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VOLUME 17 NUMBER 2 • NOVEMBER 2020

57

SA JOURNAL OF DIABETES & VASCULAR DISEASE

Report

Independent of the population-specific BMI thresholds determining

overweight and obesity, visceral fat distribution has been found to

elevate the risk of mortality.

1

What are the benefits of weight loss in diabetes

prevention and therapy?

The progression of T2DM can be arrested and often reversed in the

first five years after diagnosis by significantly reducing body weight

(≥ 10%); the metabolic dysregulation and inflammatory processes

that predispose to T2DM can frequently be corrected.

5

The Finnish Diabetes Prevention Study

7

showed that in pre-

diabetic individuals, intensive dietary and exercise programmes

Fig. 1.

Pathways from obesity to diabetes.

6

decreased the overall risk of diabetes by 58% (Fig. 2). Similarly,

the Diabetes Prevention Program

8

showed that moderate weight

loss with lifestyle intervention in an obese population with

impaired glucose tolerance could reduce the incidence of diabetes

by 58%, whereas metformin alone reduced diabetes incidence

by only 31% (Fig. 3).

The American Cancer Society’s Cancer Prevention Study I

indicated that intentional weight loss of 10 kg in those with T2DM

reduced total mortality by approximately 25%. Other clinical

trials have demonstrated that a loss of 5–10% of body weight

in diabetes patients demonstrates beneficial effects at one year

(Table 1).

9-12

Fig. 2.

Finnish Diabetes Prevention Study: intensive dietary and exercise

intervention decreases overall risk of diabetes.

Fig. 3.

Diabetes Prevention Programme: lifestyle modification is superior to

metformin for the prevention of T2DM.

Obesity

Permanent elevation of FFA

Inhibits glucose transport activity

Predominant utilisation of lipids by muscle

Accumulation of TG in liver and beta-cells

i

Glucose uptake by muscle

i

Glycogen synthesis in skeletal muscle

i

INSULIN RESISTANCE

DIABETES

INSULIN DEFICIENCY

i

Insulin secretion

Impairs insulin sensitivity

Oxidative stress and systemic inflammation

Hepatic and islet dysfunction

(lipotoxicity)

h

Insulin secretion

(sustained hyperinsulinaemia)

Chronic hyperglycaemia

(glucotoxicity)