Fasting Serum IGFBP-1 as a Marker of Insulin Resistance in Diverse School Age Groups.


Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
2022
Historique:
received: 21 12 2021
accepted: 14 03 2022
entrez: 19 5 2022
pubmed: 20 5 2022
medline: 21 5 2022
Statut: epublish

Résumé

The known markers of insulin resistance in obese children are well studied. However, they require serial measurements and complicated calculations. The objective is to study IGFBP-1 and its relation with other known risk measures. The study included 98 New York City school students of diverse ethnic/racial backgrounds (57 males and 41 females), 11-15 years of age. Subjects were enrolled in a cross-sectional study, and anthropometric measures were collected. They underwent fasting intravenous glucose tolerance tests (IVGTT), and glucose, insulin, lipids, IGFBP-1, adiponectin and inflammatory markers were collected. The subjects were stratified into 3 groups based upon the BMI Z-score. Out of all the subjects, 65.3% were in the group with a BMI Z-score <1 SDS, 16.3% subjects were in the group with a BMI Z-score of 1 to 2 SDS, and 18.4% of the subjects were in the group with a BMI Z-score of more than 2 SDS. The group with a BMI Z-score of more than 2 SDS had increased waist circumference (WC), body fat, increased fasting insulin, and triglycerides (TG). This group had decreased levels of adiponectin and HDL and low IGFBP-1 as compared to the group with BMI <1 SDS. The group with a BMI Z-score of 1 to 2 SDS had a decreased level of IGFBP-1 as compared to the group with a BMI Z-score less than 1 SDS. IGFBP-1 inversely correlated with age, WC, BMI, body fat, TG, and insulin levels. IGFBP-1 positively correlated with adiponectin and HDL levels. IGFBP-1 in children can identify the presence of insulin resistance in the group with BMI 1 to 2 SDS, even before the known markers of insulin resistance such as elevated triglycerides and even before decreased HDL and adiponectin levels are identified.

Identifiants

pubmed: 35586622
doi: 10.3389/fendo.2022.840361
pmc: PMC9108162
doi:

Substances chimiques

Adiponectin 0
Biomarkers 0
IGFBP1 protein, human 0
Insulin 0
Insulin-Like Growth Factor Binding Protein 1 0
Triglycerides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

840361

Informations de copyright

Copyright © 2022 Bhangoo, Gupta, Shelov, Carey, Accacha, Fennoy, Altshuler, Lowell, Rapaport, Rosenfeld, Speiser, Ten and Rosenbaum.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The reviewer EG declared a shared affiliation with the author RR to the handling editor at the time of review.

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Auteurs

Amrit Bhangoo (A)

Division of Pediatric Endocrinology, Children's Hospital of Orange County, Orange, CA, United States.

Rishi Gupta (R)

Division of Pediatric Endocrinology, Children's Hospital of Orange County, Orange, CA, United States.
Department of Pediatrics, Division of Pediatric Gastroenterology and Endocrinology, University of Rochester Medical Center, Rochester, NY, United States.

Steve P Shelov (SP)

Department of Pediatrics, Winthrop University Hospital, Mineola, NY, United States.

Dennis E Carey (DE)

Division of Pediatric Endocrinology, Northwell Health, Lake Success, NY, United States.

Siham Accacha (S)

Department of Pediatrics, Winthrop University Hospital, Mineola, NY, United States.

Ilene Fennoy (I)

Division of Pediatric Endocrinology, New York Presbyterian Morgan Stanley Children's Hospital, New York, NY, United States.

Lisa Altshuler (L)

Program for Medical Education Innovations & Research (PrMeir), New York University (NYU) Grossman School of Medicine, New York, NY, United States.

Barbara Lowell (B)

Laboratory of Diabetes, Obesity and Other Metabolic Disorders, Feinstein Institutes for Medical Research, Northwell Health, Manhasset, NY, United States.

Robert Rapaport (R)

Division of Pediatric Endocrinology and Diabetes at Mount Sinai Kravis Children's Hospital, New York, NY, United States.

Warren Rosenfeld (W)

Department of Pediatrics, Winthrop University Hospital, Mineola, NY, United States.

Phyllis W Speiser (PW)

Cohen Children's Medical Center of NY and Zucker School of Medicine, New Hyde Park, NY, United States.

Svetlana Ten (S)

Division of Pediatric Endocrinology, Richmond University Medical Center, Staten Island, NY, United States.

Michael Rosenbaum (M)

Department of Pediatrics, Division of Molecular Genetics, New York Presbyterian Medical Center, New York, NY, United States.

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