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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 25, No 5, September/October 2014

230

AFRICA

observation was made regarding the proportions of patients with

hypertensive retinopathy among those with and without CKD

(89.3 vs 83.3%) (

χ

2

=

0.12,

p

=

0.73). The association of CKD with

hypertensive retinopathy was not significant for all retinopathy

stages combined (

χ

2

=

0.17,

p

=

0.68, OR

=

1.7, 95% CI: 0.4–6.6)

or for each retinopathy stage taken individually (

χ

2

=

0.03–2.82,

p

=

0.09–0.85). Compared to patients without hypertensive

retinopathy, those with stages 3 and 4 hypertensive retinopathy

were 3.3 and 13.3 times more likely to have CKD, respectively.

There were 85.7% of patients with hypertensive retinopathy

among those who suffered from stroke (28 patients, Table

3). This proportion was not significantly different from the

83.2% of patients with hypertensive retinopathy among those

without stroke (

χ

2

>

0.001,

p

=

0.99). Patients with hypertensive

retinopathy were as likely as those without retinopathy to have

stroke (18 vs 15.4%) (

χ

2

=

0.34,

p

=

0.56). No association was

found between stroke and hypertensive retinopathy regardless

of retinopathy stage (

χ

2

<

0.01,

p

=

0.96, OR

=

1.2; 95% CI:

0.4–3.8) and for individual retinopathy stages (

χ

2

=

0.02–1.06,

p

=

0.30–0.88).

A subset of data of 75 patients with complete documentation

was used to perform a multivariate logistic regression analysis

that included age, gender, BMI, alcohol consumption, smoking,

diabetes, arterial pressures (systolic, diastolic and pulse), current

blood pressure-lowering treatment, LVH, CKD and stroke as

candidate explanatory variables, and hypertensive retinopathy

as outcome variable after controlling for diabetes. The results,

shown in Table 4, indicate that CKD was the most significant

predictor of hypertensive retinopathy, with OR of 4.4 compared

to CKD-free patients. Age

>

50 years and smoking appeared to

decrease the risk of hypertensive retinopathy; the effects were

negligible but significant.

Discussion

Hypertension is an important cause of morbidity and mortality

in the general population in Western countries, and recent

surveys in sub-Saharan Africa have reported high prevalences

of hypertension ranging between 19 and 50% in both urban

and rural populations.

19,20

If left untreated, hypertension may

result in considerable damage to the cardiovascular, renal

and cerebrovascular systems, leading to such complications as

myocardial infarction, CKD and cerebrovascular accident.

While significant efforts have been invested to demonstrate

the benefits of antihypertensive treatment, it is critical for

better management to know both to what extent the various

hypertension-related TODs are interrelated, and the risk factors

for hypertension-related damage. Because studies in this regard

are limited in sub-SaharanAfrica, we investigated the relationship

between hypertensive retinopathy and LVH, CKD and stroke

among Congolese patients. We also assessed the determinants of

hypertensive retinopathy.

It has been hypothesised that both hypertension-related

retinal and renal vascular changes share common pathogenetic

mechanisms. As a result, earlier studies have consistently reported

an association between the presence of retinal vascular changes

associated with hypertension and lower GFR.

21-23

Surprisingly,

our results suggest otherwise, which may be ascribed to the small

study population.

Signs of hypertensive retinopathy have also long been

recognised as risk indicators of LVH, both in population- and

hospital-based studies.

24-26

For example, in the Chronic Renal

Insufficiency Cohort (CRIC) study,

26

there was an association

between severity of hypertensive retinopathy and the incidence

of any cardiovascular disease. Similarly, a follow up of the

National Health and Nutrition Survey (NHANES I) reported

an increased risk of cardiovascular disease in people with

hypertensive ocular fundus retinal vascular changes.

27

The lack of association between hypertensive retinopathy

and LVH found in our study echoes the findings of other earlier

studies.

28,29

While there is a general agreement on the association

between hypertensive retinopathy and all types of hypertensive

cardiovascular diseases,

26,27,30

our study only focused on LVH,

which may explain the lack of association. Overall, our findings

corroborate those of earlier studies that the risk of developing

LVH increases significantly with the severity of hypertensive

retinopathy.

Table 1. Association between hypertensive retinopathy

and left ventricular hypertrophy (LVH)

Retinopa-

thy grade

With LVH

(%)

Without

LVH (%)

OR

(95% CI)

Chi-

square

p

-value

0

7 (13.5)

12 (26.7)

1

1

19 (36.5)

21 (46.7) 1.6 (0.5–4.8)

0.24 0.62

2

10 (19.2)

5 (11.1) 3.4 (0.8–14.2) 1.91 0.17

3

13 (25.0)

5 (11.1) 4.5 (1.1–17.9) 3.34 0.07

4

3 (5.8)

2 (4.4)

2.6 (0.3–19.3) 0.18 0.67

OR: odd ratio, CI: confidence interval.

Table 2. Association between hypertensive retinopathy

and chronic kidney disease (CKD)

Retinopa-

thy grade

With CKD

(%)

Without

CKD (%)

OR

(95% CI)

Chi-

square

p

-value

0

3 (10.7)

10 (16.6)

1

1

9 (32.1)

26 (43.3)

1.2 (0.3–5.2)

0.04 0.85

2

2 (7.1)

13 (21.7)

0.5 (0.07–3.7)

0.03 0.86

3

10 (35.7)

10 (16.7)

3.3 (0.7–15.9)

1.4 0.24

4

4 (14.3)

1 (1.7)

13.3 (1.1–169.1) 2.8 0.09

OR: odd ratio, CI: confidence interval.

Table 3. Association between hypertensive

retinopathy and stroke

Retinopa-

thy grade

With

stroke (%)

Without

stroke (%)

OR

(95% CI)

Chi-

square

p

-value

0

4 (14.3)

22 (16.8)

1

-

-

1

11 (39.3)

56 (42.7) 1.1 (0.3–3.8)

0.04 0.85

2

6 (21.4)

12 (9.2)

2.8 (0.7–11.7) 1.1 0.30

3

4 (14.3)

33 (25.2) 0.7 (0.2–2.9)

0.02 0.88

4

3 (10.7)

8 (6.1)

2.1 (0.4–11.3) 0.2 0.70

OR: odd ratio, CI: confidence interval.

Table 4. Significant determinants of hypertensive retinopathy

Parameters

β

p

-value

OR (95% CI)

Constant

–0.88

0.23

0.41

Chronic kidney disease

1.49

0.018 4.4 (1.29–15.21)

Age

>

50 years

–1.46

0.046 0.23 (0.06–0.97)

Smoking

–2.02

0.035

0.1 (0.02–0.9)

OR: odd ratio, CI: confidence interval.