Incidence of juvenile-onset Crohn's disease in Scotland: Association with northern latitude and affluence

被引:126
|
作者
Armitage, EL
Aldhous, MC
Anderson, N
Drummond, HE
Riemersma, RA
Ghosh, S
Satsangi, J
机构
[1] Univ Edinburgh, Western Gen Hosp, Dept Med Sci, Gastrointestinal Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Univ Edinburgh, Dept Publ Hlth Sci, Edinburgh EH4 2XU, Midlothian, Scotland
[3] Univ Edinburgh, Cardiovasc Res Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[4] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Dept Gastroenterol, London, England
基金
英国医学研究理事会;
关键词
D O I
10.1053/j.gastro.2004.06.024
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: The incidence of Crohn's disease in Scottish children has increased steadily over 30 years. Many studies have investigated genetic influence or possible links with childhood events. We aimed to study sociodemographic and/or geographic distribution of juvenile=onset Crohn's disease in Scotland. Methods: Using a previously established and validated database covering the entire Scottish population, 580 Scottish children (<16 years of age at symptom onset) with inflammatory bowel disease incident between 1981 and 1995 were identified. Postcodes of incident cases were classed for geographic location and material deprivation. Incidence rates (/100,000/year) were sex standardized to the 1991 census population. The effects of sex, geographic location, time, and deprivation category were estimated from a multifactorial Poisson regression model. Results: The incidence of juvenile-onset Crohn's disease was 2.3 (95% CI: 2.0-2.5) for the time period 1981 to 1995 and was significantly higher in northern (3.1, 95% CI: 2.6-3.8) than in southern Scotland (2.1, 95% CI: 1.9-2.4, P<0.001). The incidence of juvenile-onset ulcerative colitis did not show north/south variation (P = 0.677). The relative risks of developing CD were significantly lower in postcode areas with deprivation categories 2-7 as compared with deprivation score 1 (most affluent, P = 0.033). This pattern was not seen for UC. Conclusions: There was an increased incidence of juvenile-onset Crohn's disease in northern compared with southern Scotland. Children from more affluent areas had a higher relative risk of developing Crohn's disease. Juvenile onset ulcerative colitis did not show north/south variation in incidence or association with affluence.
引用
收藏
页码:1051 / 1057
页数:7
相关论文
共 50 条
  • [21] Juvenile-onset Parkinson's Disease With Psychosis: Diagnostic and Therapeutic Challenges
    Selvaraj, Bannupriya
    Ramamurthy, Parthasarathy
    Sundaram, Shobana
    Thilakan, Pradeep
    INDIAN JOURNAL OF PSYCHOLOGICAL MEDICINE, 2024,
  • [22] Brain structure in juvenile-onset Huntington disease
    Tereshchenko, Alexander
    Magnotta, Vincent
    Epping, Eric
    Mathews, Katherine
    Espe-Pfeifer, Patricia
    Martin, Erin
    Dawson, Jeffrey
    Duan, Wenzhen
    Nopoulos, Peg
    NEUROLOGY, 2019, 92 (17) : E1939 - E1947
  • [23] Cardiac abnormalities in a transgenic model of juvenile-onset Huntington's disease
    Mihm, MJ
    Amann, DM
    Schanbacher, BL
    Hoyt, KR
    Bauer, JA
    PEDIATRIC RESEARCH, 2003, 53 (04) : 34A - 34A
  • [24] SAFETY AND EFFICACY OF ETANERCEPT IN CHILDREN WITH JUVENILE-ONSET BEHCET'S DISEASE
    Cantarini, L.
    Tinazzi, I.
    Caramaschi, P.
    Bellisai, F.
    Brogna, A.
    Galeazzi, M.
    INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 2009, 22 (02) : 551 - 555
  • [25] DISTRIBUTION OF JUVENILE-ONSET DIABETES CASES IN SCOTLAND (1968-1976)
    PATTERSON, CC
    SMITH, PG
    MANN, JI
    THOROGOOD, M
    HEASMAN, MA
    CLARKE, JA
    DIABETOLOGIA, 1981, 20 (06) : 673 - 673
  • [26] Longitudinal Clinical and Biological Characteristics in Juvenile-Onset Huntington's Disease
    Schultz, Jordan L.
    Langbehn, Douglas R.
    Al-Kaylani, Hend M.
    van der Plas, Ellen
    Koscik, Timothy R.
    Epping, Eric A.
    Espe-Pfeifer, Patricia B.
    Martin, Erin P.
    Moser, David J.
    Magnotta, Vincent A.
    Nopoulos, Peggy C.
    MOVEMENT DISORDERS, 2023, 38 (01) : 113 - 122
  • [27] JUVENILE-ONSET BEHCET'S DISEASE: CLINICAL AND GENETIC FEATURES COMPARED WITH ADULT ONSET-DISEASE
    Ben Salem, T.
    Naceur, I.
    Tougorti, M.
    Ben Ghorbel, I.
    Lamloum, M.
    Houman, M. H.
    ANNALS OF THE RHEUMATIC DISEASES, 2016, 75 : 1095 - 1095
  • [28] Juvenile-onset Behcet's syndrome and mimics
    Pain, Clare E.
    CLINICAL IMMUNOLOGY, 2020, 214
  • [29] Estimated incidence of juvenile-onset recurrent respiratory papillomatosis in Korea
    Oh, Jin-Kyoung
    Choi, Hwa Young
    Han, Minji
    Jung, Yuh-Seog
    Lee, Sang Joon
    Ki, Moran
    EPIDEMIOLOGY AND HEALTH, 2021, 43
  • [30] Adult-onset and Juvenile-onset Still's Disease: A Comparative Study of Both Sides
    Aicha, Ben Tekaya
    Emna, Hannech
    Olfa, Saidane
    Selma, Bouden
    Leila, Rouached
    Rawda, Tekaya
    Ines, Mahmoud
    Slim, Abdelmoula
    Leila, Abdelmoula
    CURRENT RHEUMATOLOGY REVIEWS, 2023, 19 (02) : 235 - 241