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Inicio Medicina Clínica Coronary heart disease and COVID-19: A meta-analysis
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Vol. 156. Núm. 11.
Páginas 547-554 (junio 2021)
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Vol. 156. Núm. 11.
Páginas 547-554 (junio 2021)
Original article
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Coronary heart disease and COVID-19: A meta-analysis
Cardiopatía coronaria y COVID-19: metaanálisis
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Chendi Lianga, Weijun Zhangb, Shuzhen Lic, Gang Qinb,
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13834143738@126.com

Corresponding author.
a Shanxi Medical University, Taiyuan, Shanxi, China
b Department of Cardiology, First Hospital of Shanxi Medical University, Taiyuan, Shanxi, China
c Baoan District Center for Disease Control and Prevention, Shenzhen, Guangdong, China
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Table 1. Basic characteristics of the included studies.
Abstract
Objective

Since the World Health Organization (WHO) announced coronavirus disease 2019 (COVID-19) had become a global pandemic on March 11, 2020, the number of infections has been increasing. The purpose of this meta-analysis was to investigate the prognosis of COVID-19 in patients with coronary heart disease.

Method

Pubmed, Embase, and Cochrane Library databases were searched to collect the literature concerning coronary heart disease and COVID-19. The retrieval time was from inception to Nov 20, 2020, using Stata version 14.0 for meta-analysis.

Results

A total of 22,148 patients from 40 studies were included. The meta-analysis revealed that coronary heart disease was associated with poor prognosis of COVID-19 (OR=3.42, 95%CI [2.83, 4.13], P<0.001). After subgroup analysis, coronary heart disease was found to be related to mortality (OR=3.75, 95%CI [2.91, 4.82], P<0.001), severe/critical COVID-19 (OR=3.23, 95%CI [2.19, 4.77], P<0.001), ICU admission (OR=2.25, 95%CI [1.34, 3.79], P=0.002), disease progression (OR=3.01, 95%CI [1.46, 6.22], P=0.003); Meta-regression showed that the association between coronary heart disease and poor prognosis of COVID-19 was affected by hypertension (P=0.004), and subgroup analysis showed that compared with the proportion of hypertension >30% (OR=2.85, 95%CI [2.33, 3.49]), the proportion of hypertension <30% (OR=4.78, 95%CI [3.50, 6.51]) had a higher risk of poor prognosis.

Conclusion

Coronary heart disease is a risk factor for poor prognosis in patients with COVID-19.

Keywords:
Coronary heart disease
COVID-19
Meta-analysis
Resumen
Objetivo

Desde que la Organización Mundial de la Salud (OMS) anunció que la enfermedad por coronavirus de 2019 (COVID-19) se había convertido en una pandemia global el 11 de marzo de 2020, se ha incrementado el número de infecciones. El objetivo de este metaanálisis fue investigar el pronóstico de la COVID-19 en pacientes con cardiopatía coronaria.

Método

Se realizó una búsqueda en las bases de datos de Pubmed, Embase y Cochrane Library para reunir la literatura relativa a cardiopatía coronaria y COVID-19. El tiempo de recuperación de datos fue desde el inicio hasta el 20 de noviembre de 2020, utilizando la versión 14.0 de Stata® para el metaanálisis.

Resultados

Se incluyó un total de 22.148 pacientes de 40 estudios. El metaanálisis reveló que la cardiopatía coronaria estaba asociada a un mal pronóstico de COVID-19 (OR: 3,42; IC 95%: 2,83-4,13; p<0,001). Tras el análisis de subgrupo, se encontró que la cardiopatía coronaria tenía relación con la mortalidad (OR: 3,75; IC 95%: 2,91-4,82; p<0,001), COVID-19 grave/crítica (OR: 3,23; IC 95%: 2,19-4,77; p<0,001), ingreso en la UCI (OR: 2,25; IC 95%: 1,34-3,79; p=0,002), progresión de la enfermedad (OR: 3,01; IC 95%: 1,46-6,22; p=0,003). La metarregresión reflejó que la asociación entre cardiopatía coronaria y mal pronóstico de la COVID-19 estaba influida por la hipertensión (p=0,004), y el análisis de subgrupo mostró que comparada con la proporción de hipertensión >30% (OR: 2,85; IC 95%: 2,33-3,49), la proporción de hipertensión <30% (OR: 4,78; IC 95%: 3,50-6,51) tenía mayor riesgo de mal pronóstico.

Conclusión

La cardiopatía coronaria es un factor de riesgo de mal pronóstico en pacientes con COVID-19.

Palabras clave:
Cardiopatía coronaria
COVID-19
Metaanálisis
Texto completo
Introduction

After the first case of coronavirus disease 2019 (COVID-19) was discovered in Wuhan, Hubei Province, China on December 8, 2019. As of November 27, 2020, a total of 61,452,584 cases have been confirmed globally, resulting in 1,440,629 deaths.1 Pathogens were severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the main manifestation were flu-like symptoms and could develop into severe respiratory failure, shock, or multiple organ failure.2,3 COVID-19 patients with underlying diseases such as diabetes, hypertension, and chronic obstructive pulmonary disease have a poor prognosis.4 However, the relationship between coronary heart disease and the prognosis of COVID-19 is still unknown. Many observational studies had been conducted to explore the factors associated with the poor prognosis of COVID-19 patients, but most of them were small sample sizes. Therefore, the purpose of this meta-analysis was to search the association between coronary heart disease and the prognosis of COVID-19 patients.

Materials and methods

The work followed PRISMA statement for systematic reviews and meta-analysis.

Search strategy

Pubmed, Embase, and Cochrane Library databases were used for literature retrieval from inception to Nov 20, 2020. The search strategy in Pubmed was: 1.((((((((((((((((((“Coronary Disease”[Mesh]) OR (“Coronary Disease”)) OR (“Coronary Diseases”)) OR (“Disease, Coronary”)) OR (“Diseases, Coronary”)) OR (“Coronary Heart Disease”)) OR (“CHD”)) OR (“Coronary Heart Diseases”)) OR (“Disease, Coronary Heart”)) OR (“Diseases, Coronary Heart”)) OR (“Heart Disease, Coronary”)) OR (“Heart Diseases, Coronary”)) OR (“Coronary Artery Disease”)) OR (“CAD”)) OR (“Artery Disease, Coronary”)) OR (“Artery Diseases, Coronary”)) OR (“Coronary Artery Diseases”)) OR (“Disease, Coronary Artery”)) OR (“Diseases, Coronary Artery”); 2.((((“COVID-19”) OR (“Coronavirus disease 2019”)) OR (“2019 novel coronavirus”)) OR (“2019-nCoV”)) OR (“SARS-CoV-2”); 3.1 ADN 2.

Inclusion and exclusion criteria

The definition of coronary heart disease in this meta-analysis were those reported in the relevant articles as coronary artery disease (CAD), coronary heart disease (CHD), or coronary disease.

Inclusion criteria: (1) The selected population was COVID-19 patients; (2) The primary outcome of the study included disease progression, severe/critical COVID-19, ICU admission, and mortality; (3) The study design should be a case–control, cross-sectional, or cohort study with detailed data of coronary heart disease for analysis; (4) The language of the study was limited to English.

Exclusion criteria: (1) Letters, comments, reviews, conference abstracts; (2)Studies describing only the children were excluded, but studies that involved both children and adults were included;

The definition of severe/critical COVID-19 was based on Diagnosis and treatment protocol for COVID-19.5

Data extraction and quality assessment

Two authors scanned the title and abstract independently to exclude irrelevant studies, and the full-text articles were read to screen out eligible studies. Two authors independently completed the data extraction and collected the basic information of the included studies (author, study design, sample size, gender, hypertension, CHD/CAD, heart failure, primary outcome, etc.). Newcastle – Ottawa (NOS) scale was used for quality assessment.6 Any differences were resolved by the third author.

Statistical analysis

Stata version 14.0 was used for meta-analysis. The pooled odds ratio (OR) with 95% confidence interval (95% CI) was calculated to evaluate the relationship between coronary heart disease and the prognosis of COVID-19. P-value <0.05 was statistically significant. Heterogeneity was assessed with I2, if the heterogeneity was significant (I2>50%), the random effect model was used. A sensitivity analysis was performed by removing outlier studies, meta-regression was used to explore the source of heterogeneity. Subgroup analysis was performed based on the primary outcome and meta-regression results (P-value <0.05). We used the funnel plot and Egger test to evaluate publication bias, when the funnel plot was symmetrical and the P-value of Egger test >0.05, publication bias was accepted. If publication bias was present, the trim and fill method was used to correct for funnel plot asymmetry caused by the publication bias and to recalculate the pooled odds ratio.

ResultsThe basic characteristics of the included studies

A total of 2246 articles were searched in the electronic database, 363 duplicate articles were excluded, 1619 articles were excluded after reading the title and abstract, 224 articles were excluded after scanning the full-text. Finally, 40 articles were involved. The literature screening process was shown in Fig. 1.

Fig. 1.

Flow chart of the screening process.

(0.28MB).

The 40 studies included 22 case–control studies, 17 cohort studies, and 1 cross-sectional study, involving 22,148 COVID-19 patients. According to the primary outcome of the study, they were divided into disease progression, severe/critical COVID-19, ICU admission, or mortality. The primary outcomes of 4 studies were ICU admission, 22 studies were mortality, 11 studies were severe/critical COVID-19, and 3 studies were disease progression. See Table 1 for the basic characteristics of the studies.

Table 1.

Basic characteristics of the included studies.

Author  Study design  Sample (nOverall age (Mean/Median) (years)  Male (%)  HTN (%)  HF (%)  CHD/CAD (%)  Primary outcome  NOS score 
Aladağ,7  Case–control  50 (15 vs. 35)  68 (68 vs. 68)  56 (40 vs. 62.86)  72 (73.33 vs. 71.43)  40 (26.67 vs. 45.71)  44 (46.67 vs. 42.86)  Mortality  7 (3/1/3) 
Barman,8  Case–control  607 (103 vs. 504)  –  55 (59 vs. 54)  44 (58 vs. 40)  –  19 (38 vs. 15)  Mortality  7 (3/1/3) 
Bruce,9  Case–control  1222 (358 vs. 864)  –  56.5 (29.9 vs. 70.1)  50.5 (56.3 vs. 48)  –  22.4 (30.1 vs. 19.3)  Mortality  7 (3/1/2) 
Cen,10  Cohort  964 (244 vs. 720)  –  47.9 (58.6 vs. 44.3)  25.9 (43 vs. 21.3)  –  5.7 (9.8 vs. 4.3)  Progression  6 (3/0/3) 
Chen,11  Case–control  1578 (903 vs. 675)  –  48.8 (49.8 vs. 47.4)  31.2 (35.3 vs. 25.6)  –  6.6 (9 vs. 3.4)  Severe/Critical  6 (3/0/3) 
Ciceri,12  Cohort  410 (95 vs. 315)  –  72.9 (73.7 vs. 72.7)  49.9 (69.9 vs. 43.9)  –  12.6 (27.2 vs. 8.3)  Mortality  6 (3/1/2) 
Cipriani,13  Case–control  109 (20 vs. 89)  71 (86 vs. 69)  67 (50 vs. 70.8)  62.4 (80 vs. 58.4)  14.7 (25 vs. 12.4)  16.5 (45 vs. 10.1)  Mortality  7 (3/1/3) 
Deng,14  Cohort  264 (52 vs. 212)  64.5 (74.5 vs. 62.5)  49.2 (63.5 vs. 45.8)  37.9 (51.9 vs. 34.4)  –  12.1 (34.6 vs. 6.6)  Mortality  6 (3/0/3) 
Gu,15  Case–control  275 (94 vs. 181)  66.4 (70.7 vs. 64.2)  62.9 (59.6 vs. 64.6)  39.6 (44.7 vs. 37)  8 (10.6 vs. 6.6)  14.5 (26.6 vs. 8.3)  Mortality  8 (4/1/3) 
Gupta,16  Cohort  200 (32 vs. 168)  –  57 (62.4 vs. 57.1)  23 (34.4 vs. 20.8)  –  4.5 (9.4 vs. 3.6)  ICU  7 (3/1/3) 
Gupta,17  Cohort  2215 (784 vs. 1431)  60.5 (66 vs. 57.4)  64.8 (68.4 vs. 62.9)  59.7 (68.9 vs. 54.6)  8.8 (12.2 vs. 7)  13 (20.2 vs. 9.1)  Mortality  6 (3/0/3) 
Hewitt,18  Cohort  1564 (425 vs. 1139)  –  57.7 (60 vs. 56.9)  51.6 (56.4 vs. 49.8)  –  22.1 (31.3 vs. 18.7)  Mortality  6 (3/1/2) 
Huang,19  Cohort  299 (16 vs. 283)  53.4 (69.2 vs. 52.5)  53.5 (68.8 vs. 52.7)  24.7 (68.8 vs. 22.3)  –  6 (25 vs. 4.9)  Mortality  7 (3/1/3) 
Iaccarino,20  Cross–sectional  1591 (188 vs. 1403)  66.5 (79.6 vs. 64.7)  64 (66.5 vs. 63.6)  54.9 (72.9 vs. 52.5)  11.8 (30.3 vs. 9.3)  13.6 (29.8 vs. 11.4)  Mortality  7 (3/1/3) 
Islam,21  Cohort  1016 (25 vs. 991)  –  64.1 (76 vs. 63.8)  14.3 (36 vs. 13.7)  –  3.9 (16 vs. 3.6)  Mortality  7 (3/1/3) 
Jackson,22  Cohort  297 (51 vs. 246)  –  49.8 (56.9 vs. 48.4)  67.7 (86.3 vs. 63.8)  10.8 (9.8 vs. 11)  11.1 (19.6 vs. 9.3)  Mortality  7 (3/1/3) 
Lagi,23  Case–control  84 (16 vs. 68)  62 (67 vs. 62)  65.5 (87.5 vs. 60.3)  36.9 (31.3 vs. 38.2)  –  14.3 (31.3 vs. 10.3)  ICU  7 (3/1/3) 
Lee,24  Case–control  694 (137 vs. 557)  –  30.5 (41.6 vs. 27.8)  18.9 (44.6 vs. 22.4)  1.4 (4 vs. 1.6)  2.4 (5.9 vs. 2.9)  Severe/Critical  6 (3/0/3) 
Lendorf,25  Cohort  111 (20 vs. 91)  68 (64 vs. 69)  60.4 (85 vs. 54.9)  34.2 (45 vs. 31.9)  7.2 (5 vs. 7.7)  17.1 (15 vs. 17.6)  ICU  6 (3/0/3) 
Li,26  Case–control  74 (14 vs. 60)  66 (71 vs. 62)  59.5 (78.6 vs. 55)  47.3 (71.4 vs. 41.7)  –  8.1 (28.6 vs. 3.3)  Mortality  7 (3/1/3) 
Liao,27  Case–control  148 (56 vs. 92)  –  50 (53.6 vs. 47.8)  20.3 (23.2 vs. 18.5)  –  4.7 (7.1 vs. 3.3)  Progression  8 (3/2/3) 
Liu,28  Cohort  2044 (957 vs. 1087)  –  48.9 (54.9 vs. 43.7)  39.7 (47.5 vs. 32.9)  –  9.8 (12.6 vs. 7.3)  Severe/Critical  6 (3/1/2) 
Liu,29  Cohort  84 (23 vs. 61)  53 (67 vs. 51)  56 (69.6 vs. 50.8)  19 (43.5 vs. 9.8)  –  9.5 (26.1 vs. 3.3)  Progression  8 (3/2/3) 
Maeda,30  Cohort  224 (57 vs. 167)  –  56.7 (54.4 vs. 57.5)  59.4 (73.7 vs. 54.5)  12.5 (16.1 vs. 11.4)  20.1 (31.6 vs. 16.2)  ICU  8 (3/2/3) 
Russo,31  Case–control  192 (35 vs. 157)  –  59.9 (57.1 vs. 60.5)  57.8 (77.1 vs. 53.5)  10.4 (17.1 vs. 8.9)  13.5 (28.6 vs. 10.2)  Mortality  7 (3/1/3) 
Serin,32  Case–control  2217 (68 vs. 2149)  –  –  20.6 (41.2 vs. 19.9)  –  7.4 (26.5 vs. 6.8)  Mortality  6 (3/0/3) 
Shang,33  Case–control  113 (49 vs. 64)  66 (73 vs. 62)  64.6 (73.5 vs. 57.8)  44.2 (53.1 vs. 37.5)  –  24.8 (40.8 vs. 12.5)  Mortality  7 (3/1/3) 
Shi,34  Case–control  671 (62 vs. 609)  63 (74 vs. 61)  48 (56.5 vs. 47.1)  29.7 (59.7 vs. 26.6)  3.3 (21 vs. 1.5)  8.9 (33.9 vs. 6.4)  Mortality  6 (3/0/3) 
Sun,35  Case–control  336 (26 vs. 310)  50 (65 vs. 48)  52.8 (76.9 vs. 50.8)  23.6 (42.3 vs. 22)  –  5.1 (19.2 vs. 3.9)  Severe/Critical  6 (3/0/3) 
Turagam,36  Cohort  140 (52 vs. 88)  61 (71 vs. 58)  72.9 (73.1 vs. 72.7)  61.4 (67.3 vs. 58)  15.7 (21.2 vs. 12.5)  25 (25 vs. 25)  Mortality  7 (3/1/3) 
Wang,37  Case–control  85 (39 vs. 46)  59.4 (65.1 vs. 53.6)  52.9 (69.2 vs. 39.1)  25.9 (41 vs. 13)  –  10.6 (20.5 vs. 2.2)  Severe/Critical  6 (3/0/3) 
Wang,38  Cohort  340 (33 vs. 307)  –  48.2 (63.6 vs. 46.6)  15.6 (39.4 vs. 13)  –  3.8 (24.2 vs. 1.6)  Mortality  7 (3/1/3) 
Wei,39  Cohort  276 (14 vs. 262)  51 (65 vs. 50)  56.2 (71.4 vs. 55.3)  17 (57.1 vs. 14.9)  –  4 (28.6 vs. 5.2)  Severe/Critical  7 (3/1/3) 
Xie,40  Case–control  62 (24 vs. 38)  –  43.5 (54.2 vs. 36.8)  38.7 (62.5 vs. 23.7)  3.2 (8.3 vs. 0)  11.3 (25 vs. 2.6)  Severe/Critical  7 (3/1/3) 
Xiong,41  Case–control  116 (55 vs. 61)  58.5 (64 vs. 56)  69 (69.1 vs. 68.9)  38.8 (47.3 vs. 31.1)  –  14.7 (23.6 vs. 6.6)  Severe/Critical  7 (3/1/3) 
Xu,42  Case–control  88 (41 vs. 47)  –  40.9 (36.6 vs. 44.7)  26.1 (31.7 vs. 21.3)  –  8 (9.8 vs. 6.4)  Severe/Critical  6 (3/0/3) 
Yuan,43  Case–control  117 (56 vs. 61)  –  47.9 (46.4 vs. 49.2)  34.2 (41.1 vs. 27.9)  –  9.4 (12.5 vs. 6.6)  Severe/Critical  8 (3/2/3) 
Zhang,44  Case–control  541 (359 vs. 182)  –  47.1 (50.1 vs. 41.2)  23.1 (28.4 vs. 12.6)  –  7.6 (10 vs. 2.7)  Severe/Critical  6 (3/0/3) 
Zhao,45  Case–control  539 (125 vs. 414)  58 (70 vs. 54)  47.3 (56.8 vs. 44.4)  26 (49.6 vs. 18.8)  –  6.9 (16 vs. 4.1)  Mortality  6 (3/0/3) 
Zhou,46  Cohort  191 (54 vs. 137)  56 (69 vs. 52)  62.3 (70.4 vs. 59.1)  30.4 (48.1 vs. 23.4)  –  7.9 (24.1 vs. 1.5)  Mortality  7 (3/1/3) 

Abbreviations: HTN, hypertension; HF, heart failure; CAD, coronary artery disease; CHD, coronary heart disease.

The NOS scores of the 40 included studies were ≥6. (See Table 1).

Coronary heart disease and outcome

The meta-analysis showed coronary heart disease was associated with poor prognosis of COVID-19 (OR=3.42, 95%CI [2.83, 4.13], P<0.001; I2=62.4%, P<0.001). (See Fig. 2).

Fig. 2.

Forest plot of the relationship between coronary heart disease and the prognosis of COVID-19.

(0.57MB).
Coronary heart disease and mortality

22 studies reported significant differences between coronary heart disease and mortality in COVID-19 patients (OR=3.75, 95%CI [2.91, 4.82], P<0.001), with moderately high heterogeneity (I2=73.1%, P<0.001). (See Fig. 2). A sensitivity analysis was carried out to exclude the study by Bruce,9 Gupta,17 Hewitt,18 Turagam,36 and Wang,38 resulting in a pooled odds ratio of 4.40 [3.56, 5.44; P<0.001] with low heterogeneity between studies [I2=25.5%, P=0.161].

Coronary heart disease and severe/critical COVID-19

11 studies reported significant differences between coronary heart disease and severe/critical COVID-19 (OR=3.23, 95%CI [2.19, 4.77], P<0.001), with moderate heterogeneity (I2=45.3%, P=0.05). (See Fig. 2). A sensitivity analysis was carried out to exclude the studies by Liu,28 and Wei,39 resulting in a pooled OR of 3.20 [2.31, 4.43; P<0.001] with no heterogeneity between studies [I2=0.0%, P=0.595].

Coronary heart disease and ICU admission

4 studies reported significant differences between coronary heart disease and ICU admission in COVID-19 patients (OR=2.25, 95%CI [1.34, 3.79], P=0.002), with no heterogeneity (I2=0.0%, P=0.393). (See Fig. 2).

Coronary heart disease and disease progression

3 studies reported significant differences between coronary heart disease and disease progression in COVID-19 patients (OR=3.01, 95%CI [1.46, 6.22], P=0.003), with low heterogeneity (I2=24.4%, P=0.266). (See Fig. 2).

Meta-regression

Due to the significant heterogeneity between coronary heart disease and poor prognosis of COVID-19 (I2=62.4%, P<0.001), we separately conducted meta-regression of study design, sample size, overall age, gender, heart failure, hypertension, and quality score to search for the source of heterogeneity. Results showed that the association between coronary heart disease and poor prognosis of COVID-19 was affected by hypertension (P=0.004), but not study design (P=0.543), sample size (P=0.103), age (P=0.121), gender (P=0.836), heart failure (P=0.120), and quality score (P=0.924).

Subgroup analysis

Meta-regression showed that hypertension (P=0.004) was the source of heterogeneity, subgroup analysis showed that compared with the proportion of hypertension >30% (OR=2.85, 95%CI [2.33, 3.49]), the proportion of hypertension <30% (OR=4.78, 95%CI [3.50, 6.51]) had a higher risk of poor prognosis. (See Fig. 3).

Fig. 3.

Subgroup analysis based on meta-regression results.

(0.6MB).
Publication bias

Because the funnel plot was asymmetric and the P-value of the Egger test <0.05, there was a publication bias in the relationship between coronary heart disease and the prognosis of COVID-19. Therefore, the trim and fill method was used to correct for funnel plot asymmetry caused by the publication bias. After adding the 10 missing hypothetical studies, the redrawn funnel plot was symmetrical and recalculated the pooled odds ratio showed that coronary heart disease was associated with poor prognosis of COVID-19 (OR=2.78, 95%CI [2.29, 3.38], P<0.001). (See Fig. 4).

Fig. 4.

Publication bias analysis. (A) For the relationship between coronary heart disease and prognosis of COVID-19, a funnel plot was used to qualitatively assess publication bias. (B) For the relationship between coronary heart disease and prognosis of COVID-19, the Egger test was used to quantitatively assess publication bias (P<0.001). (C) Trim and fill funnel plot was symmetrical after addition of 10 missing hypothetical studies.

(0.2MB).
Discussion

We included a total of 40 studies in our meta-analysis, which showed that coronary heart disease was associated with poor prognosis of COVID-19, with statistically significant outcomes for mortality, disease progression, severe/critical COVID-19, and ICU admission. After correcting for publication bias, recalculation of pooled odds ratio showed that coronary heart disease was still associated with poor prognosis of COVID-19 (OR=2.78, 95%CI [2.29, 3.38], P<0.001).

At the same time, we used meta-regression to explore the source of heterogeneity. When study design, sample size, overall age, gender, heart failure, hypertension and quality score were analyzed, it found that hypertension (P=0.004) influenced the association between coronary heart disease and poor prognosis of COVID-19. Subgroup analysis showed that compared with the proportion of hypertension >30% (OR=2.85, 95%CI [2.33, 3.49]), the proportion of hypertension <30% (OR=4.78, 95%CI [3.50, 6.51]) had a higher risk of poor prognosis.

As the primary receptor for SARS-CoV-2 to enter target cells, angiotensin-converting enzyme 2 (ACE2) is found in lung cells, heart cells, renal epithelial cells, intestinal mucosal cells, immune cells, and cerebral neuronal cells, etc.3 SARS-CoV-2 can invade human cells through the interaction between spike protein and the extracellular domain of ACE2, and induce cytokine storm by down-regulating ACE2 on the infected cellular surface in various ways.47 However, the imbalance between ACE and ACE2 in lung and myocardial tissues, which is manifested as the increase of ACE activity and the decrease of ACE2 activity, can induce myocardial inflammation and acute respiratory distress syndrome.48,49 Chen50 found that the high expression of ACE2 in pericytes might be the target of SARS-CoV-2 invading cardiac cells, which could cause the dysfunction of capillary endothelial cells and induced the disorder of micro-circulation. The myocardial inflammation and microvascular dysfunction caused by SARS-CoV-2 will aggravate the imbalance between cardiac reserve and metabolic demand in patients with coronary heart disease, further promote the rupture of coronary plaques.49 This may be the reason why COVID-19 patients with coronary heart disease are more likely to have a poor prognosis.

The use of angiotensin receptor blocker (ARB) and angiotensin-converting enzyme inhibitor (ACEI) in animal experiments can reduce lung injury caused by SARS-COV infection. But on the other hand, the use of large doses of ACEI/ARB can up-regulate ACE2 expression in animal studies, thereby arising concern about whether ACEI/ARB can increase the risk of COVID-19.51 Feng et al.52 included a multicenter study and found that COVID-19 patients taking ACEI/ARB were more in the moderate group than severe and the critical group. Meng et al.53 included 42 COVID-19 patients with hypertension to evaluate the effect of ACEI/ARB and found ACEI/ARB could reduce inflammatory response by inhibiting the level of IL-6 in peripheral blood. Besides, Meng et al.53 also found ACEI/ARB could reduce the peak viral load and increased the count of CD3 and CD8 T cells in peripheral blood to avoid the consumption of peripheral T cells. This evidence supports that ACEI/ARB can improve the prognosis of COVID-19 patients with hypertension. Our meta-analysis showed a higher proportion of hypertension among COVID-19 patients with coronary heart disease seemed to have a better prognosis. The possible reason was the use of ACEI/ARB drugs in patients with hypertension. Unfortunately, due to the limitation of data, the association between COVID-19 patients with coronary heart disease and ACEI/ARB drugs was not analyzed. The influence of ACEI/ARB on the prognosis of COVID-19 patients still needs further study.

In conclusion, people with pre-existing coronary heart disease are more likely to have more severe COVID-19 disease, as compared to people without coronary heart disease. The association is affected by hypertension. Therefore, people with coronary heart disease should pay more attention to self-prevention to avoid infection with the virus, and doctors should also give more notice to COVID-19 patients with coronary heart disease to avoid the occurrence of adverse events.

Limitations

The restrictions of this meta-analysis are as follows: 1. The factors of coronary heart disease included in this analysis were simply combined with the data without adjusting the confounding factors; 2. Due to the limitation of data, the association between COVID-19 patients with coronary heart disease and ACEI/ARB drugs was not analyzed.

Conclusion

Coronary heart disease is a risk factor for poor prognosis in COVID-19 patients. The relationship was more powerful in studies with a lower proportion of hypertensive patients.

Funding

This work was supported by special projects for the guidance of the transformation of scientific and technological achievements in Shanxi Province (Project number: 201804D131045) and the transformation and cultivation projects of scientific and technological achievements in colleges and universities of Shanxi Province (Project number: 2020CG028).

Author contributions

GQ proposed and designed the study. CDL and WJZ contributed to literature research and data extraction. CDL performed statistical analysis. CDL and WJZ drafted the manuscript. SZL played a guiding role in this meta-analysis. GQ contributed to the revision of the manuscript and determined the final version.

Conflicts of interest

None declared.

References
[1]
Coronavirus update (Live): 61,452,584 Cases and 1,440,629 Deaths from COVID-19 Virus Pandemic – Worldometer.
(2020),
[2]
S.E. Park.
Epidemiology, virology, and clinical features of severe acute respiratory syndrome – coronavirus-2 (SARS-CoV-2; Coronavirus Disease-19).
Clin Exp Pediatr, 63 (2020), pp. 119-124
[3]
A.O. Docea, A. Tsatsakis, D. Albulescu, O. Cristea, O. Zlatian, M. Vinceti, et al.
A new threat from an old enemy: re-emergence of coronavirus (Review).
Int J Mol Med, 45 (2020), pp. 1631-1643
[4]
B. Wang, R. Li, Z. Lu, Y. Huang.
Does comorbidity increase the risk of patients with COVID-19: evidence from meta-analysis.
Aging (Albany NY), 12 (2020), pp. 6049-6057
[5]
National Health Commission of the People's Republic of China.
Diagnosis and treatment protocol for COVID-19 (trial version 7).
Infect Dis Inf, 33 (2020), pp. 1-6
[6]
A. Stang.
Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses.
Eur J Epidemiol, 25 (2010), pp. 603-605
[7]
N. Aladağ, R.D. Atabey.
The role of concomitant cardiovascular diseases and cardiac biomarkers for predicting mortality in critical COVID-19 patients.
[8]
H.A. Barman, A. Atici, I. Sahin, G. Alici, E. Aktas Tekin, Ö.F. Baycan, et al.
Prognostic significance of cardiac injury in COVID-19 patients with and without coronary artery disease.
Coron Artery Dis, (2020),
[9]
E. Bruce, F. Barlow-Pay, R. Short, A. Vilches-Moraga, A. Price, A. McGovern, et al.
Prior routine use of non-steroidal anti-inflammatory drugs (NSAIDs) and important outcomes in hospitalised patients with COVID-19.
J Clin Med, 9 (2020), pp. 2586
[10]
Y. Cen, X. Chen, Y. Shen, X.H. Zhang, Y. Lei, C. Xu, et al.
Risk factors for disease progression in patients with mild to moderate coronavirus disease 2019 – a multi-centre observational study.
Clin Microbiol Infect, 26 (2020), pp. 1242-1247
[11]
Y. Chen, Y. Ke, X. Liu, Z. Wang, R. Jia, W. Liu, et al.
Clinical features and antibody response of patients from a COVID-19 treatment hospital in Wuhan, China.
J Med Virol, (2020),
[12]
F. Ciceri, A. Castagna, P. Rovere-Querini, F. De Cobelli, A. Ruggeri, L. Galli, et al.
Early predictors of clinical outcomes of COVID-19 outbreak in Milan, Italy.
Clin Immunol, 217 (2020), pp. 108509
[13]
A. Cipriani, F. Capone, F. Donato, L. Molinari, D. Ceccato, A. Saller, et al.
Cardiac injury and mortality in patients with Coronavirus disease 2019 (COVID-19): insights from a mediation analysis.
Intern Emerg Med, 27 (2020), pp. 1-9
[14]
P. Deng, Z. Ke, B. Ying, B. Qiao, L. Yuan.
The diagnostic and prognostic role of myocardial injury biomarkers in hospitalized patients with COVID-19.
Clin Chim Acta, 510 (2020), pp. 186-190
[15]
T. Gu, Q. Chu, Z. Yu, B. Fa, A. Li, L. Xu, et al.
History of coronary heart disease increased the mortality rate of patients with COVID-19: a nested case–control study.
BMJ Open, 10 (2020), pp. e038976
[16]
N. Gupta, P. Ish, R. Kumar, N. Dev, S.R. Yadav, N. Malhotra, et al.
Evaluation of the clinical profile, laboratory parameters and outcome of two hundred COVID-19 patients from a tertiary centre in India.
Monaldi Arch Chest Dis, (2020), pp. 90
[17]
S. Gupta, S.S. Hayek, W. Wang, L. Chan, K.S. Mathews, M.L. Melamed, et al.
Factors associated with death in critically ill patients with coronavirus disease 2019 in the US.
JAMA Intern Med, 180 (2020), pp. 1-12
[18]
J. Hewitt, B. Carter, A. Vilches-Moraga, T.J. Quinn, P. Braude, A. Verduri, et al.
The effect of frailty on survival in patients with COVID-19 (COPE): a multicentre, European, observational cohort study.
Lancet Public Health, 5 (2020), pp. e444-e451
[19]
J. Huang, A. Cheng, R. Kumar, Y. Fang, G. Chen, Y. Zhu, et al.
Hypoalbuminemia predicts the outcome of COVID-19 independent of age and co-morbidity.
J Med Virol, 92 (2020), pp. 2152-2158
[20]
G. Iaccarino, G. Grassi, C. Borghi, C. Ferri, M. Salvetti, M. Volpe.
Age and multimorbidity predict death among COVID-19 patients: results of the SARS-RAS study of the Italian society of hypertension.
Hypertension, 76 (2020), pp. 366-372
[21]
M.Z. Islam, B.K. Riaz, A.N.M.S. Islam, F. Khanam, J. Akhter, R. Choudhury, et al.
Risk factors associated with morbidity and mortality outcomes of COVID-19 patients on the 28th day of the disease course: a retrospective cohort study in Bangladesh.
Epidemiol Infect, 148 (2020), pp. e263
[22]
B.R. Jackson, J.A.W. Gold, P. Natarajan, J. Rossow, R. Neblett Fanfair, J. da Silva, et al.
Predictors at admission of mechanical ventilation and death in an observational cohort of adults hospitalized with COVID-19.
Clin Infect Dis, (2020),
[23]
F. Lagi, M. Piccica, L. Graziani, I. Vellere, A. Botta, M. Tilli, et al.
Early experience of an infectious and tropical diseases unit during the coronavirus disease (COVID-19) pandemic, Florence, Italy, February to March 2020.
Euro Surveill, 25 (2020), pp. 2000556
[24]
J.Y. Lee, S.W. Hong, M. Hyun, J.S. Park, J.H. Lee, Y.S. Suh, et al.
Epidemiological and clinical characteristics of coronavirus disease 2019 in Daegu, South Korea.
Int J Infect Dis, 98 (2020), pp. 462-466
[25]
M.E. Lendorf, M.K. Boisen, P.L. Kristensen, E.C.L. Løkkegaard, S.M. Krog, L. Brandi, et al.
Characteristics and early outcomes of patients hospitalised for COVID-19 in North Zealand, Denmark.
Dan Med J, 67 (2020),
[26]
J. Li, G. Xu, H. Yu, X. Peng, Y. Luo, C. Cao.
Clinical characteristics and outcomes of 74 patients with severe or critical COVID-19.
Am J Med Sci, 360 (2020), pp. 229-235
[27]
Y. Liao, Y. Feng, B. Wang, H. Wang, J. Huang, Y. Wu, et al.
Clinical characteristics and prognostic factors of COVID-19 patients progression to severe: a retrospective, observational study.
Aging (Albany NY), 12 (2020), pp. 18853-18865
[28]
D. Liu, P. Cui, S. Zeng, S. Wang, X. Feng, S. Xu, et al.
Risk factors for developing into critical COVID-19 patients in Wuhan, China: a multicenter, retrospective, cohort study.
E Clin Med, 25 (2020), pp. 100471
[29]
Y.P. Liu, G.M. Li, J. He, Y. Liu, M. Li, R. Zhang, et al.
Combined use of the neutrophil-to-lymphocyte ratio and CRP to predict 7-day disease severity in 84 hospitalized patients with COVID-19 pneumonia: a retrospective cohort study.
Ann Transl Med, 8 (2020), pp. 635
[30]
T. Maeda, R. Obata, D.O.D. Rizk, T. Kuno.
The association of interleukin-6 value, interleukin inhibitors, and outcomes of patients with COVID-19 in New York City.
J Med Virol, (2020),
[31]
V. Russo, M. Di Maio, E. Attena, A. Silverio, F. Scudiero, D. Celentani, et al.
Clinical impact of pre-admission antithrombotic therapy in hospitalized patients with COVID-19: a multicenter observational study.
Pharmacol Res, 159 (2020), pp. 104965
[32]
I. Serin, N.D. Sari, M.H. Dogu, S.D. Acikel, G. Babur, A. Ulusoy, et al.
A new parameter in COVID-19 pandemic: initial lactate dehydrogenase (LDH)/Lymphocyte ratio for diagnosis and mortality.
J Infect Public Health, 13 (2020), pp. 1664-1670
[33]
Y. Shang, T. Liu, Y. Wei, J. Li, L. Shao, M. Liu, et al.
Scoring systems for predicting mortality for severe patients with COVID-19.
E Clin Med, 24 (2020), pp. 100426
[34]
S. Shi, M. Qin, Y. Cai, T. Liu, B. Shen, F. Yang, et al.
Characteristics and clinical significance of myocardial injury in patients with severe coronavirus disease 2019.
Eur Heart J, 41 (2020), pp. 2070-2079
[35]
L. Sun, F. Song, N. Shi, F. Liu, S. Li, P. Li, et al.
Combination of four clinical indicators predicts the severe/critical symptom of patients infected COVID-19.
J Clin Virol, 128 (2020), pp. 104431
[36]
M.K. Turagam, D. Musikantow, M.E. Goldman, A. Bassily-Marcus, E. Chu, P. Shivamurthy, et al.
Malignant arrhythmias in patients with COVID-19: incidence, mechanisms, and outcomes.
Circ Arrhythm Electrophysiol, 13 (2020), pp. e008920
[37]
C.Z. Wang, S.L. Hu, L. Wang, M. Li, H.T. Li.
Early risk factors of the exacerbation of coronavirus disease 2019 pneumonia.
J Med Virol, 92 (2020), pp. 2593-2599
[38]
K. Wang, P. Zuo, Y. Liu, M. Zhang, X. Zhao, S. Xie, et al.
Clinical and laboratory predictors of in-hospital mortality in patients with coronavirus disease-2019: a cohort study in Wuhan, China.
Clin Infect Dis, 71 (2020), pp. 2079-2088
[39]
Y. Wei, W. Zeng, X. Huang, J. Li, X. Qiu, H. Li, et al.
Clinical characteristics of 276 hospitalized patients with coronavirus disease 2019 in Zengdu District, Hubei Province: a single-center descriptive study.
BMC Infect Dis, 20 (2020), pp. 549
[40]
Y. Xie, Q. You, C. Wu, S. Cao, G. Qu, X. Yan, et al.
Impact of cardiovascular disease on clinical characteristics and outcomes of coronavirus disease 2019 (COVID-19).
Circ J, 84 (2020), pp. 1277-1283
[41]
S. Xiong, L. Liu, F. Lin, J. Shi, L. Han, H. Liu, et al.
Clinical characteristics of 116 hospitalized patients with COVID-19 in Wuhan, China: a single-centered, retrospective, observational study.
BMC Infect Dis, 20 (2020), pp. 787
[42]
X. Xu, M.Q. Yu, Q. Shen, L.Z. Wang, R.D. Yan, M.Y. Zhang, et al.
Analysis of inflammatory parameters and disease severity for 88 hospitalized COVID-19 patients in Wuhan, China.
Int J Med Sci, 17 (2020), pp. 2052-2062
[43]
X. Yuan, W. Huang, B. Ye, C. Chen, R. Huang, F. Wu, et al.
Changes of hematological and immunological parameters in COVID-19 patients.
Int J Hematol, 112 (2020), pp. 553-559
[44]
J. Zhang, S. Lu, X. Wang, X. Jia, J. Li, H. Lei, et al.
Do underlying cardiovascular diseases have any impact on hospitalised patients with COVID-19?.
Heart, 106 (2020), pp. 1148-1153
[45]
Y. Zhao, H.X. Nie, K. Hu, X.J. Wu, Y.T. Zhang, M.M. Wang, et al.
Abnormal immunity of non-survivors with COVID-19: predictors for mortality.
Infect Dis Poverty, 9 (2020), pp. 108
[46]
F. Zhou, T. Yu, R. Du, G. Fan, Y. Liu, Z. Liu, et al.
Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study.
Lancet, 395 (2020), pp. 1054-1062
[47]
S. Groß, C. Jahn, S. Cushman, C. Bär, T. Thum.
SARS-CoV-2 receptor ACE2-dependent implications on the cardiovascular system: From basic science to clinical implications.
J Mol Cell Cardiol, 144 (2020), pp. 47-53
[48]
R.M. Wösten-van Asperen, R. Lutter, P.A. Specht, G.N. Moll, J.B. van Woensel, C.M. van der Loos, et al.
Acute respiratory distress syndrome leads to reduced ratio of ACE/ACE2 activities and is prevented by angiotensin-(1-7) or an angiotensin II receptor antagonist.
J Pathol, 225 (2011), pp. 618-627
[49]
T.Y. Xiong, S. Redwood, B. Prendergast, M. Chen.
Coronaviruses and the cardiovascular system: acute and long-term implications.
Eur Heart J, 41 (2020), pp. 1798-1800
[50]
L. Chen, X. Li, M. Chen, Y. Feng, C. Xiong.
The ACE2 expression in human heart indicates new potential mechanism of heart injury among patients infected with SARS-CoV-2.
Cardiovasc Res, 116 (2020), pp. 1097-1100
[51]
H. Kai, M. Kai.
Interactions of coronaviruses with ACE2, angiotensin II, and RAS inhibitors-lessons from available evidence and insights into COVID-19.
Hypertens Res, 43 (2020), pp. 648-654
[52]
Y. Feng, Y. Ling, T. Bai, Y. Xie, J. Huang, J. Li, et al.
COVID-19 with different severities: a multicenter study of clinical features.
Am J Respir Crit Care Med, 201 (2020), pp. 1380-1388
[53]
J. Meng, G. Xiao, J. Zhang, X. He, M. Ou, J. Bi, et al.
Renin-angiotensin system inhibitors improve the clinical outcomes of COVID-19 patients with hypertension.
Emerg Microbes Infect, 9 (2020), pp. 757-760
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