Dipeptidyl peptidase IV (DDP IV) in NASH patients

被引:116
作者
Balaban, Yasemin H. [1 ]
Korkusuz, Petek [2 ]
Simsek, Halis [1 ]
Gokcan, Hale [3 ]
Gedikoglu, Gokhan [4 ]
Pinar, Ash [5 ]
Hascelik, Gulsen [6 ]
Asan, Esin [2 ]
Hamaloglu, Erhan [7 ]
Tatar, Gonca [1 ]
机构
[1] Abant Izzet Baysal Univ, Izzet Baysal Fac Med, Dept Internal Med, Div Gastroenterol, Bolu, Turkey
[2] Hacettepe Univ, Dept Histol & Embryol, Ankara, Turkey
[3] Baskent Univ, Div Gastroenterol, Dept Internal Med, TR-06490 Ankara, Turkey
[4] Hacettepe Univ, Dept Pathol, Ankara, Turkey
[5] Hacettepe Univ, Childrens Hosp, Clin Chem Lab, Ankara, Turkey
[6] Hacettepe Univ, Dept Microbiol & Clin Microbiol, Ankara, Turkey
[7] Hacettepe Univ, Dept Gen Surg, Ankara, Turkey
关键词
CD26; dipeptidyl peptidase IV; non-alcoholic steatohepatitis; metabolic syndrome;
D O I
10.1016/S1665-2681(19)31905-2
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective(s): Non-alcoholic steatohepatitis (NASH) is a chronic liver disease with unknown etiology. The insulin resistance, immune mechanisms and oxidative stress are the main factors in its pathogenesis. Dipeptidyl peptidase IV (DPPIV) or CD26 is a protein with endocrine and immune functions. This study aimed to elicudate the changes related to DPPIV in NASH patients. Methods: Serum and urinary DPPIV activities were measured in 31 NASH patients and 17 healthy controls. The liver biopsies of 29 patients were immunolabeled for CD26. Results: The mean age of patients were 46 +/- 11 years and 14 (45%) of them were female. The serum DPPIV activity was higher in patients (57.3 +/- 7.8 U/L) than controls (43.6 +/- 10.6 U/L) (p < 0.0001), and correlated with the histopathological grade (p = 0.038, r = 0.373) and hepatosteatosis (p = 0.018, r = 0.423) but not with stage (p = 0.286), class (p = 0.286) or CD26 staining (p = 0.743). The urinary DPPIV activity was similar in patients (1.52 +/- 0.94 U/mmol creatinine) and controls (1.37 +/- 0.68 U/mmol creatinine) (p = 0.861). Three acinar zones of liver had equal CD26 expression (p = 0.076). The intensity of CD26 immunostaining was correlated with histopathological grade (p = 0.001) and hepatosteatosis (p = 0.003) but no correlation with stage or class could be detected (p = 0.610 and 0.956, respectively). In Conclusions: The serum DPPIV activity and the staining intensity of CD26 in liver are correlated with histopathologic grade of NASH and hepatosteatosis. DPPIV can be proposed as a novel candidate with several potential functions in NASH pathogenesis.
引用
收藏
页码:242 / 250
页数:9
相关论文
共 35 条
[11]   Serum dipeptidyl peptidase IV (DPP IV, CD26) activity in chronic hepatitis C [J].
Firneisz, G ;
Lakatos, PL ;
Szalay, F .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2001, 36 (08) :877-880
[12]   Antidiabetic thiazolidinediones inhibit collagen synthesis and hepatic stellate cell activation in vivo and in vitro [J].
Galli, A ;
Crabb, DW ;
Ceni, E ;
Salzano, R ;
Mello, T ;
Svegliati-Baroni, G ;
Ridolfi, F ;
Trozzi, L ;
Surrenti, C ;
Casini, A .
GASTROENTEROLOGY, 2002, 122 (07) :1924-1940
[13]   Regulation of epithelial and lymphocyte cell adhesion by adenosine deaminase-CD26 interaction [J].
Ginés, S ;
Mariño, M ;
Mallol, J ;
Canela, EI ;
Morimoto, C ;
Callebaut, C ;
Hovanessian, A ;
Casadó, V ;
Lluis, C ;
Franco, R .
BIOCHEMICAL JOURNAL, 2002, 361 :203-209
[14]   Incretin mimetics and dipeptidyl peptidase-IV inhibitors: A review of emerging therapies for type 2 diabetes [J].
Kendall, David M. ;
Kim, Dennis ;
Maggs, David .
DIABETES TECHNOLOGY & THERAPEUTICS, 2006, 8 (03) :385-396
[15]   IMMUNOMODULATING EFFECT OF URSODEOXYCHOLIC ACID THERAPY IN PATIENTS WITH PRIMARY BILIARY-CIRRHOSIS [J].
KURKTSCHIEV, D ;
SUBAT, S ;
ADLER, D ;
SCHENTKE, KU .
JOURNAL OF HEPATOLOGY, 1993, 18 (03) :373-377
[16]   Dipeptidyl-Peptidase IV from Bench to Bedside: An Update on Structural Properties, Functions, and Clinical Aspects of the Enzyme DPP IV [J].
Lambeir, AM ;
Durinx, C ;
Scharpé, S ;
De Meester, I .
CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 2003, 40 (03) :209-+
[17]   Lower activity of serum peptidases in abstinent alcohol-dependent patients [J].
Maes, M ;
Lin, AH ;
Bonaccorso, S ;
Vandoolaeghe, E ;
Song, C ;
Goossens, F ;
De Meester, I ;
DeGroote, J ;
Neels, H ;
Scharpé, S ;
Janca, A .
ALCOHOL, 1999, 17 (01) :1-6
[18]   Nonalcoholic fatty liver disease - A feature of the metabolic syndrome [J].
Marchesini, G ;
Brizi, M ;
Bianchi, G ;
Tomassetti, S ;
Bugianesi, E ;
Lenzi, M ;
McCullough, AJ ;
Natale, S ;
Forlani, G ;
Melchionda, N .
DIABETES, 2001, 50 (08) :1844-1850
[19]   ALTERED ZONAL EXPRESSION OF THE CD26 ANTIGEN (DIPEPTIDYL PEPTIDASE-IV) IN HUMAN CIRRHOTIC LIVER [J].
MATSUMOTO, Y ;
BISHOP, GA ;
MCCAUGHAN, GW .
HEPATOLOGY, 1992, 15 (06) :1048-1053
[20]   Molecular pathogenesis of liver disease: an approach to hepatic inflammation, cirrhosis and liver transplant tolerance [J].
McCaughan, GW ;
Gorrell, MD ;
Bishop, GA ;
Abbott, CA ;
Shackel, NA ;
McGuinness, PH ;
Levy, MT ;
Sharland, AF ;
Bowen, DG ;
Yu, D ;
Slaitini, L ;
Church, WB ;
Napoli, J .
IMMUNOLOGICAL REVIEWS, 2000, 174 :172-191