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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 28, No 1, January/February 2017

26

AFRICA

pregnant women (

p

<

0.001), respectively. Significant differences

were observed for BPWA (

p

<

0.01) and augmentation index at

75 bpm (

p

<

0.0001) between the four groups.

For BPWA, Dunn’s multiple comparison test revealed a

significant difference only between HIV-negative normotensive

and HIV-negative pre-eclamptic pregnant women (

p

<

0.01).

For augmentation index, significant differences were observed

between HIV-negative normotensive and HIV-positive

pre-eclamptic pregnant women (

p

<

0.001) and between

HIV-negative normotensive and HIV-negative pre-eclamptic

pregnant women (

p

<

0.001), as shown in Fig. 5. RHI was lower

in HIV-positive normotensive and HIV-positive pre-eclamptic

women than in normotensive HIV-negative women, although

this did not reach statistical significance (

p

=

0.1195).

Discussion

In this study, we set out to assess whether PAT (through

RHI) demonstrates endothelial dysfunction in pre-eclampsia.

The RHI was found to be significantly lower in patients with

pre-eclampsia compared to normotensive controls. Since RHI

is endothelium dependent, these results indicate that there is

indeed endothelial dysfunction in rural African women with

pre-eclampsia, therefore confirming what has been reported

in other populations. To our knowledge, this is the first report

involving rural black African women.

Endothelial dysfunction is known to be the central mechanism

in the pathophysiology of pre-eclampsia.

3

Several reports have

demonstrated that FMD is significantly reduced in patients with

pre-eclampsia when compared with normotensive controls,

18-20

confirming that pre-eclampsia is associated with endothelial

dysfunction. Although FMD measurement is still regarded

as the gold standard for assessing endothelial function in

pregnancy, it has several limitations, including the need for an

experienced sonographer, a good-quality ultrasound machine,

and the need for intra-arterial injections. It is therefore not easy

to adapt the method for use in assessing endothelial function in

large numbers of patients in a clinic setting.

We have shown in this study that the EndoPAT 2000 can

be used successfully to assess endothelial function in pregnant

subjects by measuring the RHI. Although the EndoPAT 2000

itself is a fairly expensive machine, it is less invasive, much easier

to use, does not require extensive training and it can be used to

assess large numbers of patients rapidly and reliably, even in a

clinic setting.

Although not many studies have tested endothelial function

in pregnancy using EndoPAT 2000, our results are in agreement

with the study done by Yinon

et al.

in 2006, who examined 17

women at the time of diagnosis of pre-eclampsia (mean gestation

32 weeks) and compared themwith 25 women with normotensive

pregnancies. They found that women with pre-eclampsia had

significantly lower RHI values (1.5

±

0.1 vs 1.8

±

0.1) compared

to uncomplicated pregnancies.

The results of this study with much larger number of subjects

clearly indicate that RHI, as measured using the EndoPAT, can

be used as an adjunct to blood pressure measurement in assessing

endothelial dysfunction in pre-eclampsia. However, as endothelial

dysfunction is known to precede clinical pre-eclampsia, the

important question is, can the EndoPAT 2000 be used for screening

and identifying patients before the onset of clinical pre-eclampsia?

Carty

15

followed up a cohort of patients in Scotland from the first

trimester all through pregnancy to postpartum, but did not find

any difference in RHI between women who went on to develop

pre-eclampsia and normotensive pregnancies, both at 16 and 28

weeks’ gestation. This, however, does not rule out the possibility

that RHI might still be useful in either early identification or

prediction of pre-eclampsia in larger studies, as the search for

predictors of pre-eclampsia continues in earnest.

If it were demonstrated that RHI, as measured by the

EndoPAT 2000, can be used as a predictor of pre-eclampsia, then

the test would become much more cost-effective and cheaper. A

prospective cohort study of normotensive pregnant women

recruited in the first or early second trimester and followed until

delivery is planned to determine whether RHI measurement can

be used as a predictor of pre-eclampsia.

When participants with early-onset pre-eclampsia were

compared with those with late-onset pre-eclampsia, there was

no statistically significant difference in RHI between patients

with early- and late-onset pre-eclampsia (

p

> 0.05). Although

the numbers are small, this finding suggests that endothelial

dysfunction is indeed present in both early- and late-onset

Systolic BP (mmHg)

0 20 40 60 80 100 120 140 160

Baseline pulse wave amplitude (au)

1600

1400

1200

1000

800

600

400

200

0

Fig. 4.

Relationship between systolic pressure and baseline

pulse-wave amplitude.

Augmentation index @ 75 bpm (%)

Normotensive

HIV+

Normotensive

HIV–

Pre-eclamptic

HIV+

Pre-eclamptic

HIV–

19

18

17

16

15

14

13

12

11

10

9

8

7

6

5

4

3

2

1

0

Fig. 5.

Augmentation index @ 75 bpm between the four HIV

groups.