Prevention of type 2 diabetes

Prevention of type 2 diabetes can be achieved with both lifestyle changes and use of medication.[1] The American Diabetes Association categorizes people with prediabetes, who have glycemic levels higher than normal but do not meet criteria for diabetes, as a high-risk group. Without intervention, people with prediabetes progress to type 2 diabetes with a 5% to 10% rate. Diabetes prevention is achieved through weight loss and increased physical activity,[2] which can reduce the risk of diabetes by 50% to 60%.[3]

Lifestyle

Many interventions to promote healthy lifestyles have been shown to prevent diabetes. A combination of diet and physical activity promotion through counselling and support programs decrease weight, improve systolic blood pressure, improve cholesterol levels and decrease risk of diabetes.[3]

Increasing physical activity may be helpful in preventing type 2 diabetes, particularly if undertaken soon after a carbohydrate-rich meal that increases blood sugar levels.[4][5][6] The American Diabetes Association (ADA) recommends maintaining a healthy weight, getting at least 2+12 hours of exercise per week (several brisk sustained walks appear sufficient), having a modest fat intake (around 30% of energy supply should come from fat),[7] and eating sufficient fiber (e.g., from whole grains).

Numerous clinical studies have shown that resistant starch increases insulin sensitivity, independent of the glycemic response of the food[8][9] and may reduce the risk of type 2 diabetes.[10] The U.S. Food and Drug Administration requires claims that resistant starch can reduce the risk of type 2 diabetes to be qualified with a declaration that scientific evidence in support of this claim is limited.[11]

Foods with low glycemic index, rich in fiber and other important nutrients, are recommended, notwithstanding insufficient evidence.[12]

Study group participants whose "physical activity level and dietary, smoking, and alcohol habits were all in the low-risk group had an 82% lower incidence of diabetes".[13]

Various sources suggest an influence of dietary fat types. Positive effects of unsaturated fats have been asserted on theoretical grounds and observed in animal feeding studies. Hydrogenated fats are universally considered harmful, mainly because of their well-known effect on cardiovascular risk factors.[14]

Numerous studies suggest connections between some aspects of type 2 diabetes with ingestion of certain foods or with some drugs. Breastfeeding may also be associated with the prevention of type 2 diabetes in mothers.[15]

Some evidence relates consumption of coffee with prevention of type 2 diabetes. However, it is unclear if coffee causes any change in the risk of diabetes. This is true regardless of if it is caffeinated/decaffeinated, consumed with/without sugar, or potboiled or not.[16]

Medications

Some studies have shown delayed progression to diabetes in predisposed patients through prophylactic use of metformin,[17][5] rosiglitazone,[18] or valsartan.[19] Lifestyle interventions are, however, more effective than metformin alone at preventing diabetes regardless of weight loss,[20] though evidence suggests that lifestyle interventions and metformin together can be effective treatment in patients who are at a higher risk of developing diabetes.[17]

A Cochrane systematic review assessed the effect of alpha-glucosidase inhibitors in people with impaired glucose tolerance, impaired fasting blood glucose, elevated glycated hemoglobin A1c (HbA1c).[21] It was found that acarbose appeared to reduce incidence of diabetes mellitus type 2 when compared to placebo; however, there was no conclusive evidence that acarbose compared to diet and exercise, metformin, placebo, no intervention improved all-cause mortality, reduced or increased risk of cardiovascular mortality, serious or non-serious adverse events, non-fatal stroke, congestive heart failure, or non-fatal myocardial infarction.[21] The same review found that there was no conclusive evidence that voglibose compared to diet and exercise or placebo reduced incidence of diabetes mellitus type 2, or any of the other measured outcomes.[21]

Many other medications are well known to modify risk of diabetes 2, although in most cases they are prescribed for reasons unrelated to diabetes 2. In patients on hydroxychloroquine for rheumatoid arthritis, incidence of diabetes was reduced by 77%, though causal mechanisms are unclear.[22] Dopamine receptor agonists are also known to improve glycemic control, reduce insulin resistance and help controlling body weight.[23]

Co-morbidities

People with mental health disorders are at a higher risk of developing type 2 diabetes. The most effective way to prevent type 2 diabetes in people with mental disorders is not clear; considerations include pharmacological interventions, behavior changes, and organizational interventions.[24]

Programmes

Several countries have established more and less successful national programmes to improve prevention and treatment of diabetes.[25] In the UK, the NHS's diabetes prevention programme Healthier You offers personalised face-to-face and digital services.[26] Assessment of the programme is ongoing, but based on the first 36,000 patients, it seems that those who complete the programme manage to reduce their blood sugar levels and lose weight.[27][28] At the same time, only 1 in 5 people complete the whole 9-month programme.[29][30] A study of 18,470 people who had been referred to the programme found that they had a 20% reduced risk of developing diabetes.[31][32]

References

  1. ^ Raina Elley C, Kenealy T (December 2008). "Lifestyle interventions reduced the long-term risk of diabetes in adults with impaired glucose tolerance". Evidence-Based Medicine. 13 (6): 173. doi:10.1136/ebm.13.6.173. PMID 19043031. S2CID 26714233.
  2. ^ Alustiza E, Perales A, Mateo-Abad M, Ozcoidi I, Aizpuru G, Albaina O, Vergara I (September 2021). "Tackling risk factors for type 2 diabetes in adolescents: PRE-STARt study in Euskadi". Anales de Pediatria. 95 (3). Anales de Pediatría: 186–196. doi:10.1016/j.anpedi.2020.11.001. PMID 34384737.
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  21. ^ a b c Moelands SV, Lucassen PL, Akkermans RP, De Grauw WJ, Van de Laar FA, et al. (Cochrane Metabolic and Endocrine Disorders Group) (December 2018). "Alpha-glucosidase inhibitors for prevention or delay of type 2 diabetes mellitus and its associated complications in people at increased risk of developing type 2 diabetes mellitus". The Cochrane Database of Systematic Reviews. 2018 (12): CD005061. doi:10.1002/14651858.CD005061.pub3. PMC 6517235. PMID 30592787.
  22. ^ Wasko MC, Hubert HB, Lingala VB, Elliott JR, Luggen ME, Fries JF, Ward MM (July 2007). "Hydroxychloroquine and risk of diabetes in patients with rheumatoid arthritis". JAMA. 298 (2): 187–193. doi:10.1001/jama.298.2.187. PMID 17622600.
  23. ^ Defronzo RA (April 2011). "Bromocriptine: a sympatholytic, d2-dopamine agonist for the treatment of type 2 diabetes". Diabetes Care. 34 (4): 789–794. doi:10.2337/dc11-0064. PMC 3064029. PMID 21447659.
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  30. ^ Howarth E, Bower PJ, Kontopantelis E, Soiland-Reyes C, Meacock R, Whittaker W, Cotterill S (December 2020). "'Going the distance': an independent cohort study of engagement and dropout among the first 100 000 referrals into a large-scale diabetes prevention program". BMJ Open Diabetes Research & Care. 8 (2): e001835. doi:10.1136/bmjdrc-2020-001835. PMC 7733095. PMID 33303493.
  31. ^ Ravindrarajah R, Sutton M, Reeves D, Cotterill S, Mcmanus E, Meacock R, et al. (February 2023). "Referral to the NHS Diabetes Prevention Programme and conversion from nondiabetic hyperglycaemia to type 2 diabetes mellitus in England: A matched cohort analysis". PLOS Medicine. 20 (2): e1004177. doi:10.1371/journal.pmed.1004177. PMC 9970065. PMID 36848393.
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