Lack of correlation of degree of villous atrophy with severity of clinical presentation of coeliac disease

被引:87
作者
Brar, P. [1 ]
Kwon, G. Y. [1 ]
Egbuna, I. I. [1 ]
Holleran, S. [1 ]
Ramakrishnan, R. [1 ]
Bhagat, G. [1 ]
Green, P. H. R. [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, Dept Med Pediat & Pathol, New York, NY 10032 USA
关键词
clinical presentation; coeliac disease; villous atrophy;
D O I
10.1016/j.dld.2006.07.014
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and aim. Both the clinical presentation and the degree of mucosal damage in coeliac disease vary greatly. In view of conflicting information as to whether the mode of presentation correlates with the degree of villous atrophy, we reviewed a large cohort of patients with coeliac disease. Patients and methods. We correlated mode of presentation (classical, diarrhoea predominant or atypical/silent) with histology of duodenal biopsies and examined their trends over time. Results. The cohort consisted of 499 adults, mean age 44.1 years, 68% females. The majority had silent coeliac disease (56%) and total villous atrophy (65%). There was no correlation of mode of presentation with the degree of villous atrophy (p = 0.25). Sixty-eight percent of females and 58% of males had a severe villous atrophy (p = 0.052). There was a significant trend over time for a greater proportion of patients presenting as atypical/silent coeliac disease and having partial villous atrophy, though the majority still had total villous atrophy. Conclusions. Among our patients the degree of villous atrophy in duodenal biopsies did not correlate with the mode of presentation, indicating that factors other than the degree of villous atrophy must account for diarrhoea in coeliac disease. (C) 2006 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:26 / 29
页数:4
相关论文
共 28 条
  • [1] Bai J. C., 1995, Acta Gastroenterologica Latinoamericana, V25, P277
  • [2] Pancreatic enzyme therapy in childhood celiac disease - A double-blind prospective randomized study
    Carroccio, A
    Iacono, G
    Montalto, G
    Cavataio, F
    Lorello, D
    Greco, L
    Soresi, M
    Notarbartolo, A
    [J]. DIGESTIVE DISEASES AND SCIENCES, 1995, 40 (12) : 2555 - 2560
  • [3] Platelet serotonin transporter in coeliac disease
    Chiaravalloti, G
    Marazziti, D
    Batistini, A
    Favilli, T
    Ughi, C
    Ceccarelli, M
    Cassano, GB
    [J]. ACTA PAEDIATRICA, 1997, 86 (07) : 696 - 699
  • [4] The value of wireless capsule endoscopy in patients with complicated celiac disease
    Culliford, A
    Daly, J
    Diamond, B
    Rubin, M
    Green, PHR
    [J]. GASTROINTESTINAL ENDOSCOPY, 2005, 62 (01) : 55 - 61
  • [5] Histology of the terminal ileum in coeliac disease
    Dickey, W
    Hughes, DF
    [J]. SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2004, 39 (07) : 665 - 667
  • [6] El-Salhy M, 1998, HISTOL HISTOPATHOL, V13, P1069, DOI 10.14670/HH-13.1069
  • [7] Prevalence of celiac disease in at-risk and not-at-risk groups in the United States - A large multicenter study
    Fasano, A
    Berti, I
    Gerarduzzi, T
    Not, T
    Colletti, RB
    Drago, S
    Elitsur, Y
    Green, PHR
    Guandalini, S
    Hill, ID
    Pietzak, M
    Ventura, A
    Thorpe, M
    Kryszak, D
    Fornaroli, F
    Wasserman, SS
    Murray, JA
    Horvath, K
    [J]. ARCHIVES OF INTERNAL MEDICINE, 2003, 163 (03) : 286 - 292
  • [8] Colonic histopathology in untreated celiac sprue or refractory sprue: Is it lymphocytic colitis or colonic lymphocytosis?
    Fine, KD
    Lee, EL
    Meyer, RL
    [J]. HUMAN PATHOLOGY, 1998, 29 (12) : 1433 - 1440
  • [9] Capsule endoscopy in celiac disease
    Green, PHR
    Rubin, M
    [J]. GASTROINTESTINAL ENDOSCOPY, 2005, 62 (05) : 797 - 799
  • [10] Coeliac disease
    Green, PHR
    Jabri, B
    [J]. LANCET, 2003, 362 (9381) : 383 - 391