Доказова панкреатологія: що ми знаємо про хронічний панкреатит до 2020 року?
DOI:
https://doi.org/10.30978/MG-2020-3-96Ключові слова:
підшлункова залоза, хронічний панкреатит, зовнішньосекреторна недостатність підшлункової залози, діагностика, лікуванняАнотація
Висвітлено досягнення сучасної панкреатології в галузі патогенезу, динаміки розвитку та лікування хронічного панкреатиту (ХП). Розглянуто дані генетичних досліджень щодо генетичних мутацій, котрі призводять до виникнення ХП. Проаналізовано також генетичні мутації, які спричиняють розвиток раку підшлункової залози (ПЗ). Наведено чинники ризику розвитку автоімунного панкреатиту. Описано особливості супутнього ураження нирок. Представлено концептуальну модель ХП, яка передбачає фазу раннього ХП. Наведено положення Міжнародного консенсусу про ранній ХП і діагностику цієї стадії ХП з використанням як клінічних/функціональних критеріїв, так і візуалізувальних методів досліджень. Розглянуто патофізіологічні особливості фіброгенезу в ПЗ. Проаналізовано результати досліджень особливостей виникнення зовнішньосекреторної недостатності ПЗ (ЗНПЗ), доцільність визначення фекальної еластази‑1 для скринінгу ЗНПЗ. Розглянуто особливості виникнення ЗНПЗ при остеопенії і кардіоваскулярних захворюваннях. Висвітлено нюанси проведення замісної ферментної терапії при стеатозі ПЗ, ожирінні, а також її вплив на якість і тривалість життя хворих на ХП із ЗНПЗ. Описано переваги застосування мінімікросфер в ентеросолюбільній оболонці та можливість купірування клінічних виявів ЗНПЗ, збільшення маси тіла, поліпшення якості життя та його тривалості при проведенні замісної ферментної терапії. Розглянуто оптимальні дози ферментних препаратів при призначенні замісної терапії. Наведено результати рандомізованих досліджень, які доводять ефективність мінімікросферичних препаратів.
Посилання
Words of wisdom about medicine and healing: the sayings, aphorisms, quotes / Ed. Ya. S. Tsimmerman. Moscow: Geotar-Media, 2015:256.
Apte M, Pirola R, Wilson J. Pancreatic stellate cell: physiologic role, role in fibrosis and cancer. Curr Opin Gastroenterol. 2015;31:416-423. doi: 10.1097/MOG.0000000000000196
Bang UC, Benfield T, Hyldstrup L et al. Mortality, cancer, and comorbidities associated with chronic pancreatitis: a Danish nationwide matched-cohort study. Gastroenterology. 2014;146(4):989-994. doi: 10.1053/j.gastro.2013.12.033
Barkin J, Barkin J. Chronic pancreatitis and bone disease. J Clin Densitom. 2019;S1094-6950 (19)30125-8. doi: 10.1016/j.jocd.2019.08.004
Birari R, Bhutani K. Pancreatic lipase inhibitors from natural sources: Unexplored potential. Drug Discov. 2007;12:879-889. doi: 10.1016/j.drudis.2007.07.024
Brennan GT, Saif MW. Pancreatic enzyme replacement therapy: a concise review. JOP. 2019;20(5):121-125.
Cohn JA, Friedman KJ, Noone PG et al. Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis. N Engl J Med. 1998;339:653-658. doi: 10.1056/NEJM199809033391002
Czako L, Takacs T, Hegyi P et al. Quality of life assessment after pancreatic enzyme replacement therapy in chronic pancreatitis. Can J Gastroenterol. 2003;17 (10):597-603. doi: 10.1155/2003/515848
D’Haese JG, Ceyhan GO, Demir IE et al. Pancreatic enzyme replacement therapy in patients with exocrine pancreatic insufficiency due to chronic pancreatitis: a 1-year disease management study on symptom control and quality of life. Pancreas. 2014;43(6):834-841. doi: 10.1097/MPA.0000000000000131
De la Iglesia-Garcia D, Vallejo-Senra N, Iglesias-Garcia J et al. Increased risk of mortality associated with pancreatic exocrine insufficiency in patients with chronic pancreatitis. J Clin Gastroenterol. 2018;52(8):e63-e72. doi: 10.1097/MCG.0000000000000917
De Martines D, Gianotten S, Wetzels J, van der Meijden W. Secondary hyperoxaluria due to pancreatic insufficiency. Netherl J Med. 2019;77(8):287-292.
Dominguez-Munoz J. Management of pancreatic exocrine insufficiency. Curr Opin Gastroenterol. 2019;35(5):455-459. doi: 10.1097/MOG.0000000000000562
Felderbauer P, Hoffmann P, Einwachter H et al. A novel mutation of the calcium sensing receptor gene is associated with chronic pancreatitis in a family with heterozygous SPINK1 mutations. BMC Gastroenterol. 2003;N. 3:34. doi: 10.1186/1471-230X-3-34
Fjeld K, Weiss FU, Lasher D et al. A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis. Nat Genet. 2015;47:518-522. doi: 10.1038/ng.3249
Frost F, Kacprowski T, Rühlemann M et al. Impaired exocrine pancreatic function associates with changes in intestinal microbiota composition and diversity. Gastroenterology. 2019;156(4):1010-1015. doi: 10.1053/j.gastro.2018.10.047
Gómez J, Molero X, Vaquero E et al. Vitamin E attenuates biochemical and morphological features associated with development of chronic pancreatitis. Am J Physiol Gastrointest Liver Physiol. 2004;287(1):G162-9. doi: 10.1152/ajpgi.00333.2003
Gubergrits N, Malecka-Panas E, Lehman GA et al. A 6-month, open-label clinical trial of pancrelipase delayed-release capsules (Creon) in patients with exocrine pancreatic insufficiency due to chronic pancreatitis or pancreatic surgery. Aliment Pharmacol Ther. 2011;33 (10):1152-1161. doi: 10.1111/j.1365-2036.2011.04631.× 18. Hohwieler M, Illing A, Hermann P et al. Human pluripotent stem cell derived acinar/ductal organoids generate human pancreas upon orthotopic transplantation and allow disease modelling. Gut. 2017;66:473-486. doi: 10.1136/gutjnl-2016-312423
Huang W, Iglesia‑García D, Baston‑Rey I et al. Exocrine pancreatic insufficiency following acute pancreatitis: systematic review and meta‑analysis. Digestive Diseases and Sciences. 2019;64:1985-2005. doi: 10.1007/s10620-019-05568-9
Ito K, Matsuura K, Mihara Y et al. Delivery of pancreatic digestive enzymes into the gastrointestinal tract by pancreatic exocrine tissue transplant. Sci Rep. 2019;9. 5922. doi: 10.1038/s41598-019-42362-z
Ito T, Ishiguro H, Ohara H et al. Evidence based clinical practice guidelines for chronic pancreatitis 2015. J Gastroenterol. 2016;51(2):85-92. doi: 10.1007/s00535-015-1149-× 22. Ito T, Kataoka K, Irisawa A et al. Prospective follow-up study of the patients with early CP or possible CP (The final report of the RCIPD chaired by Shimosegawa T). The RCIPD Report. 2015;145e9.
Kleeff J, Whitcomb DC, Shimosegawa T et al. Chronic pancreatitis. Nat Rev Dis Primers. 2017;3. 17060. doi: 10.1038/nrdp.2017.60
Kume K, Masamune A, Ariga H, Shimosegawa T. Alcohol consumption and the risk for developing pancreatitis: a case-control study in Japan. Pancreas. 2015;44:53-58. doi: 10.1097/MPA.0000000000000256
Kuno A, Yamada T, Masuda K et al. Angiotensin-converting enzyme inhibitor attenuates pancreatic inflammation and fibrosis in male Wistar Bonn/Kobori rats. Gastroenterology. 2003;124(4):1010-1019. doi: 10.1053/gast.2003.50147
Layer P, Kashirskaya N, Gubergrits N. Contribution of pancreatic enzyme replacement therapy to survival and quality of life in patients with pancreatic exocrine insufficiency. World J Gastroenterol. 2019;25 (20):2430-2441. doi: 10.3748/wjg.v25.i20.2430
Lin Y, Tamakoshi A, Hayakawa T, Ogawa M, Ohno Y. Cigarette smoking as a risk factor for chronic pancreatitis: a case-control study in Japan. Research Committee on Intractable Pancreatic Diseases. Pancreas. 2000;21:109-114. doi: 10.1097/00006676-200008000-00001
Löhr JM, Domínguez-Muñoz E, Rosendahl J et al. United European Gastroenterology evidence based guidelines for the diagnosis and therapy of chronic pancreatitis (HaPanEU). United European Gastroenterology Journal. 2017;5(2):153-199. doi: 10.1177/2050640616684695
Lowenfels A, Maisonneuve P, Cavallini G et al. Pancreatitis and the risk of pancreatic cancer. International Pancreatitis Study Group. Engl J Med. 1993;328:1433-1437. doi: 10.1056/NEJM199305203282001
Masamune A, Nakano E, Hamada S, Kakuta Y, Kume K, Shimosegawa T. Common variants at PRSS1-PRSS2 and CLDN2-MORC4 loci associate with chronic pancreatitis in Japan. Gut. 2015;64:345-1346. doi: 10.1136/gutjnl-2015-309802
Masamune A, Nakano E, Kume K, Kakuta Y, Ariga H, Shimosegawa T. Identification of novel missense CTRC variants in Japanese patients with chronic pancreatitis. Gut. 2013;62:653-654. doi: 10.1136/gutjnl-2012-303860
Motoo Y. Antiproteases in the treatment of chronic pancreatitis. JOP. 2007;9(4):533-537.
Nagashio Y, Ueno H, Imamura M et al. Inhibition of transforming growth factor beta decreases pancreatic fibrosis and protects the pancreas against chronic injury in mice. Lab Invest. 2004;84 (12):1610-1618. doi: 10.1038/labinvest.3700191
Nikolic S, Dugic A, Steiner C et al. Chronic pancreatitis and the heart disease: Still terra incognita?. World J Gastroenterol. 2019;25 (44):6561-6570. doi: 10.3748/wjg.v25.i44.6561
Pei Y, Ai T, Deng Z et al. Impact of plant extract on the gastrointestinal fate of nutraceutical-loaded nano emulsions: Phytic acid inhibits lipid digestion but enhances curcumin bio accessibility. Food Funct. 2019;10:3344-3355. doi: 10.1039/c9fo00545e
Ramesh H, Reddy N, Bhatia S et al. A 51-week, open-label clinical trial in India to assess the efficacy and safety of pancreatin 40000 enteric-coated minimicrospheres in patients with pancreatic exocrine insufficiency due to chronic pancreatitis. Pancreatology. 2013;13(2):133-139. doi: 10.1016/j.pan.2013.01.009
Reding T, Bimmler D, Perren A et al. A selective COX-2 inhibitor suppresses chronic pancreatitis in an animal model (WBN/Kob rats): significant reduction of macrophage infiltration and fibrosis. Gut. 2006;55(8):1165-1173. doi: 10.1136/gut.2005.077925
Ribichini E, Stigliano S, Rossi S et al. Role of fibre in nutritional management of pancreatic diseases. Nutrients. 2019;11. 2219. doi: 10.3390/nu11092219
Rosendahl J, Witt H, Szmola R et al. Chymotrypsin C (CTRC) variants that diminish activity or secretion are associated with chronic pancreatitis. Nat Genet. 2008;40:78-82. doi: 10.1038/ng.2007.44
Safdi M, Bekal PK, Martin S et al. The effects of oral pancreatic enzymes (Creon 10 capsule) on steatorrhea: a multicenter, placebo-controlled, parallel group trial in subjects with chronic pancreatitis. Pancreas. 2006;33(2):156-162. doi: 10.1097/01.mpa.0000226884.32957.5e
Satouchi K, Matsushita S. Purification and properties of a lipase inhibiting protein from soy bean cotyledons. Agric Biol Chem. 1976;40:889-897. doi: 10.1271/bbb1961.40.889
Sharer N, Schwarz M, Malone G et al. Mutations of the cystic fibrosis gene in patients with chronic pancreatitis. N Engl J Med. 1998;339:645-652. doi: 10.1056/NEJM199809033391001
Shimizu K, Shiratori K, Kobayashi M, Kawamata H. Troglitazone inhibits the progression of chronic pancreatitis and the profibrogenic activity of pancreatic stellate cells via a PPARgamma-independent mechanism. Pancreas. 2004;29(1):67-74. doi: 10.1097/00006676-200407000-00058
Shimosegawa T. A new insight into chronic pancreatitis. Tohoku J Exp Med. 2019;248:225-238. doi: 10.1620/tjem.248.225
Shobassy M, Husainat N, Tabash A et al. Endoscopic ultrasound findings in patients diagnosed with exocrine pancreatic insufficiency by low fecal elastase-1. Gastroenterology Research and Practice. 2019:5. doi: 10.1155/2019/5290642
Singh G, Suresh S, Bayineni V, Kadeppagari R. Lipase inhibitors from plants and their medical applications. Int J Pharm Pharm Sci. 2015;7:1-5.
Szmola R, Sahin-Tóth M. Chymotrypsin C (caldecrin) promotes degradation of human cationic trypsin: identity with Rinderknecht’s enzyme Y. Proc Natl Acad Sci. 2007;104:11227-11232. doi: 10.1073/pnas.0703714104
Tahtaci M, Algın O, Karakan T et al. Can pancreatic steatosis affect exocrine functions of pancreas?. Turk J Gastroenterol. 2018;29:588-594. doi: 10.5152/tjg.2018.17696
The Pancreas: An Integrated Textbook of Basic Science, Medicine and Surgery / Ed. By HG. Beger, A. L. Warshaw, R. H. Hruban et al. Oxford: Willey Blackwell, 2018:1173.
Thorat V, Reddy N, Bhatia S et al. Randomised clinical trial: the efficacy and safety of pancreatin enteric-coated minimicrospheres (Creon 40000 MMS) in patients with pancreatic exocrine insufficiency due to chronic pancreatitis — a double-blind, placebo-controlled study. Aliment Pharmacol Ther. 2012;36(5):426-436. doi: 10.1111/j.1365-2036.2012.05202.× 51. Toskes P et al. Efficacy of a novel pancreatic enzyme product, EUR-1008 (Zenpep), in patients with exocrine pancreatic insufficiency due to chronic pancreatitis. Pancreas. 2011;40(3):376-382. doi: 10.1097/MPA.0b013e31820b971c
Ueda J, Tanaka M, Ohtsuka T et al. Research Committee of Intractable Diseases of the Pancreas. Surgery for chronic pancreatitis decreases the risk for pancreatic cancer: a multicenter retrospective analysis. Surgery. 2013;153:357-364. doi: 10.1016/j.surg.2012.08.005
Vallejo-Senra N, de la Inglesia-Garcia D, Lopez-Lopez A et al. Cardiovascular risk (CVR) associated with pancreatic exocrine insufficiency (PEI) in patients with chronic pancreatitis (CP). 48th European Pancreatic Club (EPC) meeting. Pancreatology. 2016;16 (3S1):S80. doi: 10.1016/j.pan.2016.05.270
van Westerloo D, Florquin S, de Boer A et al. Therapeutic effects of troglitazone in experimental chronic pancreatitis in mice. Am J Pathol. 2005;166(3):721-728. doi: 10.1016/S0002-9440 (10)62293-6
Vujasinovic M, Hedström A, Maisonneuve P et al. Zinc deficiency in patients with chronic pancreatitis. World J Gastroenterol. 2019;25(5):600-607. doi: 10.3748/wjg.v25.i5.600
Vujasinovic M, Kunst G, Breznikar B et al. Is pancreatic exocrine insufficiency a cause of malabsorption in patients after bariatric surgery?. JOP. 2016;17:241-244.
Vujasinovic M, Pozzi Mucelli R, Valente R et al. Kidney Involvement in patients with type 1 autoimmune pancreatitis. J Clin Med. 2019;18(2):E258. doi: 10.3390/jcm8020258
Vujasinovic M, Valente R, Maier P et al. Diagnosis, treatment and long-term outcome of autoimmune pancreatitis in Sweden. Pancreatology. 2018;18(8):900-904. doi: 10.1016/j.pan.2018.09.003
Vujasinovic M, Valente R, Thorel A et al. Pancreatic exocrine insufficiency after bariatric surgery. Nutrients. 2017;9:1241. doi: 10.3390/nu9111241
Whitcomb DC, Frulloni L, Garg P et al. Chronic pancreatitis: an international draft consensus proposal for a new mechanistic definition. Pancreatology. 2016;16(2):218-224. doi: 10.1016/j.pan.2016.02.001
Whitcomb DC, Lehman GA, Vasileva G et al. Pancrelipase delayed-release capsules (CREON) for exocrine pancreatic insufficiency due to chronic pancreatitis or pancreatic surgery: a double-blind randomized trial. Am J Gastroenterol. 2010;105 (10):2276-2286. doi: 10.1038/ajg.2010.201
Whitcomb DC, Shimosegawa T, Chari ST et al. International consensus statements on early chronic Pancreatitis. Recommendations from the working group for the international consensus guidelines for chronic pancreatitis in collaboration with The International Association of Pancreatology, American Pancreatic Association, Japan Pancreas Society, Pancreas. Fest Working Group and European Pancreatic Club. Pancreatology. 2018;18:516-527. doi: 10.1016/j.pan.2018.05.008
Whitcomb DC, Gorry MC, Preston RA et al. Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene. Nat Genet. 1996;14:141-145. doi: 10.1038/ng1096-141
Whitcomb DC, LaRusch J, Krasinskas AM et al. Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. Nat Genet. 2012;44:1349-1354. doi: 10.1038/ng.2466
Whitcomb DC, Preston RA, Aston CE et al. A gene for hereditary pancreatitis maps to chromosome 7q35. Gastroenterology. 1996;110:1975-1980. doi: 10.1053/gast.1996.v110.pm8964426
Winny M, Paroglou V, Bektas H et al. Insulin dependence and pancreatic enzyme replacement therapy are independent prognostic factors for long-term survival after operation for chronic pancreatitis. Surgery. 2014;155(2):271-279. doi: 10.1016/j.surg.2013.08.012
Witt H, Beer S, Rosendahl J et al. Variants in CPA1 are strongly associated with early onset chronic pancreatitis. Nat Genet. 2013;45:1216-1220. doi: 10.1038/ng.2730
Witt H, Luck W, Hennies HC et al. Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis. Nat Genet. 2000;25:213-216. doi: 10.1038/76088
Yamada T, Kuno A, Masuda K et al. Candesartan, an angiotensin II receptor antagonist, suppresses pancreatic inflammation and fibrosis in rats. J Pharmacol Exp Ther. 2003;307(1):17-23. doi: 10.1124/jpet.103.053322
Zha M, Xu W, Jones P et al. Isolation and characterization of human islet stellate cells. Exp Cell Res. 2016;314:61-66. doi: 10.1016/j.yexcr.2015.11.002
Zhang Y, Cui L, Fang F. Chronic high-fat diets induce oxide injuries and fibrogenesis of pancreatic cells in rats X. 42nd European Pancreatic Club (EPC) meeting. Pancreatology. 2010;10:273. doi: 10.1097/MPA.0b013e3181744b50
Zheng Q, Koike K, Han L et al. New biologically active triterpenoid saponins from Scabiosa tschiliensis. J Nat Prod 2004;67:604-613. doi: 10.1021/np0304722
Zou WB, Boulling A, Masamune A et al. No association between CEL-HYB hybrid allele and chronic pancreatitis in Asian populations. Gastroenterology. 2016;150:1558-1560. doi: 10.1053/j.gastro.2016.02.071