» Articles » PMID: 30599480

Association Between Hemoglobin Glycation Index and Cardiometabolic Risk Factors in Korean Pediatric Nondiabetic Population

Overview
Specialty Pediatrics
Date 2019 Jan 3
PMID 30599480
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: The hemoglobin glycation index (HGI) represents the degree of nonenzymatic glycation and has been positively associated with cardiometabolic risk factors (CMRFs) and cardiovascular disease in adults. This study aimed to investigate the association between HGI, components of metabolic syndrome (MS), and alanine aminotransferase (ALT) in a pediatric nondiabetic population.

Methods: Data from 3,885 subjects aged 10-18 years from the Korea National Health and Nutrition Examination Survey (2011-2016) were included. HGI was defined as subtraction of predicted glycated hemoglobin (HbA1c) from measured HbA1c. Participants were divided into 3 groups according to HGI tertile. Components of MS (abdominal obesity, fasting glucose, triglycerides, high-density lipoprotein cholesterol, and blood pressure), and proportion of MS, CMRF clustering (≥2 of MS components), and elevated ALT were compared among the groups.

Results: Body mass index (BMI) z-score, obesity, total cholesterol, ALT, abdominal obesity, elevated triglycerides, and CMRF clustering showed increasing HGI trends from lower-to-higher tertiles. Multiple logistic regression analysis showed the upper HGI tertile was associated with elevated triglycerides (odds ratio, 1.65; 95% confidence interval, 1.18-2.30). Multiple linear regression analysis showed HGI level was significantly associated with BMI z-score, HbA1c, triglycerides, and ALT. When stratified by sex, age group, and BMI category, overweight/obese subjects showed linear HGI trends for presence of CMRF clustering and ALT elevation.

Conclusion: HGI was associated with CMRFs in a Korean pediatric population. High HGI might be an independent risk factor for CMRF clustering and ALT elevation in overweight/obese youth. Further studies are required to establish the clinical relevance of HGI for cardiometabolic health in youth.

Citing Articles

A genome-wide association study identifies genetic determinants of hemoglobin glycation index with implications across sex and ethnicity.

House J, Breeyear J, Akhtari F, Evans V, Buse J, Hempe J Front Endocrinol (Lausanne). 2024; 15:1473329.

PMID: 39530122 PMC: 11551017. DOI: 10.3389/fendo.2024.1473329.


Association of haemoglobin glycation index with outcomes in patients with acute coronary syndrome: results from an observational cohort study in China.

Li J, Xin Y, Li J, Zhou L, Qiu H, Shen A Diabetol Metab Syndr. 2022; 14(1):162.

PMID: 36316759 PMC: 9620631. DOI: 10.1186/s13098-022-00926-6.


Association Between Hemoglobin Glycation Index and Risk of Cardiovascular Disease and All Cause Mortality in Type 2 Diabetic Patients: A Meta-Analysis.

Wu J, Liang D, Xie Y, Chen M, Chen H, Sun D Front Cardiovasc Med. 2021; 8:690689.

PMID: 34124211 PMC: 8193090. DOI: 10.3389/fcvm.2021.690689.


The Relationship Between Hemoglobin Glycation Variation Index and Vitamin D in Type 2 Diabetes Mellitus.

Li Z, Wang F, Jia Y, Guo F, Chen S Diabetes Metab Syndr Obes. 2021; 14:1937-1948.

PMID: 33958883 PMC: 8096423. DOI: 10.2147/DMSO.S310672.


Association of hemoglobin glycation index and its interaction with obesity/family history of hypertension on hypertension risk: a community-based cross-sectional survey.

Mi J, Song J, Zhao Y, Wu X BMC Cardiovasc Disord. 2020; 20(1):477.

PMID: 33148181 PMC: 7640660. DOI: 10.1186/s12872-020-01762-0.


References
1.
Kelley D, Goodpaster B . Skeletal muscle triglyceride. An aspect of regional adiposity and insulin resistance. Diabetes Care. 2001; 24(5):933-41. DOI: 10.2337/diacare.24.5.933. View

2.
Rohlfing C, Wiedmeyer H, Little R, Grotz V, Tennill A, England J . Biological variation of glycohemoglobin. Clin Chem. 2002; 48(7):1116-8. View

3.
Hempe J, Gomez R, McCarter Jr R, Chalew S . High and low hemoglobin glycation phenotypes in type 1 diabetes: a challenge for interpretation of glycemic control. J Diabetes Complications. 2002; 16(5):313-20. DOI: 10.1016/s1056-8727(01)00227-6. View

4.
McCarter R, Hempe J, Gomez R, Chalew S . Biological variation in HbA1c predicts risk of retinopathy and nephropathy in type 1 diabetes. Diabetes Care. 2004; 27(6):1259-64. DOI: 10.2337/diacare.27.6.1259. View

5.
Cohen R, Snieder H, Lindsell C, Beyan H, Hawa M, Blinko S . Evidence for independent heritability of the glycation gap (glycosylation gap) fraction of HbA1c in nondiabetic twins. Diabetes Care. 2006; 29(8):1739-43. DOI: 10.2337/dc06-0286. View