Type 2 & other diabetes

Very‐low‐calorie diet‐based intensive lifestyle intervention for remission of type 2 diabetes: Real‐world experience in a South Asian population

Diabet MedPublished Retrospective cohort study

Authors' conclusion

VDRP is effective in achieving T2D remission amongst Sri Lankan adults with recently diagnosed T2D and obesity. Over half of the participants followed the programme and over 75% would recommend it to others, indicating good acceptability.

Study context

Population
Sri Lankan adults (>18 years) with T2D for <3 years and BMI over 25 kg/m²; mean age 38.4 years, men 68%, mean baseline HbA1c 86.9 mmol/mol87 followed programme
Participants
170 adults
Exposure
Very Low-calorie Diet (VLCD)-based Diabetes Remission Programme followers vs non-followers
  • VDRP followersn = 87
  • VDRP non-followersn = 83reference
Outcome
Diabetes remission: HbA1c <6.5% at least 3 months after stopping glucose-lowering medications
Methodological detailsreal-world, single diabetes practice
  • Real-world
  • Single diabetes practice

Main finding

As reported in the abstract

Achieving DR (HbA1c <6.5% ≥3 months after stopping glucose-lowering medications)

Adjusted hazard ratio

9.3

95% CI 2.2–16.4

P = 0.002

Events by group

Between Followed VDRP and Did not follow VDRP
aHR 9.3 (95% CI 2.2–16.4); P = 0.002

Observational data: associations, not effects.

Further findings

Events

OutcomeVDRP followersVDRP non-followers
Normoglycaemia (HbA1c <6.5%) while continuing glucose-lowering medication2020
  • Normoglycaemia (HbA1c <6.5%) while continuing glucose-lowering medication: 20/87 vs 20/85

Acceptability

Followed the programme
87 (51%)
Reason for not following: too restrictive dietary quantity
92%
Reason for not following: difficulties finding recommended food items
67%
Would recommend VDRP to others
79%

Original publication

Very‐low‐calorie diet‐based intensive lifestyle intervention for remission of type 2 diabetes: Real‐world experience in a South Asian population. Diabet Med. Published 8 August 2024. doi:10.1111/dme.15422

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