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Pharmacodynamics of Metformin in Pregnant Women With Gestational Diabetes Mellitus and Nonpregnant Women With Type 2 Diabetes Mellitus.
Shuster, Diana L; Shireman, Laura M; Ma, Xiaosu; Shen, Danny D; Flood Nichols, Shannon K; Ahmed, Mahmoud S; Clark, Shannon; Caritis, Steve; Venkataramanan, Raman; Haas, David M; Quinney, Sara K; Haneline, Laura S; Tita, Alan T; Manuck, Tracy A; Thummel, Kenneth E; Morris Brown, Linda; Ren, Zhaoxia; Brown, Zane; Easterling, Thomas R; Hebert, Mary F.
Affiliation
  • Shuster DL; PRA Health Sciences, Clinical Pharmacology-Scientific Affairs, Lenexa, Kansas, USA.
  • Shireman LM; University of Washington, Departments of Pharmaceutics, Obstetrics & Gynecology, and Pharmacy, Seattle, Washington, USA.
  • Ma X; Global PK/PD & Pharmacometrics, Eli Lilly and Company, Indianapolis, Indiana, USA.
  • Shen DD; University of Washington, Departments of Pharmaceutics, Obstetrics & Gynecology, and Pharmacy, Seattle, Washington, USA.
  • Flood Nichols SK; Madigan Army Medical Center, Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Tacoma, Washington, USA.
  • Ahmed MS; University of Texas Medical Branch in Galveston, Department of Obstetrics & Gynecology, Galveston, Texas, USA.
  • Clark S; University of Texas Medical Branch in Galveston, Department of Obstetrics & Gynecology, Galveston, Texas, USA.
  • Caritis S; University of Pittsburgh, Department of Obstetrics & Gynecology, Pittsburgh, Pennsylvania, USA.
  • Venkataramanan R; University of Pittsburgh, Departments of Pharmacy, Pharmaceutical Sciences and Pathology, Pittsburgh, Pennsylvania, USA.
  • Haas DM; Indiana University, Departments of Obstetrics & Gynecology and Pediatrics, Indianapolis, Indiana, USA.
  • Quinney SK; Indiana University, Departments of Obstetrics & Gynecology and Pediatrics, Indianapolis, Indiana, USA.
  • Haneline LS; Indiana University, Departments of Obstetrics & Gynecology and Pediatrics, Indianapolis, Indiana, USA.
  • Tita AT; University of Alabama at Birmingham, Department of Obstetrics & Gynecology, Birmingham, Alabama, USA.
  • Manuck TA; University of North Carolina, Department of Obstetrics & Gynecology, Chapel Hill, North Carolina, USA.
  • Thummel KE; University of Washington, Departments of Pharmaceutics, Obstetrics & Gynecology, and Pharmacy, Seattle, Washington, USA.
  • Morris Brown L; RTI International, Environmental and Health Science Unit, Biostatistics and Epidemiology Division, Rockville, Maryland, USA.
  • Ren Z; Obstetric and Pediatric Pharmacology and Therapeutic Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland, USA.
  • Brown Z; University of Washington, Departments of Pharmaceutics, Obstetrics & Gynecology, and Pharmacy, Seattle, Washington, USA.
  • Easterling TR; University of Washington, Departments of Pharmaceutics, Obstetrics & Gynecology, and Pharmacy, Seattle, Washington, USA.
  • Hebert MF; University of Washington, Departments of Pharmaceutics, Obstetrics & Gynecology, and Pharmacy, Seattle, Washington, USA.
J Clin Pharmacol ; 60(4): 540-549, 2020 04.
Article in En | MEDLINE | ID: mdl-31742716
Gestational diabetes mellitus is a condition similar to type 2 diabetes mellitus (T2DM) in that patients are unable to compensate for the degree of insulin resistance, and both conditions are often treated with metformin. The comparative pharmacodynamic response to metformin in these 2 populations has not been studied. This study characterized insulin sensitivity, ß-cell responsivity, and disposition index following a mixed-meal tolerance test utilizing a minimal model of glucose, insulin, and C-peptide kinetics before and during treatment with metformin. The study included women with gestational diabetes mellitus (n = 34), T2DM (n = 14), and healthy pregnant women (n = 30). Before treatment, the gestational diabetes mellitus group had significantly higher baseline (45%), dynamic (68%), static (71%), and total ß-cell responsivity (71%) than the T2DM group. Metformin significantly increased insulin sensitivity (51%) as well as disposition index (97%) and decreased mixed-meal tolerance test peak glucose concentrations (8%) in women with gestational diabetes mellitus after adjustment for gestational age-dependent effects; however, in women with T2DM metformin only significantly affected peak glucose concentrations (22%) and had no significant effect on any other parameters. Metformin had a greater effect on the change in disposition index (Δ disposition index) in women with gestational diabetes mellitus than in those with T2DM (P = .01). In conclusion, response to metformin in women with gestational diabetes mellitus is significantly different from that in women with T2DM, which is likely related to the differences in disease severity.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetes, Gestational / Diabetes Mellitus, Type 2 / Hypoglycemic Agents / Metformin Type of study: Clinical_trials / Observational_studies Limits: Adolescent / Adult / Female / Humans / Middle aged / Pregnancy Language: En Journal: J Clin Pharmacol Year: 2020 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetes, Gestational / Diabetes Mellitus, Type 2 / Hypoglycemic Agents / Metformin Type of study: Clinical_trials / Observational_studies Limits: Adolescent / Adult / Female / Humans / Middle aged / Pregnancy Language: En Journal: J Clin Pharmacol Year: 2020 Document type: Article Affiliation country: United States Country of publication: United kingdom