Theodoros Kelesidis

Dr. Theodoros Kelesidis

orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
19 January 2010 in Annals of Internal Medicine
Verified
Journal Article
Closed access
TKTheodoros Kelesidis
Theodoros Kelesidis
IKIosif Kelesidis
Iosif Kelesidis
SCSharon Chou
Sharon Chou
CMChristos S. Mantzoros
Christos S. Mantzoros
Leptin is a hormone secreted by adipose tissue that helps regulate energy homeostasis, neuroendocrine function, and metabolism. Recent studies suggest that leptin is an indicator of energy deficien... Leptin is a hormone secreted by adipose tissue in direct proportion to amount of body fat. The circulating leptin levels serve as a gauge of energy stores, thereby directing the regulation of energ...

28 March 2006 in British Journal of Cancer
Verified
Journal Article
Open access
PDF file
IKI Kelesidis
I Kelesidis
TKTheodoros Kelesidis
Theodoros Kelesidis
CMChristos S. Mantzoros
Christos S. Mantzoros
Recent studies have demonstrated that obesity is a significant risk factor for the development of several malignancies, but the mechanisms underlying this relationship remain to be fully elucidated. Adiponectin, an adipocyte secreted endogenous insulin sensitizer, appears to play an important role not only in glucose and lipid metabolism but also in the development and progression of several obesity-related malignancies. In this review, we present recent findings on the association of adiponectin with several malignancies as well as recent data on underlying molecular mechanisms that provide novel insights into the association between obesity and cancer risk. We also identify important research questions that remain unanswered.

11 November 2011 in Therapeutic Advances in Gastroenterology
Verified
Journal Article
Closed access
TKTheodoros Kelesidis
Theodoros Kelesidis
CPCharalabos Pothoulakis
Charalabos Pothoulakis
Several clinical trials and experimental studies strongly suggest a place for Saccharomyces boulardii as a biotherapeutic agent for the prevention and treatment of several gastrointestinal diseases. S. boulardii mediates responses resembling the protective effects of the normal healthy gut flora. The multiple mechanisms of action of S. boulardii and its properties may explain its efficacy and beneficial effects in acute and chronic gastrointestinal diseases that have been confirmed by clinical trials. Caution should be taken in patients with risk factors for adverse events. This review discusses the evidence for efficacy and safety of S. boulardii as a probiotic for the prevention and therapy of gastrointestinal disorders in humans.

4 September 2012 in Journal of Antimicrobial Chemotherapy
Verified
Journal Article
Open access
PDF file
BGBing Gu
Bing Gu
TKTheodoros Kelesidis
Theodoros Kelesidis
Sotirios TsiodrasSotirios Tsiodras
Sotirios Tsiodras
JHJanet Hindler
Janet Hindler
RHRomney M. Humphries
Romney M. Humphries
The oxazolidinone antibiotic linezolid has demonstrated potent antimicrobial activity against Gram-positive bacterial pathogens, including methicillin-resistant staphylococci. This article systematically reviews the published literature for reports of linezolid-resistant Staphylococcus (LRS) infections to identify epidemiological, microbiological and clinical features for these infections. Linezolid remains active against >98% of Staphylococcus, with resistance identified in 0.05% of Staphylococcus aureus and 1.4% of coagulase-negative Staphylococcus (CoNS). In all reported cases, patients were treated with linezolid prior to isolation of LRS, with mean times of 20.0 ± 47.0 months for S. aureus and 11.0 ± 8.0 days for CoNS. The most common mechanisms for linezolid resistance were mutation (G2576T) to the 23S rRNA (63.5% of LRSA and 60.2% of LRCoNS) or the presence of a transmissible cfr ribosomal methyltransferase (54.5% of LRSA and 15.9% of LRCoNS). The emergence of linezolid resistance in Staphylococcus poses significant challenges to the clinical treatment of infections caused by these organisms, and in particular CoNS.

1 April 2007 in The Journal of Clinical Endocrinology & Metabolism
Verified
Journal Article
Open access
PDF file
STShelley S Tworoger
Shelley S Tworoger
AEA. Heather Eliassen
A. Heather Eliassen
TKTheodoros Kelesidis
Theodoros Kelesidis
GCGraham A Colditz
Graham A Colditz
WWWalter C. Willett
Walter C. Willett
SHSusan E. Hankinson
Susan E. Hankinson
Introduction: Previous retrospective case-control studies suggest that adiponectin, an obesity-related hormone, is inversely associated with breast cancer risk, particularly in postmenopausal women; however, no prospective studies exist. Therefore, we conducted a prospective case-control study nested within the Nurses’ Health Study (NHS) and NHSII cohorts examining the association between plasma adiponectin concentrations and breast cancer risk. Materials and Methods: Blood samples were collected from 1989 through 1990 (NHS) and 1996 through 1999 (NHSII); adiponectin was measured by RIA. The analysis included 1477 breast cancer cases diagnosed after blood collection and before June 2000 (NHS) or June 2003 (NHSII) who had one or two controls (n = 2196) matched on age, menopausal status, postmenopausal hormone (PMH) use, fasting, and time of day and month of blood collection. We adjusted for body mass index at age 18, weight change from age 18 to blood draw, family history of breast cancer, history of benign breast disease, duration of PMH use, ages at menarche and first birth, and parity. Results: Although we observed no association between adiponectin and breast cancer risk overall, there was a nearly significant interaction by menopausal status (P = 0.08), with a relative risk, top vs. bottom quartile of 0.73 (95% confidence interval, 0.55–0.98; P trend = 0.08) among postmenopausal women and 1.30 (95% confidence interval, 0.80–2.10; P trend = 0.09) for premenopausal women. Among postmenopausal women, adiponectin appeared more strongly inversely associated in women who never used PMH (P heterogeneity = 0.05) and women with low circulating estradiol levels (P heterogeneity = 0.05). Discussion: Our results suggest that adiponectin may be inversely associated with postmenopausal breast cancer risk, particularly in a low-estrogen environment.

1 June 2010 in Clinical Immunology
Verified
Journal Article
Closed access
TKTheodoros Kelesidis
Theodoros Kelesidis
OYOtto Yang
Otto Yang