Could Dietary Modification Independent of Energy Balance Influence the Underlying Pathophysiology of Type 2 Diabetes? Implications for Type 2 Diabetes Remission.
Nicola D GuessPublished in: Diabetes therapy : research, treatment and education of diabetes and related disorders (2022)
High-quality clinical trial data demonstrate that remission is possible for people living with type 2 diabetes (T2D) if they lose a large amount of weight (≥ 10 kg). Durable remission appears predicated on the long-term maintenance of weight loss. Unfortunately, long-term follow-up data from lifestyle-based weight loss programmes show that, on average, most people regain at least some of the weight lost. In addition, restoration of a diminished first-phase insulin response also appears necessary for durable remission, and this becomes less likely as T2D progresses. A pragmatic approach to enhance the effects of weight loss on durable remission is to consider whether dietary components could help control blood glucose, independent of caloric balance. This manuscript reviews current evidence on weight-neutral effects of diet on blood glucose, including high-protein, low-carbohydrate, high-fibre and plant-based diets, with a particular focus on the effect of nutrition on the underlying pathophysiology of T2D, including the first-phase insulin response. The importance of mechanistic data in enhancing our understanding of dietary strategies in T2D remission is described, and suggestions are made for future advances in remission research.
Keyphrases
- weight loss
- glycemic control
- blood glucose
- type diabetes
- bariatric surgery
- disease activity
- roux en y gastric bypass
- gastric bypass
- ulcerative colitis
- clinical trial
- physical activity
- electronic health record
- rheumatoid arthritis
- systemic lupus erythematosus
- weight gain
- obese patients
- big data
- insulin resistance
- body mass index
- blood pressure
- metabolic syndrome
- open label
- randomized controlled trial
- small molecule
- artificial intelligence
- phase ii
- binding protein