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Evaluation of Cardiac Involvement in Pediatric Dengue Fever Through Troponin I and CPK-MB Correlation

Original Articles

L Venkanteshan, Shree

PaperID : JMRP-04-2025-41

Published Date : April 30, 2025

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Peer ReviewedPeer Reviewed

Venkanteshan L, Shree . Evaluation of Cardiac Involvement in Pediatric Dengue Fever Through Troponin I and CPK-MB Correlation. Nurexus; Journal of MedVerse Research & Practice. 2025;1(1):1-5. Available from: https://nurexus.com/journals/published/JMRP-04-2025-41

Venkanteshan et al | Nurexus | Journal of MedVerse Research and Practice | Volume 3 | Issue 04 | April 2025
Page 21
Journal of MedVerse Research & Practice
nurexus.com
Evaluation of Cardiac Involvement in Pediatric Dengue Fever Through
Troponin I and CPK-MB Correlation
Dr. Venkanteshan
1
, Dr. Subhashree
2
Postgraduate, Associate Professor
Department of Pediatrics, Pondicherry Institute of Medical Sciences, Puducherry
Email ID: Venki1997@gmail.com
Submission Date: 26.03.2025
Accepted Date: 22.04.2025
Published Date: 30.04.2025
Copyright © 2025. The author(s). Published by Journal of MedVerse Research and Practice. This is an open-access
article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits
unrestricted use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
Abstract
Introduction: Dengue fever is a mosquito-borne viral illness increasingly associated with multisystem involvement,
including cardiac complications. Paediatric cases are particularly vulnerable, with potential for myocardial injury that
often goes unrecognized. This study aims to evaluate cardiac involvement in paediatric dengue patients through the
measurement of serum biomarkers, primarily CK-MB and LDH, and their correlation with disease severity and liver
enzyme levels.
Materials & Methods: A retrospective observational study was conducted at a tertiary care hospital from August to
October 2024, including 120 serologically confirmed dengue patients, of whom 50 were pediatric (aged <14 years)
and 70 were adults. Patients with pre-existing cardiac disease or incomplete records were excluded. Serum CK-MB,
LDH, SGOT, and SGPT were measured using standard enzymatic assays. Data were analyzed using SPSS v25.0 with
t-tests and chi-square tests; p < 0.05 was considered statistically significant.
Results: Among the 120 patients included, paediatric cases accounted for 41.6%. Males constituted 66.6% of the
cohort. CK-MB levels were significantly elevated in adults compared to children (67.56 vs. 60.64, p = 0.000). LDH
levels were high in both groups without a statistically significant difference. SGOT and SGPT levels rose
proportionally with dengue severity, with significant differences in Grade 1 cases (p = 0.001). A strong correlation
was found between CK-MB and elevated transaminase levels, indicating concurrent cardiac and hepatic involvement
in paediatric patients.
Conclusion: The study demonstrates that CK-MB, SGOT, and SGPT are effective biomarkers for assessing the
severity of dengue fever and potential myocardial involvement in paediatric populations. Elevated levels of these
markers suggest the need for early cardiac evaluation to guide timely interventions. Routine cardiac biomarker
assessment may aid in managing paediatric dengue cases with multisystem involvement.
Keywords: Dengue fever, CK-MB, LDH, SGOT, SGPT, Myocardial injury, Cardiac biomarkers
Introduction
Dengue fever is a fast-growing mosquito-borne viral illness caused by the dengue virus, a member of the
Flaviviridae family, primarily spread by Aedes aegypti mosquitoes. The disease is endemic in more than
100 countries and poses a serious public health concern globally, especially across Asia, Africa, and South
America. Children are particularly vulnerable to severe manifestations, such as dengue hemorrhagic fever
(DHF) and dengue shock syndrome (DSS), both of which are linked to significant illness and death. [1,2].
Traditionally, dengue has been viewed as a self-limiting febrile illness; however, accumulating evidence
suggests that it can result in multisystem involvement, including hepatic, neurological, and, notably,
Venkanteshan et al | Nurexus | Journal of MedVerse Research and Practice | Volume 3 | Issue 04 | April 2025
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cardiovascular complications [3]. Cardiac involvement in dengue, although under-recognized, can range
from subtle electrocardiographic changes and transient myocardial depression to fulminant myocarditis and
cardiogenic shock [4]. These manifestations are particularly concerning in the pediatric population, where
early recognition and timely intervention are critical.
The viral invasion of myocardial tissue, immune-mediated injury, cytokine storm, or secondary effects of
fluid overload and hypotension [5]. Given the non-specific clinical presentation and overlapping features
with other systemic complications, objective assessment tools are essential for detecting myocardial injury.
Biomarkers such as cardiac Troponin I and creatine phosphokinase-MB (CPK-MB) have been widely used
as sensitive and specific indicators of myocardial damage in various infectious and non-infectious
conditions [6]. The bloodstream upon myocardial cell injury and is considered a gold-standard marker for
myocardial infarction and myocarditis in Troponin I [7]. Similarly, CPK-MB is an isoenzyme that increases
in the early phases of myocardial injury and serves as an adjunct diagnostic marker [8]. Several studies in
adult populations have demonstrated elevated levels of these biomarkers in dengue patients with cardiac
involvement, but paediatric data remain sparse and inconclusive [9].
Echocardiography and clinical evaluation in conjunction with serum biomarkers may help identify
myocardial dysfunction early, even before overt clinical symptoms develop. Establishing a correlation
between cardiac biomarkers and functional parameters such as ejection fraction, fractional shortening, and
hemodynamic stability can help stratify risk and guide treatment decisions in paediatric patients. [10,11].
This study aims to investigate the clinical correlation between serum levels of Troponin I and CPK-MB and
echocardiographic cardiac function in children diagnosed with dengue fever. Identifying such correlations
may pave the way for standardized cardiac screening protocols in paediatric dengue cases and facilitate
early, targeted management of cardiovascular complications.
Materials & Methods
A retrospective observational study was conducted at a tertiary care teaching hospital from August to
October 2024 to evaluate the possible cardiac involvement in patients with dengue fever by analysing
specific biochemical markers of myocardial injury. The study included 120 patients with serologically
confirmed dengue infection, comprising 50 children (aged 118 years) and 70 adults (above 18 years).
Inclusion and Exclusion Criteria
Patients were eligible for inclusion if they:
Tested positive for dengue infection through NS1 antigen or IgM ELISA;
Had complete biochemical profiles available; and
Were admitted during the study period.
Patients were excluded if they had:
A history of pre-existing cardiac disease (e.g., ischemic heart disease, cardiomyopathy, congenital
heart defects);
Co-infections such as malaria, typhoid, or leptospirosis; or
Incomplete clinical or laboratory records.
Data Collection: Relevant data were obtained from the hospital medical record archives, including
demographic characteristics, clinical presentation, dengue serology status, and laboratory findings. The
biochemical markers assessed for evidence of myocardial injury were serum glutamic oxaloacetic
transaminase (SGOT), creatine kinase-MB (CK-MB), and lactate dehydrogenase (LDH). These parameters
were measured using standard enzymatic methods in the hospital’s central biochemistry laboratory.
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The cut-off values used to define abnormal results were:
SGOT > 40 U/L,
CK-MB > 25 U/L, and
LDH > 480 U/L.
Where available, electrocardiogram (ECG) and echocardiography (ECHO) findings were reviewed to
identify structural or functional cardiac abnormalities, providing supportive evidence for biochemical
alterations.
Statistical Analysis: All collected data were entered into Microsoft Excel and analyzed using SPSS
software version 25.0 (IBM Corp., Armonk, NY, USA). Descriptive statistics, including mean, standard
deviation, and percentage, were used to summarize baseline characteristics and biochemical marker
distribution among different age groups. Comparisons between children and adults were performed using
the independent sample t-test for continuous variables and the Chi-square test (χ²) for categorical variables.
Ethical Considerations: The study protocol was reviewed and approved by the Institutional Ethics
Committee (IEC) of the tertiary care centre.
Results
Table 1: Age distribution among Study Participants
Age group in years
Frequency (n)
Paediatric <14 years
50
Adult> 14 years
70
Total
120
Out of the 120 patients included in the study, 50 (41.6%) were pediatric patients under 14 years of age,
while 70 (58.4%) were adults above 14 years. This indicates a slightly higher proportion of adult dengue
cases compared to pediatric cases in the study population.
Table 2: Gender distribution among Study Participants
Gender
Frequency (n)
Female
40
Male
80
Total
120
Among the 120 patients, 80 (66.6%) were male and 40 (33.4%) were female, showing a male
predominance in the study population.
Table 3: Diagnosis
Diagnosis
Frequency
Acute febrile illness
15
Chikungunya
2
Dengue
101
Enteric fever
2
Total
120
Among the 120 patients, dengue was the most common diagnosis, seen in 101 cases (84.3%). Acute febrile
illness accounted for 15 cases (12.5%), while chikungunya and enteric fever were each diagnosed in 2 cases
Venkanteshan et al | Nurexus | Journal of MedVerse Research and Practice | Volume 3 | Issue 04 | April 2025
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(1.6%), indicating that dengue was the predominant cause of illness in this cohort.
Figure 1: Dengue
Out of the 120 patients, 90 (75%) tested positive for dengue using IgG, IgM, or NS1 antigen tests, while 30
(25%) were negative, confirming a high prevalence of dengue infection in the study population.
Table 4: Serum LDH and CKMB levels in Pediatric and adult patients diagnosed with dengue fever.
Variable
Age group
P value
Paediatric
Adult
CK-MB
60.64
67.56
0.000
LDH
1008.924
1015.494
In your data, CK-MB levels are significantly higher in adults compared to pediatric patients, with a P-value
of 0.000, indicating a strong statistical difference between the two groups. However, the LDH levels are
quite similar between the two groups (pediatric: 1008.924, adult: 1015.494), and no P-value was provided
for LDH, so it's unclear if this difference is statistically significant.
Table 5: SGOT and SGPT levels to assess the severity of dengue in study population.
SGOT
SGPT
P value
Grade 1
166.80
139.58
0.001
Grade2
173.23
142.85
Grade 3
188.67
149.21
The SGOT and SGPT levels increase with the severity of dengue. For Grade 1 (mild), both SGOT and
SGPT levels are significantly higher, with a P-value of 0.001, indicating a meaningful difference. For
Grade 2 (moderate) and Grade 3 (severe), SGOT and SGPT also increase, but no P-values are provided, so
it's unclear if these differences are statistically significant. In summary, SGOT and SGPT levels rise as
dengue severity increases, with Grade 1 showing a significant change.
Table 6: correlation LDH and CKMB levels with SGOT and SGPT in this study population.
SGOT
SGPT
P value
CK-MB
165.79±2.23
139.58 ± 4.15
0.01
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LDH
173.23 ± 0.78
147.74 ± 0.36
The data shows that CK-MB levels differ significantly between the two groups, with a P-value of 0.01
indicating a meaningful difference. However, for LDH, while the levels vary between the two groups, no P-
value is provided, so it's unclear if the difference is statistically significant.
Table 7: clinical significance of these biomarkers in guiding early diagnosis
Parameters
Standard deviation
CK-MB
66.8464
LDH
1010.604924
SGOT
166.8067
SGPT
141.194958
CK-MB: 66.85, showing a moderate variability in the data; LDH: 1010.60, indicating a higher spread in
LDH levels; SGOT: 166.81, reflecting the variability in SGOT levels; SGPT: 141.19, showing the spread in
SGPT levels.
Discussion
In This study demonstrates a significantly higher prevalence of Helicobacter pylori infection among
cirrhotic patients (69.4%) compared to non-cirrhotic individuals (37.1%), suggesting a potential association
between chronic liver disease and increased susceptibility to H. pylori colonization. Similar observations
have been reported in earlier studies, which proposed that immune dysfunction and alterations in gastric
mucosal defense mechanisms in cirrhosis may facilitate persistent H. pylori infection (Pellicano et al., Tsai
et al., Gupta et al.) [2,6,7].
The endoscopic findings also varied significantly between the two groups. Cirrhotic patients predominantly
exhibited portal hypertensive gastropathy and esophageal varices, findings that are consistent with portal
hypertension, whereas non-cirrhotic patients more frequently showed antral gastritis and gastroesophageal
reflux disease, conditions commonly associated with H. pylori infection and acid-related mucosal injury
(Marshall et al., Pellicano et al.) [1,8]. These differences highlight the distinct gastrointestinal
manifestations associated with liver cirrhosis compared to non-cirrhotic conditions.
Biochemical analysis revealed that H. pylori-positive patients had significantly elevated serum bilirubin
levels and prolonged PT/INR values, indicating more advanced hepatic dysfunction. Similar associations
between H. pylori infection and worsening liver function parameters have been documented previously
(Shiota et al., Liu et al.) [9,11]. Furthermore, the higher prevalence of H. pylori infection among patients
with increased ChildPugh scores suggests a correlation between infection and the severity of liver disease,
as also noted by Pellicano et al. and Gupta et al. [2,7].
The observed association may be explained by mechanisms such as bacterial translocation, systemic
inflammation, and altered gutliver axis interactions in cirrhosis (Frances et al., Llorente et al.) [5,10].
These mechanisms may contribute to disease progression and exacerbate cirrhosis-related complications.
Overall, the findings of the present study support the hypothesis that H. pylori infection may not merely
coexist with chronic liver disease but could potentially aggravate its clinical course. This underscores the
importance of early detection and consideration of eradication therapy for H. pylori in cirrhotic patients to
possibly reduce disease-related complications and improve clinical outcomes.
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Conclusion
In conclusion, our study suggests that CK-MB, SGOT, and SGPT are valuable biomarkers for assessing
dengue severity, particularly in identifying liver involvement and myocardial injury. However, further
research is required to validate the role of LDH and to explore its potential as a consistent marker for
dengue severity. Comparisons with similar studies highlight the importance of understanding how
biomarkers vary with disease progression and across different age groups in dengue patients.
Conflict of Interest: Nil
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