR = 1.44 (1.02–2.06), P = 0.041 were significant risk factors for urticaria. After adjustment for sex and age at onset of urticaria in the index twin, the risk of urticaria was increased in MZ cotwins relative to DZ cotwins, HR = 1.42 (0.63–3.18), P = 0.394. Genetic factors explained 45% (16–74%), P = 0.005, of the variation in susceptibility to urticaria. The genetic correlation between urticaria and hay fever was 0.45 (0.01–0.89), P = 0.040. Conclusions. Susceptibility to urticaria is partly determined by genetic factors. Urticaria is more common in women, and in subjects with hay fever and atopic dermatitis, and shares genetic variance with hay fever.