Evidence map›Paper›PMID 26089610›Full record

ArticleIndian journal of clinical biochemistry : IJCB2015

Association of Aberrations in One Carbon Metabolism with Intimal Medial Thickening in Patients with Type 2 Diabetes Mellitus.

R Dhananjayan, T Malati, Y Rupasree, Vijay Kumar Kutala

Abstract read
In one paragraph

Article in Indian journal of clinical biochemistry : IJCB, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

R DhananjayanDepartment of Biochemistry, ACS Medical College & Hospital, Velappanchavadi, Chennai, 600 077 Tamil Nadu India.
T MalatiDepartment of Biochemistry, Nizam's Institute of Medical Sciences, Hyderabad, 500 082 Andhra Pradesh India.
Y RupasreeClinical Pharmacology and Therapeutics, Nizam's Institute of Medical Sciences, Hyderabad, 500 082 Andhra Pradesh India.
Vijay Kumar KutalaClinical Pharmacology and Therapeutics, Nizam's Institute of Medical Sciences, Hyderabad, 500 082 Andhra Pradesh India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present work was aimed to study the association of one carbon genetic variants, hyperhomocysteinemia and oxidative stress markers, i.e., serum nitrite, plasma malondialdehyde (MDA) and glutathione (GSH) on intimal medial thickening (IMT) in patients with type 2 diabetes mellitus (T2D). A total number of 76 subjects from ACS Medical College and Hospital, Chennai, India were included in the study, i.e., Group I (n = 42) of T2D and Group II (n = 34) of age- and sex matched healthy controls. The glycated haemoglobin was measured by ion-exchange resin method; plasma homocysteine by Enzyme Linked Immunosorbant Assay method; serum nitrite (nitric oxide, NO), plasma MDA and GSH by spectrophotometric methods; the IMT by high frequency ultrasound. The polymorphisms of one carbon genetic variants were genotyped using polymerase chain reaction-restriction fragment length polymorphism and amplified fragment length polymorphism methods. Results indicate that methyltetrahydrofolate homocysteine methyl transferase (MTR) A2756G allele was found to be protective in T2D and the other variants were not significantly associated with T2D. Glutamate carboxypeptidase II (GCP II) C1561T (r = 0.34; p = 0.05) and methylene tetrahydrofolate reductase (MTHFR) C677T (r = 0.35; 0.04) showed positive correlation with plasma homocysteine in T2D cases. In this study, MTR A2756G allele was found to be protective in T2D; GCP II C1561T and MTHFR C677T showed positive association with plasma homocysteine in T2D cases. Among all the genetic variants, MTR A2756G was found influence IMT. RFC 1 G80A and TYMS 5'-UTR 2R3R showed synergistically interact with MTR A2756G in influencing increase in IMT.

Indexed as

Diabetes mellitusHomocysteineIMTOne carbon metabolismOxidative stress

Identifiers

PMID26089610
PMCPMC4469063

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