Effect of augmented glycation in mobilization of plasma free fatty acids in type 2 diabetes mellitus.


Journal

Diabetes & metabolic syndrome
ISSN: 1878-0334
Titre abrégé: Diabetes Metab Syndr
Pays: Netherlands
ID NLM: 101462250

Informations de publication

Date de publication:
Historique:
received: 29 04 2020
revised: 12 06 2020
accepted: 09 07 2020
pubmed: 7 8 2020
medline: 10 7 2021
entrez: 7 8 2020
Statut: ppublish

Résumé

Type 2 Diabetes Mellitus (T2DM) is known to be associated with an increase in total plasma free fatty acid (FFA) concentration. The present study was conducted to determine the changes in plasma fatty acids at different levels of glycation in type 2 diabetes mellitus. The study involved 50 subjects having different levels of glycation (HbA1c 4.9-15.0%) and further categorized in 5 groups [group 1 (HbA1c <6%), group 2 (HbA1c 6-7%), group 3 (HbA1c 7.1-9%), group 4 (HbA1c (9.1-12%) and group 5 (HbA1c >12%)] with 10 subjects in each group. A total of 19 free fatty acids were detected by gas chromatography-mass spectrometry (GC-MS) analysis in the plasma samples. The levels of lauric acid (C12:0) and stearic acid (C18:0) were significantly raised at an advanced stage of glycation (HbA1c 9.1-15%). Long-chain fatty acids, pentadecanoic acid (C15:0) and palmitic acid (C16:0) levels were elevated in hyperglycemia as compared to normoglycaemic subjects (HbA1c <6%). Moreover, levels of mono and polyunsaturated fatty acids, oleic acid (C18:1) and linoleic acid (C18:2, w6) were significantly decreased in patients with increased levels of glycation (HbA1c 6-15%). GC-MS is a novel way to study the plasma fatty acid profiling and findings of this study suggest that monitoring alterations in plasma FFA profile may be of prognostic value.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Type 2 Diabetes Mellitus (T2DM) is known to be associated with an increase in total plasma free fatty acid (FFA) concentration. The present study was conducted to determine the changes in plasma fatty acids at different levels of glycation in type 2 diabetes mellitus.
METHODS METHODS
The study involved 50 subjects having different levels of glycation (HbA1c 4.9-15.0%) and further categorized in 5 groups [group 1 (HbA1c <6%), group 2 (HbA1c 6-7%), group 3 (HbA1c 7.1-9%), group 4 (HbA1c (9.1-12%) and group 5 (HbA1c >12%)] with 10 subjects in each group.
RESULTS RESULTS
A total of 19 free fatty acids were detected by gas chromatography-mass spectrometry (GC-MS) analysis in the plasma samples. The levels of lauric acid (C12:0) and stearic acid (C18:0) were significantly raised at an advanced stage of glycation (HbA1c 9.1-15%). Long-chain fatty acids, pentadecanoic acid (C15:0) and palmitic acid (C16:0) levels were elevated in hyperglycemia as compared to normoglycaemic subjects (HbA1c <6%). Moreover, levels of mono and polyunsaturated fatty acids, oleic acid (C18:1) and linoleic acid (C18:2, w6) were significantly decreased in patients with increased levels of glycation (HbA1c 6-15%).
CONCLUSION CONCLUSIONS
GC-MS is a novel way to study the plasma fatty acid profiling and findings of this study suggest that monitoring alterations in plasma FFA profile may be of prognostic value.

Identifiants

pubmed: 32755839
pii: S1871-4021(20)30276-9
doi: 10.1016/j.dsx.2020.07.028
pii:
doi:

Substances chimiques

Biomarkers 0
Blood Glucose 0
Fatty Acids, Nonesterified 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1385-1389

Informations de copyright

Copyright © 2020 Diabetes India. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Kailash Chandra (K)

Department of Biochemistry, HIMSR, Jamia Hamdard, New Delhi, India.

Vineet Jain (V)

Department of Medicine, HIMSR, Jamia Hamdard, New Delhi, India.

Masood Azhar (M)

Department of Quality Assurance, Delhi Institute of Pharmaceutical Sciences and Research, University of Delhi, India.

Washim Khan (W)

Bioactive Natural Product Laboratory, Department of Pharmacognosy and Phytochemistry, SPER, Jamia Hamdard, New Delhi, India.

Ozair Alam (O)

Dept. of Pharmaceutical Chemistry, SPER, Jamia Hamdard, India.

Sayeed Ahmad (S)

Bioactive Natural Product Laboratory, Department of Pharmacognosy and Phytochemistry, SPER, Jamia Hamdard, New Delhi, India.

Swatantra Kumar Jain (SK)

Department of Biochemistry, HIMSR, Jamia Hamdard, New Delhi, India. Electronic address: sk608@rediffmail.com.

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Classifications MeSH