scispace - formally typeset
M

Maria Teresa Guagnano

Researcher at University of Chieti-Pescara

Publications -  119
Citations -  2898

Maria Teresa Guagnano is an academic researcher from University of Chieti-Pescara. The author has contributed to research in topics: Body mass index & Medicine. The author has an hindex of 24, co-authored 103 publications receiving 2403 citations.

Papers
More filters
Journal ArticleDOI

Platelet activation in obese women: role of inflammation and oxidant stress.

TL;DR: Android obesity is associated with enhanced lipid peroxidation and persistent platelet activation and these abnormalities are driven by inflammatory triggers related to the degree of abdominal adiposity and are, at least in part, reversible with a successful weight-loss program.
Journal ArticleDOI

Platelet activation in obesity and metabolic syndrome.

TL;DR: The complex interactions between platelets and the pathogenic events occurring in obesity and MS are addressed, trying to translate this body of mechanistic information into a clinically relevant read‐out, in order to establish novel strategies in the prevention/treatment of atherothrombosis.
Journal ArticleDOI

Association of inflammation markers with impaired insulin sensitivity and coagulative activation in obese healthy women

TL;DR: The results are the first to document an in vivo relationship between insulin sensitivity and coagulative activation in obesity and the elevated TGF-beta 1 levels detected in the obese population may provide a biochemical link between insulin resistance and an increased risk for cardiovascular disease.
Journal ArticleDOI

Effect of Thyroid Function on LDL Oxidation

TL;DR: In hyperthyroid patients, the increased lipid peroxidation was strictly related to free thyroxine levels, whereas in hypothyroidism it was strongly influenced by serum lipids.
Journal ArticleDOI

Insulin Resistance as a Determinant of Platelet Activation in Obese Women

TL;DR: Insulin resistance is a major determinant of platelet activation in female obesity, independently of adiponectin, CRP, CD40L, and lipid patterns.