Effects of the Norfolk diabetes prevention lifestyle intervention (NDPS) on glycaemic control in screen-detected type 2 diabetes: a randomised controlled trial

Sampson, Michael and Clark, Allan and Bachmann, Max and Garner, Nikki and Irvine, Lisa and Howe, Amanda and Greaves, Colin and Auckland, Sara and Smith, Jane and Turner, Jeremy and Rea, Dave and Rayman, Gerry and Dhatariya, Ketan and John, W. Garry and Barton, Garry and Usher, Rebecca and Ferns, Clare and Pascale, Melanie and Auckland, Sara and Bachmann, Max and Barton, Garry and Clark, Allan and Dhatariya, Ketan and Ferns, Clare and Garner, Nikki and Greaves, Colin and Goldson, Andy and Hadley-Brown, Martin and Howe, Amanda and Irvine, Lisa and John, Garry and Pascale, Melanie and Rea, David and Smith, Jane and Usher, Jeremy Turner Rebecca and Wallace, Tara (2021) Effects of the Norfolk diabetes prevention lifestyle intervention (NDPS) on glycaemic control in screen-detected type 2 diabetes: a randomised controlled trial. BMC Medicine, 19 (1). ISSN 1741-7015

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Abstract

The purpose of this trial was to test if the Norfolk Diabetes Prevention Study (NDPS) lifestyle intervention, recently shown to reduce the incidence of type 2 diabetes in high-risk groups, also improved glycaemic control in people with newly diagnosed screen-detected type 2 diabetes.

Methods
We screened 12,778 participants at high risk of type 2 diabetes using a fasting plasma glucose and glycosylated haemoglobin (HbA1c). People with screen-detected type 2 diabetes were randomised in a parallel, three-arm, controlled trial with up to 46 months of follow-up, with a control arm (CON), a group-based lifestyle intervention of 6 core and up to 15 maintenance sessions (INT), or the same intervention with additional support from volunteers with type 2 diabetes trained to co-deliver the lifestyle intervention (INT-DPM). The pre-specified primary end point was mean HbA1c compared between groups at 12 months.

Results
We randomised 432 participants (CON 149; INT 142; INT-DPM 141) with a mean (SD) age of 63.5 (10.0) years, body mass index (BMI) of 32.4 (6.4) kg/m2, and HbA1c of 52.5 (10.2) mmol/mol. The primary outcome of mean HbA1c at 12 months (CON 48.5 (9.1) mmol/mol, INT 46.5 (8.1) mmol/mol, and INT-DPM 45.6 (6.0) mmol/mol) was significantly lower in the INT-DPM arm compared to CON (adjusted difference −2.57 mmol/mol; 95% CI −4.5, −0.6; p = 0.007) but not significantly different between the INT-DPM and INT arms (−0.55 mmol/mol; 95% CI −2.46, 1.35; p = 0.57), or INT vs CON arms (−2.14 mmol/mol; 95% CI −4.33, 0.05; p = 0.07). Subgroup analyses showed the intervention had greater effect in participants < 65 years old (difference in mean HbA1c compared to CON −4.76 mmol/mol; 95% CI −7.75, −1.78 mmol/mol) than in older participants (−0.46 mmol/mol; 95% CI −2.67, 1.75; interaction p = 0.02). This effect was most significant in the INT-DPM arm (−6.01 mmol/mol; 95% CI −9.56, −2.46 age < 65 years old and −0.22 mmol/mol; 95% CI −2.7, 2.25; aged > 65 years old; p = 0.007). The use of oral hypoglycaemic medication was associated with a significantly lower mean HbA1c but only within the INT-DPM arm compared to CON (−7.0 mmol/mol; 95% CI −11.5, −2.5; p = 0.003).

Item Type: Article
Subjects: ArticleGate > Medical Science
Depositing User: APLOS Lib
Date Deposited: 27 Jun 2022 03:36
Last Modified: 27 Jun 2022 03:36
URI: http://ebooks.pubstmlibrary.com/id/eprint/90

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