Evidence map›Paper›PMID 40775313›Full record

ArticleBMC pediatrics2025

Identifying inherited metabolic disorders in children: the role of elevated creatine kinase.

Merve Yoldaş Çelik, Burcu Köşeci

Abstract read
In one paragraph

Article in BMC pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Merve Yoldaş ÇelikAdana City Training and Research Hospital, Department of Pediatric Metabolism and Nutrition, Adana, Turkey. drmerveyoldas@yahoo.com.ORCID 0000-0003-0015-9807
Burcu KöşeciAdana City Training and Research Hospital, Department of Pediatric Metabolism and Nutrition, Adana, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionElevated creatine kinase (CK) levels are key indicators of muscle injury and are commonly used in the differential diagnosis of pediatric disorders, particularly inherited metabolic disorders (IMDs). However, variability in CK elevation and the absence of standardized diagnostic thresholds complicate its clinical interpretation. This study aimed to evaluate the diagnostic utility of CK levels in distinguishing IMDs from other etiologies and to identify clinical and biochemical patterns that could facilitate earlier recognition of IMDs.

methodsWe retrospectively analyzed 1,660 pediatric patients seen at a metabolic clinic, identifying 320 (19.3%) who had CK measurements. Among them, 99 patients (30.9%) had elevated CK levels (> 171 U/L). These patients were divided into three diagnostic groups: idiopathic, IMD-diagnosed, and other diseases. "Idiopathic" referred to cases without a confirmed diagnosis. Biochemical parameters (CK, AST, LDH) were compared, and receiver operating characteristic (ROC) analysis was performed.

resultsThirteen patients (15.1%) were diagnosed with IMDs. The IMD group showed significantly higher CK and AST levels compared to the idiopathic group (p < 0.05). ROC analysis indicated that a CK cut-off of 617.5 U/L had a sensitivity of 61.5% and specificity of 88.0% for identifying IMDs. However, CK alone could not effectively distinguish other diseases from idiopathic cases. Advanced metabolic investigations and comprehensive clinical evaluations were essential for accurate diagnosis.

conclusionWhile CK levels offer useful preliminary diagnostic information, they must be interpreted alongside advanced metabolic testing and clinical findings for reliable diagnosis. This study emphasizes the value of a multidisciplinary approach in assessing elevated CK levels in pediatric patients and calls for further research to optimize diagnostic pathways.

Indexed as

Creatine KinaseMetabolic DiseasesMetabolism, Inborn ErrorsAdolescentAspartate AminotransferasesBiomarkersChildChild, PreschoolDiagnosis, DifferentialFemaleHumansInfantL-Lactate DehydrogenaseMaleRetrospective StudiesROC CurveAspartate AminotransferasesBiomarkersCreatine KinaseL-Lactate DehydrogenaseBiochemical markersCKCreatine kinaseInherited metabolic disordersMetabolic myopathiesMultisystem ınvolvement

Identifiers

PMID40775313
PMCPMC12333054

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.