期刊论文详细信息
BMC Gastroenterology
Histological evaluation of duodenal biopsies from coeliac patients: the need for different grading criteria during follow-up
Stefano Ferrero4  Leda Roncoroni2  Letterio Runza1  Dario Conte3  Silvano Bosari3  Maria Teresa Bardella2  Carolina Tomba3  Enea Zini1  Luca Elli2 
[1]Pathology Unit, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Via F. Sforza 28, Milan, 20100, Italy
[2]Center for the Prevention and Diagnosis of Coeliac Disease, Gastroenterology and Endoscopy Unit - Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Via F. Sforza 28, Milan, 20100, Italy
[3]Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Via Festa del Perdono 7, Milan, 20100, Italy
[4]Department of Biomedical, Surgical and Dental Sciences, Università degli Studi di Milano, Via Festa del Perdono 7, Milan, 20100, Italy
关键词: Malabsorption;    Histopathology;    Small Intestine;    Coeliac Disease;   
Others  :  1234377
DOI  :  10.1186/s12876-015-0361-8
 received in 2014-11-23, accepted in 2015-10-01,  发布年份 2015
PDF
【 摘 要 】

Background

Coeliac disease is characterised by villous atrophy, which usually normalises after gluten withdrawal. Sometimes the revaluation of duodenal histology is required during follow-up, even if the methodology for comparing duodenal histology before and after introducing a gluten-free diet is not yet established. Our aim was to evaluate a novel criterion to compare duodenal histology in coeliac disease before and after gluten withdrawal.

Methods

Duodenal biopsies from coeliac patients were retrospectively reviewed to compare duodenal histology at diagnosis and after at least one year on a gluten-free diet. Two different methods were used: the first was represented by the classical Marsh-Oberhuber score, the second compared the areas covered by each Marsh-Oberhuber grade and expressed as percentages, the final grade being calculated from the analysis of ten power fields per duodenal biopsy.

Results

Sixty-nine patients (17 males 52 females, age at diagnosis 36 ± 15 years) who underwent duodenal biopsies, were considered. According to the classical Marsh-Oberhuber scale, 32 patients did not present atrophy during follow-up while 37 showed duodenal atrophy, among whom 26 improved the grade of severity and 11 retained the same one. Of these latter, according to the second method, eight patients were considered improved, two showed a worsened duodenal damage and only one remained unchanged; the evaluation changed in 91 % of cases.

Conclusions

The proposed semi-quantitative approach (i.e. the second method) for the evaluation of histology at follow-up provides additional information about the progression/regression of the mucosal damage.

【 授权许可】

   
2015 Elli et al.

【 预 览 】
附件列表
Files Size Format View
20151129043905512.pdf 1598KB PDF download
Fig. 3. 216KB Image download
Fig. 2. 14KB Image download
Fig. 1. 10KB Image download
【 图 表 】

Fig. 1.

Fig. 2.

Fig. 3.

【 参考文献 】
  • [1]Elli L, Discepolo V, Bardella MT, Guandalini S: Does Gluten Intake Influence the Development of Celiac Disease-associated Complications? J Clin Gastroenterol 2014, 48(1):13-20.
  • [2]Schuppan D, Junker Y, Barisani D: Celiac disease: from pathogenesis to novel therapies. Gastroenterol 2009, 137(6):1912-33.
  • [3]Ciccocioppo R, Di Sabatino A, Bauer M, Della Riccia DN, Bizzini F, Biagi F, Cifone MG, Corazza GR, Schuppan D: Matrix metalloproteinase pattern in celiac duodenal mucosa. Lab Invest 2005, 85(3):397-407.
  • [4]Fasano A, Catassi C: Clinical practice. Celiac disease. N Engl J Med 2012, 367(25):2419-26.
  • [5]Jamma S, Rubio-Tapia A, Kelly CP, Murray J, Najarian R, Sheth S, Schuppan D, Dennis M, Leffler DA: Celiac crisis is a rare but serious complication of celiac disease in adults. Clin Gastroenterol Hepatol 2010, 8(7):587-90.
  • [6]Marsh MN: Grains of truth: evolutionary changes in small intestinal mucosa in response to environmental antigen challenge. Gut 1990, 31(1):111-4.
  • [7]Oberhuber G, Granditsch G, Vogelsang H: The histopathology of coeliac disease: time for a standardized report scheme for pathologists. Eur J Gastroenterol Hepatol 1999, 11(10):1185-94.
  • [8]Corazza GR, Villanacci V, Zambelli C, Milione M, Luinetti O, Vindigni C, Chioda C, Albarello L, Bartolini D, Donato F: Comparison of the interobserver reproducibility with different histologic criteria used in celiac disease. Clin Gastroenterol Hepatol 2007, 5(7):838-43.
  • [9]Bardella MT, Velio P, Cesana BM, Prampolini L, Casella G, Di Bella C, Lanzini A, Gambarotti M, Bassotti G, Villanacci V: Coeliac disease: a histological follow-up study. Histopathol 2007, 50(4):465-71.
  • [10]Kaukinen K, Peraaho M, Lindfors K, Partanen J, Woolley N, Pikkarainen P, Karvonen AL, Laasanen T, Sievanen H, Maki M, et al.: Persistent small bowel mucosal villous atrophy without symptoms in coeliac disease. Aliment Pharmacol Ther 2007, 25(10):1237-45.
  • [11]Ludvigsson JF, Leffler DA, Bai JC, Biagi F, Fasano A, Green PH, Hadjivassiliou M, Kaukinen K, Kelly CP, Leonard JN, et al.: The Oslo definitions for coeliac disease and related terms. Gut 2014, 62(1):43-52.
  • [12]Bednarska O, Ignatova S, Dahle C, Strom M: Intraepithelial lymphocyte distribution differs between the bulb and the second part of duodenum. BMC Gastroenterol 2013, 13:111. BioMed Central Full Text
  • [13]Marsh MN: Gluten, major histocompatibility complex, and the small intestine. A molecular and immunobiologic approach to the spectrum of gluten sensitivity ('celiac sprue'). Gastroenterol 1992, 102(1):330-54.
  • [14]Leffler D, Schuppan D, Pallav K, Najarian R, Goldsmith JD, Hansen J, Kabbani T, Dennis M, Kelly CP: Kinetics of the histological, serological and symptomatic responses to gluten challenge in adults with coeliac disease. Gut 2013, 62(7):996-1004.
  • [15]Lahdeaho ML, Kaukinen K, Laurila K, Vuotikka P, Koivurova OP, Karja-Lahdensuu T, Marcantonio A, Adelman DC, Maki M: Glutenase ALV003 Attenuates Gluten-Induced Mucosal Injury in Patients With Celiac Disease. Gastroenterol 2014, 146(7):1649-58.
  • [16]Taavela J, Koskinen O, Huhtala H, Lahdeaho ML, Popp A, Laurila K, Collin P, Kaukinen K, Kurppa K, Maki M: Validation of morphometric analyses of small-intestinal biopsy readouts in celiac disease. PLoS One 2013., 8(10) Article ID e76163
  • [17]Cummins AG, Alexander BG, Chung A, Teo E, Woenig JA, Field JB, Thompson FM, Roberts-Thomson IC: Morphometric evaluation of duodenal biopsies in celiac disease. Am J Gastroenterol 2011, 106(1):145-50.
  • [18]Al-toma A, Verbeek WH, Mulder CJ: The management of complicated celiac disease. Dig Dis 2007, 25(3):230-6.
  • [19]Lanzini A, Lanzarotto F, Villanacci V, Mora A, Bertolazzi S, Turini D, Carella G, Malagoli A, Ferrante G, Cesana BM, et al.: Complete recovery of intestinal mucosa occurs very rarely in adult coeliac patients despite adherence to gluten-free diet. Aliment Pharmacol Ther 2009, 29(12):1299-308.
  • [20]Vaira V, Roncoroni L, Barisani D, Gaudioso G, Bosari S, Bulfamante G, Doneda L, Conte D, Tomba C, Bardella MT, et al.: microRNA profiles in coeliac patients distinguish different clinical phenotypes and are modulated by gliadin peptides in primary duodenal fibroblasts. Clin Sci (Lond) 2014, 126(6):417-23.
  • [21]Kaukinen K, Sulkanen S, Maki M, Collin P: IgA-class transglutaminase antibodies in evaluating the efficacy of gluten-free diet in coeliac disease. Eur J Gastroenterol Hepatol 2002, 14(3):311-5.
  • [22]Catassi C, Fabiani E, Iacono G, D'Agate C, Francavilla R, Biagi F, Volta U, Accomando S, Picarelli A, De Vitis I, et al.: A prospective, double-blind, placebo-controlled trial to establish a safe gluten threshold for patients with celiac disease. Am J Clin Nutr 2007, 85(1):160-6.
  • [23]Gabrovska D, Kocna P, Rysova J, Borovska D, Tlaskalova-Hogenova H: Monitoring of daily gliadin intake in patients on gluten-free diets. Prague Med Rep 2011, 112(1):5-17.
  • [24]Abdulkarim AS, Burgart LJ, See J, Murray JA: Etiology of nonresponsive celiac disease: results of a systematic approach. Am J Gastroenterol 2002, 97(8):2016-21.
  • [25]Leffler DA, Dennis M, Hyett B, Kelly E, Schuppan D, Kelly CP: Etiologies and predictors of diagnosis in nonresponsive celiac disease. Clin Gastroenterol Hepatol 2007, 5(4):445-50.
  • [26]Macdonald WC, Brandborg LL, Flick AL, Trier JS, Rubin CE: Studies of Celiac Sprue. Iv. the Response of the Whole Length of the Small Bowel to a Gluten-Free Diet. Gastroenterology 1964, 47:573-89.
  • [27]Marsh MN, Crowe PT: Morphology of the mucosal lesion in gluten sensitivity. Baillieres Clin Gastroenterol 1995, 9(2):273-93.
  • [28]Ravelli A, Bolognini S, Gambarotti M, Villanacci V: Variability of histologic lesions in relation to biopsy site in gluten-sensitive enteropathy. Am J Gastroenterol 2005, 100(1):177-85.
  • [29]Ravelli A, Villanacci V, Monfredini C, Martinazzi S, Grassi V, Manenti S: How patchy is patchy villous atrophy?: distribution pattern of histological lesions in the duodenum of children with celiac disease. Am J Gastroenterol 2010, 105(9):2103-10.
  • [30]Kemppainen T, Kroger H, Janatuinen E, Arnala I, Kosma VM, Pikkarainen P, Julkunen R, Jurvelin J, Alhava E, Uusitupa M: Osteoporosis in adult patients with celiac disease. Bone 1999, 24(3):249-55.
  • [31]Soni S, Badawy SZ: Celiac disease and its effect on human reproduction: a review. J Reprod Med 2010, 55(1–2):3-8.
  文献评价指标  
  下载次数:19次 浏览次数:31次