The relationship between gastroesophageal reflux disease and severity of lung damage in systemic sclerosis


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅或者付费存取

详细

Objective. To investigate the incidence and severity of gastroesophageal reflux disease (Gerd) and a potential relationship with severity of lung damage in systemic sclerosis. Material and methods. 56 patients (mean age 46±і4 years) with diffuse and limited form of systemic sclerosis were allocated to groups on the basis of the presence or absence of gastroesophageal reflux disease (The Montreal Classification). To detect the presence and evaluate severity of lung damage, all patients underwent standard clinical and diagnostic investigations, including gastroduodenoscopy, contrast esophagography and high resolution chest ct. Results. GERD was found in 27 of 56 (48.2%) patients. Of them, 24 patients were on continuous therapy with proton pump inhibitors and 3 received them for exacerbations. Among 23 patients who underwent esophagogastroduodenoscopy, 1 patient had erosive GERD, 11 patients - non-erosive GERD (esophageal mucosa hyperemia) and 11 were found to have esophageal functional changes (endoscopy-negative stage). All studied patients had moderate esophageal damage. According to Savary-Miller classification of reflux esophagitis severity, 1 patient had grade I reflux esophagitis; there were no cases of grades II, III and IV reflux esophagitis. Almost all GERD patients (26 of 27) had dysphagia, while it was observed only in 11 patients without GERD. Esophageal motility disturbances according to contrast esophagography were found in 20 of 25 (80%) patients with GERD compared to 5 of 24 (20.8%) without Gerd. Clinically significant dyspnea (NYHA>II) was detected twice as often in patients with GERD compared with patients without GERD (at 92.6% compared to 44.8%, RESPECTIVELY, P=0.0002). DYSPNEA (NYHA III) was detected 4 times more often in patients with GERD compared with patients without Gerd (44.4% compared to 1 0.3%, respectively, p=0,006). severe INTERSTITIAL LUNG DISEASE (OVER 20%) ACCORDING TO GOH ET al. staging system was significantly more common in PATIENTS WITH Gerd (74. 1 % COMPARED TO 37,5% WITHOUT Gerd, P=0.018). Conclusion. GERD is a common co-morbidity in systemic sclerosis. The study findings showed that more severe LUNG DISEASE WAS ASSOCIATED WITH GERD SUGGESTING A POTENTIAL CONTRIBUTION OF GERD TO THE DEVELOPMENT AND PROGRESSION OF PULMONARY FIBROSIS IN PATIENTS WITH SYSTEMIC SCLEROSIS.

全文:

受限制的访问

参考

  1. Ревматология: национальное руководство. Под ред Е.Л. Насонова, В.А. Насоновой М.: ГЭОТАР-Медиа, 2010. 720 с.
  2. Коган Е.А., Коренев Б.М., Попова Е.Н., Фомин В.В и др. Интерстициальные болезни легких. М., Литтерра. 2007. 416 с.
  3. Ананьева Л.П., Теплова Л.В., Лесняк В.Н., Конева О.А., Овсянникова О.Б., Старовойтова М.Н., Десинова О.В. Клиническая оценка проявлений интерстициального поражения легких при системной склеродермии по данным компьютерной томографии высокого разрешения. Научнопрактическая ревматология. 2011; 2: 30-39.
  4. Гусева Н.Г. Системная склеродермия: клиника, диагностика, лечение. Российский журнал кожных и венерических болезней. 2002; 4: 5-15.
  5. Каратеев А.Е., Мовсисян М.М., Ананьева Л.П., Раденска-лоповок С.Г. Патология пищевода при системной склеродермии: данные клиникоэндоскопического обследования. Научно-практическая ревматология. 2012; 1: 54-59.
  6. Чучалин А.Г. Клинические рекомендации. Пульмонология. М., ГЭОТАРМедиа. 2007. 37 с.
  7. Гриппи М.А. Патофизиология легких. М., Бином. 2005.
  8. Bassotti G., Battaglia E., Debernardi V., Germani U., Quiriconi F., Dughera L., Buonafede G., Puiatti P., Morelli A., Spinozzi F., Mioli P.R., Emanuelli G. Esophageal dysfunction in scleroderma: relationship with disease subsets. Arthritis Rheum. 1997; 40: 2252-2259.
  9. Bouros D., Wells A.U., Nicholson A.G., Colby T.V., Polychronopoulos V., Pantelidis P., Haslam P.L., Vassilakis D.A., Black C.M., du Bois R.M. Histopathologic subsets of fibrosing alveolitis in patients with systemic sclerosis and their relationship to outcome. Am. J. Respir. Crit. Care Med. 2002; 165(12): 1581-1586.
  10. Christmann R.B., Wells A.U., Capelozzi V.L., Silver R.M. Gastroesophageal reflux incites interstitial lung disease in systemic sclerosis: clinical, radiologic, histopathologic, and treatment evidence. Semin. Arthritis Rheum. 2010; 40(3): 241-249.
  11. Clements P., Goldin J., Kleerup E., Furst D.E., Elashoff R.M., Tashkin D.P., Roth M.D. Regional differences in bronchoalveolar lavage and thoracic high-resolution computed tomography results in dyspno patients with systemic sclerosis. Arthr. Rheum. 2004; 50: 1909-1917.
  12. de Souza R.B., Borges C.T., Capelozzi V.L., Parra E.R., Jatene F.B., Kavakama J., Kairalla R.A., Bonfa E. Centrilobularfibrosis: an underrecognized pattern in systemic sclerosis. Respiration. 2009; 77(4): 389-397.
  13. Desai S.R., Veeraraghavan S., Hansell D.M., Nikolakopolou A., Goh N.S., Nicholson A.G., Colby T.V., Denton C.P., Black C.M., du Bois R.M., Wells A.U. CT features of lung disease in patients with systemic sclerosis: comparison with idiopathic pulmonary fibrosis and nonspecific interstitial pneumonia. Radiology. 2004; 232(2): 560-567.
  14. Downing T.E., Sporn T.A., Bollinger R.R., Davis R.D., Parker W., Lin S.S. Pulmonary histopathology in an experimental model of chronic aspiration is independent of acidity. Exp. Biol. Med. (Maywood). 2008; 14: 1202-1212.
  15. Ebert E.C. Esophageal disease in scleroderma. J. Clin. Gastroenterol. 2006; 40: 769-775.
  16. Ebert E.C. Gastric and enteric involvement in progressive systemic sclerosis. J. Clin. Gastroenterol. 2008; 42: 5-12.
  17. Geirsson A.J., Wollheim F.A., Akesson A. Disease severity of 100 patients with systemic sclerosis over a period of 14 years: using a modified Medsger scale. Ann. Rheum. Dis. 2001; 60(12): 1117-1122.
  18. Gilson M., Zerkak D., Wipff J., Dusser D., Dinh-Xuan A.T., Abitbol V., Chaussade S., Legmann P., Kahan A., Allanore Y. Prognostic factors for lung function in systemic sclerosis: prospective study of 105 cases. Eur. Respir J. 2010; 35(1): 112-117.
  19. Goh N.S., Desai S.R., Veeraraghavan S., Hansell D.M., Copley S.J., Maher T.M., Corte T.J., Sander C.R., Ratoff J., Devaraj A., Bozovic G., Denton C.P., Black C.M., du Bois R.M., Wells A.U. Interstitial lung disease in systemic sclerosis: a simple staging system. Am. J. Respir. Crit. Care Med. 2008; 177(11): 1248-1254.
  20. Goldin J.G., Lynch D.A., Strollo D.C., Suh R.D., Schraufnagel D.E., Clements P.J., Elashoff R.M., Furst D.E., Vasunilashorn S., McNitt-Gray M.F., Brown M.S., Roth M.D., Tashkin D.P.; Scleroderma Lung Study Research Group. High-resolution CT scan findings in patients with symptomatic scleroderma-related interstitial lung disease. Chest. 2008; 134(2): 358-367.
  21. Greenwald G.I., Tashkin D.P., Gong H., Simmons M., Duann S., Furst D.E., Clements P. Longitudinal changes in lung function and respiratory symptoms in progressive systemic sclerosis. Prospective study. Am. J. Med. 1987; 83(1): 83-92.
  22. Guttadauria M., Ellman H., Emmanuel G., Kaplan D., Diamond H. Pulmonary function in scleroderma. Arthritis Rheum. 1977; 20: 1071-1079.
  23. Harrison N.K., Myers A.R., Corrin B. et al. Structural features of interstitial lung disease in systemic sclerosis // Am. Rev. Respir. Dis. 1991. 144(3 Pt 1). P. 706-713.
  24. Highland K.B., Silver R.M. Clinical aspects of lung involvement: lessons from idiopathic pulmonary fibrosis and the scleroderma lung study. Curr. Rheumatol. 2005; 7(2): 135-141.
  25. Ioannidis J.P., Vlachoyiannopoulos P.G., Haidich A.B., Medsger T.A. Jr, Lucas M., Michet C.J., Kuwana M., Yasuoka H., van den Hoogen F., Te Boome L., van Laar J.M., Verbeet N.L., Matucci-Cerinic M., Georgountzos A., Moutsopoulos H.M. Mortality in systemic sclerosis: an international metaanalysis of individual patient data. Am. J. Med. 2005; 118: 2-10.
  26. Jaffin B.W., Chang P., Spiera H. Fecal incontinence inscleroderma. Clinical features, anorectal manometric findings, and their therapeutic implications. J. Clin. Gastroenterol. 1997; 25: 513-517.
  27. Kaloudi О., Miniati I., Alari S. Interstitial lung disease in systemic sclerosis. Intern. Emerg. Med. 2007; 2(4): 250-255.
  28. Kay L., Jorgensen T., Jensen K.H. The epidemiology ofirritable bowel syndrome in a random population: prevalence, incidence, natural history and risk factors. J. Intern. Med. 1994; 236: 23-30.
  29. Khanna D., Clements P.J., Furst D.E., Tashkin D.P. Current concepts in disease-modifying therapy for systemic sclerosis-associated interstitial lung disease: lessons from clinical trials. Curr. Rheumatol. Rep. 2009; 11: 111-119.
  30. Khanna D., Hays R.D., Park G.S., Braun-Moscovici Y., Mayes M.D., McNearney T.A., Hsu V., Clements P.J., Furst D.E. Development of a preliminary scleroderma gastrointestinal tract 1.0 Quality of Life Instrument. Arthritis Rheum. 2007; 57: 1280-1286.
  31. Kim D.S., Yoo В., Lee J.S., Kim E.K., Lim C.M., Lee S.D., Koh Y., Kim W.S., Kim W.D., Colby T.V., Kitiaichi M. The major histopathologic pattern of pulmonary fibrosis in scleroderma is nonspecific interstitial pneumonia. Sarcoidosis Vasc. Diffuse Lung Dis. 2002; 19(2): 121-127.
  32. Lahcene M., Oumnia N., Matougui N., Boudjella M., Tebaibia A., Touchene B. Esophageal dysmotility is scleroderma: a prospective study of 183 cases. Gastroenterol Clin. Biol. 2009; 33: 466-469.
  33. Marcisz C., Kucharz E.J., Brzezinska-Wcislo L., Kotulska A., Jonderko G. Pulmonary functional abnormalities in asymptomatic patients with systemic sclerosis. Eur. J. Intern. Med. 2003; 14(3): 162-165.
  34. Marie I., Dominique S., Levesque H., Ducrotté P., Denis P., Hellot M.F., Courtois H. Esophageal involvement and pulmonary manifestations in systemic sclerosis. Arthritis Rheum. 2001; 45: 346-354.
  35. McNearney T.A., Reveille J.D., Fischbach M., Friedman A.W., Lisse J.R., Goel N., Tan F.K., Zhou X., Ahn C., Feghali-Bostwick C.A., Fritzler M., Arnett F.C., Mayes M.D. Pulmonary involvement in systemic sclerosis: associations with genetic,serologic, sociodemographic, and behavioral factors. Arthr. Rheum. 2007; 57(2): 318-326.
  36. Morgan С., Knight С., Lunt M., Black C.M., Silman A.J. Predictors of end stage lung disease in a cohort of patients with scleroderma. Ann. Rheum. Dis. 2003; 62(2): 146-150.
  37. Nishimagi E., Tochimoto A., Kawaguchi Y., Satoh T., Kuwana M., Takagi K., Ichida H., Kanno T., Soejima M., Baba S., Kamatani N., Hara M. Characteristics of patients with early systemic sclerosis and severe gastrointestinal tract involvement. J. Rheumatol. 2007; 34: 2050-2055.
  38. Thoua N.M., Bunce C., Brough G., Forbes A., Emmanuel A.V., Denton C.P. Assessment of gastrointestinal symptoms in patients with systemic sclerosis in a UK tertiary referral centre. Rheumatology (Oxford). 2010; 49(9): 1770-1775.
  39. Parra E.R., Otani L.H., de Carvalho E.F., Ab'Saber A., Capelozzi V.L. Systemic sclerosis and idiopathic interstitial pneumonia: histomorphometric differences in lung biopsies. J. Bras. Pneumol. 2009; 35(6): 529-540.
  40. Peters-Golden M., Wise R.A., Schneider P., Hochberg M., Stevens M.B., Wigley F. Clinical and demographic predictors of loss of pulmonary function in systemic sclerosis. Medicine Baltimore. 1984; 63(4): 221-231.
  41. Remy-Jardin M., Remy J., Wallaert B. Pulmonary involvement in progressive systemic sclerosis sequential evaluation with CT, pulmonary tests and broncho-alveolar lavage. Radiology. 1993; 188: 499-506.
  42. Ruangjutipopan S., Kasitanon N., Louthrenoo W., Sukitawut W., Wichainun R. Causes of death and poor survival prognostic factors in thai patients with systemic sclerosis. J. Med. Assoc. Thai. 2002; 85(11): 1204-1209.
  43. Sallam H., McNearney T.A., Chen J.D. Systematic review: pathophysiology and management of gastrointestinaldysmotility in systemic sclerosis (scleroderma). Aliment Pharmacol. Ther. 2006; 23: 691-712.
  44. Savarino E., Bazzica M., Zentilin P., Pohl D., Parodi A., Cittadini G., Negrini S., Indiveri F., Tutuian R., Savarino V., Ghio M. Gastroesophagealreflux and pulmonary fibrosis in scleroderma: a study using pH-impedance monitoring. Am. J. Respir. Crit. Care Med. 2009; 179: 408-413. g

补充文件

附件文件
动作
1. JATS XML
##common.cookie##