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34

VOLUME 17 NUMBER 1 • JULY 2020

CASE REPORT

SA JOURNAL OF DIABETES & VASCULAR DISEASE

Diabetes predisposes patients to atrial fibrillation

Diabetes also increases the risk for the development of AF. Two

cohort studies, the first based on Framingham data and the

second on a large American register from the Veterans’ Health

Administration Hospitals, have associated diabetes with increased

AF risk. The Framingham data reflected a 40% increased risk of AF

and there was a doubling of risk in the American study (Fig. 4).

5,6

In T2DM patients with AF, there is a substantially increased risk of

death and cardiovascular events. This was shown in the ADVANCE

trial of 11 140 T2DM patients, including 7% with AF. In this study,

AF impacted on the outcome of both all-cause mortality and major

cerebrovascular events over five years (Fig. 5).

7

Fig. 4.

Diabetes predisposes patients to AF.

5,6

Fig. 5.

AF and T2DM frequently co-exist and are associated with subsequent

increased risk of death and cerebrovascular events.

7

The risk for development of AF is further increased in the patient

with CKD and the metabolic syndrome, which is characterised

by dysglycaemic traits other than diabetes (Fig. 6).

8

This stresses

the need for clinicians to screen not only their T2DM patients’

glucose levels, but for all relevant risk factors, and to consider

appropriate interventions, including nonvitamin K antagonist oral

anticoagulants (NOACs) for the management of AF.

Risk reduction in T2DM patients with AF using NOACs

The RELOADED study of diabetic patients with non-valvular AF

(NVAF) using rivaroxaban showed a trend towards risk reduction

for end-stage renal disease and a slower progression to acute

kidney injury (AKI). There was no increase in ischaemic/systemic

embolism, intracranial haemorrhage and fatal bleeding with the

use of rivaroxaban (Fig. 7).

9

Follow-up of patients, using ICD10 diagnostic codes for diabetes

and AF and prescription information from MarketScan and other

real-world data sets, evaluated progression to renal dysfunction

(AKI, stage 5 CKD or haemodialysis) of those patients newly initiated

Fig. 6.

The metabolic syndrome and CKD increase risk of AF.

8

Kaplan-Meier curves

showing the cumulative event-free survival for AF in

patients classified into four groups based on the presence/absence of metabolic

syndrome and CKD. *The associations were tested using a Cox proportional

hazards model adjusted for age, sex, alcohol consumption, smoking status and

physical activity.

Fig. 7.

RELOADED: Trend towards risk reductions observed in T2DM patients

with NVAF using NOACs.

9

Fig. 8.

Risk of major adverse renal outcomes in diabetic patients with AF

receiving rivaroxaban vs warfarin.

10

Retrospective analysis of US MarketScan

claims data for patients with NVAF and diabetes, newly initiating therapy with

rivaroxaban (

n

= 10 017) or warfarin (

n

= 11 665). Patients with CKD stage 5 or

on haemodialysis were excluded.

NOAC vs phenprocoumon (n=8 545)

HR (95% CI)

HR (95% CI)

Rate per 100 PYs

Rivaroxaban Warfarin

HR (95% CI)

HR (95% CI)