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Table 1: Effects of diabetes medicines (excluding insulin) on HbA 1c<br />

, cardiovascular co-morbidities, progression of kidney disease,<br />

weight and risk of hypoglycaemia. Adapted from the American Diabetes Association (<strong>2020</strong>) 19<br />

Medicine<br />

lowering HbA 1c<br />

CVD<br />

HF<br />

chronic kidney<br />

disease<br />

Efficacy for<br />

Cardiovascular effects Renal effects:<br />

progression of<br />

Effects on<br />

weight<br />

Risk of<br />

hypoglycaemia<br />

Metformin<br />

High<br />

Potential<br />

benefit<br />

Neutral<br />

Neutral<br />

Neutral with<br />

potential for<br />

modest loss<br />

Low<br />

Sulfonylureas High Neutral Neutral Neutral Gain High<br />

Pioglitazone<br />

High<br />

Potential<br />

benefit<br />

Increased risk Neutral Gain Low<br />

Vildagliptin Intermediate Neutral Neutral Neutral Neutral Low<br />

SGLT-2<br />

inhibitor * †<br />

Intermediate<br />

Benefit:<br />

empagliflozin,<br />

canagliflozin<br />

Benefit:<br />

empagliflozin,<br />

canagliflozin,<br />

dapagliflozin<br />

Benefit:<br />

empagliflozin,<br />

canagliflozin,<br />

dapagliflozin<br />

Loss<br />

Low<br />

GLP-1 receptor<br />

agonist * †<br />

High<br />

Benefit;<br />

lixisenatide is<br />

neutral<br />

Neutral<br />

Benefit:<br />

liraglutide<br />

Loss<br />

Low<br />

* Not funded<br />

† Preferred choice to add to metformin in patients with cardiovascular disease, heart failure or chronic kidney disease 19<br />

When to seek further advice<br />

Consider discussing patients with a diabetes specialist if<br />

appropriate management and adherence to treatment is<br />

ineffective in controlling progression of disease, e.g. HbA 1c<br />

> 75<br />

mmol/mol, declining renal function, significant albuminuria or<br />

other uncontrolled diabetes or cardiovascular complications.<br />

For the original and extended version of this article see:<br />

“A rising tide of type 2 diabetes in younger people: what can<br />

primary care do” (available at: https://bpac.org.nz/2018/<br />

diabetes.aspx)<br />

References<br />

1. Ng M, Fleming T, Robinson M, et al. Global, regional, and national prevalence of<br />

overweight and obesity in children and adults during 1980-2013: a systematic<br />

analysis for the Global Burden of Disease Study 2013. Lancet 2014;384:766–81.<br />

doi:10.1016/S0140-6736(14)60460-8<br />

2. Ministry of Health NZ. Living well with diabetes. Ministry of Health NZ<br />

2015. Available from: www.health.govt.nz/publication/living-well-diabetes<br />

(Accessed Jul, <strong>2020</strong>).<br />

3. Coppell KJ, Mann JI, Williams SM, et al. Prevalence of diagnosed and<br />

undiagnosed diabetes and prediabetes in New Zealand: findings from the<br />

2008/09 Adult Nutrition Survey. N Z Med J 2013;126:23–42.<br />

4. Huo X, Gao L, Guo L, et al. Risk of non-fatal cardiovascular diseases in earlyonset<br />

versus late-onset type 2 diabetes in China: a cross-sectional study. Lancet<br />

Diabetes Endocrinol 2016;4:115–24. doi:10.1016/S2213-8587(15)00508-2<br />

5. Dabelea D, Stafford JM, Mayer-Davis EJ, et al. Association of type 1<br />

diabetes vs type 2 diabetes diagnosed during childhood and adole<strong>sce</strong>nce<br />

with complications during teenage years and young adulthood. JAMA<br />

2017;317:825–35. doi:10.1001/jama.2017.0686<br />

6. Al-Saeed AH, Constantino MI, Molyneaux L, et al. An inverse relationship<br />

between age of type 2 diabetes onset and complication risk and mortality:<br />

the impact of youth-onset type 2 diabetes. Diabetes Care 2016;39:823–9.<br />

doi:10.2337/dc15-0991<br />

www.bpac.org.nz<br />

Best Practice Journal – SCE Issue 1 13

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