Over the past few months, COVID-19, the pandemic disease caused by severe acute respiratory
syndrome coronavirus 2, has been associated with a high rate of infection and lethality,
especially in patients with comorbidities such as obesity, hypertension, diabetes,
and immunodeficiency syndromes.
1
These cardiometabolic and immune impairments are common comorbidities of Cushing's
syndrome, a condition characterised by excessive exposure to endogenous glucocorticoids.
In patients with Cushing's syndrome, the increased cardiovascular risk factors, amplified
by the increased thromboembolic risk, and the increased susceptibility to severe infections,
are the two leading causes of death.
2
In healthy individuals in the early phase of infection, at the physiological level,
glucocorticoids exert immunoenhancing effects, priming danger sensor and cytokine
receptor expression, thereby sensitising the immune system to external agents.
3
However, over time and with sustained high concentrations, the principal effects of
glucocorticoids are to produce profound immunosuppression, with depression of innate
and adaptive immune responses. Therefore, chronic excessive glucocorticoids might
hamper the initial response to external agents and the consequent activation of adaptive
responses. Subsequently, a decrease in the number of B-lymphocytes and T-lymphocytes,
as well as a reduction in T-helper cell activation might favour opportunistic and
intracellular infection. As a result, an increased risk of infection is seen, with
an estimated prevalence of 21–51% in patients with Cushing's syndrome.
4
Therefore, despite the absence of data on the effects of COVID-19 in patients with
Cushing's syndrome, one can make observations related to the compromised immune state
in patients with Cushing's syndrome and provide expert advice for patients with a
current or past history of Cushing's syndrome.
Fever is one of the hallmarks of severe infections and is present in up to around
90% of patients with COVID-19, in addition to cough and dyspnoea.
1
However, in active Cushing's syndrome, the low-grade chronic inflammation and the
poor immune response might limit febrile response in the early phase of infection.
2
Conversely, different symptoms might be enhanced in patients with Cushing's syndrome;
for instance, dyspnoea might occur because of a combination of cardiac insufficiency
or weakness of respiratory muscles.
2
Therefore, during active Cushing's syndrome, physicians should seek different signs
and symptoms when suspecting COVID-19, such as cough, together with dysgeusia, anosmia,
and diarrhoea, and should be suspicious of any change in health status of their patients
with Cushing's syndrome, rather than relying on fever and dyspnoea as typical features.
The clinical course of COVID-19 might also be difficult to predict in patients with
active Cushing's syndrome. Generally, patients with COVID-19 and a history of obesity,
hypertension, or diabetes have a more severe course, leading to increased morbidity
and mortality.
1
Because these conditions are observed in most patients with active Cushing's syndrome,
2
these patients might be at an increased risk of severe course, with progression to
acute respiratory distress syndrome (ARDS), when developing COVID-19. However, a key
element in the development of ARDS during COVID-19 is the exaggerated cellular response
induced by the cytokine increase, leading to massive alveolar–capillary wall damage
and a decline in gas exchange.
5
Because patients with Cushing's syndrome might not mount a normal cytokine response,
4
these patients might parodoxically be less prone to develop severe ARDS with COVID-19.
Moreover, Cushing's syndrome and severe COVID-19 are associated with hypercoagulability,
such that patients with active Cushing's syndrome might present an increased risk
of thromboembolism with COVID-19. Consequently, because low molecular weight heparin
seems to be associated with lower mortality and disease severity in patients with
COVID-19,
6
and because anticoagulation is also recommended in specific conditions in patients
with active Cushing's syndrome,
7
this treatment is strongly advised in hospitalised patients with Cushing's syndrome
who have COVID-19. Furthermore, patients with active Cushing's syndrome are at increased
risk of prolonged duration of viral infections, as well as opportunistic infections,
particularly atypical bacterial and invasive fungal infections, leading to sepsis
and an increased mortality risk,
2
and COVID-19 patients are also at increased risk of secondary bacterial or fungal
infections during hospitalisation.
1
Therefore, in cases of COVID-19 during active Cushing's syndrome, prolonged antiviral
treatment and empirical prophylaxis with broad-spectrum antibiotics1, 4 should be
considered, especially for hospitalised patients (panel
).
Panel
Risk factors and clinical suggestions for patients with Cushing's syndrome who have
COVID-19
Reduction of febrile response and enhancement of dyspnoea
Rely on different symptoms and signs suggestive of COVID-19, such as cough, dysgeusia,
anosmia, and diarrhoea.
Prolonged duration of viral infections and susceptibility to superimposed bacterial
and fungal infections
Consider prolonged antiviral and broad-spectrum antibiotic treatment.
Impairment of glucose metabolism (negative prognostic factor)
Optimise glycaemic control and select cortisol-lowering drugs that improve glucose
metabolism. Hypertension (negative prognostic factor) Optimise blood pressure control
and select cortisol-lowering drugs that improve blood pressure.
Thrombosis diathesis (negative prognostic factor)
Start antithrombotic prophylaxis, preferably with low-molecular-weight heparin treatment.
Surgery represents the first-line treatment for all causes of Cushing's syndrome,8,
9 but during the pandemic a delay might be appropriate to reduce the hospital-associated
risk of COVID-19, any post-surgical immunodepression, and thromboembolic risks.
10
Because immunosuppression and thromboembolic diathesis are common Cushing's syndrome
features,2, 4 during the COVID-19 pandemic, cortisol-lowering medical therapy, including
the oral drugs ketoconazole, metyrapone, and the novel osilodrostat, which are usually
effective within hours or days, or the parenteral drug etomidate when immediate cortisol
control is required, should be temporarily used.
9
Nevertheless, an expeditious definitive diagnosis and proper surgical resolution of
hypercortisolism should be ensured in patients with malignant forms of Cushing's syndrome,
not only to avoid disease progression risk but also for rapidly ameliorating hypercoagulability
and immunospuppression;
9
however, if diagnostic procedures cannot be easily secured or surgery cannot be done
for limitations of hospital resources due to the pandemic, medical therapy should
be preferred. Concomitantly, the optimisation of medical treatment for pre-existing
comorbidities as well as the choice of cortisol-lowering drugs with potentially positive
effects on obesity, hypertension, or diabates are crucial to improve the eventual
clinical course of COVID-19.
Once patients with Cushing's syndrome are in remission, the risk of infection is substantially
decreased, but the comorbidities related to excess glucocorticoids might persist,
including obesity, hypertension, and diabetes, together with thromboembolic diathesis.
2
Because these are features associated with an increased death risk in patients with
COVID-19,
1
patients with Cushing's syndrome in remission should be considered a high-risk population
and consequently adopt adequate self-protection strategies to minimise contagion risk.
In conclusion, COVID-19 might have specific clinical presentation, clinical course,
and clinical complications in patients who also have Cushing's syndrome during the
active hypercortisolaemic phase, and therefore careful monitoring and specific consideration
should be given to this special, susceptible population. Moreover, the use of medical
therapy as a bridge treatment while waiting for the pandemic to abate should be considered.