Evidence map›Paper›PMID 42071887›Full record

ArticleMedicine2026

Alarin as a potential biomarker in childhood obesity: Evidence from a case-control study.

Ilknur Kaba, Musa Yilmaz, Havva Nur Peltek Kendirci

Abstract read
In one paragraph

Article in Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Ilknur KabaDepartment of Pediatrics, Hitit University Faculty of Medicine, Corum, Turkey.ORCID 0000-0003-0969-7548
Musa YilmazDepartment of Medical Biochemistry, Hitit University Faculty of Medicine, Corum, Turkey.ORCID 0000-0001-9557-678
Havva Nur Peltek KendirciDepartment of Pediatric Endocrinology, Hitit University Faculty of Medicine, Corum, Turkey.ORCID 0000-0001-7398-765

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies on Alarin, a newly identified orexigenic adipokine, have mainly focused on adults, while research investigating Alarin levels and its association with obesity in children remains limited. The aim of this study was to measure Alarin levels in children and adolescents with obesity and investigate their relationship with various metabolic parameters, as well as explore how these associations may differ by age group and gender. This prospective case-control study included 30 children with obesity (body mass index [BMI] standard deviation score [SDS] > +2) and 49 age- and gender-matched controls (BMI SDS between -1.9 and +1.9). Participants were recruited at the pediatric endocrinology outpatient clinic between April 2022 and April 2023. Clinical data, including chronological age, physical examination findings, and laboratory test results (alanine transaminase [ALT], aspartate transaminase [AST], total cholesterol, triglycerides, low-density lipoprotein cholesterol [LDL-C], high-density lipoprotein cholesterol [HDL-C], fasting blood glucose, and insulin levels), were collected from the hospital's information management system. The presence and severity of hepatosteatosis were assessed by abdominal ultrasound. Insulin resistance (IR) was determined using the HOMA-IR index, with a cutoff value of 2.5 for prepubertal patients and 3.16 for pubertal patients. The mean age of the participants was 11.6 ± 3.5 years (range: 4.5-17.7 years), with 58.2% (n = 46) being female. Serum Alarin, LDL-C, γ-glutamyl transferase (GGT), insulin, and HOMA-IR levels were significantly higher in the obesity group (P < .05). In the obese group, Alarin levels showed positive correlations with age, BMI SDS, fasting glucose, and presence of hepatic steatosis (P < .05). No significant correlations were found in the control group. The study found elevated Alarin levels in children and adolescents with obesity, similar to previous findings in adults. This suggests that Alarin may play a role in energy homeostasis and insulin resistance in childhood obesity. The results contribute to a deeper understanding of obesity's molecular mechanisms of obesity and may help to identify new therapeutic targets for preventing obesity-related complications and metabolic diseases.

Indexed as

Galanin-Like PeptidePediatric ObesityAdolescentBiomarkersBlood GlucoseBody Mass IndexCase-Control StudiesChildFemaleHumansInsulin ResistanceMaleProspective StudiesalarinBiomarkersBlood GlucoseGalanin-Like PeptideadolescentsAlarinchildreninsulin resistanceobesity

Identifiers

PMID42071887
PMCPMC13124430

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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.