Retrospective Study Open Access
Copyright ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Oct 16, 2022; 10(29): 10435-10450
Published online Oct 16, 2022. doi: 10.12998/wjcc.v10.i29.10435
Age-adjusted NT-proBNP could help in the early identification and follow-up of children at risk for severe multisystem inflammatory syndrome associated with COVID-19 (MIS-C)
Moises Rodriguez-Gonzalez, Division of Pediatric Cardiology, Puerta del Mar University Hospital, Cadiz 11009, Spain
Ana Castellano-Martinez, Division of Pediatric Nephrology, Puerta del Mar University Hospital, Cadiz 11009, Spain
ORCID number: Moises Rodriguez-Gonzalez (0000-0002-5587-435X); Ana Castellano-Martinez (0000-0001-7563-1235).
Author contributions: Rodriguez-Gonzalez M and Castellano-Martinez A collected the data, performed the statistical analysis, and wrote the manuscript; Both authors have read and approved the final manuscript.
Institutional review board statement: As retrospective data were collected from clinical reviews only, consent from patients and parents or guardians was not obtained. As the data analysis was retrospective and no additional data were collected beyond those required for standard medical care, a full ethics review was not required.
Informed consent statement: As retrospective data in this study were collected from clinical reviews only, consent from patients and parents or guardians was not obtained.
Conflict-of-interest statement: We have no financial relationships or any other conflict of interest to disclose.
Data sharing statement: No additional data are available.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Ana Castellano-Martinez, MD, Doctor, Research Scientist, Division of Pediatric Nephrology, Puerta del Mar University Hospital, Ana de Viya Avenue 21st, Cadiz 11009, Spain. anacastellanomartinez@gmail.com
Received: March 24, 2022
Peer-review started: March 24, 2022
First decision: June 16, 2022
Revised: June 17, 2022
Accepted: September 1, 2022
Article in press: September 1, 2022
Published online: October 16, 2022

Abstract
BACKGROUND

Multisystem inflammatory syndrome in children (MIS-C) has emerged as a new disease associated with COVID-19 that presents in acute critically ill children with acute cardiovascular dysfunction.

AIM

To determine whether the age-adjusted N-terminal pro-brain natriuretic peptide (NT-proBNP) value (Z-log-NT-proBNP) is associated with severe MIS-C and myocardial dysfunction.

METHODS

A retrospective study was conducted which included children with MIS-C managed at our institution between April 1, 2020, and February 28, 2022. We divided the population into groups depending on severity based on pediatric intensive care unit (PICU) admission. We compared Z-log-NT-proBNP values across these groups and analyzed Z-log-NT-proBNP dynamics during the one-month follow-up.

RESULTS

We included 17 participants [median age 3 (2-9) years] and seven (41%) required PICU admission. All (100%) of these cases presented very high (Z-log > 4) levels of NT-proBNP at the time of admission compared to only 5 (50%) patients with non-severe MIS-C (P = 0.025). NT-proBNP was significantly correlated with high-sensitive Troponin I levels (P = 0.045), Ross modified score (P = 0.003) and left ventricle ejection fraction (P = 0.021).

CONCLUSION

Raised NT-proBNP, specifically very high values (Z-log-NT-proBNP > 4) could help in the early identification of MIS-C patients with myocardial dysfunction requiring inotropic support and PICU admission.

Key Words: Multisystem inflammatory syndrome associated with COVID-19, COVID-19, SARS-CoV-2, NT-proBNP, Echocardiography, Myocardial dysfunction, Children

Core Tip: Multisystem inflammatory syndrome in children (MIS-C) is a rare but serious condition associated with coronavirus disease 2019 in which the cardiovascular system is frequently impaired, with more than half of children presenting with heart failure and myocardial dysfunction secondary to the inflammatory response. N-terminal pro-brain natriuretic peptide (NT-proBNP) is a promising biomarker for the detection of cardiac dysfunction in conditions where heart failure and inflammation coexist, but its use in pediatrics is limited by its strong age-dependency. Therefore, we think that the use of age-adjusted NT-proBNP values could help to identify those children with risk for severe MIS-C.



INTRODUCTION

The coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been a stressful and challenging situation globally. Since its onset in early 2020 it has led to widespread morbidity and mortality worldwide, and it is noteworthy that a new disease has emerged: COVID-19-associated multi-systemic inflammatory response syndrome in children (MIS-C). Reports across the world of children presenting with hyperinflammatory shock, myocardial dysfunction, and multiorgan involvement, sharing clinical characteristics with Kawasaki disease and toxic shock syndrome, led the World Health Organization (WHO) to identify these cases as having a novel condition and to define MIS-C criteria for diagnosis[1].

MIS-C is a relatively rare disease affecting 0.6% of children with COVID-19[2]; most were previously healthy children with a mild-symptomatic/asymptomatic COVID-19. Prior to the description of MIS-C, the pediatric population was not considered to be at serious risk of developing severe COVID-19 and complications compared with adult patients[1]. Although MIS-C is characterized by multisystem involvement, acute cardiovascular dysfunction is a prominent and critical manifestation. This significant cardiovascular compromise includes vasoplegic and cardiogenic shock, severe valve regurgitation, ventricular dysfunction, and coronary artery dilatation[2-7]. Remarkably, a high proportion of children with MIS-C present as acute critically ill children, requiring admission to the pediatric intensive care unit (PICU) in more than half of cases, most requiring inotropic support and even extracorporeal membrane oxygenation (ECMO) in a few of them. Furthermore, the mortality rate is estimated at around 1%, higher than the 0.1%-0.6% mortality rate for pediatric COVID-19 reported before MIS-C[8-10].

Despite this critical presentation, the clinical outcomes of MIS-C are favorable. Fortunately, most children recover rapidly from their acute presentation after initiating immunomodulatory therapy, with complete resolution of cardiac alterations. Cardiac sequelae in mild myocardial dysfunction or coronary artery alterations were present in up to 5%-10% of cases at the time of hospital discharge[8-10]. Studies with long-term follow-up periods of 6-9 mo, assessing cardiac function by speckle tracking echocardiography and myocardial fibrosis by cardiac MRI, have shown complete cardiac recovery in most children[11-15].

As the long-term prognosis seems excellent, prompt initiation of anti-inflammatory therapy and cardiovascular support in the acute phase is crucial for a successful, rapid, and complete recovery. Therefore, identifying early markers of cardiac dysfunction would be helpful for both directed therapy and identifying MIS-C patients at the highest risk for deterioration. As echocardiography is a non-widely available technique in all emergency departments and requires training and experience for proper application, it would be interesting to investigate laboratory markers of more widespread use that identify patients with MIS-C in whom there may be echocardiographic alterations. Using cardiac biomarkers such as N-terminal (1–76) pro-brain natriuretic peptide (NT-proBNP) seems to be a promising tool. NT-proBNP secretion from the ventricular myocardium is up-regulated by myocardial stress in situations of myocardial volume/pressure over-load[16]. Thus, it is an excellent biomarker for heart failure and myocardial dysfunction on echocardiography[17-19]. Notably, its secretion is also influenced by the inflammatory response[20,21]. NT-proBNP is increasingly used as a biomarker in pediatric conditions that combine myocardial stress and inflammatory diseases, such as sepsis or Kawasaki disease[22-24]. Therefore, it is not surprising that NT-proBNP levels are markedly raised in almost all patients with MIS-C, where the proposed mechanism for the cardiovascular dysfunction is myocardial inflammation related to systemic inflammation with a cytokine storm[4,8,11,25,26].

An increasing number of studies have reported the characteristics of cardiac markers in MIS-C patients. Some investigations suggested that the patients requiring PICU admission present with the highest peak NT-proBNP values at the time of hospitalization[4]. However, all studies exploring the role of NT-proBNP in MIS-C use heterogeneous and fixed or static cut-off points based on adult reference values for diagnosing congestive heart failure in adults (150-300 pg/mL)[27]. This is a significant limitation, as pediatric NT-proBNP values are strongly age-dependent, with a continuous decrease from birth to adolescence, with a constant decline from infant to adult, being more marked in the neonatal period and the first year of life[28,29]. This age dependence makes it impossible to compare absolute NT-proBNP values in age-heterogeneous populations such as MIS-C[28]. Recently, Palm et al[29] introduced NT-proBNP values adjusted for the age in days, providing continuous reference values across all the pediatric age intervals, which is a more physiological approach. These authors also demonstrated the superiority of the age-adjusted approach compared with the use of absolute values to detect severe myocardial dysfunction in a pediatric population with congenital heart diseases. Therefore, the age-adjusted (Z-log-NT-proBNP) system could provide uniformity to research studies using NT-proBNP.

This study describes the dynamics of NT-proBNP and echocardiographic alterations in our MIS-C case series during the first month of disease. The primary objective is to determine whether the Z-log-NT-proBNP values are associated with severity and echocardiographic alterations during the acute phase of the disease.

MATERIALS AND METHODS
Design, setting, and participants

This is a retrospective case series study conducted in the Pediatric Cardiology Division of our institution, a tertiary-level university hospital in Cadiz, Spain. We included children aged less than 16 years meeting classification criteria for MIS-C according to the World Health Organization definition (Table 1)[1] between April 1, 2020, and February 28, 2022. All patients were managed following current international recommendations[30] at the discretion of the attending pediatrician. We excluded patients with a known underlying or new diagnosis of heart disease during hospitalization and patients lost to follow-up, or those with incomplete data. As retrospective data were collected from clinical reviews only, consent from patients, parents, or guardians was not obtained. As the data analysis was retrospective and no additional data were collected beyond those required for standard medical care, a full ethics review was not required.

Table 1 World Health Organization case definition for Multisystem inflammatory syndrome in children.
All criteria must be met
Age 0 to 19 yr
Fever ≥ 3 d
Clinical signs of multisystem involvement (at least 2 of the following):
Rash, bilateral non purulent conjunctivitis, or mucocutaneous inflammation (oral, hands, or feet)
Hypotension or shock
Cardiac dysfunction, pericarditis, valvulitis, or coronary abnormalities (including echocardiographic findings or elevated troponin/BNP)
Evidence of coagulopathy (prolonged PT or PTT; elevated D-dimer)
Acute gastrointestinal symptoms (diarrhea, vomiting, or abdominal pain)
Elevated markers of inflammation (e.g., ESR, CRP, or procalcitonin)
No other obvious microbial cause of inflammation, including bacterial sepsis and staphylococcal/streptococcal toxic shock syndromes
Evidence of SARS-CoV-2 infection with any of the following:
Positive SARS-CoV-2 RT-PCR
Positive serology
Positive antigen test
Contact with an individual with COVID-19 either laboratory confirmation of SARS-CoV-2 infection by RT-PCR, serology, or antigen test, or known COVID-19 exposure within 4 weeks before symptom onset
Cardiac management and follow-up

All MIS-C patients managed in our institution were evaluated by the Pediatric Cardiology Division through a physical exam, ECG, cardiac biomarkers (High Sensitivity-Troponin I (hs-TnI) and NT-proBNP), and 2D-Doppler echocardiography at least at four different time points: (1) First 24 h of admission; (2) 24 h after administering immunomodulatory therapy; (3) Hospital discharge; and (4) 1-mo post-admission. The start and discontinuation of any cardiac medication were carried out at the discretion of the attending pediatric cardiologist, following local protocols and international guidelines for cardiogenic shock and heart failure[19]. Further cardiac controls were performed for each patient during admission and post-discharge follow-up based on their clinical state and evolution. These data were not collected for the present study. Cardiac MRI was not performed on any patient during the acute or subacute phase.

Data collection

Our institution's electronic clinical records were reviewed by one investigator (ACM), who abstracted data for each time point described previously. Information collected included patient demographics and preexisting comorbidities, clinical presentation, laboratory findings, imaging findings, microbiological investigations, treatment, and outcomes.

Main cardiac measurements and definitions

Heart failure: Clinical heart failure status was defined based on the age-based Ross modified score[31]. In this score, each age range (0–3 mo, 4–12 mo, 1–3 years, 4–8 years, and 9–18 years) has ten variables with scores of 0, 1, or 2 possible for a range of 0 to 20. The scoring system can be used as a continuous data set for comparison with outcomes, or it can be categorized by points assessed as Ross classes I (0–5; no heart failure), II (6–10; mild heart failure), III (11–15; moderate heart failure) and IV (16–20; severe heart failure).

Raised hs-TnI: hs-TnI was the biomarker used in our institution to assess myocardial injury or ischemia. hs-cTnI levels were measured in ng/L using the Architect i1000SR platform (Abbott Diagnostics®, Spain) with 1.1–1.9 ng/L of a lower detection limit, 2.5% intra-run variation, and < 4% inter-run variation). In the absence of clear pediatric reference values for hs-cTnI, we defined myocardial injury as the presence of serum levels plus 50 ng/L, the reported 75th percentile for this assay in infants and children[32].

Raised NT-proBNP: NT-proBNP was the biomarker used in our institution to assess myocardial strain. NT-proBNP levels were measured in pg/mL using the Alere NT-proBNP for Alinity I assay (Abbott Diagnostics®, Spain). The intra-assay and inter-assay coefficients of variation were 1.9% to 2.9% and 2.6% to 5.4%, respectively, with an analytical range of 8.3 to 35 000 pg/mL. As reference values for children are markedly age-dependent, we calculated Z-log-NT-proBNP values adjusted for age as recommended by Palm et al[29], and Z-log > 1.96 was considered high NT-proBNP. We anticipated that all patients in our case series had Z-log-NT-proBNP > 1.96. For the statistical analysis, we defined very high NT-proBNP as Z-log-NT-proBNP > 4 (double of average values for age).

Abnormal echocardiographic findings: Standard techniques to obtain M-mode, two-dimensional, and Doppler echocardiograms were performed in all patients by the senior pediatric cardiologist as recommended in the guidelines for pediatric echocardiography[33]. Images were obtained using IE33 (Phillips®) or Aplio i-series (Canon Medical Systems®) machines with a 5, 8, or 12-MHz sectorial transducer. This study focused on left and right ventricular function and coronary artery dimensions, as these are the main cardiac alterations previously described in MIS-C patients. Left ventricular (LV) dysfunction was defined as an LV ejection fraction (LVEF) < 55%, and graded as mild (LVEF 45% to 54%), moderate (LVEF 35% to 44%), or severe (LVEF < 35%). Right ventricular (RV) dysfunction was defined as tricuspid annular plane systolic excursion (TAPSE) < 2 Z-score for body surface area[34]. In cases where LVEF or TAPSE were unavailable, ventricular dysfunction definition was based on the qualitative grade of hypokinesis. Coronary artery dilation was defined as diameter > 2 Z-scores for body surface area (BSA) by the published reference standard in the affected segment[35], and graded as dilation 2.0–2.49, small aneurysm > 2.5 to < 5, medium aneurysm > 5 to < 10, and large aneurysm > 10.

Cardiac sequelae: All children with MIS-C who had any abnormal cardiac measurement of those described above at the time of discharge or after one month were defined as cardiac sequelae.

Research endpoints: The research endpoints in this study were: (1) Development of severe MIS-C during hospitalization was defined as the need for PICU admission; (2) The presence of abnormal echocardiography at admission; and (3) The presence of cardiac sequelae. The study population was divided into two groups based on the predefined research endpoints. The analysis focused on comparing cardiac biomarkers values across these groups and the cardiac dynamics throughout the follow-up.

Statistical analysis

Descriptive statistics were used to summarize our population's baseline key features and outcomes. The hs-TnI values were log-transformed and standardized to account for widely varying ranges, and Z-log-NT-proBNP values were calculated as previously described. These values of cardiac biomarkers were those used in statistical analysis and graphics. Continuous data were expressed as median and interquartile range values. Categorical data were expressed as frequencies and proportions (%). Continuous variables were analyzed using the nonparametric U-Mann Whitney test as normality was not assumed with the sample size of our case series. Categorical variables were analyzed using the chi-square and Fisher's exact test. Spearman rank correlation coefficients were used to identify relationships between continuous variables. Differences in repeated cardiac measurements between the four-time points used in this study were assessed using the Wilcoxon signed rank-sum test. Due to the limited sample size of this study, we were unpowered to establish cut-off points to identify outcomes. For all analyses, P values of < 0.05 were considered significant. Due to the potential for type I error because of multiple comparisons, our findings should be interpreted as exploratory. All statistical analyses were performed with Stata v.16 software (StataCorp, College Station, TX, United States).

RESULTS
Baseline characteristics

This case series included 17 MIS-C participants [9 (53%) males; 14 (82%) white race] with a median age of 3 (2-9) years. Tables 2 and 3 summarize baseline clinical, laboratory, and echocardiographic data at admission. Sixteen (94%) cases were previously healthy children. Four cases (24%) were diagnosed with COVID in the previous 4-8 wk, and in 15 (88%), we documented IgG antibodies to SARS-CoV-2, and 7 (41%) had positive RT-PCR tests. No other microbial cause of the illness was identified in these patients.

Table 2 Demographic data and clinical presentation of the study population.
N = 17
Results
Age (yr)23 (2-9)
Weight (kg)217 (12-34)
Gender (male)19 (53)
Ethnicity (white)114 (82)
Comorbidity11 (6)
Known previous COVID-19 disease (4-8 wk before)14 (24)
Contact with known COVID-19 case17 (41)
IgG antibodies to SARS-CoV-2115 (88)
SARS-CoV-2 RT-PCR positive test17 (41)
Fever117 (100)
Days of fever24 (3-4)
Cutaneous rash17 (41)
Conjunctivitis17 (41)
Lymphadenopathy15 (29)
Palmar or plantar erythema13 (17)
Changes in oral mucosa16 (35)
Respiratory symptoms13 (17)
Hypoxemia12 (12)
SpO2 (%)298 (97-99)
Gastrointestinal symptoms110 (58)
Neurological symptoms13 (17)
Heart failure (age-based Ross score > 5)111 (65)
Cardiogenic/Vasoplegic shock13 (17)
Tachycardia113 (76)
Heart rate (bpm)2150 (120-160)
Hypotension14 (23)
Systolic arterial pressure (mmHg)297 (75-106)
Diastolic arterial pressure (mmHg)260 (40-68)
Table 3 Baseline laboratory and echocardiographic data of the study population.
N = 17
Results
Leukocytes (/µL)29930 (83490-12250)
Leukocytosis14 (23)
Lymphocytes (/µL)21480 (680-3100)
Lymphopenia19 (53)
Hemoglobin (g/dL)210.7 (8-12.2)
Anemia18 (47)
Thrombocytes (/µL)2161000 (120000-238000)
Thrombocytopenia15 (29)
Dimer D (ng/mL)23504 (3284-5290)
Coagulopathy17 (41)
CRP (mg/L)2171 (121-201)
Procalcitonin (ng/mL)23.2 (1.4-10.2)
Ferritin (ng/mL)2789 (552-978)
Creatinine (mg/dL)20.5 (0.4-0.57)
Urea (mg/dL)223 (19-31)
AKI12 (11)
Sodium (mEq/L)2134 (131-137)
Hyponatremia18 (47)
GPT (U/L)240 (25-66)
Hypertransaminemia16 (35)
pH27.37 (7.34-7.4)
pCO2 (mmHg)237 (33-39)
HCO3 (mmol/L)223 (21-24)
Acidosis14 (23)
NT-proBNP (pg/mL)25221 (2638-10020)
NT-proBNP (Z-log value adjusted for age)24.62 (4.46-5.23)
High NT-proBNP (Z-log for age > 2)117 (100)
Very high NT-proBNP (Z-log for age > 4)112 (71)
hs-TnI (ng/L)235 (10-116)
High hs-TnI (> 50 ng/L)15 (29)
LVEF (%)2
LV dysfunction, n (%)1
Maximal CA diameter (Z-score)2
CA dilation1

All patients presented with fever with a median duration of 4 (3-4) days before hospitalization, with mucocutaneous inflammatory (41%) and gastrointestinal symptoms (58%) as the common non-cardiac manifestations. Eleven (65%) cases were diagnosed with heart failure by the age-based Ross modified score. Of these, 5 (29%) had severe heart failure, and 3 (17%) were in cardiogenic shock at presentation.

At the time of hospitalization, 8 (47%) patients had anemia, 5 (29%) thrombocytopenia, and 9 (53%) lymphopenia, and all laboratory markers of an inflammatory response (C-reactive protein (CRP), procalcitonin, ferritin, and Dimer-D) were markedly elevated (Table 2). With regard to cardiac biomarkers, both NT-proBNP (median values of 5221 (2638-10020) pg/mL) and hs-TnI (35 (10-116) ng/L) were markedly raised. All patients presented with high (Z-log > 2) NT-proBNP, most of them (71%) with very-high (Z-log > 4) plasma levels, whereas 5 (29%) participants showed hs-TnI concentrations indicative of myocardial injury.

Abnormal echocardiographic findings were found in 10 (58%) cases; 9 (53%) patients had LV dysfunction, 2 (11%) of them with concomitant RV dysfunction. On admission, the medial LVEF was 58 (48-65)%; in 2 (11%) patients, the myocardial dysfunction was graded as severe and in the other 2 (11%) as moderate. There was mild coronary artery dilation (Zscore 2-2.5) in 3 (17%) patients. ECG was performed in all patients, with sinus tachycardia in 14 (82%) and T-wave inversion at left precordial leads in 2 (11%) cases). Chest X-ray was performed in 12 (70%) children and was considered abnormal in 3 (17%), 2 cases with cardiomegaly, and 1 (6%) case with lung edema. Abdominal ultrasound was carried out in 8 (47%) participants with unspecific lymphadenopathy and ileocolitis as the main findings.

Treatment and outcomes

Treatment was provided as recommended in the standard treatment guidelines for MIS-C. All our patients showed an excellent short-term clinical course in this study and were discharged after 7 (5-10) days of hospitalization. Table 4 summarizes the treatment and outcomes of the study population. Immunomodulatory therapy was administered to all patients. Steroids plus intravenous immunoglobulin (IVIG) were used in 14 (82%), and only steroids were used in 2 (11 %) cases. In 4 (23%) children, the inflammatory response was not controlled with first-line therapy and required a biological medication; anakinra in 3 (17%) cases and tocilizumab in 1 (6%) case leading to rapid control of the hyperinflammatory state. All patients continued steroids until fever disappeared and all inflammatory markers were in the normal ranges. Aspirin was used in most (88%) cases, whereas anticoagulation with low molecular weight heparin was administered only in 3 (17%) critically ill patients presenting with shock and myocardial dysfunction. Empirical broad-spectrum antibiotics were started in many patients (88%) at the time of hospitalization and were discontinued after the blood and urine cultures were noted to be sterile. Ten (53%) children required diuretics to relieve congestive heart failure, and in 6 (35%), therapy against myocardial remodeling (enalapril + carvedilol) was started. Of these patients, 8 (59%) continued on cardiac medications at discharge, and all were tapered off after one month of hospitalization in the outpatient clinic. There were no arrhythmic events, and no anti-arrhythmic medication was needed.

Table 4 Treatment and clinical outcomes of the study population.
N = 17
Results
IVIG114 (82)
Steroids116 (94)
Aspirin115 (88)
LWH13 (17)
Anakinra13 (17)
Tocilizumab11 (6)
Antibiotics115 (88)
Diuretics110 (53)
Beta blockers16 (35)
ACEIs16 (35)
Antiarrhythmics10 (0)
Oxygen (nasal cannula)12 (11)
CPAP11 (6)
Mechanical ventilation11 (6)
Inotropics17 (41)
ECMO10 (0)
Resistance to immunomodulatory therapy14 (23)
PICU admission17 (41)
PICU stay (days)23.5 (3-4.5)
LOS hospitalization (days)27 (5-10)
Heart failure at discharge11 (6)
Myocardial dysfunction at discharge11 (6)
Coronary artery dilation at discharge12 (11)
Raised hs-TnI or NT-proBNP at discharge19 (53)
Cardiac medications at discharge18 (47)
Any cardiac sequelae or medications at 1 month follow-up10 (0)
Death10 (0)

Seven (41%) participants required PICU admission (median PICU stay of 3.5 (3-4.5 days) and administration of inotropic support in the severe MIS-C group. Milrinone was used alone in 3 (17%) cases, milrinone in combination with norepinephrine in 3 (17%) cases, and levosimendan combined with norepinephrine in 1 (6%) case. No patients required ECMO support for the management of cardiogenic shock. Respiratory therapy included invasive ventilation in 1 patient (6%), continuous positive airway pressure in 1 patient (6%), and conventional oxygen therapy in 2 patients (11%). Two (11%) patients presented acute kidney injury without requiring renal replacement therapy. There were no deaths.

Dynamics of cardiac abnormalities

Regarding the dynamic changes of cardiac abnormalities, we observed a significant rapid, gradual, and continuous clinical, laboratory, and echocardiographic improvement in our patients following immunomodulatory therapy administration. This improvement was coupled with the disappearance of fever and a marked decrease of the remaining laboratory inflammatory markers (data not shown). Cardiac abnormalities observed on the four-time points assessed in this study are detailed in Table 5 and Figure 1.

Figure 1
Figure 1 Bar (left panel) and box-plot (right panel) diagrams showing the dynamics of different cardiac measurements. A: Ross modified score; B: High Sensitivity-Troponin I; C: N-terminal pro-brain natriuretic peptide; D: Left ventricular ejection fraction; obtained at 4 different time points in this study. NT-proBNP: N-terminal pro-brain natriuretic peptide; LVEF: Left ventricular ejection fraction.
Table 5 Dynamics of cardiac parameters during the follow-up in this study. Comparison between groups regarding duration of respiratory support.
Cardiac parameter
Admission
24 h after AIT
Discharge
After 1-mo fu.
NT-proBNP (Z-log value adjusted for age)24.62 (4.46-5.23)3.78 (3.26-4.87)11.79 (0.66-2.5)10.72 (0.21-1.29)1
Log (10)-Hs-TnI (ng/L)235 (10-116)13 (5-35)110 (10-13)110 (10-10)
LVEF (%)258 (48-65)68 (65-70)170 (66-72)70 (68-71)
Coronary arteries maximal dimension (Z-score for BSA)21.39 (0.56-2.66)1.2 (0.77-1.5)1 (0.5-1.2)10.8 (0.51-1.2)
Age-based Ross classification for heart failure in children28 (4-12)3 (2-7)10 (0-0)10 (0-0)

After 24 h of treatment, heart failure persisted in 7 (63%) children, but with no severe cases and a significant decrease in the age-based Ross modified score from 8 (4-12) points to 3 (2-7) points (P < 0.001) in parallel with significant enhancement of LVEF from 58 (48-65)% to 68 (65-70)% (P < 0.001), with 6 (35%) cases of mild and 1 (6%) case of moderate LV dysfunction, and complete resolution of RV dysfunction. There was also a significant decrease in the plasma levels of both cardiac biomarkers. At this time point, NT-proBNP decreased from Z-log of 4.62 (4.46-5.23) to Z-log of 3.78 (3.26-4.87) (P = 0.001), with very high levels still observed in 5 (29%) cases; and hs-TnI decreased from 35 (10-116) ng/L to 13 (5-35) ng/L (P = 0.008), with raised levels in 4 (23%) cases.

At discharge, we documented a continuous significant (P < 0.001) improvement in all these cardiac measurements and coronary artery dimensions concerning the previous time points assessed. However, some cardiac abnormalities remained: 1 (6%) case of mild heart failure with mild LV dysfunction, the patient presenting with the most severe disease and decreased LVEF; 2 (11%) cases of mild coronary artery dilation; 3 (17%) cases of raised hs-TnI in 3 (17%) levels and 9 (53%) cases of high (Z-log>2) NT-proBNP levels.

In the follow-up visit at the pediatric cardiologist outpatient clinic one month after hospitalization, we documented complete normalization of the cardiac state, without cardiac sequelae in any of the patients.

Cardiac biomarkers to assess severe MIS-C and echocardiographic abnormalities

The group with severe MIS-C was composed of the 7 (41%) patients that required PICU admission and inotropic support. Compared with those cases with non-severe MIS-C, these patients presented with a higher Ross modified score (P = 0.003), lower LVEF (P = 0.034), and higher Z-log-NT-proBNP (P = 0.016) (Table 6 and Figure 2). There were no differences regarding hs-TnI levels, coronary dimensions, demographics, days of fever, and any laboratory marker of inflammation (all P > 0.05). Focusing on NT-proBNP, we were not powered to assess sensitive laboratory cutoffs of NT-proBNP predictive of severe MIS-C. Therefore, we assessed the association of high NT-proBNP with severe MIS-C as a dichotomous variable. We observed that 7/7 (100%) patients with severe MIS-C had very high (Z-log > 4) levels of NT-proBNP at the time of admission compared to only 5 (50%) patients with non-severe MIS-C (P = 0.025). We also found that our patients' NT-proBNP levels were associated with other cardiac abnormalities. Specifically, NT-proBNP was significantly correlated with hs-TnI levels (P = 0.045), Ross modified score (P = 0.003), and LVEF (P = 0.021), but not with the maximal coronary artery diameter (Table 7 and Figure 3).

Figure 2
Figure 2 Box-plot diagrams showing the comparison of left ventricular ejection fraction (left panel) and N-terminal pro-brain natriuretic peptide (right panel) between groups of multisystem inflammatory syndrome in children severity. PICU: Pediatric intensive care unit.
Figure 3
Figure 3 Scatter-plot diagrams. A: The association between N-terminal pro-brain natriuretic peptide and Ross modified score; B: High Sensitivity-Troponin I; C: Left ventricular ejection fraction.
Table 6 Comparison of clinical, laboratory and echocardiographic characteristics according to the need of pediatric intensive care unit admission and inotropic support during hospitalization.
Variable
PICU admission (n = 7; 41%)
No PICU admission (n = 10; 59%)
P value
Age (mo)26 (1-12)2.5 (2-8)NS.
Male sex18 (53)14 (56)NS.
Weight (kg)35 (71)4 (40)NS.
Days of fever24 (2-5)4 (3-4)NS.
Age-based Ross score216 (11-19)4 (2-8)0.003
Lymphocytes (/µL)21240 (720-5940)1552 (1260-3100)NS.
CRP (mg/L)2171 (120-237)167 (131-201)NS.
Procalcitonin (ng/mL)23.6 (1.3-21.6)2.5 (1.4-8.8)NS.
Ferritin (ng/mL)2814 (552-2789)750 (517-878)NS.
Dimer D (ng/mL)23436 (2461-9434)4728 (3284-5290)NS.
NT-proBNP (Z-log for age)25.41 (4.62-6.51)4.48 (4-5)0.016
Troponin I (ng/L)240 (10-909)27 (10-43)NS.
LVEF (%)248 (45-65)62.5 (57-67)0.034
Maximal CA diameter (Z-score)21.2 (0.55-1.4)1.5 (0.5-3)NS.
Table 7 Correlation analysis of the relationship between N-terminal pro-brain natriuretic peptide and all the cardiac continuous variables explored in this study.
NT-proBNP (Z-log value adjusted for age)
Correlation coefficient
P value
hs-TnI (ng/L)0.470.045
Age-based Ross score for heart failure0.760.003
LVEF (%)-0.550.021
Maximal CA diameter-0.21NS.
DISCUSSION

In this article, we describe the evolution of cardiac biomarker elevation and echocardiographic findings in 17 MIS-C cases focusing on NT-proBNP dynamics during both the acute phase and recovery. Our cohort's spectrum of cardiac involvement is similar to the larger MIS-C case series. We observed a high rate of echocardiographic abnormalities in the acute phase in our patients, with 53% of cases presenting with myocardial dysfunction. These alterations improved rapidly after immunomodulatory treatment, with 94% of cases asymptomatic and normal LV function at hospital discharge and recovered completely after one month of follow-up. In one of the first multicenter studies focusing on cardiovascular manifestations in MIS-C, Valverde et al analyzed 286 children and found that LV dysfunction was present in 34% on admission but recovered to normal in 80% during hospitalization[4]. The more extensive case series of MIS-C published (n = 539) also found reduced left ventricular systolic function in 34.2%, with a complete normalization in 91% within 30 d and 99.4% by 90 d[7]. A recent single-center study (n = 46) by Penner et al[36] showed normalization of LVEF in all patients by six months. Matsubara et al[13] recently showed using speckle tracking echocardiography in 60 children with MIS-C that there is no persistent subclinical dysfunction after three months. Capone et al[6] reported that 62% and 52% of MIS-C cases required PICU admission and inotropic support for myocardial dysfunction, respectively.

In addition to being very frequent, myocardial dysfunction was associated with severe MIS-C disease in our patients and had prognostic implications. All patients who required PICU had myocardial dysfunction on admission echocardiography. Valverde et al[4] described the children requiring intensive care unit admission as having significantly reduced LV systolic ventricular function. Sanil et al[37], in a longitudinal observational study of 54 patients with MIS-C, reported that impaired LV function at initial presentation indicates a higher risk of an adverse acute clinical course and persistent subclinical left ventricular dysfunction at the 10-wk follow-up could be applied to identify higher-risk children with MIS-C.

The previously mentioned observations highlight the relevance of identifying myocardial dysfunction in MIS-C patients, and based on our findings, NT-proBNP could be an adequate tool for this purpose. The association of higher levels of NT-proBNP with myocardial dysfunction and severe MIS-C requiring PICU and inotropic support has been previously described in larger studies. Abrams et al[38] analyzed 1080 cases of MIS-C. They determined that PICU admission, LV dysfunction, and the need for inotropic support were associated with increased concentrations of C-reactive protein, troponin, ferritin, D-dimer, NT-proBNP, or interleukin-6, or reduced platelet or lymphocyte counts. A recent meta-analysis on the role of cardiac biomarkers in MIS-C that included 1613 patients from 24 studies determined that NT-proBNP was the only cardiac biomarker able to differentiate between patients with severe/non-severe MIS-C[39]. However, there is no evidence on the best cut-off point to use in this context.

Our study is novel in using Z-log-NT-proBNP for the first time to assess the severity and echocardiographic abnormalities in MIS-C, overcoming the main limitation of using this biomarker in children, its strong age dependence. Using this approach, we observed that all our patients presented with raised levels of NT-proBNP (Z-log-NT-proBNP > 2) and that 71% were twice the average for their age (Z-log-NT-proBNP > 4). These data point to the importance of NT-proBNP as a biomarker in the differential diagnosis of MIS-C with other conditions with lesser potential severity with which it shares clinical and laboratory findings (acute appendicitis, Kawasaki disease, exanthematous fevers...). Notably, Z-log-NT-proBNP showed a moderate to strong correlation with all the cardiac alterations measured in this study (except for coronary artery dilation): LVEF, the Ross modified score and hs-TnI levels. Furthermore, it is also noteworthy that all patients admitted to the PICU and required inotropic support had Z-log-NT-proBNP > 4 on admission. Z-log-NT-proBNP is increasingly used in congenital heart disease, where it is a suitable marker of severity[40]. Specifically, Palm et al[29], in a recent study that included 138 children with a wide age range (1 day-7.5 years), concluded that patients with very high NT-proBNP values (Z-log-NT-proBNP > 3) were at higher risk of developing major adverse events during follow-up, highlighting a negative predictive value of 96% for a cut-off point Z-log-NT-proBNP < 1.96 (average for the age). The small sample size limits our ability to calculate the diagnostic accuracy of NT-proBNP for these outcomes. However, based on our observations, Z-log-NT-proBNP > 4 may be more indicative of concerning echocardiographic findings associated with illness severity, including reduced LVEF and the need for PICU admission for inotropic support. Therefore, it could be an appropriate starting point to explore in future prospective studies with larger sample sizes.

Finally, another interesting finding in our case series is the delayed improvement of NT-proBNP levels regarding myocardial function normalization. We observed that 94% of our patients were free of symptoms of congestive heart failure and with normal LVEF at discharge, whereas 53% still presented biochemical signs of myocardial stress with a Z-log-NT-proBNP > 1.96. NT-proBNP secretion is stimulated by myocardial stress and the systemic inflammatory response in MIS-C[20,25,26]. Several reasons could explain the persistence of elevated NT-proBNP levels in patients with normal myocardial function. Subtle systemic inflammatory responses may persist, although this is unlikely as all patients had normal inflammatory marker levels at discharge. More likely, this is due to the persistence of subclinical myocardial dysfunction. Although myocardial function recovered when measured by standard methods such as LVEF, recent studies using speckle tracking imaging demonstrated that subclinical LV dysfunction persists in these patients for at least 1-3 mo after hospitalization[13,15,36]. Therefore, NT-proBNP could be used as a laboratory marker of this subclinical dysfunction, aiding in the appropriate monitoring of cardiovascular complications in these patients during their post-hospitalization follow-up, especially in centers where speckle tracking echocardiography is not available.

The main limitations of this study include the single-center nature, retrospective design, and small sample size. In addition, laboratory values of NT-proBNP are assay-dependent and cannot be compared between centers using different laboratory methods for its determination. Finally, the follow-up period was limited to 1 mo, and we did not perform advanced imaging techniques (speckle tracking echocardiography or cardiac MRI) to determine subclinical myocardial impairment. This approach prevents us from establishing a long-term prognosis and ensuring that there are no mid-term myocardial alterations in MIS-C patients.

CONCLUSION

Our experience supports previous findings that MIS-C presents a high rate of myocardial involvement, impacting the severity of the disease. This myocardial involvement appears to recover quickly and with near-complete normalization of cardiac function a few days after immunomodulatory therapy and administration of cardiovascular support. Therefore, the early identification of cardiac dysfunction is crucial to start prompt treatment modalities and prevent cardiovascular complications. Based on our observations, NT-proBNP seems to be a promising biomarker for the initial screening and monitoring of myocardial dysfunction during the acute phase, where Z-log-NT-proBNP > 4 may be more indicative of concerning echocardiographic findings associated with illness severity; also, it could have a role in the post-hospitalization follow-up of these patients. Using Z-log-NT-proBNP values would provide constant reference values of NT-proBNP in children with MIS-C and would lead to consistency in data analysis across centers worldwide.

ARTICLE HIGHLIGHTS
Research background

Multisystem inflammatory syndrome in children (MIS-C) emerged as a severe new disease associated with coronavirus disease 2019. One of the most critical issues is the high prevalence of cardiovascular involvement in these children, leading to a high percentage of cardiogenic shock, myocardial dysfunction secondary to the inflammatory response, and the need for inotropic support and extracorporeal membrane oxygenation (ECMO).

Research motivation

MIS-C is a severe new entity, and we still know very little about it. Therefore, it is necessary to communicate the experience in the management of these patients as well as to generate scientific evidence on all aspects of MIS-C that allow the best management of these patients.

Research objectives

This study was designed to identify clinical and laboratory markers of severity in this new disease. MIS-C is a condition with cardiac involvement in almost all cases. Therefore, we decided to analyze whether NT-proBNP, one of the most widely used cardiac biomarkers in routine clinical practice, was capable of identifying the most severe cases that required admission to the pediatric intensive care unit (PICU) and administration of inotropic support. We also aimed to determine whether NT-proBNP was an adequate follow-up parameter in this setting.

Research methods

A retrospective study was conducted which included children with MIS-C managed at our institution between April 1, 2020, and February 28, 2022. We divided the population into groups of severity based on PICU admission. We compared Z-log-NT-proBNP values adjusted for age in days across these groups and analyzed Z-log-NT-proBNP dynamics throughout the one-month follow-up.

Research results

We included 17 participants (median age 3 (2-9) years) and seven (41%) required PICU admission. All (100%) of these cases presented very high (Z-log > 4) levels of NT-proBNP at the time of admission compared to only 5 (50%) patients with non-severe MIS-C (P = 0.025). NT-proBNP was significantly correlated with high-sensitivity Troponin I levels (P = 0.045), Ross modified score (P = 0.003) and left ventricle ejection fraction (P = 0.021). NT-proBNP was raised in all of our patients at admission, and we observed a significant rapid, gradual, and continuous decrease in our patients following immunomodulatory therapy administration. In the follow-up visit at the pediatric cardiologist outpatient clinic one month after of the hospitalization, we documented complete normalization of the cardiac state, without cardiac sequelae in any of the patients.

Research conclusions

Raised NT-proBNP, specifically very high values (Z-log-NT-proBNP > 4), could help identify MIS-C patients with myocardial dysfunction requiring inotropic support and PICU admission. NT-proBNP could also have a role in the post-hospitalization follow-up of these patients to monitor their cardiovascular recovery.

Research perspectives

NT-proBNP is a promising biomarker for the initial screening and monitoring of myocardial dysfunction during the acute phase of MIS-C. However, its use in pediatrics is limited by its strong age dependency. Using Z-log-NT-proBNP values could provide constant reference values of NT-proBNP in children with MIS-C and would lead to consistency in data analysis across centers worldwide. NT-proBNP could also be used as a laboratory marker of subclinical myocardial dysfunction, aiding in the appropriate monitoring of cardiovascular complications in these patients during their post-hospitalization follow-up, especially in centers where speckle tracking echocardiography is not available. Therefore, this study could be an appropriate starting point to explore in future prospective studies with larger sample sizes and to confirm our results.

Footnotes

Provenance and peer review: Invited article; Externally peer reviewed.

Peer-review model: Single blind

Specialty type: Pediatrics

Country/Territory of origin: Spain

Peer-review report’s scientific quality classification

Grade A (Excellent): 0

Grade B (Very good): 0

Grade C (Good): C, C

Grade D (Fair): 0

Grade E (Poor): 0

P-Reviewer: Gupta MK, Germany; Sitkin S, Russia S-Editor: Liu JH L-Editor: Webster JR P-Editor: Liu JH

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