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Stratified glucose-lowering response to vildagliptin and pioglitazone by obesity and hypertriglyceridemia in a randomized crossover trial.
Brandon, Rebecca; Jiang, Yannan; Yeu, Rui Qian; Tweedie-Cullen, Ry; Smallman, Kate; Doherty, Glenn; Macaskill-Smith, Kerry A; Doran, Rebekah J; Clark, Penny; Moffitt, Allan; Merry, Troy; Nehren, Norma; King, Frances; Hindmarsh, Jennie Harré; Leask, Megan Patricia; Merriman, Tony R; Orr-Walker, Brandon; Shepherd, Peter R; Paul, Ryan; Murphy, Rinki.
Afiliação
  • Brandon R; Department of Medicine, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.
  • Jiang Y; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.
  • Yeu RQ; Department of Statistics, Faculty of Sciences, The University of Auckland, Auckland, New Zealand.
  • Tweedie-Cullen R; National Institute for Health Innovation, School of Population Health, The University of Auckland, Auckland, New Zealand.
  • Smallman K; Department of Medicine, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.
  • Doherty G; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.
  • Macaskill-Smith KA; Department of Medicine, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.
  • Doran RJ; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.
  • Clark P; Diabetes Foundation Aotearoa, Auckland, New Zealand.
  • Moffitt A; Tongan Health Society, Auckland, New Zealand.
  • Merry T; Ventures/Pinnacle Incorporated, Hamilton, New Zealand.
  • Nehren N; Ventures/Pinnacle Incorporated, Hamilton, New Zealand.
  • King F; Ventures/Pinnacle Incorporated, Hamilton, New Zealand.
  • Hindmarsh JH; Procare Primary Health Organisation, Auckland, New Zealand.
  • Leask MP; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.
  • Merriman TR; Discipline of Nutrition, University of Auckland, Auckland, New Zealand.
  • Orr-Walker B; Te Hiku Hauora, Northland District Health Board, Kaitaia, New Zealand.
  • Shepherd PR; Ngati Porou Hauora, Tairawhiti, New Zealand.
  • Paul R; Ngati Porou Hauora, Tairawhiti, New Zealand.
  • Murphy R; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.
Front Endocrinol (Lausanne) ; 13: 1091421, 2022.
Article em En | MEDLINE | ID: mdl-36699039
ABSTRACT

Background:

Understanding which group of patients with type 2 diabetes will have the most glucose lowering response to certain medications (which target different aspects of glucose metabolism) is the first step in precision medicine.

Aims:

We hypothesized that people with type 2 diabetes who generally have high insulin resistance, such as people of Maori/Pacific ethnicity, and those with obesity and/or hypertriglyceridemia (OHTG), would have greater glucose-lowering by pioglitazone (an insulin sensitizer) versus vildagliptin (an insulin secretagogue).

Methods:

A randomised, open-label, two-period crossover trial was conducted in New Zealand. Adults with type 2 diabetes, HbA1c>58mmol/mol (>7.5%), received 16 weeks of either pioglitazone (30mg) or vildagliptin (50mg) daily, then switched to the other medication over for another 16 weeks of treatment. Differences in HbA1c were tested for interaction with ethnicity or OHTG, controlling for baseline HbA1c using linear mixed models. Secondary outcomes included weight, blood pressure, side-effects and diabetes treatment satisfaction.

Results:

346 participants were randomised (55% Maori/Pacific) between February 2019 to March 2020. HbA1c after pioglitazone was lower than after vildagliptin (mean difference -4.9mmol/mol [0.5%]; 95% CI -6.3, -3.5; p<0.0001). Primary intention-to-treat analysis showed no significant interaction effect by Maori/Pacific vs other ethnicity (1.5mmol/mol [0.1%], 95% CI -0.8, 3.7), and per-protocol analysis (-1.2mmol/mol [0.1%], 95% CI -4.1, 1.7). An interaction effect (-4.7mmol/mol [0.5%], 95% CI -8.1, -1.4) was found by OHTG status. Both treatments generated similar treatment satisfaction scores, although there was greater weight gain and greater improvement in lipids and liver enzymes after pioglitazone than vildagliptin.

Conclusions:

Comparative glucose-lowering by pioglitazone and vildagliptin is not different between Maori/Pacific people compared with other New Zealand ethnic groups. Presence of OHTG predicts greater glucose lowering by pioglitazone than vildagliptin. Clinical trial registration www.anzctr.org.au, identifier (ACTRN12618001907235).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hipertrigliceridemia / Tiazolidinedionas / Diabetes Mellitus Tipo 2 / Inibidores da Dipeptidil Peptidase IV Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hipertrigliceridemia / Tiazolidinedionas / Diabetes Mellitus Tipo 2 / Inibidores da Dipeptidil Peptidase IV Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article