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22

VOLUME 12 NUMBER 1 • JULY 2015

RESEARCH ARTICLE

SA JOURNAL OF DIABETES & VASCULAR DISEASE

The results of these and other studies have resulted in treatment

guidelines recommending progressively lower LDL-C targets.

21-23

However, studies from all over the world have demonstrated

that many patients on lipid-lowering therapy do not reach their

recommended lipid targets.

24-26

The South African Heart Association

(SA Heart) together with the Lipid and Atherosclerosis Society

of Southern Africa (LASSA) therefore recently emphasised that

intensive management of dyslipidaemia could significantly reduce

the South African CVD health burden.

21

The DYSlipidaemia International Study (DYSIS) is a cross-sectional,

observational study that has examined the efficacy of lipid-lowering

therapies in patients from various regions of the world, including

Canada and Europe (11 countries), in order to better characterise

predictive factors for dyslipidaemia and CVD.

24,25

Here, as part of

DYSIS, we have analysed residual dyslipidaemia in statin-treated

South African patients

.

Methods

As part of DYSIS, this epidemiological, observational, cross-sectional

study was conducted in South Africa between 1 November and 9

December 2011. Data for the study were collected in the South

African private healthcare sector by 16 physicians; 50%were primary-

care physicians and 50% were specialised office-based physicians

(e.g. cardiologists).

Prior to study initiation, the relevant local ethical reviewcommittees

approved the study protocol and all patients gave written informed

consent before enrolling in the study. Key eligibility criteria were: (1)

age of at least 45 years, (2) receiving stable statin therapy for at least

3 months, and (3) fasting for at least 12 hours at the time of visit

while on statin therapy. Participating physicians were instructed to

include all eligible and consenting patients consecutively.

Patient demographic, lifestyle and clinical characteristics were

documented. Lipid levels (total cholesterol, LDL-C, HDL-C and

triglycerides) were measured using the CardioChek

®

device (http://

www.cardiocheck.com)

at the time of patient enrollment to reliably

collect lipid measurements uniformly at all sites. The LDL-C test

strip provided measures LDL-C directly across a range of 1.29–5.18

mmol/l in about two minutes.

Additionally, the lipid-lowering regimen at the time of the most

recent blood sample was recorded for each patient (in particular,

statin type and daily dose) as well as any information regarding

other lipid-modifying therapies. The potency of different types of

statins was normalised using a calculation that allows benchmarking

against six different simvastatin dose levels (5, 10, 20, 40, 80

Table 1.

Patient characteristics, risk categories and lipid parameters in different ethnic groups

All patients

(

n

= 1 029)

Caucasian

(

n

= 582; 56.6%)

Black

(

n

= 226; 22.0%)

Asian

(

n

= 99; 9.6%)

Mixed ancestry

(

n

= 122; 11.9%)

Age (years) (mean ± SD)

65.4 ± 10.8

69.0 ± 11.0

60.0 ± 8.9

61.8 ± 9.0

60.9 ± 7.4

Family history of premature CHD (%)

26.7

34.0

1.8

44.4

23.0

Current smokers (%)

10.7

11.2

5.3

11.1

18.0

Hypertension (%)

76.8

69.8

93.3

64.6

89.3

Systolic BP (mmHg) (mean ± SD)

134.4 ± 20.0

134.9 ± 20.4

135.2 ± 19.4

129.0 ± 17.1

134.9 ± 20.7

Diastolic BP (mmHg) (mean ± SD)

79.7 ± 11.0

79.6 ± 11.1

79.6 ± 11.5

78.3 ± 9.6

81.2 ± 10.5

Waist circumference (cm) (mean ± SD)

100.7 ± 15.1

99.5 ± 16.5

105.0 ± 13.4

96.1 ± 9.6

101.8 ± 12.5

BMI (kg/m

2

) (mean ± SD)

29.6 ± 6.4

28.6 ± 6.4

32.8 ± 6.5

27.0 ± 4.5

30.4 ± 5.6

BMI > 30 kg/m

2

(%)

42.2

36.8

61.9

22.2

47.5

CVD (%)

36.2

41.1

9.7

51.5

49.2

Diabetes mellitus (%)

40.4

25.6

71.2

44.4

50.8

Metabolic syndrome (IDF) (%)

67.2

59.8

83.2

59.8

78.7

ESC risk level (2011)*

Very high-risk patient (%)

73.5

69.9

77.9

73.7

82.0

High-risk patient (%)

8.9

11.2

4.0

11.1

5.7

Moderate-risk patient (%)

13.5

15.6

11.5

9.1

10.7

Low-risk patient (%)

4.1

3.3

6.6

6.1

1.6

South African guidelines

Very high-risk patient (%)

68.6

61.2

77.9

73.5

82.8

High-risk patient (%)

9.2

11.7

6.2

8.2

3.3

Moderate-risk patient (%)

21.6

26.6

15.9

15.3

13.9

Low-risk patient (%)

0.6

0.5

0.0

3.1

0.0

Lipids (mmol/l) (mean ± SD)

LDL-C

2.3 ± 1.1

2.2 ± 1.0

2.1 ± 1.0

2.6 ± 1.2

2.7 ± 1.1

HDL-C

1.3 ± 0.4

1.3 ± 0.4

1.4 ± 0.4

1.3 ± 0.4

1.3 ± 0.5

Total cholesterol

4.4 ± 1.3

4.4 ± 1.2

4.4 ± 1.4

4.7 ± 1.6

4.7 ± 1.3

Triglycerides [median (IQR)]

1.6 (1.1–2.3)

1.5 (1.1–2.2)

1.7 (1.2–2.4)

1.7 (1.2–2.7)

1.5 (1.1–2.4)

Blood glucose

FBG (mmol/l) [median (IQR)]

4.9 (4.3–6.4)

4.6 (4.2–5.4)

6.2 (4.7–9.0)

5.3 (4.2–7.0)

5.6 (4.7–7.2)

HbA

1c

(%) diabetics [median (IQR)]

7.4 (6.6–8.8)

7.1 (6.0–8.0)

8.2 (6.8–9.9)

7.8 (7.0–8.7)

7.4 (7.0–8.8)

CHD, coronary heart disease; BP, blood pressure; BMI, body mass index; CVD, cardiovascular disease; DM, diabetes mellitus; IDF, International Diabetes

Federation.