» Articles » PMID: 24222450

Can Proopiomelanocortin Methylation Be Used As an Early Predictor of Metabolic Syndrome?

Overview
Journal Diabetes Care
Specialty Endocrinology
Date 2013 Nov 14
PMID 24222450
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: The objectives of this study were to compare early predictive marker of the metabolic syndrome with proopiomelanocortin (POMC) methylation status and to determine the association among birth weight, ponderal index, and cord blood methylation status.

Research Design And Methods: We collected pregnancy outcome data from pregnant women, cord blood samples at delivery, and blood from children (7-9 years old; n = 90) through a prospective cohort study at Ewha Womans University, MokDong Hospital (Seoul, Korea), from 2003-2005. POMC methylation was assessed by pyrosequencing. We divided subjects into three groups according to cord blood POMC methylation: the low methylation (<10th percentile), mid-methylation, and high methylation (>90th percentile) groups. We analyzed the association of POMC methylation status at birth with adiposity and metabolic components using ANCOVA and multiple linear regression analysis.

Results: Birth weights (P = 0.01) and ponderal indices (P = 0.01) in the high POMC methylation group were significantly lower than in the mid-POMC methylation group. In terms of metabolic components of childhood, blood triglycerides (57.97, 67.29 vs. 113.89 mg/dL; P = 0.03, 0.01) and insulin (7.10, 7.64 vs. 10.13 μIU/mL; P = 0.05, 0.02) at childhood were significantly higher in the high POMC methylation group than in the low and mid-POMC methylation group.

Conclusions: High POMC methylation in cord blood was associated with lower birth weight, and children with high POMC methylation in cord blood showed higher triglycerides and higher insulin concentrations in blood. Thus, POMC methylation status in cord blood may be an early predictive marker of future metabolic syndrome.

Citing Articles

Epigenetics and Gut Microbiota Crosstalk: A potential Factor in Pathogenesis of Cardiovascular Disorders.

Mehta V, Nagu P, Inbaraj B, Sharma M, Parashar A, Sridhar K Bioengineering (Basel). 2022; 9(12).

PMID: 36551003 PMC: 9774431. DOI: 10.3390/bioengineering9120798.


Elevated methylation of the vault RNA2-1 promoter in maternal blood is associated with preterm birth.

You Y, Kwon E, Hwang H, Choi S, Choi S, Kim Y BMC Genomics. 2021; 22(1):528.

PMID: 34246240 PMC: 8272312. DOI: 10.1186/s12864-021-07865-y.


Altered DNA methylation pattern reveals epigenetic regulation of Hox genes in thoracic aortic dissection and serves as a biomarker in disease diagnosis.

Liu P, Zhang J, Du D, Zhang D, Jin Z, Qiu W Clin Epigenetics. 2021; 13(1):124.

PMID: 34103071 PMC: 8186232. DOI: 10.1186/s13148-021-01110-9.


Cohort profile: the Ewha Birth and Growth Study.

Lee H, Park B, Min J, Choi E, Kim U, Park H Epidemiol Health. 2021; 43:e2021016.

PMID: 33677859 PMC: 8060523. DOI: 10.4178/epih.e2021016.


Long-term effects of pro-opiomelanocortin methylation induced in food-restricted dams on metabolic phenotypes in male rat offspring.

Lee S, Kwon E, You Y, Du J, Jo I, Kim Y Obstet Gynecol Sci. 2020; 63(3):239-250.

PMID: 32489968 PMC: 7231940. DOI: 10.5468/ogs.2020.63.3.239.