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

被引:4
作者
Brandon, Rebecca [1 ,2 ]
Jiang, Yannan [3 ,4 ]
Yeu, Rui Qian [1 ,2 ]
Tweedie-Cullen, Ry [1 ,2 ]
Smallman, Kate [5 ]
Doherty, Glenn [6 ]
Macaskill-Smith, Kerry A. [7 ]
Doran, Rebekah J. [7 ]
Clark, Penny [7 ]
Moffitt, Allan [8 ]
Merry, Troy [2 ,9 ]
Nehren, Norma [10 ]
King, Frances [11 ]
Hindmarsh, Jennie Harre [11 ]
Leask, Megan Patricia [2 ,12 ,13 ]
Merriman, Tony R. [2 ,12 ,13 ]
Orr-Walker, Brandon [14 ]
Shepherd, Peter R. [2 ,15 ]
Paul, Ryan [2 ,16 ]
Murphy, Rinki [1 ,2 ]
机构
[1] Univ Auckland, Fac Med & Hlth Sci, Dept Med, Auckland, New Zealand
[2] Maurice Wilkins Ctr Mol Biodiscovery, Auckland, New Zealand
[3] Univ Auckland, Fac Sci, Dept Stat, Auckland, New Zealand
[4] Univ Auckland, Natl Inst Hlth Innovat, Sch Populat Hlth, Auckland, New Zealand
[5] Diabet Fdn Aotearoa, Auckland, New Zealand
[6] Tongan Hlth Soc, Auckland, New Zealand
[7] Ventures Pinnacle Inc, Hamilton, New Zealand
[8] Procare Primary Hlth Org, Auckland, New Zealand
[9] Univ Auckland, Discipline Nutr, Auckland, New Zealand
[10] Northland Dist Hlth Board, Te Hiku Hauora, Kaitaia, New Zealand
[11] Ngati Porou Hauora, Tairawhiti, New Zealand
[12] Univ Otago, Dept Biochem, Dunedin, New Zealand
[13] Univ Alabama Birmingham, Div Clin Immunol & Rheumatol, Birmingham, AL USA
[14] Middlemore Clin Trials, Auckland, New Zealand
[15] Univ Auckland, Sch Med Sci, Dept Mol Med & Pathol, Auckland, New Zealand
[16] Univ Waikato, Dept Med, Waikato, New Zealand
关键词
dipeptidyl peptidase inhibitor; Maori; Pacific; pioglitazone; precision medicine; stratified drug response; thiazolidinedione; obesity; MYOCARDIAL-INFARCTION; TYPE-2; ROSIGLITAZONE; EFFICACY; GAMMA; RISK;
D O I
10.3389/fendo.2022.1091421
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundUnderstanding 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. AimsWe 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). MethodsA 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. Results346 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. ConclusionsComparative 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.
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