This editorial refers to ‘Association of hypertension and antihypertensive treatment with COVID-19 mortality: a retrospective observational study’, by C. Gao et al., on page 2058.

Arterial hypertension is the leading cause of death in the world and very frequently is accompanied by other comorbidities such as diabetes, obesity, chronic kidney disease (CKD), and established cardiovascular disease of different types. Patients suffering from infection by SARS-CoV2 frequently present arterial hypertension and these accompanying comorbidities. Data recently published have shown that the presence of associated conditions such as cardiovascular disease, diabetes, and hypertension increases the risk of COVID-19 complications in 45.4% of adults in the USA (see: https://medicalxpress.com/news/2020-04-percent-adults-complications-covid-.html). Similar percentages probably exist in Europe and are facilitated by the elevated age of the population that is accompanied by the highest prevalence of hypertension, cardiovascular disease, diabetes, and CKD. Data from China indicate that the situation differs because the percentage of subjects with COVID-19 older than 65 years is only ∼15%.1 However, the data contained in the article by Gao et al. in this issue of the European Heart Journal show that the mean age of deceased patients is 70.96 years.2 The data of Gao et al. show that hypertensive patients demonstrate a two-fold relative increase in the risk of COVID-19 mortality, particularly if they do not receive antihypertensive treatment. Therefore, these data confirm that the risk of death in the COVID-19 pandemic is particularly increased in hypertensive patients especially when advanced age is present, facilitated by cardiovascular comorbidities.2

Another aspect of interest in hypertensive patients is the presence of CKD that is frequently accompanied by the same comorbidities mentioned above and as a consequence by an increase in morbidity and mortality.3 Data on renal damage have not been reported frequently albeit acute kidney injury has been described in a small percentage of patients with severe consequences of SARS-CoV2 infection that was accompanied by a very high mortality.4 Thus, renal protection has to be considered to minimize the fatality rate in severe COVID-19 patients and this includes an adequate control of blood pressure.

It is well established that patients with arterial hypertension, diabetes, established cardiovascular disease, obesity, and CKD need to be treated with renin–angiotensin–aldosterone system (RAAS) blockers in order to attain an adequate blood pressure control and a simultaneous facilitation of prevention of organ damage in the heart, the brain, the vessels, and the kidneys (Figure 1). Thus, patients receiving this type of therapy who become infected by SARS-CoV2 theoretically should continue with this treatment to which drugs for COVID-19 should be added. However, some initial publications indicated that the use of angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) could be a potential risk factor for fatal COVID-19.5  ,  6 This concept was based on the fact that the angiotensin-converting enzyme 2 (ACE2) receptor permitted the entry of SARS-CoV2 into cells.7 The study by Gao et al. reviewing the association of hypertension and antihypertensive treatment with COVID-19 mortality shows that patients with RAAS blockers were not exposed to a higher risk of mortality.2 In fact, a relevant number of papers have demonstrated similar results, and professional scientific societies, in particular those devoted to arterial hypertension, and experts8  ,  9 have advised that ACEIs and ARBs should not be discontinued in patients infected by SARS-CoV2. Clinical trials are under way to test the safety and efficacy or RAAS blockers, including ACEIs and ARBs, in COVID-19 patients.8  ,  9 However, RAAS blockers, together with calcium channel blockers, beta-blockers, and diuretics, have been shown not to promote COVID-19 infection or its severity.10 Interestingly, a recent publication11 has considered that the early administration of the combination of a neprilysin inhibitor and an ARB (sacubitril/valsartan) could be useful in COVID-19 patients due to the anti-inflammatory properties of sacubitril. Another interesting aspect of the study by Gao et al. is that after pooling previously published data in a study-level meta-analysis, patients taking RAAS blockers were shown to be potentially associated with a decreased risk in mortality. A positive effect on the damage promoted by COVID-19 could be attributed to an elevated expression of ACE2 according to experimental data in animals.8 Therefore, studies investigating the potential good effects of RAAS blockers including mineralocorticoid receptor antagonists and sacubitril/valsartan are required, because it is not only the fact that we do not have to abandon RAAS blockers that patients were already receiving but the possibility that these drugs could be considered as a specific treatment for COVID-19 patients could be a reality. Furthermore, the withdrawal of RAAS blockers in these COVID-19 patients would increase the morbidity and mortality risk given the myocardial damage that may occur in COVID-19.12

Figure 1

Summary of the findings in the article of Gao et al.2 showing that in COVID-19 patients, RAAS blockers have to be continued to ensure maintained advantages for the brain, kidney, heart, and vessels of this type of therapy for which potential advantages over coagulation and consequences of COVID-19 could be obtained.

Finally, another positive aspect of RAAS blockers is their antithrombotic properties13  ,  14 that could ameliorate the frequent thrombotic or thrombo-embolic complications of COVID-19.15 In fact, hyperinflammation and derangement of the RAAS in COVID-19 could contribute to clinically suspected hypercoagulopathy and microvascular immunothrombosis14 (Figure 1).

In summary, as can be seen in Figure 1, the study Gao et al.2 contains data obtained in an adequately controlled retrospective analysis proving the absence of the need to withdraw RAAS blockers and opening the door for a specific indication to improve the prognosis of COVID-19 patients by different mechanisms and independently of the presence of elevated blood pressure.

Conflict of interest: none declared.

The opinions expressed in this article are not necessarily those of the Editors of the European Heart Journal or of the European Society of Cardiology.

Footnotes

doi:10.1093/eurheartj/ehaa433.

References

1

Guan
 
WJ
,
Ni
 
ZY
,
Hu
 
Y
,
Liang
 
WH
,
Ou
 
CQ
,
He
 
JX
,
Liu
 
L
,
Shan
 
H
,
Lei
 
CL
,
Hui
 
DSC
,
Du
 
B
,
Li
 
LJ
,
Zeng
 
G
,
Yuen
 
KY
,
Chen
 
RC
,
Tang
 
CL
,
Wang
 
T
,
Chen
 
PY
,
Xiang
 
J
,
Li
 
SY
,
Wang
 
JL
,
Liang
 
ZJ
,
Peng
 
YX
,
Wei
 
L
,
Liu
 
Y
,
Hu
 
YH
,
Peng
 
P
,
Wang
 
JM
,
Liu
 
JY
,
Chen
 
Z
,
Li
 
G
,
Zheng
 
ZJ
,
Qiu
 
SQ
,
Luo
 
J
,
Ye
 
CJ
,
Zhu
 
SY
,
Zhong
 
NS
,
China Medical Treatment Expert Group for Covid-19. Clinical characteristics of coronavirus disease 2019 in China
.
N Engl J Med
 
2020
;
382
:
1708
1720
.

2

Gao
 
C
,
Cai
 
Y
,
Zhang
 
K
,
Zhou
 
L
,
Zhang
 
Y
,
Zhang
 
X
,
Li
 
Q
,
Li
 
W
,
Yang
 
S
,
Zhao
 
X
,
Zhao
 
Y
,
Wang
 
H
,
Liu
 
Y
,
Yin
 
Z
,
Zhang
 
R
,
Wnag
 
R
,
Yang
 
M
,
Hui
 
C
,
Wijns
 
W
,
McEvoy
 
W
,
Soliman
 
O
,
Onuma
 
Y
,
Serruys
 
PW
,
Tao
 
L
,
Li
 
F.
 
Association of hypertension and antihypertensive treatment with COVID-19 mortality: a retrospective observational study
.
Eur Heart J
 
2020
;
41
:2058–2066.

3

Ruilope
 
LM
,
Bakris
 
GL.
 
Renal function and target organ damage in hypertension
.
Eur Heart J
 
2011
;
32
:
1599
604
.

4

Yang
 
X
,
Yu
 
Y
,
Xu
 
J
,
Shu
 
H
,
Xia
 
J
,
Liu
 
H
,
Wu
 
Y
,
Zhang
 
L
,
Yu
 
Z
,
Fang
 
M
,
Yu
 
T
,
Wang
 
Y
,
Pan
 
S
,
Zou
 
X
,
Yuan
 
S
,
Shang
 
Y.
 
Clinical course and outcomes of critically ill patients with SARS-CoV-2 pneumonia in Wuhan, China: a single-centered, retrospective, observational study
.
Lancet Respir Med
 
2020
;
8
:
475
481
.

5

Sommerstein
 
R
,
Kochen
 
MM
,
Messerli
 
FH
,
Gräni
 
C.
 
Coronavirus disease 2019 (COVID-19): do angiotensin-converting enzyme inhibitors/angiotensin receptor blockers have a biphasic effect?
 
J Am Heart Assoc
 
2020
;
9
:
e016509
.

6

Fang
 
L
,
Karakiulakis
 
G
,
Roth
 
M.
 
Are patients with hypertension and diabetes mellitus at increased risk for COVID-19 infection?
 
Lancet Respir Med
 
2020
;
8
:
e21
.

7

Zheng
 
YY
,
Ma
 
YT
,
Zhang
 
JY
,
Xie
 
X.
 
COVID-19 and the cardiovascular system
.
Nat Rev Cardiol
 
2020
;
17
:
259
260
.

8

Danser
 
AHJ
,
Epstein
 
M
,
Batlle
 
D.
 
Renin–angiotensin system blockers and the COVID-19 pandemic: at present there is no evidence to abandon renin–angiotensin system blockers
.
Hypertension
 
2020
;
75
:
1382
1385
.

9

Vaduganathan
 
M
,
Vardeny
 
O
,
Michel
 
T
,
McMurray
 
JJV
,
Pfeffer
 
MA
,
Solomon
 
SD.
 
Renin–angiotensin–aldosterone system inhibitors in patients with Covid-19
.
N Engl J Med
 
2020
;
382
:
1653
1659
.

10

Reynolds
 
HR
,
Adhikari
 
S
,
Pulgarin
 
C
,
Troxel
 
AB
,
Iturrate
 
E
,
Johnson
 
SB
,
Hausvater
 
A
,
Newman
 
JD
,
Berger
 
JS
,
Bangalore
 
S
,
Katz
 
SD
,
Fishman
 
GI
,
Kunichoff
 
D
,
Chen
 
Y
,
Ogedegbe
 
G
,
Hochman
 
JS.
 
Renin–angiotensin–aldosterone system inhibitors and risk of Covid-19
.
N Engl J Med
 
2020
;doi: 10.1056/NEJMoa2008975.

11

Acanfora
 
D
,
Ciccone
 
MM
,
Scicchitano
 
P
,
Acanfora
 
C
,
Casucci
 
G.
 
Neprilysin inhibitor–angiotensin II receptor blocker combination (sacubitril/valsartan): rationale for adoption in SARS-CoV-2 patients
.
Eur Heart J Cardiovasc Pharmacother
 
2020
;
6
:
135
136
.

12

Murray
 
E
,
Tomaszewski
 
M
,
Guzik
 
TJ.
 
Binding of SARS-CoV-2 and angiotensin-converting enzyme 2: clinical implications
.
Cardiovasc Res
 
2020
;
116
:
e87
e89
.

13

Dézsi
 
CA
,
Szentes
 
V.
 
Effects of angiotensin-converting enzyme inhibitors and angiotensin receptor blockers on prothrombotic processes and myocardial infarction risk
.
Am J Cardiovasc Drugs
 
2016
;
16
:
399
406
.

14

Henry
 
BM
,
Vikse
 
J
,
Benoit
 
S
,
Favaloro
 
EJ
,
Lippi
 
G.
 
Hyperinflammation and derangement of renin–angiotensin–aldosterone system in COVID-19: a novel hypothesis for clinically suspected hypercoagulopathy and microvascular immunothrombosis
.
Clin Chim Acta
 
2020
;
507
:
167
173
.

15

Bikdeli
 
B
,
Madhavan
 
MV
,
Jimenez
 
D
,
Chuich
 
T
,
Dreyfus
 
I
,
Driggin
 
E
,
Nigoghossian
 
C
,
Ageno
 
W
,
Madjid
 
M
,
Guo
 
Y
,
Tang
 
LV
,
Hu
 
Y
,
Giri
 
J
,
Cushman
 
M
,
Quéré
 
I
,
Dimakakos
 
EP
,
Gibson
 
CM
,
Lippi
 
G
,
Favaloro
 
EJ
,
Fareed
 
J
,
Caprini
 
JA
,
Tafur
 
AJ
,
Burton
 
JR
,
Francese
 
DP
,
Wang
 
EY
,
Falanga
 
A
,
McLintock
 
C
,
Hunt
 
BJ
,
Spyropoulos
 
AC
,
Barnes
 
GD
,
Eikelboom
 
JW
,
Weinberg
 
I
,
Schulman
 
S
,
Carrier
 
M
,
Piazza
 
G
,
Beckman
 
JA
,
Steg
 
PG
,
Stone
 
GW
,
Rosenkranz
 
S
,
Goldhaber
 
SZ
,
Parikh
 
SA
,
Monreal
 
M
,
Krumholz
 
HM
,
Konstantinides
 
SV
,
Weitz
 
JI
,
Lip
 
GYH.
 
COVID-19 and thrombotic or thromboembolic disease: implications for prevention, antithrombotic therapy, and follow-up
.
J Am Coll Cardiol
 
2020
;doi: 10.1016/j.jacc.2020.04.031.

This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)