key: cord-0768665-j8y9gt2o
authors: Kato, Verstrepen; Laure, Baisier; Harald, De Cauwer
title: Neurological manifestations of COVID-19, SARS and MERS
date: 2020-06-19
journal: Acta Neurol Belg
DOI: 10.1007/s13760-020-01412-4
sha: 70f4c59a93097fee06e844f5eebcce4c1bdeed0f
doc_id: 768665
cord_uid: j8y9gt2o

Since December 2019, the world is affected by an outbreak of a new disease named COVID-19, which is an acronym of ‘coronavirus disease 2019’. Coronaviruses (CoV) were assumed to be associated with mild upper respiratory tract infections, such as common cold. This perception changed in time due to occurrence of the Severe Acute Respiratory Syndrome (SARS) caused by SARS-CoV in 2002 and the Middle East Respiratory Syndrome (MERS) caused by MERS-CoV in 2012, both inducing an epidemic severe viral pneumonia with potentially respiratory failure and numerous extra-pulmonary manifestations. The novel coronavirus, SARS-CoV-2, is likewise a causative pathogen for severe viral pneumonia with the risk of progression to respiratory failure and systemic manifestations. In this review, we will give a summary of the neurological manifestations due to SARS and MERS, as those might predict the neurological outcome in the novel COVID-19. Additionally, we provide an overview of the current knowledge concerning neurological manifestations associated with COVID-19, to the extent that literature is already available as the pandemic is still ongoing.

Viruses of the Coronaviridae family are positive-sensed, single-stranded RNA viruses. They are broadly distributed in different animal species including avian host, cats, dogs, bats, camels, cattle and mice. Among these viruses, some are pathogenic to human [1] [2] [3] .

In humans, CoV infections were primarily associated with upper respiratory tract and gastrointestinal tract infections. However, the last 2 decades the world was affected by several viral epidemics, such as Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) in 2002−2003 and Middle East Respiratory Syndrome Coronavirus (MERS-CoV) in 2012, both resulting in high mortality rate, respectively, 10% and 35%.

Since December 2019, the world is affected by an outbreak of a new disease named COVID-19, which is an acronym of 'coronavirus disease 2019'. It is caused by a novel coronavirus (CoV), named SARS-CoV-2, due to similarities with the Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) [1] .

All three infections show a broad spectrum of clinical manifestation, varying from asymptomatic or mild disease to severe illness with risk of progress to respiratory failure due to viral pulmonary infection [4, 5] .

It is known that human coronaviruses can reach the central nervous system (CNS) and that they could be associated with neurological symptoms [6] . Several cases of neurological involvement during SARS and MERS and the potential mechanisms have already been described in literature [4] [5] [6] [7] .

Conversely, despite the current global outbreak with many more patients affected, little is known about neurological manifestations in COVID-19 after 6 months. In this review, we will give an overview of these neurological manifestations reported due to SARS and MERS as this might be of great importance in dealing with the novel COVID-19. Additionally, we present a summary of the current knowledge-still evolving in literature-on neurological manifestations associated with SARS-CoV-2-infection.

The authors searched PubMed/MEDLINE databases in March 2020. Articles related to the topic were identified by following terms: "Severe Acute Respiratory Syndrome", "Middle East Respiratory Syndrome", Coronavirus disease 2019", "Neurology", "MERS", "SARS", "COVID-19", "Stroke", "Epilepsy", "Guillain-Barré Syndrome", "Encephalitis", "Myelitis", "Meningitis", "Neurological Sequels", "Polyneuropathy" and "Carotid Dissection".

We used a date restriction ranging from the 1 st of January 2002 until present. There were limited linguistic restrictions (articles in English, Dutch, French and German were eligible for inclusion).

"Middle East Respiratory Syndrome" and "Neurology" identified 53 articles, of which 20 articles were retained based on review of title and abstract to select material for potential review. "Severe Acute Respiratory Syndrome" and "Neurology" revealed 102 articles, "Coronavirus disease 2019 and Neurology" revealed 1 article, "MERS" and "Neurology" 109 articles, "SARS" and "Neurology" 25 articles, "COVID-19" and "Neurology" 5 articles, ("SARS" OR "MERS" OR "COVID-19") and "Stroke" 17 articles, ("SARS" OR "MERS" OR "COVID-19") and "Epilepsy" 15 articles, ("SARS" OR "MERS" OR "COVID-19") and Guillain-Barré syndrome" 3 articles, ("SARS" OR "MERS" OR "COVID-19") and "Myelitis" 23 articles, ("SARS" OR "MERS" OR "COVID-19") and "Carotid dissection" 1 articles, but after reviewing the titles and abstracts, no additional articles were retained. ("SARS" OR "MERS" OR "COVID-19") and "Encephalitis" revealed 252 articles, of which 6 articles were selected for the review based on title and abstract. ("SARS" OR "MERS" OR "COVID-19") and "Meningitis revealed 45 articles, of which 1 article was a potential result for the review. However, this article was only accessible in Danish and was not retained for this review. ("SARS" OR "MERS" OR "COVID-19") and "Neurological sequels" revealed 47 articles, of which 3 were selected for the review. ("SARS" OR "MERS" OR "COVID-19") and "Polyneuropathy" delivered 7 results, of which 1 was retained.

The manuscripts that were considered as suitable for the review were evaluated via full text review. Interesting articles for our review noticed in the references of these articles, were used for additional information.

Human coronaviruses (HCoV) are known to have neurotropic and neuro-invasive capabilities. Desforges et al. hypothesize human coronaviruses are neurovirulent, as they could contribute in short-and long-term neurological disorders such as encephalomyelitis and multiple sclerosis [6] [7] [8] . The presence of HCoV RNA in the human CNS confirms these properties [9] .

Viruses, in general, may enter the brain and spinal cord via hematogenous or retrograde neuronal distribution. It is already known that HCoV can also spread from the respiratory tract to the central nervous system (CNS) through transneuronal and hematogenous routes [10] .

HCoV may persist in human brains, so it is assumed that long-term sequelae can develop related to emergence or aggravation of chronic neurological diseases, as it is already described for the human coronaviruses HCOV-229E and HCOV-OC43. The latter have been detected in various neurological diseases, including multiple sclerosis [9] . Several recent articles report associated cases of encephalitis, acute flaccid paralysis and other neurological symptoms, such as Guillain-Barré syndrome or ADEM, as possible complications of a HCoV infection [6] .

In this article, we will focus on the neurological manifestations described in SARS, MERS, and COVID-19.

SARS may present with non-specific symptoms such as persistent fever, non-productive cough, myalgia, dyspnoea and headache. In roughly 20% of the patients, the initial presentation got complicated with acute respiratory distress syndrome [6] . Aside from the respiratory tract, SARS-CoV infection may also target intestinal mucosal cells, renal tubular epithelial cells and neurons as well as cells from the lymphoid and reticuloendothelial system. As a consequence, extrapulmonary features including watery diarrhoea and vomiting may also be part of the clinical presentation. Furthermore, dizziness, nausea, decrease in general well-being and confusion have also been reported [5] .

The clinical presentation of MERS may also be nonspecific. Runny nose, sore throat, low-grade fever and myalgia can present before the viremia becomes detectable [4, 11] . In case of severe disease, progression to acute respiratory distress may occur. Extrapulmonary manifestations including gastrointestinal symptoms and acute kidney failure have been reported in case of severe illness, as well as neurological manifestations [11] .

Common clinical features of COVID-19 include fever, cough, sore throat, headache, fatigue, myalgia, anosmia and dyspnoea. The infection may evolve into pneumonia, respiratory failure, multiple organ failure and death due to extreme rise in inflammatory cytokines [1, 12] .

Current data, mainly from Chinese brain autopsy studies, confirm CNS invasion by SARS-CoV [13, 14] .

Cases described in the articles mentioned below concerning neurological manifestations reported during SARS-CoVinfection are rendered in Table 1 [3] . Another impact of the SARS-epidemic was the adverse effect on seizure control due to withdrawal of anti-epileptic drug treatment as many patients avoided hospital visits [16] .

Neuromuscular disorders in SARS are predominantly lateonset sequelae and include critical-illness polyneuropathy and myopathy [17] .

Muscle weakness and elevated serum creatine kinase levels occur in more than 30% of patients with SARS [18] . In patients with fatal SARS, Leung et al. examined post-mortem histological muscle samples and described a myopathy, either resulting from critical illness myopathy or from the immune response against SARS-CoV [19] .

Critical illness myopathy and critical illness polyneuropathy can both occur in a context entitled the systemic inflammatory response syndrome (SIRS). SIRS is a term comprising sepsis and multiple organ failure, which can both be aspects of SARS-CoV-infections and be related to excessive production of tumour necrosis factor alfa and nitric oxide in the macrophages [20] [21] [22] Rhabdomyolysis has previously been associated with many infectious diseases, but it is rarely seen in SARS-CoVinfection [23] . In a case series, rhabdomyolysis correlated with renal failure and was considered to be a severe manifestation of SARS. Therefore, creatine kinase levels of SARSpatients should be monitored thoroughly [24] .

In contrast to frequent occurrence of anosmia in early stages of COVID-19 (see below), it is anecdotal in SARS and only described in late stage of the disease. Nevertheless, olfactory function test should be part of routine work-up for patients with SARS [25] .

Five cases of large artery ischaemic stroke were described in SARS. It is suggested that a pro-coagulant state could be present in patients with SARS [26, 27] . This could contribute to large cerebral arterial thromboembolism, together with factors as systemic hypotension and cardiac dysfunction. However, stroke is not uncommon in critically ill patients with co-morbidity. Furthermore, it is believed that the use of intravenous immunoglobulins, used to treat SARS, could play a role in SARS-related stroke. Hyperviscosity induced by intravenous immunoglobulins in patients already prone to hypercoagulable state due to viral infection and the inflammatory response, could play a key role in stroke [26, 27] .

Chronic post-SARS syndrome was described by Moldofsky et al. The syndrome is characterized by persistent fatigue, diffuse myalgia, weakness, depression, nonrestorative sleep with associated REM-related apneas/hypopneas, an elevated sleep EEG cyclical alternating pattern and alpha EEG sleep anomaly [28] .

Other authors suggest that prolonged fatigue and malaise may be linked to peripheral and autonomic nervous system dysfunction. Chronic fatigue may be present months after recovery from acute illness. One study shows autonomic dysfunction to be present in 50% of recovered SARSpatients. Subclinical orthostatic hemodynamic disturbances would lead to fatigue and dizziness [29, 30] .

Cases described in the articles mentioned below concerning neurological manifestations reported during MERS-CoVinfection are rendered in Table 2 . 

Although it is exceptional, the CNS could be involved by MERS-CoV infection, mostly due to auto-immune reaction through autoreactive T-cells which recognize viral and myelin antigens as similar molecules, rather than to viral infection itself [31] [32] [33] .

A retrospective study in Saudi Arabia stated that about 25% of MERS patients developed confusion and 8.6% experienced a seizure [34] .

Another case series of three patients with altered level of consciousness varying from confusion to coma, ataxia and focal motor deficit, describes diffuse CNS disease with MRI showing new onset, widespread, bilateral hyperintense lesions on T2-weighted imaging within white matter and subcortical areas of different lobes, basal ganglia, corpus callosum, pons, cerebellum and upper cervical cord with only non-specific increased protein level in CSF.

Final working diagnoses in the three patients were respectively acute disseminated encephalomyelitis, acute bilateral non-occlusive stroke due to MERS-CoV vasculopathy and encephalitis [35] .

The negative CSF for MERS-CoV RT-PCR might be due to the timing of the test, the lack of meningeal involvement as shown on MRI, or the virus being located intra-neuronally as reported with SARS-CoV [36] .

Intracerebral haemorrhage as result of thrombocytopenia, disseminated intravascular coagulation and platelet dysfunction, is very rare [32] .

In 2007, Al-Hameed et al. described the case of a female health care worker who developed a sudden-onset diabetes insipidus and spontaneous massive intracranial haemorrhage with intra-ventricular extension and tonsillar herniation. Her platelet count and coagulation profile did not show any abnormalities. As mentioned in the table, the woman was obese. The severity of MERS in obese patients can be explained as dipeptidyl peptidase 4 (DPP4), a transmembrane protein involved in cell entry of viruses such as MERS-CoV, is overexpressed in obese patients [37, 38] .

Only one case of a 28-year-old male, an orthopaedic resident, was reported. After a long stay in intensive care, he suffered from weakness in both legs and inability to walk, along with numbness and tingling in stocking distribution. He was diagnosed with critical illness polyneuropathy [32] .

Kim et al. published a case report of four patients who developed neurological manifestations during treatment of Table 3 [39] . Interferon alpha-2a is a possible causative drug for peripheral neuropathy, sensory neuropathy, vasculitic neuropathy, Bell's palsy, Guillain Barré Syndrome, chronic inflammatory demyelinating polyneuropathy and autonomic polyneuropathy [40] [41] [42] . Lopinavir/ritonavir is another possible causative drug for peripheral neuropathy [43] . Ribavirine is not associated with peripheral neuropathy [42] .

Similar to SARS-CoV, SARS-CoV-2 profits from the angiotensin converting enzyme 2 receptor (ACE2-R) to infiltrate in the intracellular space. It has been described that the brain expresses ACE2-R, which have been detected in glial cells and neurons as well as endothelial cells and smooth muscle cells. Therefore, these cells and neurons are potential targets of COVID-19 [44] COVID-19 may reach the central nervous system via the systemic circulation or via the cribriform plate of the ethmoid bone during an early or later phase of the infection as has been reported in SARS-CoV [45] Once the neuronal tissues are reached, the interaction between SARS-CoV-2 and ACE2-R can initiate a cycle of viral growth with co-occurrence of neuronal damage without substantial inflammation as has been seen with cases of SARS-CoV [45] .

What does this mean in the clinical setting?

These are similar to SARS and MERS and merely non-specific including dizziness, nausea, vomiting, and headache [46, 47] . Hypogeusia and hyposmia are frequently reported and have become a cardinal factor in the early diagnosis of COVID-19 [46] .

Most probably, this is caused by direct invasion of the olfactory bulb when SARS-CoV-2 makes its entry into the skull via the cribriform plate [44] .

A recent German report states that it seems to be well distinguishable from a post-infectious olfactory disorder following rhinitis or another upper respiratory tract infection: most of the patients describe a rather sudden, almost complete loss of odour (i.e. mostly anosmia, less often hyposmia). COVID-19 patients are less likely to have other nasal [48] .

By the end of April 2020, after 4 months of evolving pandemic, Guillain Barré syndrome (GBS) was reported in less than ten COVID-19-patients, but more cases are in press.

Most of the cases occurred in the early stage of COVID-19 in patients presenting with only minor respiratory symptoms at onset of GBS. Although it is notable that the disease severity for both the GBS and pneumonia can deteriorate simultaneously [49] [50] [51] .

One report described GBS in a patient without any respiratory symptoms, but with loss of smell and taste preceding GBS [52] .

A variety of cerebrovascular disorders has been recently reported, probably due to endothelial dysfunction, or hypercoagulability in COVID-19 patients.

These disorders include ischemic stroke, intracerebral hemorrhage, and cerebral venous sinus thrombosis [44, [54] [55] [56] . Cerebrovascular disease was associated with poor outcome (more respiratory distress, more multi-organ dysfunction, and higher mortality) of COVID-19 patients [56] .

The three major outbreaks of corona viruses (SARS-CoV, MERS-CoV, and SARS-CoV-2) show similarities in neurological manifestations, but also some differences.

Due to the hospital emergency plan and the splitting of hospitals in hot zones versus cold zones to prevent hospital clusters of corona-infection, neurological work up is limited to bedside clinical evaluation, spinal fluid analysis and CT scan. MRI imaging is mostly located in the cold zone, thus limited available for infected patients. A surveillance of neurological manifestations (Guillain-Barré syndrome, meningoencephalitis, stroke…) in these patients is warranted as is surveillance for thromboembolic sequelae (pulmonary embolism, stroke). Many patients present with fever, respiratory symptoms, but also headache, anosmia, dizziness. However, spinal tap is not routinely performed and literature on spinal fluid analysis is very sparse. An explanation for the lack of CSF-data would be that there is currently no validated test to detect SARS-CoV-2 in CSF. A multidisciplinary approach and more neurology consultations in the emergency department and COVID-19-wards could prevent under-diagnosing of neurological complications and thus insufficient treatment. Rapid diagnosis and proper treatment of Guillain-Barré syndrome, critical illness polyneuropathy, stroke, and other neurological disorders could have a positive impact on outcome. As the COVID-19 pandemic is evolving, our knowledge on the neurological manifestations of COVID-19 is also evolving. Although the current pandemic is of a much higher scale than SARS and MERS, and far more neurological cases could be expected, the thusfar available literature about neurological manifestation of COVID-19 is rather limited. This review will hopefully contribute to increased alertness for both neurologists and non-neurologists involved in the care of COVID-19 patients.

Conflict of interest All the authors report no disclosure nor conflict of interest relevant to the manuscript. All authors report no financial disclosure.

Ethical approval This manuscript does not contain any studies with human participants or animals performed by any of the authors.

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