Stratified glucose-lowering response to vildagliptin and pioglitazone by obesity and hypertriglyceridemia in a randomized crossover trial.

Troy Merry, Rinki Murphy, Ryan Paul, Peter R Shepherd, Brandon Orr-Walker, Tony R Merriman, Megan Patricia Leask, Jennie Harré Hindmarsh, Frances King, Norma Nehren, Rebecca Brandon, Allan Moffitt, Penny Clark, Rebekah J Doran, Kerry A Macaskill-Smith, Glenn Doherty, Kate Smallman, Ry Tweedie-Cullen, Rui Qian Yeu, Yannan Jiang

Journal: Frontiers in endocrinology 2023;13():1091421

PMID: 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 Māori/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% Māori/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 Māori/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 Māori/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).

Copyright © 2023 Brandon, Jiang, Yeu, Tweedie-Cullen, Smallman, Doherty, Macaskill-Smith, Doran, Clark, Moffitt, Merry, Nehren, King, Hindmarsh, Leask, Merriman, Orr-Walker, Shepherd, Paul and Murphy.

Address: Department of Medicine, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.; Department of Statistics, Faculty of Sciences, The University of Auckland, Auckland, New Zealand.; National Institute for Health Innovation, School of Population Health, The University of Auckland, Auckland, New Zealand.; Diabetes Foundation Aotearoa, Auckland, New Zealand.; Tongan Health Society, Auckland, New Zealand.; Ventures/Pinnacle Incorporated, Hamilton, New Zealand.; Procare Primary Health Organisation, Auckland, New Zealand.; Discipline of Nutrition, University of Auckland, Auckland, New Zealand.; Te Hiku Hauora, Northland District Health Board, Kaitaia, New Zealand.; Ngāti Porou Hauora, Tairāwhiti, New Zealand.; Department of Biochemistry, University of Otago, Dunedin, New Zealand.; Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, United States.; Middlemore Clinical Trials, Auckland, New Zealand.; Department of Molecular Medicine and Pathology, School of Medical Sciences, The University of Auckland, Auckland, New Zealand.; Department of Medicine, University of Waikato, Waikato, New Zealand.
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