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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 32, No 4, July/August 2021

180

AFRICA

0.002, group A vs group D;

p

= 0.001, group B vs group C;

p

=

0.009, group B vs

group D;

p

= 0.011, group C vs

group D;

p

=

0.018) (Fig. 1).

The ROC curves showed that the area under the curve,

optimal cut-off value, sensitivity and specificity of NLR for

MACE in patients with CHF and AF were 0.879 (95% CI:

0.801–0.978,

p

< 0.001), 3.12, 72.39% and 86.18%, respectively

(Fig. 2).

Discussion

CHF is a clinically common and frequently occurring disease.

The proportion of patients with HF in the total population is

as high as 2–3%, even in developed countries.

7

AF is a common

type of arrhythmia and also has a high rate of incidence. HF and

AF often co-exist, and the rate of incidence of AF in patients

with HF is up to 54%. There is a positive correlation between

the degree of HF and the rate of incidence of AF, and the rate

of incidence of AF in HF patients in NYHA class IV is 10 times

that in patients in class I.

8

There has been a consensus in multiple studies that the

long-term prognosis of patients with HF and AF is poor. Both

chronic diseases seriously affect the quality of life of patients and

impose a heavy burden on the medical system.

9

However, there

are no reliable methods for predicting the prognosis of patients

with CHF and AF. Therefore, we urgently need to find new

markers to improve the early identification of adverse prognostic

events and improve the quality of life of such patients.

AF leads to a decline and even disappearance of atrial

systolic function in patients with HF, it causes irreversible

embolism and a systemic inflammatory response, and reduces

lymphocyte counts in patients, ultimately resulting in a steady

increase in NLR in the blood.

10

It has been confirmed in a large

Table 2. Multivariate logistic regression analysis of

independent predictive factors for MACE

β

SE Wald p-value

OR (95% CI)

Age

< 60

1.000

≥ 60

2.304 0.467 22.657 0.008 10.291 (3.789–24.315)

Smoking history

No

1.000

Yes

2.644 0.854 0.212 0.323 2.32 (0.021–6.544)

Diabetes mellitus

No

1.000

Yes

0.542 0.343 1.743 0.001 1.622 (1.311–3.245)

LDL-C

< 2.30 mmol/l

1.000

> 2.30 mmol/l

0.020 0.010 2.6987 0.001 2.022 (1.987–2.056)

NLR

< 3.50

1.000

> 3.50

1.501 0.341 19.412 < 0.001 4.159 (2.378–8.814)

LVEF

< 50%

1.000

> 50%

–0.432 0.308 58.802 < 0.001 0.657(0.365–0.802)

FPG

< 7.1 mmol/l

1.000

> 7.1 mmol/l

0.759 0.218 11.242 0.014 2.142 (1.391–3.132)

NYHA heart

function class

I + II

1.000

III + IV

0.987 0.458 0.102 0.005 1.854 (2.654–4.654)

FPG: fasting plasma glucose; LDL-C: low-density lipoprotein cholesterol;

LVEF: left ventricular ejection fraction; MACE: major adverse cardiovascular

event; NLR: neutrophil-to-lymphocyte ratio; NYHA: New York Heart Associa-

tion.

Table 3. Prognosis of patients with different NLR values

Group A

(

n

= 62)

Group B

(

n

= 62)

Group C

(

n

= 62)

Group D

(

n

= 62)

χ

2

p

-value

Acute myocardial

infarction

1

5

8

10

8.488 0.037

Congestive heart

failure

1

3

2

2

1.033 0.793

Ischaemic stroke

1

1

1

1

0.000 1.000

Peripheral artery

occlusion

2

2

1

1

0.683 0.877

Recurrent angina

3

3

1

1

2.067 0.559

Severe arrhythmia

2

3

6

10

8.064 0.045

Cardiac death

2

4

8

11

8.674 0.034

Total

12

21

27

36 20.803 < 0.001

NLR: neutrophil-to-lymphocyte ratio.

Time (month)

Group A

Group B

Group C

Group D

0

0

20

20

40

60

80

100

40

60

Survival rate (%)

Fig. 1.

Survival analysis of patients with different NLR values

undergoing MACE. MACE: major adverse cardiovas-

cular event; NLR: neutrophil-to-lymphocyte ratio.

Sensitivity

1 - Specificity

1.0

1.0

0.8

0.8

0.6

0.6

0.4

0.4

0.2

0.2

0.0

0.0

Fig. 2.

Predictive value of NLR for MACE. MACE: major

adverse cardiovascular event; NLR: neutrophil-to-

lymphocyte ratio.