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Journal of Pathology and Infectious Diseases  •  Vol 3  •  Issue 2  •  2020 1
INTRODUCTION
A
drenal insufficiency (AI) is a treatable disorder that
can be life-threatening if its diagnosis is missed.
[1]
Many symptoms and signs of AI may overlap
with those of coronavirus disease 2019 (COVID-19) such
as hypotension, diarrhea, vomiting, and hyponatremia.[1,2]
Unfortunately, the status of adrenal function is unclear
in COVID-19. In turn, in patients who already have AI,
the prevalence of COVID-19 is unknown. In one Italian
survey of 121 patients with AI (n = 40 with primary AI,
and n = 81 with secondary AI), COVID-19 was reported in
one patient with primary AI, that is, 0.8% prevalence.[3]
The
main purpose of this manuscript is to review all pertinent
studies that evaluated AI among patients with COVID-19.
These studies included case reports, imaging, and autopsy
investigations.
CASE REPORTS
Only 4 case reports were found in the literature that
described new-onset AI in patients with COVID-19.[4-7]
Overview of these reports is summarized in Table 1. In the
first case Frankel et al.[4]
from Israel reported a 66-year-
old woman with a history of primary antiphospholipid
syndrome (APLS) who was hospitalized for COVID-19.
Her main symptoms included diffuse abdominal tenderness
due to bilateral adrenal hemorrhage.[4]
AI was confirmed by
undetectable serum cortisol levels that failed to respond to
stimulation by a synthetic adrenocorticotrophic hormone
(ACTH).[4]
The authors attributed this case of primary AI to
adrenal hemorrhage due to thrombosis of adrenal veins caused
both by APLS and COVID-19.[4]
In the second report from
France, Maria et al.[5]
described another patient with primary
APLS who also presented with abdominal pain in addition
to diffuse thrombosis in the lower extremity. However, the
MINI-REVIEW
Assessment of Adrenal Function in COVID-19
Nasser Mikhail, Soma Wali
Department of Medicine, Division of Endocrinology, Olive-View-UCLA Medical Center, David-Geffen School of
Medicine, California, USA
ABSTRACT
Adrenal insufficiency (AI) is a life-threatening but readily treatable condition. The prevalence of AI in coronavirus
disease 2019 (COVID-19) is unknown. The objective of this article is to review data regarding AI in COVID-19. We
performed a PubMed search in English, Spanish, and French until November 25, 2020. Search terms included AI,
adrenal hemorrhage, adrenal infarction, COVID-19. We found only 4 case reports of new-onset AI possibly triggered
by COVID-19. Two cases were due to bilateral adrenal hemorrhage, a third patient had pituitary apoplexy, and the
fourth case presented with severe hyponatremia. A computed tomography series reported acute adrenal infarction as an
incidental finding in 23% of 219 patients with severe and critical COVID-19. Autopsy studies have shown microscopic
lesions in the adrenal glands of 46% of patients who died from severe COVID-19. No cases of AI were described after
the withdrawal of dexamethasone (6 mg/d for up to 10 days) given to treat patients with COVID-19. We conclude that
AI is uncommonly reported in patients with COVID-19 and is likely underdiagnosed. Most cases are due to hemorrhagic
infarction of the adrenals or pituitary gland. Further studies are needed to evaluate adrenal function in patients with
COVID-19.
Key words: Adrenal infarction, adrenal insufficiency, coagulopathy, coronavirus disease 2019, pituitary
Address for correspondence:
Nasser Mikhail, MD, MSc, Chief Endocrinology Division, Department of Medicine, Olive-View UCLA Medical Center,
14445 Olive-View Dr, Sylmar, CA 91342, USA
https://doi.org/10.33309/2639-8893.030201 www.asclepiusopen.com
© 2020 The Author(s). This open access article is distributed under a Creative Commons Attribution (CC-BY) 4.0 license.
Mikhail and Wali: Adrenal function in COVID-19
2 Journal of Pathology and Infectious Diseases  •  Vol 3  •  Issue 2  •  2020
authors did not report the method of biochemical confirmation
of AI. Nevertheless, replacement glucocorticoid therapy was
given to the patient.[5]
In the third report, Gravalos et al.[6]
from Spain described
the case of a 59-year-old man admitted to the hospital with
COVID-19 and severe hyponatremia [Table 1]. Work-up
of hyponatremia revealed secondary AI due to pituitary
apoplexy, a form of hemorrhagic infarction in a pituitary
tumor.[5]
In the fourth case, Heidarpour et al.[7]
from Iran
reported a 69-year-old man with COVID-19 admitted
with COVID-19 pneumonia and refractory hypotension.
The authors diagnosed acute AI based on the assumption
that serum cortisol levels, although within normal limits,
were inappropriate in the face of the stress of COVID-19
pneumonia.[7]
Taken together, these 4 reports suggest that new-onsetAI may
occur in the setting of COVID-19. Although the underlying
mechanisms are unclear, it is possible that the coagulopathy
that characterizes COVID-19 could have triggered adrenal
vein thrombosis,[4,5]
or pituitary apoplexy.[5]
Thus, AI appears
to be an uncommon complication of COVID-19, but it
manifests itself in the presence of a predisposing factor, such
as pre-existing APLS or pituitary adenoma.[4-6]
Meanwhile,
the case of AI reported by Heiderpour et al.[7]
suggests that
refractory hypotension may occur in association with severe
COVID-19, similar to other causes of severe sepsis. Indeed,
the short-term clinical course of the 4 patients described
above responded favorably to hydrocortisone therapy and no
one died [Table 1].
Imaging studies
Leyendecker et al.[8]
evaluated the frequency of acute adrenal
infarction by unenhanced computed tomography (CT) of
chest performed in 219 French patients with severe and
critical COVID-19. The authors found that 51 of the 219
(23%) of patients had CT signs of acute adrenal infarction on
their initial chest CT, and in 45 of these 51 patients (88%),
the adrenal infarction was bilateral.[8]
In addition, the authors
mentioned that 4 patients with bilateral adrenal infarction
had “biological” AI defined as a triad of hyperkalemia
(5mmol/L),hyponatremia(130mmol/L)andhypoglycemia
(3.9 mmol/L).[8]
Moreover, rates of intensive care unit
(ICU) admissions were significantly greater in patients with
adrenal infarction compared with those without infarction,
67% and 45%, respectively (P  0.05).[8]
Yet, mortality rates
were similar, 27% in each group of patients.[8]
These data
suggest that a common finding in severe and critical cases of
COVID-19 is adrenal infarction. The latter may be related to
Table 1: Studies reporting new-onset adrenal insufficiency (AI) in patients with COVID-19
Reference Frankel et al.[4]
Gravalos et al.[6]
Heiderpour et al.[7]
Maria et al.[5]
Patient age/sex 66-year-old F 59-year-old M 69-year-old M 48-year-old man
Main symptom Diffuse abdominal pain Vomiting, abdominal
pain, confusion
Refractory hypotension Sudden abdominal
pain, thrombosis of
dorsalis pedis artery
Lowest serum
sodium levels
129 mEq/L (135–145) 102 mEq/L (135–145) 135 mEq/L (normal
range not reported)
Not reported
Serum cortisol 1µg/dl (normal range
not reported)
3.1 µg/dl (4.8–19.5) 12 µg/dl (normal range
not reported)
Not reported
ACTH 207 pmol/L (1.6–13.9) 4.6 pg/ml (7–60) Not reported Not reported
Imaging CT suggested bilateral
adrenal hemorrhage
MRI of sella turcica
showed pituitary
apoplexy in a
macroadenoma
Not done CT showed bilateral
adrenal hemorrhage
Treatment of AI IV hydrocortisone (dose
not reported) followed by
prednisone 10 mg/d +
fludrocortisone 0.1 mg/d
Hypertonic saline (3%) IV.
Hydrocortisone
100 mg IV q12, then
100 mg infusion over 24 h
IV hydrocortisone
100 mg followed by
1 mg/h. Maintenance
10 mg prednisolone
orally qday
Not detailed
“substitutive therapy
for adrenal function”
Outcome Discharge after 11 days Had transsphenoidal
decompression of
apoplexy
After 53 days, patient’s
condition was “good” on
supplemental oxygen
Discharge after
27 days
Comments Patient had history of
primary anti-phospholipid
syndrome
Long-term outcome was
not mentioned
Long-term outcome was
not mentioned
Patient had history
of primary anti-
phospholipid
syndrome
F: Female, M: Male, ACTH: Adrenocorticotrophic hormone, CT: Computed tomography, MRI: Magnetic resonance imaging, IV: Intravenous
Mikhail and Wali: Adrenal function in COVID-19
Journal of Pathology and Infectious Diseases  •  Vol 3  •  Issue 2  •  2020 3
COVID-19 coagulopathy.[9,10]
Meanwhile, the observation by
Leyendecker et al.[8]
that only a minority of patients (4 of 219,
or 1.8%) exhibit the laboratory abnormalities characteristic
of AI suggest that many cases of AI associated with severe
COVID-19 are either subclinical and/or underdiagnosed.
Autopsy studies
In 28 patients who died from severe COVID-19, Santana
et al.[11]
showed that 12 patients (43%) had adrenal lesions.
The most common observed lesions were necrosis found in
7 cases, followed by cortical lipid degeneration and adrenal
hemorrhage, whereas vascular thrombosis was seen in one
patient.[11]
The authors attributed these pathological lesions
to COVID-19.[11]
Interestingly, there was no biochemical
evidence of AI before death as serum cortisol levels
measured 24–48 h before death were appropriate for the
levels of patients’ stress.[11]
In another smaller autopsy
study of 5 patients who died from COVID-19. Iuga et al.[12]
reported acute fibrinoid necrosis of small vessels of adrenal
glands. No significant inflammation, infarcts, or thrombi
were appreciated.[12]
Interestingly, in the previous 2 autopsy
studies, the causative virus of COVID-19, that is, the severe
acute respiratory syndrome coronavirus 2, was not isolated
from any autopsy specimen.[11,12]
Effect of glucocorticoid therapy on adrenal
function in COVID-19
In the RECOVERY trial conducted in the UK, the
investigators randomized hospitalized patients with
COVID-19 into two groups in a 2:1 ratio; the larger group
(n = 4,321) received usual care while the smaller group
(n = 2,104) received usual care plus low-dose dexamethasone
6 mg/d orally or intravenously for up to 10 days in
an open-label fashion.[13]
Significantly fewer patients
assigned to dexamethasone reached the primary outcome
of 28-day mortality compared with usual care, 21.6% and
24.8%, respectively; relative risk 0.83; 95% CI 0.74–0.92
(P  0.001).[13]
The RECOVERY dexamethasone protocol is
currently followed throughout the world and was supported
by the World Health Organization.[14]
It is unknown whether
dexamethasone doses and duration in the RECOVERY trial
can cause secondary (iatrogenic) AI by suppression of the
hypothalamic-pituitary-adrenal axis.[1]
To the authors’ best
knowledge, no cases of AI or adrenal crises were reported
following the termination of this dexamethasone course in
patients with COVID-19. The latter observation is likely
due to the relatively small dose (6 mg/d) and short-duration
(10 days) of dexamethasone treatment in the RECOVERY
trial. However, it is wise to be aware of the possibility of
the development of AI or crisis in the weeks following the
withdrawal of dexamethasone. Thus, if any symptoms or
signs of AI occur during this time frame (e.g., unexplained
hypotension, vomiting, abdominal pain, diarrhea, and new-
onset hyponatremia), the authors suggest drawing serum
cortisol or performing the cosyntropin (synthetic ACTH)
stimulation test and start empiric glucocorticoids (e.g.,
100 mg hydrocortisone intravenously) pending the results of
cortisol and cosyntropin stimulation test.
CONCLUSIONS AND CURRENT
NEEDS
No doubt, our knowledge about AI in COVID-19 is still in
its stage of infancy. Available data suggest that AI is rarely
documented in patients with COVID-19 admitted to the
hospital and is likely underreported. Three of 4 cases of AI
reported have underlying pathology that predisposes patients
with COVID-19 to develop AI, namely APLS or a pituitary
tumor.[4-6]
However, imaging and autopsy investigations
suggest that adrenal infarction and pathologic involvements
of adrenals are not uncommon in patients with severe
COVID-19.[8,11,12]
Aprospective study is underway to examine
the impact of COVID-19 on adrenal function by measuring
serum levels of cortisol and ACTH in patients with severe
COVID-19.[15]
The results of this study should clarify the
prevalence of adrenal dysfunction in patients with severe
COVID-19. In the meantime, physicians should be aware of
the symptoms and signs of AI and adrenal crisis that may be
obscured by those of COVID-19.
REFERENCES
1.	 Charmandari E, Nicolaides NC, Chrousos GP. Adrenal
insufficiency. Lancet 2014;383:2152-67.
2.	 Guan WJ, Ni ZY, Hu Y, Liang WH, Ou CQ, He JX, et al.
Clinical characteristics of coronavirus disease 2019 in China.
N Engl J Med 2020;382:1708-20.
3.	 Martino M, Aboud N, Cola MF, Giancola G, Ciarloni A,
Salvio G, et al. Impact of COVID-19 pandemic on
psychophysical stress in patients with adrenal insufficiency:
The CORTI-COVID study. J Endocrinol Invest 2020;18:1-10.
4.	 Frankel M, Feldman I, Levine M, Frank Y, Bogot NR,
Benjaminov O, et al. Bilateral adrenal hemorrhage in
coronavirus disease 2019 patient: A case report. J Clin
Endocrinol Metab 2020;105:1-5.
5.	 Maria AT, Cau I, Benejean JM, Nutz A, Schiffmann A, Biron-
Andrean C, et al. Flare of antiphospholipid syndrome in the
course of COVID-19. TH Open 2020;4:e207-10.
6.	 Gravalos T, Conde AR, Del Pozo R, De La Flor Merino JC,
Reyes LM. An unusual case of severe acute hyponatremia in
patient with COVID-19 infection. Nefrologia 2020;40:356-8.
7.	 Heidarpour M, Vakhshoori M, Abbasi S, Shafie D, Rezaei N.
Adrenal insufficiency in coronavirus disease 2019: A case
report. J Med Case Rep 2020;14:134.
8.	 Leyendecker P, Ritter S, Riou M, Wackenthaler A, Meziani F,
Roy C, et al. Acute adrenal infarction as an incidental CT
finding and a potential prognosis factor in severe SARS-CoV-2
infection: A retrospective cohort analysis on 219 patients. Eur
Radiol 2020;2020:1-6.
9.	 Klok FA, Kruip MJ, van der Meer NJ, Arbous MS,
Gommers DA, Kant KM, et al. Incidence of thrombotic
Mikhail and Wali: Adrenal function in COVID-19
4 Journal of Pathology and Infectious Diseases  •  Vol 3  •  Issue 2  •  2020
complications in critically ill ICU patients with COVID-19.
Thromb Res 2020;191:145-7.
10.	 Terpos E, Ntanasis-Stathopoulos I, Elalamy I, Kastritis E,
Sergentanis TN, Politou M, et al. Hematological findings and
complications of COVID-19. Am J Hematol 2020;95:834-47.
11.	 Santana FM, Borba MG, Baía-da-Silva DC, Val F,
Alexandre MA, Brito-Sousa JD, et al. Case report: Adrenal
pathology findings in severe COVID-19: An autopsy study.
Am J Trop Med Hyg 2020;103:1604-7.
12.	 Iuga AC, Marboe CC, Yilmaz M, Lefkowitch JH, Gauran C,
Lagana SM, et al. Adrenal vascular changes in COVID-19
autopsies. Arch Pathol Lab Med 2020;144:1159-60.
13.	 Horby P, LimWS, Emberson JR, Mafham M, Bell JL, Linsell L,
et al, RECOVERY Collaborative Group. Dexamethasone in
hospitalized patients with covid-19-preliminary report. N Engl
J Med 2020. [ahead of print].
14.	 WHO Welcomes Preliminary Results About Dexamethasone
use in Treating Critically ill COVID-19 Patients. Available
from: https://www.who.int/news/item/16-06-2020-who-
welcomes-preliminary-results-about-dexamethasone-use-
in-treating-critically-ill-covid-19-patients. [Last accessed on
2020 Jun 28].
15.	 Pal R. COVID-19, hypothalamic-pituitary-adrenal axis and
clinical implications. Endocrine 2020;68:251-2.
How to cite this article: Mikhail N, Wali S. Assessment
of Adrenal Function in Covid-19. J Pathol Infect Dis
2020;3(2):1-4.

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Assessment of Adrenal Function in COVID-19

  • 1. Journal of Pathology and Infectious Diseases  •  Vol 3  •  Issue 2  •  2020 1 INTRODUCTION A drenal insufficiency (AI) is a treatable disorder that can be life-threatening if its diagnosis is missed. [1] Many symptoms and signs of AI may overlap with those of coronavirus disease 2019 (COVID-19) such as hypotension, diarrhea, vomiting, and hyponatremia.[1,2] Unfortunately, the status of adrenal function is unclear in COVID-19. In turn, in patients who already have AI, the prevalence of COVID-19 is unknown. In one Italian survey of 121 patients with AI (n = 40 with primary AI, and n = 81 with secondary AI), COVID-19 was reported in one patient with primary AI, that is, 0.8% prevalence.[3] The main purpose of this manuscript is to review all pertinent studies that evaluated AI among patients with COVID-19. These studies included case reports, imaging, and autopsy investigations. CASE REPORTS Only 4 case reports were found in the literature that described new-onset AI in patients with COVID-19.[4-7] Overview of these reports is summarized in Table 1. In the first case Frankel et al.[4] from Israel reported a 66-year- old woman with a history of primary antiphospholipid syndrome (APLS) who was hospitalized for COVID-19. Her main symptoms included diffuse abdominal tenderness due to bilateral adrenal hemorrhage.[4] AI was confirmed by undetectable serum cortisol levels that failed to respond to stimulation by a synthetic adrenocorticotrophic hormone (ACTH).[4] The authors attributed this case of primary AI to adrenal hemorrhage due to thrombosis of adrenal veins caused both by APLS and COVID-19.[4] In the second report from France, Maria et al.[5] described another patient with primary APLS who also presented with abdominal pain in addition to diffuse thrombosis in the lower extremity. However, the MINI-REVIEW Assessment of Adrenal Function in COVID-19 Nasser Mikhail, Soma Wali Department of Medicine, Division of Endocrinology, Olive-View-UCLA Medical Center, David-Geffen School of Medicine, California, USA ABSTRACT Adrenal insufficiency (AI) is a life-threatening but readily treatable condition. The prevalence of AI in coronavirus disease 2019 (COVID-19) is unknown. The objective of this article is to review data regarding AI in COVID-19. We performed a PubMed search in English, Spanish, and French until November 25, 2020. Search terms included AI, adrenal hemorrhage, adrenal infarction, COVID-19. We found only 4 case reports of new-onset AI possibly triggered by COVID-19. Two cases were due to bilateral adrenal hemorrhage, a third patient had pituitary apoplexy, and the fourth case presented with severe hyponatremia. A computed tomography series reported acute adrenal infarction as an incidental finding in 23% of 219 patients with severe and critical COVID-19. Autopsy studies have shown microscopic lesions in the adrenal glands of 46% of patients who died from severe COVID-19. No cases of AI were described after the withdrawal of dexamethasone (6 mg/d for up to 10 days) given to treat patients with COVID-19. We conclude that AI is uncommonly reported in patients with COVID-19 and is likely underdiagnosed. Most cases are due to hemorrhagic infarction of the adrenals or pituitary gland. Further studies are needed to evaluate adrenal function in patients with COVID-19. Key words: Adrenal infarction, adrenal insufficiency, coagulopathy, coronavirus disease 2019, pituitary Address for correspondence: Nasser Mikhail, MD, MSc, Chief Endocrinology Division, Department of Medicine, Olive-View UCLA Medical Center, 14445 Olive-View Dr, Sylmar, CA 91342, USA https://doi.org/10.33309/2639-8893.030201 www.asclepiusopen.com © 2020 The Author(s). This open access article is distributed under a Creative Commons Attribution (CC-BY) 4.0 license.
  • 2. Mikhail and Wali: Adrenal function in COVID-19 2 Journal of Pathology and Infectious Diseases  •  Vol 3  •  Issue 2  •  2020 authors did not report the method of biochemical confirmation of AI. Nevertheless, replacement glucocorticoid therapy was given to the patient.[5] In the third report, Gravalos et al.[6] from Spain described the case of a 59-year-old man admitted to the hospital with COVID-19 and severe hyponatremia [Table 1]. Work-up of hyponatremia revealed secondary AI due to pituitary apoplexy, a form of hemorrhagic infarction in a pituitary tumor.[5] In the fourth case, Heidarpour et al.[7] from Iran reported a 69-year-old man with COVID-19 admitted with COVID-19 pneumonia and refractory hypotension. The authors diagnosed acute AI based on the assumption that serum cortisol levels, although within normal limits, were inappropriate in the face of the stress of COVID-19 pneumonia.[7] Taken together, these 4 reports suggest that new-onsetAI may occur in the setting of COVID-19. Although the underlying mechanisms are unclear, it is possible that the coagulopathy that characterizes COVID-19 could have triggered adrenal vein thrombosis,[4,5] or pituitary apoplexy.[5] Thus, AI appears to be an uncommon complication of COVID-19, but it manifests itself in the presence of a predisposing factor, such as pre-existing APLS or pituitary adenoma.[4-6] Meanwhile, the case of AI reported by Heiderpour et al.[7] suggests that refractory hypotension may occur in association with severe COVID-19, similar to other causes of severe sepsis. Indeed, the short-term clinical course of the 4 patients described above responded favorably to hydrocortisone therapy and no one died [Table 1]. Imaging studies Leyendecker et al.[8] evaluated the frequency of acute adrenal infarction by unenhanced computed tomography (CT) of chest performed in 219 French patients with severe and critical COVID-19. The authors found that 51 of the 219 (23%) of patients had CT signs of acute adrenal infarction on their initial chest CT, and in 45 of these 51 patients (88%), the adrenal infarction was bilateral.[8] In addition, the authors mentioned that 4 patients with bilateral adrenal infarction had “biological” AI defined as a triad of hyperkalemia (5mmol/L),hyponatremia(130mmol/L)andhypoglycemia (3.9 mmol/L).[8] Moreover, rates of intensive care unit (ICU) admissions were significantly greater in patients with adrenal infarction compared with those without infarction, 67% and 45%, respectively (P 0.05).[8] Yet, mortality rates were similar, 27% in each group of patients.[8] These data suggest that a common finding in severe and critical cases of COVID-19 is adrenal infarction. The latter may be related to Table 1: Studies reporting new-onset adrenal insufficiency (AI) in patients with COVID-19 Reference Frankel et al.[4] Gravalos et al.[6] Heiderpour et al.[7] Maria et al.[5] Patient age/sex 66-year-old F 59-year-old M 69-year-old M 48-year-old man Main symptom Diffuse abdominal pain Vomiting, abdominal pain, confusion Refractory hypotension Sudden abdominal pain, thrombosis of dorsalis pedis artery Lowest serum sodium levels 129 mEq/L (135–145) 102 mEq/L (135–145) 135 mEq/L (normal range not reported) Not reported Serum cortisol 1µg/dl (normal range not reported) 3.1 µg/dl (4.8–19.5) 12 µg/dl (normal range not reported) Not reported ACTH 207 pmol/L (1.6–13.9) 4.6 pg/ml (7–60) Not reported Not reported Imaging CT suggested bilateral adrenal hemorrhage MRI of sella turcica showed pituitary apoplexy in a macroadenoma Not done CT showed bilateral adrenal hemorrhage Treatment of AI IV hydrocortisone (dose not reported) followed by prednisone 10 mg/d + fludrocortisone 0.1 mg/d Hypertonic saline (3%) IV. Hydrocortisone 100 mg IV q12, then 100 mg infusion over 24 h IV hydrocortisone 100 mg followed by 1 mg/h. Maintenance 10 mg prednisolone orally qday Not detailed “substitutive therapy for adrenal function” Outcome Discharge after 11 days Had transsphenoidal decompression of apoplexy After 53 days, patient’s condition was “good” on supplemental oxygen Discharge after 27 days Comments Patient had history of primary anti-phospholipid syndrome Long-term outcome was not mentioned Long-term outcome was not mentioned Patient had history of primary anti- phospholipid syndrome F: Female, M: Male, ACTH: Adrenocorticotrophic hormone, CT: Computed tomography, MRI: Magnetic resonance imaging, IV: Intravenous
  • 3. Mikhail and Wali: Adrenal function in COVID-19 Journal of Pathology and Infectious Diseases  •  Vol 3  •  Issue 2  •  2020 3 COVID-19 coagulopathy.[9,10] Meanwhile, the observation by Leyendecker et al.[8] that only a minority of patients (4 of 219, or 1.8%) exhibit the laboratory abnormalities characteristic of AI suggest that many cases of AI associated with severe COVID-19 are either subclinical and/or underdiagnosed. Autopsy studies In 28 patients who died from severe COVID-19, Santana et al.[11] showed that 12 patients (43%) had adrenal lesions. The most common observed lesions were necrosis found in 7 cases, followed by cortical lipid degeneration and adrenal hemorrhage, whereas vascular thrombosis was seen in one patient.[11] The authors attributed these pathological lesions to COVID-19.[11] Interestingly, there was no biochemical evidence of AI before death as serum cortisol levels measured 24–48 h before death were appropriate for the levels of patients’ stress.[11] In another smaller autopsy study of 5 patients who died from COVID-19. Iuga et al.[12] reported acute fibrinoid necrosis of small vessels of adrenal glands. No significant inflammation, infarcts, or thrombi were appreciated.[12] Interestingly, in the previous 2 autopsy studies, the causative virus of COVID-19, that is, the severe acute respiratory syndrome coronavirus 2, was not isolated from any autopsy specimen.[11,12] Effect of glucocorticoid therapy on adrenal function in COVID-19 In the RECOVERY trial conducted in the UK, the investigators randomized hospitalized patients with COVID-19 into two groups in a 2:1 ratio; the larger group (n = 4,321) received usual care while the smaller group (n = 2,104) received usual care plus low-dose dexamethasone 6 mg/d orally or intravenously for up to 10 days in an open-label fashion.[13] Significantly fewer patients assigned to dexamethasone reached the primary outcome of 28-day mortality compared with usual care, 21.6% and 24.8%, respectively; relative risk 0.83; 95% CI 0.74–0.92 (P 0.001).[13] The RECOVERY dexamethasone protocol is currently followed throughout the world and was supported by the World Health Organization.[14] It is unknown whether dexamethasone doses and duration in the RECOVERY trial can cause secondary (iatrogenic) AI by suppression of the hypothalamic-pituitary-adrenal axis.[1] To the authors’ best knowledge, no cases of AI or adrenal crises were reported following the termination of this dexamethasone course in patients with COVID-19. The latter observation is likely due to the relatively small dose (6 mg/d) and short-duration (10 days) of dexamethasone treatment in the RECOVERY trial. However, it is wise to be aware of the possibility of the development of AI or crisis in the weeks following the withdrawal of dexamethasone. Thus, if any symptoms or signs of AI occur during this time frame (e.g., unexplained hypotension, vomiting, abdominal pain, diarrhea, and new- onset hyponatremia), the authors suggest drawing serum cortisol or performing the cosyntropin (synthetic ACTH) stimulation test and start empiric glucocorticoids (e.g., 100 mg hydrocortisone intravenously) pending the results of cortisol and cosyntropin stimulation test. CONCLUSIONS AND CURRENT NEEDS No doubt, our knowledge about AI in COVID-19 is still in its stage of infancy. Available data suggest that AI is rarely documented in patients with COVID-19 admitted to the hospital and is likely underreported. Three of 4 cases of AI reported have underlying pathology that predisposes patients with COVID-19 to develop AI, namely APLS or a pituitary tumor.[4-6] However, imaging and autopsy investigations suggest that adrenal infarction and pathologic involvements of adrenals are not uncommon in patients with severe COVID-19.[8,11,12] Aprospective study is underway to examine the impact of COVID-19 on adrenal function by measuring serum levels of cortisol and ACTH in patients with severe COVID-19.[15] The results of this study should clarify the prevalence of adrenal dysfunction in patients with severe COVID-19. In the meantime, physicians should be aware of the symptoms and signs of AI and adrenal crisis that may be obscured by those of COVID-19. REFERENCES 1. Charmandari E, Nicolaides NC, Chrousos GP. Adrenal insufficiency. Lancet 2014;383:2152-67. 2. Guan WJ, Ni ZY, Hu Y, Liang WH, Ou CQ, He JX, et al. Clinical characteristics of coronavirus disease 2019 in China. N Engl J Med 2020;382:1708-20. 3. Martino M, Aboud N, Cola MF, Giancola G, Ciarloni A, Salvio G, et al. Impact of COVID-19 pandemic on psychophysical stress in patients with adrenal insufficiency: The CORTI-COVID study. J Endocrinol Invest 2020;18:1-10. 4. Frankel M, Feldman I, Levine M, Frank Y, Bogot NR, Benjaminov O, et al. Bilateral adrenal hemorrhage in coronavirus disease 2019 patient: A case report. J Clin Endocrinol Metab 2020;105:1-5. 5. Maria AT, Cau I, Benejean JM, Nutz A, Schiffmann A, Biron- Andrean C, et al. Flare of antiphospholipid syndrome in the course of COVID-19. TH Open 2020;4:e207-10. 6. Gravalos T, Conde AR, Del Pozo R, De La Flor Merino JC, Reyes LM. An unusual case of severe acute hyponatremia in patient with COVID-19 infection. Nefrologia 2020;40:356-8. 7. Heidarpour M, Vakhshoori M, Abbasi S, Shafie D, Rezaei N. Adrenal insufficiency in coronavirus disease 2019: A case report. J Med Case Rep 2020;14:134. 8. Leyendecker P, Ritter S, Riou M, Wackenthaler A, Meziani F, Roy C, et al. Acute adrenal infarction as an incidental CT finding and a potential prognosis factor in severe SARS-CoV-2 infection: A retrospective cohort analysis on 219 patients. Eur Radiol 2020;2020:1-6. 9. Klok FA, Kruip MJ, van der Meer NJ, Arbous MS, Gommers DA, Kant KM, et al. Incidence of thrombotic
  • 4. Mikhail and Wali: Adrenal function in COVID-19 4 Journal of Pathology and Infectious Diseases  •  Vol 3  •  Issue 2  •  2020 complications in critically ill ICU patients with COVID-19. Thromb Res 2020;191:145-7. 10. Terpos E, Ntanasis-Stathopoulos I, Elalamy I, Kastritis E, Sergentanis TN, Politou M, et al. Hematological findings and complications of COVID-19. Am J Hematol 2020;95:834-47. 11. Santana FM, Borba MG, Baía-da-Silva DC, Val F, Alexandre MA, Brito-Sousa JD, et al. Case report: Adrenal pathology findings in severe COVID-19: An autopsy study. Am J Trop Med Hyg 2020;103:1604-7. 12. Iuga AC, Marboe CC, Yilmaz M, Lefkowitch JH, Gauran C, Lagana SM, et al. Adrenal vascular changes in COVID-19 autopsies. Arch Pathol Lab Med 2020;144:1159-60. 13. Horby P, LimWS, Emberson JR, Mafham M, Bell JL, Linsell L, et al, RECOVERY Collaborative Group. Dexamethasone in hospitalized patients with covid-19-preliminary report. N Engl J Med 2020. [ahead of print]. 14. WHO Welcomes Preliminary Results About Dexamethasone use in Treating Critically ill COVID-19 Patients. Available from: https://www.who.int/news/item/16-06-2020-who- welcomes-preliminary-results-about-dexamethasone-use- in-treating-critically-ill-covid-19-patients. [Last accessed on 2020 Jun 28]. 15. Pal R. COVID-19, hypothalamic-pituitary-adrenal axis and clinical implications. Endocrine 2020;68:251-2. How to cite this article: Mikhail N, Wali S. Assessment of Adrenal Function in Covid-19. J Pathol Infect Dis 2020;3(2):1-4.