key: cord-0711611-auo0ya18
authors: Akbar, Mohammad Rizki; Pranata, Raymond; Wibowo, Arief; Lim, Michael Anthonius; Sihite, Teddy Arnold; Martha, Januar Wibawa
title: The prognostic value of elevated creatine kinase to predict poor outcome in patients with COVID-19 - A systematic review and meta-analysis
date: 2021-02-11
journal: Diabetes Metab Syndr
DOI: 10.1016/j.dsx.2021.02.012
sha: d24867f4dc9b3003b7ec4ce38f72c934d1a5df98
doc_id: 711611
cord_uid: auo0ya18

BACKGROUND AND AIMS: Creatine kinase (CK), a marker of muscle damage, is potentially associated with a more severe COVID-19. In this systematic review and meta-analysis, we aim to evaluate the association between the elevated CK and severity and mortality in COVID-19. METHODS: We performed a systematic literature search on PubMed, Scopus, and Embase up until January 26, 2020. The main outcome was poor outcome, a composite of mortality and severe COVID-19. RESULTS: There are 2471 patients from 14 studies included in this systematic review and meta-analysis. The incidence of elevated CK in this pooled analysis was 17% (11%, 22%) and the incidence of poor outcome in this pooled analysis was 27% (19%, 34%). Elevated CK was associated with poor outcome in patients with COVID-19 (OR 3.01 [2.21, 4.10], p < 0.001; I(2): 10.2%). The effect estimate did not vary with age (p = 0.610), male (p = 0.449), hypertension (p = 0.490), and diabetes (p = 0.457). Elevated CK has a sensitivity of 0.24 (0.17, 0.32), specificity of 0.91 (0.86, 0.94), PLR of 2.6 (1.9, 3.7), NLR of 0.84 (0.78, 0.90), DOR of 3 (2, 5), and AUC of 0.62 (0.57, 0.66) for predicting poor outcome in patients with COVID-19. In this pooled analysis, elevated CK confers to a 49% probability for poor outcome and a non-elevated CK confers to a 24% probability. Subgroup analysis and univariate meta-regression indicates that the sensitivity and specificity does not vary with age, male, hypertension, and diabetes. CONCLUSION: Elevated CK was associated with increased mortality and severity in patients with COVID-19. PROSPERO: CRD42021233435.

More than a year since the coronavirus disease 2019 (COVID- 19) was first discovered in Wuhan (China), the pandemic has infected nearly 100 million people. [1] The clinical features of patients range from asymptomatic to fatal. Those with a severe course of disease may develop acute respiratory syndrome (ARDS) with respiratory failure, heart failure, coagulopathy, sepsis, and multiorgan failure, requiring close care in the intensive care unit and mechanical ventilation. [2] the sorting of patients must be decided carefully given the limitations of human and medical resources.

Several inflammatory markers, including D-dimer, procalcitonin, ferritin, and C-reactive protein, frequently elevated with increasing disease severity. [3] Creatine kinase (CK), which is a marker of muscle damage, was also often found to be elevated in deceased patients and those with severe disease. [4, 5] Therefore, higher CK could be used as a prognostic marker to indicate more severe clinical picture of COVID-19. In this systematic review and metaanalysis, we aim to evaluate the association between the elevated CK and severity and mortality in COVID-19.

This is a Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines compliant meta-analysis. This study is registered in PROSPERO (ID: CRD42021233435).

The inclusion criteria were: 1) retrospective and prospective observational studies 2)

reporting COVID-19 patients 3) elevated and non-elevated CK and 2) mortality/severe COVID-19/need for intensive unit care (ICU)/invasive mechanical ventilation (IMV).

Studies were excluded if it fulfils one of the following criteria: 1) preprints, 2) conference abstracts, 3) case reports, 4) abstract-only publication, 5) review articles.

We performed a systematic literature search on PubMed, Scopus, and Embase with keywords "SARS-CoV-2" OR "2019-nCoV" OR"COVID-19" AND "creatine kinase" up until 26 January 2020. Duplicates were then removed and the title/abstracts were screened by two independent authors. Discrepancies in this process were resolved by discussion.

Data extraction of the included studies were performed by two authors independently. The data of interest includes the author, design of the study, baseline characteristics, cut-off for elevated CK, and the outcome of interest.

The key exposure was elevated CK, defined as elevation of CK beyond cut-off point reported in each studies. The main outcome was poor outcome, a composite of mortality and severe COVID-19. Severe COVID-19 was defined as patients with COVID-19 who fulfill the criteria for severe CAP or the need for ICU care or IMV. The effect estimate was odds ratio (OR).

Sensitivity, specificity, positive and negative likelihood ratio (PLR & NLR), diagnostic odds ratio (DOR), and area under curve (AUC) analysis were performed.

We performed risk of bias assessment using the Newcastle-Ottawa Scale (NOS), this was performed by two independent authors and discrepancies were resolved by discussion.

Prevalence was pooled using the meta-analysis of proportion. DerSimonian-Laird method was selected to perform random-effects meta-analysis to generate OR and its 95% CI. A pvalue <0.05 was considered as significant. I-squared (I 2 ) and Cochran Q test were performed J o u r n a l P r e -p r o o f to evaluate heterogeneity, a value of <50% or p < 0.10 indicates substantial heterogeneity.

Sensitivity, specificity, PLR, NLR, DOR, and AUC were generated to evaluate the prognostic value. To assess small-study effects and publication bias, deek's funnel-plot analysis and

Deek's asymmetry test were performed. REML meta-regression was performed for the main outcome, using baseline characteristics as moderator. STATA 16 (Stata Corp) was used to perform meta-analysis.

There are 2,471 patients from 14 studies included in this systematic review and metaanalysis. [6] [7] [8] [9] [10] [11] [12] [13] [14] [15] [16] [17] [18] [19] The baseline characteristics of the included studies can be accessed in Table   1 . The incidence of elevated CK in this pooled analysis was 17% (11%, 22%) and the incidence of poor outcome in this pooled analysis was 27% (19%, 34%). This meta-analysis indicates that elevated CK was associated with increased poor outcome with a sensitivity of 24% and specificity of 91%. Thus elevated CK is best used as a rule-in test rather than rule-out test.

Several parameters and comorbidities may affect the prognosis in patients with COVID-19. [20] [21] [22] [23] [24] Meta-regression analysis showed that the association between elevated CK and poor outcome was not affected by age, male, hypertension, and diabetes. Although it is important to evaluate chronic kidney disease and cardiovascular disease as variables, there are insufficiently reported to enable meta-regression analysis.

The majority of symptomatic patients present with respiratory tract symptoms or related complications. They tend to present as a viral pneumonia with fever, cough, fatigue, dyspnoea, and sometimes complaint musculoskeletal or neurological symptoms such as headache, muscle pain, joint aches, and smell impairment. [4, 5] However, a study [25] reported myalgia as the initial presentation in 22% of cases. One study [25] found that skeletal muscle pain and increased serum CK (>200 U/L) were significantly more common in severe cases [26] , while another study [27] reported a higher prevalence of muscle pain in milder cases.

Rhabdomyolysis, a syndrome characterized by muscle weakness, pain, and red coloured urine, is a possible but rare complication in COVID-19 patients. CK and troponin, enzymes located in the muscle tissue, will rise sharply due skeletal muscle damage and necrosis in rhabdomyolysis. [28] Therefore, patients with severe muscle damage may experience multiorgan dysfunction, including more severe kidney and liver abnormalities. The new coronavirus may possibly cause viral myositis, as seen previously in other coronavirus infections, such as severe acute respiratory syndrome (SARS), and other influenza infections (influenza A and B). [29] It is understood that the novel coronavirus (2019-nCoV or SARS-CoV-2) uses angiotensin converting enzyme 2 (ACE-2) receptor to enter human respiratory cells and cause infection. Due to its presence in various tissues, it is possible that the virus directly invades the skeletal muscle and nervous system via the same pathway. the Immune-mediated pathway might also contribute to cause muscle injury in COVID-19 patients. Moreover, muscle atrophy due to disuse and/or critical illness myopathy and/or polyneuropathy may occur and cause weakness in critically ill patients. [4] In addition, dehydration and hypovolaemia in COVID-19 patients may contribute to renal impairment and subsequent increase in CK levels. [30] It is therefore plausible to suggest CK monitoring in COVID-19 patients, especially when they complain of muscle pain and weakness.

Whether the increase in CK levels is caused by viral myositis, immune hyperactivation, toxic effect of cytokines, or other mechanisms is unclear. Electromyography (EMG), muscle imaging, and muscle histopathology are rarely performed in COVID-19 cases, let alone carrying out a PCR test for detection of SARS-CoV-2 in muscle tissue. A muscle-biopsy specimen of a patient [31] with COVID-19 and myopathy shows evidence of virus-induced type 1 interferonopathy. The specimen revealed mild perivascular inflammatory infiltration in a few vessels without regenerating or necrotic fibers or perifascicular atrophy.

Immunohistochemical analysis did not detect SARS-CoV-2 in the muscle, but showcased abnormal expression of major-histocompatibility-complex class I antigen on sarcoplasm and sarcolemma and abnormal presence of myxovirus resistance protein A on muscle fibers and J o u r n a l P r e -p r o o f capillaries. This type I interferon-inducible protein is released in response to viral infections, including SARS-CoV-2, and its deposition is an early sign of dermatomyositis, followed by characteristic perifascicular atrophy.

Another report of COVID-19 patient [29] with myalgia, proximal weakness (limb, bulbar, and fascial muscles), increased serum CK, and muscle edema on MRI. Diagnosed with myositis and myasthenia gravis, the muscle biopsy demonstrated perivascular inflammation with endomysial extension, regenerating fibers, and upregulation of HLA Class ABC expression on non-necrotic fibers. Histochemiscally, the enzyme cytochrome oxidase/succinic dehydrogenase were unremarkable. On electron microscopy, vacuolar change and curvilinear bodies indicating hydroxychloroquine were absent.

Elevated CK signifies poor prognosis in patients with COVID-19, however, due to low sensitivity; it cannot be used to rule out poor prognosis. Thus, elevated CK is better combined with other variables to form a prediction model rather than used alone.

There is a possibility of publication bias in which only positive studies are being published.

There is also slight variation in cut-off points. Some of important variables such as 

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