Skip to main content
Erschienen in: Clinical Rheumatology 6/2022

17.02.2022 | Original Article

Persistent enlargement of the pancreatic gland after glucocorticoid therapy increases the risk of relapse in IgG4-related autoimmune pancreatitis

verfasst von: Hui Lu, Linyi Peng, Liang Zhu, Ruie Feng, Jiaxin Zhou, Zheng Liu, Jieqiong Li, Xuan Luo, Yu Peng, Chenman Qin, Yunyun Fei, Yan Zhao, Xiaofeng Zeng, Yamin Lai, Wen Zhang

Erschienen in: Clinical Rheumatology | Ausgabe 6/2022

Einloggen, um Zugang zu erhalten

Abstract

Objectives

This study aims to clarify the relationship between the changes of pancreatic size after glucocorticoid (GC) therapy and relapse in IgG4-related autoimmune pancreatitis (AIP).

Methods

We prospectively enrolled 205 newly diagnosed IgG4-related AIP patients. 145 patients were followed up for more than 3 years. These patients were divided into three groups according to the changes of pancreatic size after treatment of 6 months: pancreatic swelling, normal size, and pancreatic atrophy. Baseline clinical and laboratory parameters were compared among three groups. Kaplan–Meier survival analysis was performed in the 134 patients based on GC therapy. Besides, Cox regression analysis and logistic regression analysis were performed to identify risk factors associated with relapse and the potential variables affecting changes of pancreatic size after treatment.

Results

Age at diagnosis, white blood cell count, and serum IgG1 level at baseline were significantly different among the three groups. After treatment of 6 months, the pancreas of most patients (n = 81, 55.9%) could return to normal size, while persistent pancreatic swelling was found in 24.1% patients (n = 35), and atrophy was observed in 20.0% of the patients (n = 29). Kaplan–Meier survival analysis presented patients with pancreatic swelling after 6 months of GC therapy were more likely to relapse in the follow-up of 3 years. Persistent pancreatic swelling after treatment and salivary gland involvement at baseline were independent risk variables associated with relapse in IgG4-related AIP patients, while GC-based therapy was a protective factor of relapse. Logistic regression analysis revealed that older age at diagnosis was associated with pancreatic atrophy and higher baseline serum IgG1 level was associated with pancreatic swelling after treatment of 6 months.

Conclusions

Patients with persistent pancreatic swelling after GC-based therapy of 6 months were more likely to relapse in the follow-up of 3 years. Older age at diagnosis and higher baseline serum IgG1 level were potential variables associated with pancreatic atrophy or swelling after treatment of 6 months.
Key Points
• Patients with persistent pancreatic swelling after glucocorticoid-based therapy were more likely to relapse in IgG4-related autoimmune pancreatitis.
• Older age at diagnosis was associated with pancreatic atrophy after glucocorticoid-based therapy.
• Higher baseline serum IgG1 level was associated pancreatic swelling after glucocorticoid-based therapy.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat Kamisawa T, Takuma K, Egawa N, Tsuruta K, Sasaki T (2010) Autoimmune pancreatitis and IgG4-related sclerosing disease. Nat Rev Gastroenterol Hepatol 7(7):401–409CrossRef Kamisawa T, Takuma K, Egawa N, Tsuruta K, Sasaki T (2010) Autoimmune pancreatitis and IgG4-related sclerosing disease. Nat Rev Gastroenterol Hepatol 7(7):401–409CrossRef
2.
Zurück zum Zitat Shimosegawa T, Chari ST, Frulloni L et al (2011) International consensus diagnostic criteria for autoimmune pancreatitis: guidelines of the International Association of Pancreatology. Pancreas 40(3):352–358CrossRef Shimosegawa T, Chari ST, Frulloni L et al (2011) International consensus diagnostic criteria for autoimmune pancreatitis: guidelines of the International Association of Pancreatology. Pancreas 40(3):352–358CrossRef
3.
Zurück zum Zitat Kuruma S, Kamisawa T, Kikuyama M et al (2019) Clinical characteristics of autoimmune pancreatitis with IgG4 related kidney disease. Adv Med Sci 64(2):246–251CrossRef Kuruma S, Kamisawa T, Kikuyama M et al (2019) Clinical characteristics of autoimmune pancreatitis with IgG4 related kidney disease. Adv Med Sci 64(2):246–251CrossRef
4.
Zurück zum Zitat Naitoh I, Nakazawa T, Ohara H et al (2010) Clinical significance of extrapancreatic lesions in autoimmune pancreatitis. Pancreas 39(1):e1-5CrossRef Naitoh I, Nakazawa T, Ohara H et al (2010) Clinical significance of extrapancreatic lesions in autoimmune pancreatitis. Pancreas 39(1):e1-5CrossRef
5.
Zurück zum Zitat Khandelwal A, Inoue D, Takahashi N (2020) Autoimmune pancreatitis: an update. Abdom Radiol (New York) 45(5):1359–1370CrossRef Khandelwal A, Inoue D, Takahashi N (2020) Autoimmune pancreatitis: an update. Abdom Radiol (New York) 45(5):1359–1370CrossRef
6.
Zurück zum Zitat Dong Y, D’Onofrio M, Hocke M et al (2018) Autoimmune pancreatitis: imaging features. Endoscopic ultrasound 7(3):196–203CrossRef Dong Y, D’Onofrio M, Hocke M et al (2018) Autoimmune pancreatitis: imaging features. Endoscopic ultrasound 7(3):196–203CrossRef
7.
Zurück zum Zitat Umehara H, Okazaki K, Masaki Y et al (2012) Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011. Mod Rheumatol 22(1):21–30CrossRef Umehara H, Okazaki K, Masaki Y et al (2012) Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011. Mod Rheumatol 22(1):21–30CrossRef
8.
Zurück zum Zitat Carruthers MN, Stone JH, Deshpande V, Khosroshahi A (2012) Development of an IgG4-RD responder index. Int J Rheumatol 259408 Carruthers MN, Stone JH, Deshpande V, Khosroshahi A (2012) Development of an IgG4-RD responder index. Int J Rheumatol 259408
9.
Zurück zum Zitat Rehnitz C, Klauss M, Singer R et al (2011) Morphologic patterns of autoimmune pancreatitis in CT and MRI. Pancreatol: Off J Int Assoc Pancreatology (IAP) [et al] 11(2):240–51CrossRef Rehnitz C, Klauss M, Singer R et al (2011) Morphologic patterns of autoimmune pancreatitis in CT and MRI. Pancreatol: Off J Int Assoc Pancreatology (IAP) [et al] 11(2):240–51CrossRef
10.
Zurück zum Zitat Vlachou PA, Khalili K, Jang HJ, Fischer S, Hirschfield GM, Kim TK (2011) Ig-related sclerosing disease autoimmune pancreatitis and extrapancreatic manifestations. Radiograph a Rev Publication Radiol Soc North Am Inc 31(5):1379–402 Vlachou PA, Khalili K, Jang HJ, Fischer S, Hirschfield GM, Kim TK (2011) Ig-related sclerosing disease autoimmune pancreatitis and extrapancreatic manifestations. Radiograph a Rev Publication Radiol Soc North Am Inc 31(5):1379–402
11.
Zurück zum Zitat Kamisawa T, Egawa N, Nakajima H, Tsuruta K, Okamoto A, Kamata N (2003) Clinical difficulties in the differentiation of autoimmune pancreatitis and pancreatic carcinoma. Am J Gastroenterol 98(12):2694–2699CrossRef Kamisawa T, Egawa N, Nakajima H, Tsuruta K, Okamoto A, Kamata N (2003) Clinical difficulties in the differentiation of autoimmune pancreatitis and pancreatic carcinoma. Am J Gastroenterol 98(12):2694–2699CrossRef
12.
Zurück zum Zitat Ishikawa T, Kawashima H, Ohno E et al (2020) Usefulness of endoscopic ultrasound-guided fine-needle biopsy for the diagnosis of autoimmune pancreatitis using a 22-gauge Franseen needle: a prospective multicenter study. Endoscopy 52(11):978–985CrossRef Ishikawa T, Kawashima H, Ohno E et al (2020) Usefulness of endoscopic ultrasound-guided fine-needle biopsy for the diagnosis of autoimmune pancreatitis using a 22-gauge Franseen needle: a prospective multicenter study. Endoscopy 52(11):978–985CrossRef
13.
Zurück zum Zitat Hirano K, Tada M, Isayama H et al (2013) High alcohol consumption increases the risk of pancreatic stone formation and pancreatic atrophy in autoimmune pancreatitis. Pancreas 42(3):502–505CrossRef Hirano K, Tada M, Isayama H et al (2013) High alcohol consumption increases the risk of pancreatic stone formation and pancreatic atrophy in autoimmune pancreatitis. Pancreas 42(3):502–505CrossRef
14.
Zurück zum Zitat Masuda A, Shiomi H, Matsuda T et al (2014) The relationship between pancreatic atrophy after steroid therapy and diabetes mellitus in patients. Pancreatol : Off J Int Assoc Pancreatol (IAP) [et al] 14(5):361–5CrossRef Masuda A, Shiomi H, Matsuda T et al (2014) The relationship between pancreatic atrophy after steroid therapy and diabetes mellitus in patients. Pancreatol : Off J Int Assoc Pancreatol (IAP) [et al] 14(5):361–5CrossRef
15.
Zurück zum Zitat Yamada Y, Masuda A, Sofue K et al (2020) Prediction of pancreatic atrophy after steroid therapy using equilibrium-phase contrast computed tomography imaging in autoimmune pancreatitis. JGH Open : Open Access J Gastroenterol Hepatol 4(4):677–683CrossRef Yamada Y, Masuda A, Sofue K et al (2020) Prediction of pancreatic atrophy after steroid therapy using equilibrium-phase contrast computed tomography imaging in autoimmune pancreatitis. JGH Open : Open Access J Gastroenterol Hepatol 4(4):677–683CrossRef
16.
Zurück zum Zitat Yunyun F, Yu P, Panpan Z et al (2019) Efficacy and safety of low dose Mycophenolate mofetil treatment for immunoglobulin G4-related disease: a randomized clinical trial. Rheumatol (Oxford) 58(1):52–60CrossRef Yunyun F, Yu P, Panpan Z et al (2019) Efficacy and safety of low dose Mycophenolate mofetil treatment for immunoglobulin G4-related disease: a randomized clinical trial. Rheumatol (Oxford) 58(1):52–60CrossRef
17.
Zurück zum Zitat Peng Y, Li JQ, Zhang PP et al (2019) Clinical outcomes and predictive relapse factors of IgG4-related disease following treatment: a long-term cohort study. J Intern Med 286(5):542–552CrossRef Peng Y, Li JQ, Zhang PP et al (2019) Clinical outcomes and predictive relapse factors of IgG4-related disease following treatment: a long-term cohort study. J Intern Med 286(5):542–552CrossRef
18.
Zurück zum Zitat Zhang W, Stone JH (2019) Management of IgG4-related disease. Lancet Rheumatol 1(1):e55–e65CrossRef Zhang W, Stone JH (2019) Management of IgG4-related disease. Lancet Rheumatol 1(1):e55–e65CrossRef
19.
Zurück zum Zitat Yamamoto M, Nojima M, Takahashi H et al (2015) Identification of relapse predictors in IgG4-related disease using multivariate analysis of clinical data at the first visit and initial treatment. Rheumatol (Oxford) 54(1):45–49CrossRef Yamamoto M, Nojima M, Takahashi H et al (2015) Identification of relapse predictors in IgG4-related disease using multivariate analysis of clinical data at the first visit and initial treatment. Rheumatol (Oxford) 54(1):45–49CrossRef
20.
Zurück zum Zitat Hart PA, Topazian MD, Witzig TE et al (2013) Treatment of relapsing autoimmune pancreatitis with immunomodulators and rituximab: the Mayo Clinic experience. Gut 62(11):1607–1615CrossRef Hart PA, Topazian MD, Witzig TE et al (2013) Treatment of relapsing autoimmune pancreatitis with immunomodulators and rituximab: the Mayo Clinic experience. Gut 62(11):1607–1615CrossRef
21.
Zurück zum Zitat Crosara S, D’Onofrio M, De Robertis R et al (2014) Autoimmune pancreatitis: multimodality non-invasive imaging diagnosis. World J Gastroenterol 20(45):16881–16890CrossRef Crosara S, D’Onofrio M, De Robertis R et al (2014) Autoimmune pancreatitis: multimodality non-invasive imaging diagnosis. World J Gastroenterol 20(45):16881–16890CrossRef
22.
Zurück zum Zitat Kreel L, Sandin B (1973) Changes in pancreatic morphology associated with aging. Gut 14(12):962–970CrossRef Kreel L, Sandin B (1973) Changes in pancreatic morphology associated with aging. Gut 14(12):962–970CrossRef
23.
Zurück zum Zitat Kubota K, Iida H, Fujisawa T et al (2007) Clinical factors predictive of spontaneous remission or relapse in cases of autoimmune pancreatitis. Gastrointest Endosc 66(6):1142–1151CrossRef Kubota K, Iida H, Fujisawa T et al (2007) Clinical factors predictive of spontaneous remission or relapse in cases of autoimmune pancreatitis. Gastrointest Endosc 66(6):1142–1151CrossRef
24.
Zurück zum Zitat Hirano K, Tada M, Isayama H et al (2007) Long-term prognosis of autoimmune pancreatitis with and without corticosteroid treatment. Gut 56(12):1719–1724CrossRef Hirano K, Tada M, Isayama H et al (2007) Long-term prognosis of autoimmune pancreatitis with and without corticosteroid treatment. Gut 56(12):1719–1724CrossRef
25.
Zurück zum Zitat Maire F, Le Baleur Y, Rebours V et al (2011) Outcome of patients with type 1 or 2 autoimmune pancreatitis. Am J Gastroenterol 106(1):151–156CrossRef Maire F, Le Baleur Y, Rebours V et al (2011) Outcome of patients with type 1 or 2 autoimmune pancreatitis. Am J Gastroenterol 106(1):151–156CrossRef
26.
Zurück zum Zitat Kamisawa T, Shimosegawa T, Okazaki K et al (2009) Standard steroid treatment for autoimmune pancreatitis. Gut 58(11):1504–1507CrossRef Kamisawa T, Shimosegawa T, Okazaki K et al (2009) Standard steroid treatment for autoimmune pancreatitis. Gut 58(11):1504–1507CrossRef
27.
Zurück zum Zitat Shiokawa M, Kodama Y, Kuriyama K et al (2016) Pathogenicity of IgG in patients with IgG4-related disease. Gut 65(8):1322–1332CrossRef Shiokawa M, Kodama Y, Kuriyama K et al (2016) Pathogenicity of IgG in patients with IgG4-related disease. Gut 65(8):1322–1332CrossRef
28.
Zurück zum Zitat Mizushima I, Yamada K, Fujii H et al (2012) Clinical and histological changes associated with corticosteroid therapy in IgG4-related tubulointerstitial nephritis. Mod Rheumatol 22(6):859–870CrossRef Mizushima I, Yamada K, Fujii H et al (2012) Clinical and histological changes associated with corticosteroid therapy in IgG4-related tubulointerstitial nephritis. Mod Rheumatol 22(6):859–870CrossRef
29.
Zurück zum Zitat Saeki T, Kawano M, Mizushima I et al (2013) The clinical course of patients with IgG4-related kidney disease. Kidney Int 84(4):826–833CrossRef Saeki T, Kawano M, Mizushima I et al (2013) The clinical course of patients with IgG4-related kidney disease. Kidney Int 84(4):826–833CrossRef
30.
Zurück zum Zitat Raissian Y, Nasr SH, Larsen CP et al (2011) Diagnosis of IgG4-related tubulointerstitial nephritis. J Am Soc Nephrol 22(7):1343–1352CrossRef Raissian Y, Nasr SH, Larsen CP et al (2011) Diagnosis of IgG4-related tubulointerstitial nephritis. J Am Soc Nephrol 22(7):1343–1352CrossRef
31.
Zurück zum Zitat Mizushima I, Yamamoto M, Inoue D et al (2016) Factors related to renal cortical atrophy development after glucocorticoid therapy in IgG4-related kidney disease: a retrospective multicenter study. Arthritis Res Ther 18(1):273CrossRef Mizushima I, Yamamoto M, Inoue D et al (2016) Factors related to renal cortical atrophy development after glucocorticoid therapy in IgG4-related kidney disease: a retrospective multicenter study. Arthritis Res Ther 18(1):273CrossRef
Metadaten
Titel
Persistent enlargement of the pancreatic gland after glucocorticoid therapy increases the risk of relapse in IgG4-related autoimmune pancreatitis
verfasst von
Hui Lu
Linyi Peng
Liang Zhu
Ruie Feng
Jiaxin Zhou
Zheng Liu
Jieqiong Li
Xuan Luo
Yu Peng
Chenman Qin
Yunyun Fei
Yan Zhao
Xiaofeng Zeng
Yamin Lai
Wen Zhang
Publikationsdatum
17.02.2022
Verlag
Springer International Publishing
Erschienen in
Clinical Rheumatology / Ausgabe 6/2022
Print ISSN: 0770-3198
Elektronische ISSN: 1434-9949
DOI
https://doi.org/10.1007/s10067-022-06091-5

Weitere Artikel der Ausgabe 6/2022

Clinical Rheumatology 6/2022 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Ist Fasten vor Koronarinterventionen wirklich nötig?

Wenn Eingriffe wie eine Koronarangiografie oder eine Koronarangioplastie anstehen, wird häufig empfohlen, in den Stunden zuvor nüchtern zu bleiben. Ein französisches Forscherteam hat diese Maßnahme hinterfragt.

Typ-2-Diabetes: Ernährungsunsicherheit vervierfacht Risiko für schwere Hypoglykämien

04.06.2024 Typ-2-Diabetes Nachrichten

Wenn ältere Menschen mit Typ-2-Diabetes Schwierigkeiten beim Beschaffen und Zubereiten von Mahlzeiten haben, geht dies mit einem deutlich gesteigerten Risiko für schwere Hypoglykämien einher.

Mehr Brustkrebs, aber weniger andere gynäkologische Tumoren mit Levonorgestrel-IUS

04.06.2024 Levonorgestrel Nachrichten

Unter Frauen, die ein Levonorgestrel-freisetzendes intrauterines System (IUS) verwenden, ist die Brustkrebsrate um 13% erhöht. Dafür kommt es deutlich seltener zu Endometrium-, Zervix- und Ovarialkarzinomen.

GLP-1-Agonist Semaglutid wirkt kardio- und nephroprotektiv

03.06.2024 Semaglutid Nachrichten

Der GLP-1-Agonist Semaglutid hat in der FLOW-Studie bewiesen, dass sich damit die Progression chronischer Nierenerkrankungen bei Patienten mit Typ-2-Diabetes bremsen lässt. Auch in kardiovaskulärer Hinsicht war die Therapie erfolgreich.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.