Serum thrombospondin‐2 level changes with liver stiffness improvement in patients with type 2 diabetes
Objective Baseline circulating thrombospondin‐2 (TSP2) level was identified as a potential novel hepatic fibrosis biomarker that associates with development and progression of hepatic fibrosis in patients with nonalcoholic fatty liver disease and type 2 diabetes. Here, we investigated whether circul...
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Published in: | Clinical endocrinology (Oxford) Vol. 100; no. 3; pp. 230 - 237 |
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Abstract | Objective
Baseline circulating thrombospondin‐2 (TSP2) level was identified as a potential novel hepatic fibrosis biomarker that associates with development and progression of hepatic fibrosis in patients with nonalcoholic fatty liver disease and type 2 diabetes. Here, we investigated whether circulating TSP2 levels changed with improvement in liver stiffness (LS), which reflects liver fibrosis on transient elastography.
Design
Serum TSP2 levels were measured in participants from a randomized, open‐label intervention study, at baseline and after 24‐weeks treatment of either dapagliflozin 10 mg (N = 30) or sitagliptin 100 mg daily (N = 30). Vibration‐controlled transient elastography was performed to evaluate the severity of hepatic fibrosis and steatosis using LS and controlled attenuation parameter (CAP), respectively.
Patients and Measurements
Among all 60 participants with similar clinical characteristics at baseline (mean HbA1c 8.9%, CAP 289 dB/m and LS 5.8 kPa), despite similar HbA1c lowering, treatment with dapagliflozin, but not sitagliptin, led to significant improvements in body weight (BW) (p = .012), CAP (p = .015) and LS (p = .011) after 24 weeks.
Results
Serum TSP2 level decreased significantly from baseline in dapagliflozin‐treated participants (p = .035), whereas no significant change was observed with sitagliptin. In correlation analysis, change in serum TSP2 levels only positively correlated with change in LS (r = .487, p = .006), but not with changes in BW, CAP or HbA1c after dapagliflozin treatment.
Conclusions
Serum TSP2 level decreased with LS after dapagliflozin treatment, and was independent of improvements in BW, glycemic control and hepatic steatosis, further supporting the potential of serum TSP2 level as a novel hepatic fibrosis biomarker in type 2 diabetes. |
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AbstractList | OBJECTIVEBaseline circulating thrombospondin-2 (TSP2) level was identified as a potential novel hepatic fibrosis biomarker that associates with development and progression of hepatic fibrosis in patients with nonalcoholic fatty liver disease and type 2 diabetes. Here, we investigated whether circulating TSP2 levels changed with improvement in liver stiffness (LS), which reflects liver fibrosis on transient elastography.DESIGNSerum TSP2 levels were measured in participants from a randomized, open-label intervention study, at baseline and after 24-weeks treatment of either dapagliflozin 10 mg (N = 30) or sitagliptin 100 mg daily (N = 30). Vibration-controlled transient elastography was performed to evaluate the severity of hepatic fibrosis and steatosis using LS and controlled attenuation parameter (CAP), respectively.PATIENTS AND MEASUREMENTSAmong all 60 participants with similar clinical characteristics at baseline (mean HbA1c 8.9%, CAP 289 dB/m and LS 5.8 kPa), despite similar HbA1c lowering, treatment with dapagliflozin, but not sitagliptin, led to significant improvements in body weight (BW) (p = .012), CAP (p = .015) and LS (p = .011) after 24 weeks.RESULTSSerum TSP2 level decreased significantly from baseline in dapagliflozin-treated participants (p = .035), whereas no significant change was observed with sitagliptin. In correlation analysis, change in serum TSP2 levels only positively correlated with change in LS (r = .487, p = .006), but not with changes in BW, CAP or HbA1c after dapagliflozin treatment.CONCLUSIONSSerum TSP2 level decreased with LS after dapagliflozin treatment, and was independent of improvements in BW, glycemic control and hepatic steatosis, further supporting the potential of serum TSP2 level as a novel hepatic fibrosis biomarker in type 2 diabetes. Objective Baseline circulating thrombospondin‐2 (TSP2) level was identified as a potential novel hepatic fibrosis biomarker that associates with development and progression of hepatic fibrosis in patients with nonalcoholic fatty liver disease and type 2 diabetes. Here, we investigated whether circulating TSP2 levels changed with improvement in liver stiffness (LS), which reflects liver fibrosis on transient elastography. Design Serum TSP2 levels were measured in participants from a randomized, open‐label intervention study, at baseline and after 24‐weeks treatment of either dapagliflozin 10 mg (N = 30) or sitagliptin 100 mg daily (N = 30). Vibration‐controlled transient elastography was performed to evaluate the severity of hepatic fibrosis and steatosis using LS and controlled attenuation parameter (CAP), respectively. Patients and Measurements Among all 60 participants with similar clinical characteristics at baseline (mean HbA1c 8.9%, CAP 289 dB/m and LS 5.8 kPa), despite similar HbA1c lowering, treatment with dapagliflozin, but not sitagliptin, led to significant improvements in body weight (BW) (p = .012), CAP (p = .015) and LS (p = .011) after 24 weeks. Results Serum TSP2 level decreased significantly from baseline in dapagliflozin‐treated participants (p = .035), whereas no significant change was observed with sitagliptin. In correlation analysis, change in serum TSP2 levels only positively correlated with change in LS (r = .487, p = .006), but not with changes in BW, CAP or HbA1c after dapagliflozin treatment. Conclusions Serum TSP2 level decreased with LS after dapagliflozin treatment, and was independent of improvements in BW, glycemic control and hepatic steatosis, further supporting the potential of serum TSP2 level as a novel hepatic fibrosis biomarker in type 2 diabetes. Baseline circulating thrombospondin-2 (TSP2) level was identified as a potential novel hepatic fibrosis biomarker that associates with development and progression of hepatic fibrosis in patients with nonalcoholic fatty liver disease and type 2 diabetes. Here, we investigated whether circulating TSP2 levels changed with improvement in liver stiffness (LS), which reflects liver fibrosis on transient elastography. Serum TSP2 levels were measured in participants from a randomized, open-label intervention study, at baseline and after 24-weeks treatment of either dapagliflozin 10 mg (N = 30) or sitagliptin 100 mg daily (N = 30). Vibration-controlled transient elastography was performed to evaluate the severity of hepatic fibrosis and steatosis using LS and controlled attenuation parameter (CAP), respectively. Among all 60 participants with similar clinical characteristics at baseline (mean HbA1c 8.9%, CAP 289 dB/m and LS 5.8 kPa), despite similar HbA1c lowering, treatment with dapagliflozin, but not sitagliptin, led to significant improvements in body weight (BW) (p = .012), CAP (p = .015) and LS (p = .011) after 24 weeks. Serum TSP2 level decreased significantly from baseline in dapagliflozin-treated participants (p = .035), whereas no significant change was observed with sitagliptin. In correlation analysis, change in serum TSP2 levels only positively correlated with change in LS (r = .487, p = .006), but not with changes in BW, CAP or HbA1c after dapagliflozin treatment. Serum TSP2 level decreased with LS after dapagliflozin treatment, and was independent of improvements in BW, glycemic control and hepatic steatosis, further supporting the potential of serum TSP2 level as a novel hepatic fibrosis biomarker in type 2 diabetes. |
Author | Fong, Carol Ho‐Yi Lam, Karen Siu‐Ling Mak, Jimmy Ho Cheung Hoo, Ruby Lai‐Chong Tan, Kathryn Choon‐Beng Wong, Ying Lui, David Tak‐Wai Xu, Aimin Lee, Alan Chun‐Hong Lee, Chi‐Ho Cheung, Chloe Yu‐Yan |
Author_xml | – sequence: 1 givenname: Jimmy Ho Cheung orcidid: 0000-0002-3241-3809 surname: Mak fullname: Mak, Jimmy Ho Cheung organization: The University of Hong Kong – sequence: 2 givenname: David Tak‐Wai surname: Lui fullname: Lui, David Tak‐Wai organization: The University of Hong Kong – sequence: 3 givenname: Carol Ho‐Yi surname: Fong fullname: Fong, Carol Ho‐Yi organization: The University of Hong Kong – sequence: 4 givenname: Chloe Yu‐Yan surname: Cheung fullname: Cheung, Chloe Yu‐Yan organization: The University of Hong Kong – sequence: 5 givenname: Ying surname: Wong fullname: Wong, Ying organization: The University of Hong Kong – sequence: 6 givenname: Alan Chun‐Hong surname: Lee fullname: Lee, Alan Chun‐Hong organization: The University of Hong Kong – sequence: 7 givenname: Ruby Lai‐Chong surname: Hoo fullname: Hoo, Ruby Lai‐Chong organization: The University of Hong Kong – sequence: 8 givenname: Aimin surname: Xu fullname: Xu, Aimin organization: The University of Hong Kong – sequence: 9 givenname: Kathryn Choon‐Beng orcidid: 0000-0001-9037-0416 surname: Tan fullname: Tan, Kathryn Choon‐Beng organization: The University of Hong Kong – sequence: 10 givenname: Karen Siu‐Ling orcidid: 0000-0001-5757-541X surname: Lam fullname: Lam, Karen Siu‐Ling organization: The University of Hong Kong – sequence: 11 givenname: Chi‐Ho surname: Lee fullname: Lee, Chi‐Ho email: pchlee@hku.hk organization: The University of Hong Kong |
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Cites_doi | 10.1159/000198235 10.2337/db06-1163 10.1038/s41598-018-19658-7 10.2337/dc19-1071 10.1053/j.gastro.2021.07.049 10.1002/hep.21496 10.3389/fendo.2020.609135 10.1007/s13300-021-01011-3 10.1002/hep.27368 10.1111/hepr.13645 10.1002/hep.31995 10.1002/hep.21178 10.1016/j.bbagen.2014.01.013 10.1158/0008-5472.CAN-05-1560 10.1038/s41598-022-23357-9 10.1152/ajpgi.00358.2018 10.1186/s12933-022-01646-x 10.1053/j.gastro.2015.04.043 10.2337/db18-1001 10.4093/dmj.2021.0319 10.1007/s12072-020-10094-2 10.2337/dc21-0131 10.1210/clinem/dgac292 10.1016/j.cgh.2018.04.043 10.1002/hep.23312 10.1186/s13098-016-0169-x 10.1152/ajprenal.00254.2009 10.1007/s10456-018-9644-3 10.2337/dc23-S004 10.1002/hep.26661 10.1152/ajpendo.00086.2017 10.1101/cshperspect.a006627 10.1007/s00535-016-1200-6 10.3390/jcm9020472 10.1111/dom.13520 10.1016/j.jhep.2016.12.022 10.1038/ajg.2012.331 10.1152/ajpgi.00339.2018 |
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References | 2021; 44 2015; 149 2017; 66 2009; 297 2019; 17 2022; 46 2009; 111 2005; 65 2021; 161 2020; 14 2016; 51 2022; 21 2021; 74 2014; 1840 2021; 51 2007; 56 2012; 107 2017; 313 2018; 8 2012; 2 2023; 46 2021; 12 2021; 11 2023 2006; 43 2019; 22 2015; 61 2019; 21 2019; 68 2020; 9 2022; 12 2014; 59 2020; 43 2019; 316 2022; 107 2007; 45 2016; 8 2010; 51 e_1_2_8_28_1 e_1_2_8_29_1 e_1_2_8_24_1 e_1_2_8_25_1 e_1_2_8_26_1 e_1_2_8_27_1 e_1_2_8_3_1 e_1_2_8_2_1 e_1_2_8_5_1 e_1_2_8_4_1 e_1_2_8_7_1 e_1_2_8_6_1 e_1_2_8_9_1 e_1_2_8_8_1 e_1_2_8_20_1 e_1_2_8_21_1 e_1_2_8_22_1 e_1_2_8_23_1 e_1_2_8_40_1 e_1_2_8_17_1 e_1_2_8_18_1 e_1_2_8_19_1 e_1_2_8_13_1 e_1_2_8_36_1 e_1_2_8_14_1 e_1_2_8_35_1 e_1_2_8_15_1 e_1_2_8_38_1 Lee CH (e_1_2_8_39_1) 2023 e_1_2_8_16_1 e_1_2_8_37_1 e_1_2_8_32_1 e_1_2_8_10_1 e_1_2_8_31_1 e_1_2_8_11_1 e_1_2_8_34_1 e_1_2_8_12_1 e_1_2_8_33_1 e_1_2_8_30_1 |
References_xml | – volume: 12 issue: 1 year: 2022 article-title: Circulating thrombospondin 2 levels reflect fibrosis severity and disease activity in HCV‐infected patients publication-title: Sci Rep – volume: 43 start-page: 1317 issue: 6 year: 2006 end-page: 1325 article-title: Development of a simple noninvasive index to predict significant fibrosis in patients with HIV/HCV coinfection publication-title: Hepatology – volume: 9 issue: 2 year: 2020 article-title: Matrix metalloproteinases in diabetic kidney disease publication-title: J Clin Med – volume: 66 start-page: 1022 issue: 5 year: 2017 end-page: 1030 article-title: Individual patient data meta‐analysis of controlled attenuation parameter (CAP) technology for assessing steatosis publication-title: J Hepatol – start-page: 1 year: 2023 end-page: 9 article-title: Circulating thrombospondin‐2 level for identifying individuals with rapidly declining kidney function trajectory in type 2 diabetes: a prospective study of the Hong Kong west diabetes registry publication-title: Nephrol Dial Transplant – volume: 44 start-page: 2089 issue: 9 year: 2021 end-page: 2097 article-title: Circulating thrombospondin‐2 as a novel fibrosis biomarker of nonalcoholic fatty liver disease in type 2 diabetes publication-title: Diabetes Care – volume: 43 start-page: 290 issue: 2 year: 2020 end-page: 297 article-title: Performance of plasma biomarkers and diagnostic panels for nonalcoholic steatohepatitis and advanced fibrosis in patients with type 2 diabetes publication-title: Diabetes Care – volume: 45 start-page: 846 issue: 4 year: 2007 end-page: 854 article-title: The NAFLD fibrosis score: a noninvasive system that identifies liver fibrosis in patients with NAFLD publication-title: Hepatology – volume: 316 start-page: G462 issue: 4 year: 2019 end-page: G472 article-title: Hepatic transcriptome signatures in patients with varying degrees of nonalcoholic fatty liver disease compared with healthy normal‐weight individuals publication-title: Am J Physiol‐Gastrointestinal Liver Physiol – volume: 161 start-page: 1657 issue: 5 year: 2021 end-page: 1669 article-title: Clinical care pathway for the risk stratification and management of patients with nonalcoholic fatty liver disease publication-title: Gastroenterology – volume: 111 start-page: e61 issue: 3 year: 2009 end-page: e66 article-title: Thrombospondin in renal disease publication-title: Nephron Exp Nephrol – volume: 107 start-page: e3230 issue: 8 year: 2022 end-page: e3240 article-title: Serum thrombospondin‐2 levels are closely associated with the severity of metabolic syndrome and metabolic associated fatty liver disease publication-title: J Clin Endocrinol Metabol – volume: 11 year: 2021 article-title: Sodium‐glucose co‐transporter 2 inhibitors for non‐alcoholic fatty liver disease in asian patients with type 2 diabetes: a meta‐analysis publication-title: Front Endocrinol – volume: 46 start-page: 843 issue: 6 year: 2022 end-page: 854 article-title: Comparison of serum ketone levels and cardiometabolic efficacy of dapagliflozin versus sitagliptin among insulin‐treated Chinese patients with type 2 diabetes mellitus publication-title: Diabetes Metab J – volume: 1840 start-page: 2396 issue: 8 year: 2014 end-page: 2402 article-title: Thrombospondin‐2 and extracellular matrix assembly publication-title: Biochim Biophys Acta General Sub – volume: 61 start-page: 1547 issue: 5 year: 2015 end-page: 1554 article-title: Fibrosis stage is the strongest predictor for disease‐specific mortality in NAFLD after up to 33 years of follow‐up publication-title: Hepatology – volume: 12 start-page: 843 issue: 3 year: 2021 end-page: 861 article-title: Empagliflozin improves liver steatosis and fibrosis in patients with Non‐Alcoholic fatty liver disease and type 2 diabetes: a randomized, double‐blind, placebo‐controlled clinical trial publication-title: Diabetes Ther – volume: 14 start-page: 889 issue: 6 year: 2020 end-page: 919 article-title: The Asian Pacific Association for the study of the liver clinical practice guidelines for the diagnosis and management of metabolic associated fatty liver disease publication-title: Hepatol Int – volume: 8 start-page: 2362 issue: 1 year: 2018 article-title: Canagliflozin, an SGLT2 inhibitor, attenuates the development of hepatocellular carcinoma in a mouse model of human NASH publication-title: Sci Rep – volume: 56 start-page: 641 issue: 3 year: 2007 end-page: 646 article-title: Contributions of inflammation and cardiac matrix metalloproteinase activity to cardiac failure in diabetic cardiomyopathy publication-title: Diabetes – volume: 68 start-page: 2016 issue: 10 year: 2019 end-page: 2023 article-title: Elevated thrombospondin 2 contributes to delayed wound healing in diabetes publication-title: Diabetes – volume: 21 start-page: 231 issue: 1 year: 2022 article-title: Prospective associations of circulating thrombospondin‐2 level with heart failure hospitalization, left ventricular remodeling and diastolic function in type 2 diabetes publication-title: Cardiovasc Diabetol – volume: 51 start-page: 454 issue: 2 year: 2010 end-page: 462 article-title: Diagnosis of fibrosis and cirrhosis using liver stiffness measurement in nonalcoholic fatty liver disease publication-title: Hepatology – volume: 46 start-page: s49 issue: supplment_1 year: 2023 end-page: s67.2 article-title: 4. Comprehensive medical evaluation and assessment of comorbidities: standards of care in diabetes—2023 publication-title: Diabetes Care – volume: 8 start-page: 45 issue: 1 year: 2016 article-title: Empagliflozin (an SGLT2 inhibitor), alone or in combination with linagliptin (a DPP‐4 inhibitor), prevents steatohepatitis in a novel mouse model of non‐alcoholic steatohepatitis and diabetes publication-title: Diabetol Metab Syndr – volume: 59 start-page: 471 issue: 2 year: 2014 end-page: 482 article-title: Hepatic gene expression profiles differentiate presymptomatic patients with mild versus severe nonalcoholic fatty liver disease publication-title: Hepatology – volume: 74 start-page: 2452 issue: 5 year: 2021 end-page: 2466 article-title: Transcriptomics identify thrombospondin‐2 as a biomarker for NASH and advanced liver fibrosis publication-title: Hepatology – volume: 297 start-page: F1299 issue: 5 year: 2009 end-page: F1309 article-title: Thrombospondin‐2 therapy ameliorates experimental glomerulonephritis via inhibition of cell proliferation, inflammation, and TGF‐β activation publication-title: Am J Physiol‐Renal Physiol – volume: 107 start-page: 1862 issue: 12 year: 2012 end-page: 1871 article-title: Liver stiffness measurement using XL probe in patients with nonalcoholic fatty liver disease publication-title: Am J Gastroenterol – volume: 313 start-page: E563 issue: 5 year: 2017 end-page: E576 article-title: Dapagliflozin slows the progression of the renal and liver fibrosis associated with type 2 diabetes publication-title: Am J Physiol‐Endocrinol Metabol – volume: 2 issue: 5 year: 2012 article-title: Molecular basis for the regulation of angiogenesis by thrombospondin‐1 and ‐2 publication-title: Cold Spring Harbor Perspect Med – volume: 51 start-page: 641 issue: 6 year: 2021 end-page: 651 article-title: Meta‐analysis of the effect of sodium–glucose cotransporter 2 inhibitors on hepatic fibrosis in patients with type 2 diabetes mellitus complicated with non‐alcoholic fatty liver disease publication-title: Hepatol Res – volume: 316 start-page: G744 issue: 6 year: 2019 end-page: G754 article-title: Multitranscriptome analyses reveal prioritized genes specifically associated with liver fibrosis progression independent of etiology publication-title: Am J Physiol‐Gastrointestinal Liver Physiol – volume: 149 start-page: 389 issue: 2 year: 2015 end-page: 397 article-title: Liver fibrosis, but no other histologic features, is associated with long‐term outcomes of patients with nonalcoholic fatty liver disease publication-title: Gastroenterology – volume: 21 start-page: 285 issue: 2 year: 2019 end-page: 292 article-title: Evaluation of the effects of dapagliflozin, a sodium‐glucose co‐transporter‐2 inhibitor, on hepatic steatosis and fibrosis using transient elastography in patients with type 2 diabetes and non‐alcoholic fatty liver disease publication-title: Diabetes, Obes Metab – volume: 51 start-page: 1141 issue: 12 year: 2016 end-page: 1149 article-title: Ipragliflozin, a sodium–glucose cotransporter 2 inhibitor, ameliorates the development of liver fibrosis in diabetic Otsuka long–evans Tokushima fatty rats publication-title: J Gastroenterol – volume: 22 start-page: 133 issue: 1 year: 2019 end-page: 144 article-title: The calcium‐binding type III repeats domain of thrombospondin‐2 binds to fibroblast growth factor 2 (FGF2) publication-title: Angiogenesis – volume: 17 start-page: 156 issue: 1 year: 2019 end-page: 163 article-title: Vibration‐controlled transient elastography to assess fibrosis and steatosis in patients with nonalcoholic fatty liver disease publication-title: Clin Gastroenterol Hepatol – volume: 65 start-page: 9338 issue: 20 year: 2005 end-page: 9346 article-title: Low‐density lipoprotein receptor–related protein contributes to the antiangiogenic activity of thrombospondin‐2 in a murine glioma model publication-title: Cancer Res – ident: e_1_2_8_36_1 doi: 10.1159/000198235 – ident: e_1_2_8_38_1 doi: 10.2337/db06-1163 – ident: e_1_2_8_33_1 doi: 10.1038/s41598-018-19658-7 – ident: e_1_2_8_5_1 doi: 10.2337/dc19-1071 – ident: e_1_2_8_24_1 doi: 10.1053/j.gastro.2021.07.049 – ident: e_1_2_8_14_1 doi: 10.1002/hep.21496 – ident: e_1_2_8_28_1 doi: 10.3389/fendo.2020.609135 – ident: e_1_2_8_31_1 doi: 10.1007/s13300-021-01011-3 – ident: e_1_2_8_3_1 doi: 10.1002/hep.27368 – ident: e_1_2_8_29_1 doi: 10.1111/hepr.13645 – ident: e_1_2_8_10_1 doi: 10.1002/hep.31995 – ident: e_1_2_8_13_1 doi: 10.1002/hep.21178 – ident: e_1_2_8_7_1 doi: 10.1016/j.bbagen.2014.01.013 – ident: e_1_2_8_19_1 doi: 10.1158/0008-5472.CAN-05-1560 – ident: e_1_2_8_11_1 doi: 10.1038/s41598-022-23357-9 – ident: e_1_2_8_22_1 doi: 10.1152/ajpgi.00358.2018 – ident: e_1_2_8_40_1 doi: 10.1186/s12933-022-01646-x – ident: e_1_2_8_4_1 doi: 10.1053/j.gastro.2015.04.043 – ident: e_1_2_8_8_1 doi: 10.2337/db18-1001 – ident: e_1_2_8_12_1 doi: 10.4093/dmj.2021.0319 – ident: e_1_2_8_25_1 doi: 10.1007/s12072-020-10094-2 – ident: e_1_2_8_2_1 doi: 10.2337/dc21-0131 – ident: e_1_2_8_9_1 doi: 10.1210/clinem/dgac292 – ident: e_1_2_8_27_1 doi: 10.1016/j.cgh.2018.04.043 – ident: e_1_2_8_16_1 doi: 10.1002/hep.23312 – ident: e_1_2_8_34_1 doi: 10.1186/s13098-016-0169-x – ident: e_1_2_8_20_1 doi: 10.1152/ajprenal.00254.2009 – ident: e_1_2_8_18_1 doi: 10.1007/s10456-018-9644-3 – ident: e_1_2_8_26_1 doi: 10.2337/dc23-S004 – ident: e_1_2_8_21_1 doi: 10.1002/hep.26661 – ident: e_1_2_8_32_1 doi: 10.1152/ajpendo.00086.2017 – ident: e_1_2_8_6_1 doi: 10.1101/cshperspect.a006627 – ident: e_1_2_8_35_1 doi: 10.1007/s00535-016-1200-6 – start-page: 1 year: 2023 ident: e_1_2_8_39_1 article-title: Circulating thrombospondin‐2 level for identifying individuals with rapidly declining kidney function trajectory in type 2 diabetes: a prospective study of the Hong Kong west diabetes registry publication-title: Nephrol Dial Transplant contributor: fullname: Lee CH – ident: e_1_2_8_37_1 doi: 10.3390/jcm9020472 – ident: e_1_2_8_30_1 doi: 10.1111/dom.13520 – ident: e_1_2_8_15_1 doi: 10.1016/j.jhep.2016.12.022 – ident: e_1_2_8_17_1 doi: 10.1038/ajg.2012.331 – ident: e_1_2_8_23_1 doi: 10.1152/ajpgi.00339.2018 |
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Baseline circulating thrombospondin‐2 (TSP2) level was identified as a potential novel hepatic fibrosis biomarker that associates with development... Baseline circulating thrombospondin-2 (TSP2) level was identified as a potential novel hepatic fibrosis biomarker that associates with development and... ObjectiveBaseline circulating thrombospondin‐2 (TSP2) level was identified as a potential novel hepatic fibrosis biomarker that associates with development and... OBJECTIVEBaseline circulating thrombospondin-2 (TSP2) level was identified as a potential novel hepatic fibrosis biomarker that associates with development and... |
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SubjectTerms | Benzhydryl Compounds Biomarkers Body weight Correlation analysis Diabetes Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - drug therapy Diabetes Mellitus, Type 2 - pathology DPP4 inhibitor Elasticity Imaging Techniques Fatty liver Fibrosis FIB‐4 Glucosides Glycated Hemoglobin Humans Liver - diagnostic imaging Liver cirrhosis Liver Cirrhosis - drug therapy Liver diseases NFS Non-alcoholic Fatty Liver Disease Patients SGLT2 inhibitor Sitagliptin Phosphate - therapeutic use Steatosis Thrombospondin Thrombospondins - therapeutic use |
Title | Serum thrombospondin‐2 level changes with liver stiffness improvement in patients with type 2 diabetes |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fcen.15010 https://www.ncbi.nlm.nih.gov/pubmed/38127469 https://www.proquest.com/docview/2921992178 https://search.proquest.com/docview/2905521570 |
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