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VOLUME 15 NUMBER 2 • NOVEMBER 2018

73

SA JOURNAL OF DIABETES & VASCULAR DISEASE

REVIEW

6. Hebert LA, Wilmer WA, Falkenhain ME, Ladson-Wofford SE, Nahman NS, Jr, Rovin

BH. Renoprotection: one or many therapies?

Kidney Int

2001;

59

(4): 1211–1226.

7. Brenner BM, Cooper ME, de Zeeuw D, Keane WF, Mitch WE, Parving HH,

et al.

Effects of losartan on renal and cardiovascular outcomes in patients with type 2

diabetes and nephropathy.

N Engl J Med

2001;

345

(12): 861–869.

8. Colhoun HM, Betteridge DJ, Durrington PN, Hitman GA, Neil HA, Livingstone

SJ,

et al

. Primary prevention of cardiovascular disease with atorvastatin in type 2

diabetes in the Collaborative Atorvastatin Diabetes Study (CARDS): multicentre

randomised placebo-controlled trial.

Lancet

2004;

364

(9435): 685–696.

9. Ruospo M, Saglimbene VM, Palmer SC, De Cosmo S, Pacilli A, Lamacchia O,

et

al.

Glucose targets for preventing diabetic kidney disease and its progression.

Cochrane Syst Rev

2017;

6

: Cd010137.

10. Gaede P, Lund-Andersen H, Parving HH, Pedersen O. Effect of a multifactorial

intervention on mortality in type 2 diabetes.

N Engl J Med

2008;

358

(6): 580–

591.

11. Harada N, Inagaki N. Role of sodium-glucose transporters in glucose uptake of

the intestine and kidney.

J Diabetes Invest

2012;

3

(4): 352–353.

12. Nair S, Wilding JP. Sodium glucose cotransporter 2 inhibitors as a new treatment

for diabetes mellitus.

J Clin Endocrinol Metab

2010;

95

(1): 34–42.

13. McMurray JJ, Gerstein HC, Holman RR, Pfeffer MA. Heart failure: a cardiovascular

outcome in diabetes that can no longer be ignored.

Lancet Diabetes Endocrinol

2014;

2

(10): 843–851.

14. Cherney DZ, Perkins BA, Soleymanlou N, Maione M, Lai V, Lee A,

et al.

Renal

hemodynamic effect of sodium-glucose cotransporter 2 inhibition in patients

with type 1 diabetes mellitus.

Circulation

2014;

129

(5): 587–597.

15. Staruschenko A. Hypertension and diabetes mellitus: the chicken and egg

problem.

Hypertension

2017;

69

(5): 787–788.

16. Sochett EB, Cherney DZ, Curtis JR, Dekker MG, Scholey JW, Miller JA. Impact

of renin angiotensin system modulation on the hyperfiltration state in type 1

diabetes.

J Am Soc Nephrol

2006;

17

(6): 1703-1709.

17. Stratton IM, Adler AI, Neil HA, Matthews DR, Manley SE, Cull CA,

et al.

Association of glycaemia with macrovascular and microvascular complications of

type 2 diabetes (UKPDS 35): prospective observational study.

Br Med J Clin Res Ed

2000;

321

(7258): 405–412.

18. Nissen SE, Wolski K. Effect of rosiglitazone on the risk of myocardial infarction and

death from cardiovascular causes.

N Engl J Med

2007;

356

(24): 2457–2471.

19. Gupta P, White WB. Cardiovascular safety of therapies for type 2 diabetes.

Exp

Opin Drug Safety

2017;

16

(1): 13–25.

20. Zinman B, Wanner C, Lachin JM, Fitchett D, Bluhmki E, Hantel S,

et al.

Empagliflozin, cardiovascular outcomes, and mortality in type 2 diabetes.

N Engl

J Med

2015;

373

(22): 2117–2128.

21. Wanner C, Inzucchi SE, Lachin JM, Fitchett D, von Eynatten M, Mattheus M,

et al.

Empagliflozin and progression of kidney disease in type 2 diabetes.

N Engl J Med

2016;

375

(4): 323–334.

22. Neal B, Perkovic V, Mahaffey KW, de Zeeuw D, Fulcher G, Erondu N,

et al.

Canagliflozin and cardiovascular and renal events in type 2 diabetes.

N Engl J

Med

2017;

377

(7): 644–657.

23. Naidoo P, Ho K, Rambiritch V, Butkow N. Sodium-glucose co-transporter inhibitor

(SGLT): a novel class of antidiabetic drugs.

S Afr J Diabetes Vasc Dis

2015;

11

:

145–148.

24. Ruanpeng D, Ungprasert P, Sangtian J, Harindhanavudhi T. Sodium-glucose

cotransporter 2 (SGLT2) inhibitors and fracture risk in patients with type 2

diabetes mellitus: A meta-analysis.

Diabetes Metab Res Rev

2017;

33

(6). Epub

2017 Jun 16.

25. Ptaszynska A, Cohen SM, Messing EM, Reilly TP, Johnsson E, Johnsson K.

Assessing bladder cancer risk in type 2 diabetes clinical trials: the Dapagliflozin

Drug Development Program as a ‘case study’.

Diabetes Ther

2015;

6

(3): 357–

375.

Statins don’t reduce cardiovascular disease risk in healthy older people

S

tatins are not associated with a reduction

in cardiovascular disease (CVD) or death

in healthy people aged over 75 years, finds a

recent study. However, in those with type 2

diabetes, statins were related to a reduction

in cardiovascular disease and death from

any cause up to the age of 85 years.

The results of the study, led by the

University Institute for Primary Care

Research Jordi Gol (IDIAPJGol) and Girona

Biomedical Research Institute (IDIBGI), do

not support the widespread use of statins

in old and very old people, but they do

support treatment in selected people, such

as those aged 75 to 84 years with type 2

diabetes, say the researchers.

Cardiovascular disease is the leading

cause of death globally, especially for those

aged 75 years and over. Statin prescriptions

to elderly patients have increased in recent

decades, and trial evidence supports statin

treatment for people aged 75 years or

older with existing heart disease (known as

secondary prevention).

Evidence on the effects of statins

for older people without heart disease

(known as primary prevention) is lacking,

particularly in those aged 85 years or older

and those with diabetes. So, researchers

based in Spain set out to assess whether

statin treatment is associated with a

reduction in cardiovascular disease and

death in old (75–84 years) and very

old (85 years and over) adults with and

without type 2 diabetes.

UsingdatafromtheCatalanprimarycare

system database (SIDIAP), they identified

46 864 people aged 75 years or more

with no history of cardiovascular disease

between 2006 and 2015. Participants

were grouped into those with and without

type 2 diabetes and as statin non-users

or new users (anyone starting statins for

the first time during the study enrolment

period). Primary care and hospital records

were then used to track cases of CVD

(including coronary heart disease, angina,

heart attack and stroke) and death from

any cause (all-cause mortality) over an

average of 5.6 years.

In participants without diabetes, statin

treatment was not associated with a

reduction in CVD or all-cause mortality in

both old and very old age groups, even

though the risk of CVD in both groups

was higher than the risk thresholds

proposed for statin use in guidelines.

In participants with diabetes, however,

statins were associated with significantly

reduced levels of CVD (24%) and all-cause

mortality (16%) in those aged 75–84 years.

But this protective effect declined after age

85 and disappeared by age 90.

This was an observational study, so no

firm conclusions can be drawn about cause

and effect, and the authors cannot not rule

out the possibility that some of their results

may be due to unmeasured (confounding)

factors.

But they point out that this was a

high-quality study with a large sample

size, reflecting real-life clinical conditions.

Therefore they concluded that their results

do not support the widespread use of

statins in old and very old populations, but

they do support treatment in those with

type 2 diabetes younger than 85 years.

In a linked editorial, Aidan Ryan at

University Hospital Southampton and

colleagues, say the biggest challenge for

clinicians is how to stratify risk among

those aged more than 75 years to

inform shared decision making. These

observational findings should be tested

further in randomised trials, they write. In

the meantime, they say ‘patient preference

remains the guiding principle while we

wait for better evidence.’

Source: Medical Brief 2018