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Effect of insulin versus triple oral therapy on the progression of hepatic steatosis in type 2 diabetes.
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- Author(s): Lingvay I;Lingvay I; Roe ED; Duong J; Leonard D; Szczepaniak LS
- Source:
Journal of investigative medicine : the official publication of the American Federation for Clinical Research [J Investig Med] 2012 Oct; Vol. 60 (7), pp. 1059-63.- Publication Type:
Comparative Study; Journal Article; Randomized Controlled Trial; Research Support, N.I.H., Extramural- Language:
English - Source:
- Additional Information
- Source: Publisher: SAGE Publications Country of Publication: England NLM ID: 9501229 Publication Model: Print Cited Medium: Internet ISSN: 1708-8267 (Electronic) Linking ISSN: 10815589 NLM ISO Abbreviation: J Investig Med Subsets: MEDLINE
- Publication Information: Publication: 2023-: [Thousand Oaks] : SAGE Publications
Original Publication: Thorofare, NJ : Slack, c1994- - Subject Terms: Disease Progression*; Diabetes Mellitus, Type 2/*complications ; Diabetes Mellitus, Type 2/*drug therapy ; Fatty Liver/*complications ; Fatty Liver/*drug therapy ; Hypoglycemic Agents/*therapeutic use ; Insulin/*therapeutic use; Administration, Oral ; Adult ; Aged ; Female ; Follow-Up Studies ; Glyburide/pharmacology ; Glyburide/therapeutic use ; Humans ; Hypoglycemic Agents/pharmacology ; Insulin/administration & dosage ; Insulin/pharmacology ; Liver/drug effects ; Liver/metabolism ; Liver/pathology ; Male ; Metformin/pharmacology ; Metformin/therapeutic use ; Middle Aged ; Pioglitazone ; Thiazolidinediones/pharmacology ; Thiazolidinediones/therapeutic use ; Triglycerides/metabolism ; Young Adult
- Abstract: Background: Hyperinsulinemia has been associated with hepatic fat deposition and ensuing insulin resistance. It is unknown if treatment with exogenous insulin in patients with type 2 diabetes, who are most prone to hepatic fat accumulation, would promote the occurrence or worsening of nonalcoholic fatty liver disease.
Methods: Patients with treatment-naive type 2 diabetes (N = 16) were treated with insulin and metformin for a 3-month lead-in period, then assigned triple oral therapy (metformin, glyburide, and pioglitazone) or continued treatment with insulin and metformin. Hepatic triglyceride content (HTC)-measured by magnetic resonance spectroscopy, serum lipids, glucose, liver function tests, and inflammatory and thrombotic biomarkers were followed for a median of 31 months.
Results: The 45% decline in HTC during the lead-in period persisted through the follow-up period with no difference between treatment groups at the end of the study (5.26 ± 4.21% in the triple oral therapy vs 7.47 ± 7.40% for insulin/metformin), whereas glycemic control was comparable.
Conclusions: Improvements in HTC with initial insulin/metformin therapy persisted through the median 31-month follow-up period regardless of the treatment. More importantly, insulin-based treatment did not appear to promote or worsen nonalcoholic fatty liver disease. - References: J Clin Endocrinol Metab. 2009 Oct;94(10):4070-6. (PMID: 19773401)
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Mod Pathol. 1998 Jun;11(6):560-5. (PMID: 9647594) - Grant Information: K23RR024470 United States RR NCRR NIH HHS; UL1 RR024982 United States RR NCRR NIH HHS; K23 RR024470 United States RR NCRR NIH HHS; 3UL1 RR024982-05S1 United States RR NCRR NIH HHS; K08 HL083101 United States HL NHLBI NIH HHS
- Accession Number: 0 (Hypoglycemic Agents)
0 (Insulin)
0 (Thiazolidinediones)
0 (Triglycerides)
9100L32L2N (Metformin)
SX6K58TVWC (Glyburide)
X4OV71U42S (Pioglitazone) - Publication Date: Date Created: 20120718 Date Completed: 20130715 Latest Revision: 20211021
- Publication Date: 20231215
- Accession Number: PMC3448864
- Accession Number: 10.2310/JIM.0b013e3182621c5f
- Accession Number: 22801247
- Source:
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