期刊文献+

Serum bile acid profiling reflects enterohepatic detoxification state and intestinal barrier function in inflammatory bowel disease 被引量:7

Serum bile acid profiling reflects enterohepatic detoxification state and intestinal barrier function in inlammatory bowel disease
暂未订购
导出
摘要 AIM: To determine free and conjugated serum bile acid (BA) levels in inflammatory bowel disease (IBD) subgroups with defined clinical manifestations. METHODS: Comprehensive serum BA profiling was performed in 358 IBD patients and 310 healthy con- trols by liquid chromatography coupled to electrospray ionization tandem mass spectrometry. RESULTS: Serum levels of hyodeoxycholic acid, the CYP3A4-mediated detoxification product of the second- ary BA lithocholic acid (LCA), was increased significantly in Crohn's disease (CD) and ulcerative colitis (UC), while most other serum BA species were decreased signifi- cantly. Total BA, total BA conjugate, and total BA glyco- conjugate levels were decreased only in CD, whereas total unconjugated BA levels were decreased only in UC. In UC patients with hepatobiliary manifestations, the conjugated primary BAs glycocholic acid, taurocholic acid, and glycochenodeoxycholic acid were as signifi- cantly increased as the secondary BAs LCA, ursodeoxy- cholic acid, and tauroursodeoxycholic acid compared to UC patients without hepatobiliary manifestations. Finally, we found that in ileocecal resected CD patients, the unconjugated primary BAs, cholic acid and chenode- oxycholic acid, were increased significantly compared to controls and patients without surgical interventions. CONCLUSION: Serum BA profiling in IBD patients that indicates impaired intestinal barrier function and increased detoxification is suitable for advanced diag- nostic characterization and differentiation of IBD sub- groups with defined clinical manifestations. AIM:To determine free and conjugated serum bile acid (BA) levels in in? ammatory bowel disease (IBD) subgroups with defi ned clinical manifestations.METHODS: Comprehensive serum BA profiling was performed in 358 IBD patients and 310 healthy controls by liquid chromatography coupled to electrospray ionization tandem mass spectrometry.RESULTS: Serum levels of hyodeoxycholic acid, the CYP3A4-mediated detoxification product of the secondary BA lithocholic acid (LCA), was increased significantly in Crohn's disease (CD) and ulcerative colitis (UC), while most other serum BA species were decreased significantly. Total BA, total BA conjugate, and total BA glycoconjugate levels were decreased only in CD, whereas total unconjugated BA levels were decreased only in UC. In UC patients with hepatobiliary manifestations, the conjugated primary BAs glycocholic acid, taurocholic acid, and glycochenodeoxycholic acid were as significantly increased as the secondary BAs LCA, ursodeoxycholic acid, and tauroursodeoxycholic acid compared to UC patients without hepatobiliary manifestations. Finally, we found that in ileocecal resected CD patients, the unconjugated primary BAs, cholic acid and chenode-oxycholic acid, were increased significantly compared to controls and patients without surgical interventions.CONCLUSION: Serum BA profiling in IBD patients that indicates impaired intestinal barrier function and increased detoxification is suitable for advanced diagnostic characterization and differentiation of IBD subgroups with defined clinical manifestations.
出处 《World Journal of Gastroenterology》 SCIE CAS CSCD 2009年第25期3134-3141,共8页 世界胃肠病学杂志(英文版)
基金 Supported by A grant from the Deutsche Forschungs-gemeinschaft (SFB585-A1/A4) the Stiftung für Pathobio-chemie und Molekulare Diagnostik (TL),the Dietmar Hopp Foundation the EU FP 6 funded SSA "ELIfe" project (The Eu-ropean Lipidomics Initiative Shaping the life sciences proposal number 013032) the EU FP 7 funded project "Lipidomic-Net" (lipid droplets as dynamic organelles of fat deposition and release:translational research towards human disease proposal number 202272)
关键词 Bile acids Liquid chromatography Tandem mass spectrometry Inflammatory bowel disease Crohn's disease Ulcerative colitis 屏障功能 胆汁酸 炎症 解毒 血清
  • 相关文献

参考文献2

二级参考文献123

  • 1[1]Veloso FT,Carvalho J,Magro F.Immune-related systemic manifestations of inflammatory bowel disease.A prospective study of 792 patients.J Clin Gastroenterol 1996; 23:29-34
  • 2[2]Das KM.Relationship of extraintestinal involvements in inflammatory bowel disease:new insights into autoimmune pathogenesis.Dig Dis Sci 1999; 44:1-13
  • 3[77]Viereck V,Emons G,Lauck V,Frosch KH,Blaschke S,Grundker C,Hofbauer LC.Bisphosphonates pamidronate and zoledronic acid stimulate osteoprotegerin production by primary human osteoblasts.Biochem Biophys Res Commun 2002;291:680-686
  • 4[78]Vidal NO,Brandstrom H,Jonsson KB,Ohlsson C.Osteoprotegerin mRNA is expressed in primary human osteoblast-like cells:down-regulation by glucocorticoids.J Endocrinol 1998; 159:191-195
  • 5[79]Redlich K,Hayer S,Maier A,Dunstan CR,Tohidast-Akrad M,Lang S,Turk B,Pietschmann P,Woloszczuk W,Haralambous S,Kollias G,Steiner G,Smolen JS,Schett G.Tumor necrosis factor alpha-mediated joint destruction is inhibited by targeting osteoclasts with osteoprotegerin.Arthritis Rheum 2002; 46:785-792
  • 6[80]Bernstein CN,Bector S,Leslie WD.Lack of relationship of calcium and vitamin D intake to bone mineral density in premenopausal women with inflammatory bowel disease.Am J Gastroenterol 2003; 98:2468-2473
  • 7[81]Schulte CM,Dignass AU,Goebell H,Roher HD,Schulte KM.Genetic factors determine extent of bone loss in inflammatory bowel disease.Gastroenterology 2000; 119:909-920
  • 8[82]Haderslev KV,Tjellesen L,Sorensen HA,Staun M.Alendronate increases lumbar spine bone mineral density in patients with Crohn's disease.Gastroenterology 2000; 119:639-646
  • 9[83]Reffitt DM,Meenan J,Sanderson JD,Jugdaohsingh R,Powell JJ,Thompson RP.Bone density improves with disease remission in patients with inflammatory bowel disease.Eur J Gastroenterol Hepatol2003; 15:1267-1273
  • 10[84]American Gastroenterological Association medical position statement:guidelines on osteoporosis in gastrointestinal diseases.Gastroenterology 2003; 124:791-794

共引文献27

同被引文献27

引证文献7

二级引证文献28

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部