Cystic fibrosis is a risk factor for celiac disease

被引:0
|
作者
Walkowiak, Jaroslaw [1 ]
Blask-Osipa, Anna [2 ]
Lisowska, Aleksandra [2 ]
Oralewska, Beata [3 ]
Pogorzelski, Andrzej [4 ]
Cichy, Wojciech [2 ]
Sapiejka, Ewa [5 ]
Kowalska, Miroslawa [6 ]
Korzon, Michal [7 ]
Szaflarska-Poplawska, Anna [8 ]
机构
[1] Poznan Univ Life Sci, Dept Dietet, Chair Human Nutr & Hyg, Poznan, Poland
[2] Poznan Univ Med Sci, Chair Pediat 1, Dept Gastroenterol & Metab, Poznan, Poland
[3] Child Mem Hlth Inst, Dept Pediat Gastroenterol Hepatol & Immunol, Warsaw, Poland
[4] Natl Inst TB & Lung Dis, Pediat Branch, Dept Bronchol & Cyst Fibrosis, Rabka, Poland
[5] Out Patient Clin CF Patients, Gdansk, Poland
[6] Out Patient Clin Patients Pulm Dis Panaceum, Koszalin, Poland
[7] Med Univ Gdansk, Dept Obstet, Gdansk, Poland
[8] Mikolaj Kopernik Univ, Chair Pediat Gastroenterol & Alergol, Coll Med Bydgoszcz, Torun, Poland
关键词
cystic fibrosis; celiac disease; antiendomysial antibodies; genetic predisposition; INTESTINAL PERMEABILITY; HIGH PREVALENCE; INFLAMMATION; CHILDREN; TIME; TRANSGLUTAMINASE; POPULATION; ANTIBODY;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: The coexistence of cystic fibrosis (CF) and celiac disease (CD) has been reported. To our knowledge there is no study directly comparing the incidence of CD in CF patients to that in the general population at the same time. There is no published data on genetic predisposition to CD in CF patients either. Therefore, in the present study we aimed to assess the genetic predisposition to CD and its incidence in CF patients comparing it to data from the general population. Patients and methods: Two hundred eighty-two CF patients were enrolled in the study. In 230 CF patients the genetic predisposition to CD (the presence of HLA-DQ2/ DQ8) was assessed. In all CF patients, serological screening for CD was conducted. In patients with positive antiendomysial antibodies (EMA) gastroduenoscopy was offered. Intestinal histology was classified according to modified Marsh criteria. The results of serological CD screening in 3235 Polish schoolchildren and HLA-DQ typing in 200 healthy subjects (HS) were used for comparison. Results: Positive EMA was found in 2.84% of the studied CF patients. The incidence of proven CD was 2.13%. The incidence of CD as well as positive serological screening were significantly more frequent in the CF group than in the general population. The frequency of CD-related HLA-DQ alleles in CF and HS did not differ. Conclusions: Genetic predisposition to celiac disease in cystic fibrosis patients is similar to that of the general population. However, our results suggest that cystic fibrosis is a risk factor for celiac disease development.
引用
收藏
页码:115 / 118
页数:4
相关论文
共 50 条
  • [31] CYSTIC FIBROSIS-RELATED LIVER DISEASE IS AN INDEPENDENT RISK FACTOR FOR MORTALITY AND INCREASED HEALTH CARE RESOURCE UTILIZATION IN CHILDREN WITH CYSTIC FIBROSIS
    Thavamani, A.
    Umapathi, K.
    Sferra, T.
    Sankararaman, S.
    PEDIATRIC PULMONOLOGY, 2020, 55 : S129 - S129
  • [32] Celiac Disease as a risk factor for the manifestation of Crohn's disease
    Shah, Ayesha
    Burger, Daniel
    Martin, Neal
    Holtmann, Gerald
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2016, 31 : 168 - 168
  • [33] Cystic Lesions of Celiac Disease
    Dilmaghani, Saam
    Sawas, Tarek
    Sweetser, Seth
    GASTROENTEROLOGY, 2021, 161 (02) : 425 - 426
  • [34] Liver disease in Cystic Fibrosis - prevalence and risk factors
    Schibli, S.
    Rose, J.
    Durie, P.
    Ellis, L.
    Tullis, E.
    Kovesi, T.
    Corey, M.
    SWISS MEDICAL WEEKLY, 2006, 136 : 14S - 14S
  • [35] Risk factors for liver disease in cystic fibrosis (CF).
    Rigby, AS
    Pirzada, OM
    Taylor, CJ
    McGaw, J
    Evans, S
    Tanner, MS
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 213 - 213
  • [36] Liver disease in cystic fibrosis: prevalence and risk factors
    Nature Clinical Practice Gastroenterology & Hepatology, 2005, 2 (4): : 165 - 165
  • [37] Several siblings with Cystic Fibrosis as a risk factor for poor outcome
    Lavie, Moran
    Shemer, Ofer
    Sarouk, Ifat
    el Bar Aluma, Bat
    Dagan, Adi
    Efrati, Ori
    Vilozni, Daphna
    RESPIRATORY MEDICINE, 2015, 109 (01) : 74 - 78
  • [38] A new risk factor predicts ABPA in patients with cystic fibrosis
    Thronicke, Anja
    Brandt, Claudia
    Schwarz, Carsten
    EUROPEAN RESPIRATORY JOURNAL, 2015, 46
  • [39] PREVALENCE OF CELIAC-DISEASE AND CYSTIC-FIBROSIS IN IRELAND, SCOTLAND, AND ENGLAND AND WALES
    DEAN, JGK
    BRITISH JOURNAL OF PREVENTIVE & SOCIAL MEDICINE, 1975, 29 (01): : 58 - 58
  • [40] CELIAC SPRUE AS A RISK FACTOR FOR GALLBLADDER DISEASE IN CHILDREN
    Morgan, Judah D.
    Krishnamurthy, Jayasree
    Walk, Ryan M.
    O'Meara, Kevin
    Nylund, Cade M.
    GASTROENTEROLOGY, 2021, 160 (06) : S584 - S584