Vaiva Lesauskaite

Prof. Vaiva Lesauskaite

orcid

Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

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

Representative Publications

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26 March 2009 in BMC Cancer
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Journal Article
Open access
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SSSaulius Svagzdys
Saulius Svagzdys
VLVaiva Lesauskaite
Vaiva Lesauskaite
DPDainius Pavalkis
Dainius Pavalkis
INIrena Nedzelskienė
Irena Nedzelskienė
DPDarius Pranys
Darius Pranys
ATAlgimantas Tamelis
Algimantas Tamelis
The extent of angiogenesis is an important prognostic factor for colorectal carcinoma, however, there are few studies concerning changes in angiogenesis with radiotherapy (RTX). Our aim was to investigate changes in tumor angiogenesis influenced by radiotherapy to assess the prognostic value of angiogenesis the microvessel density (MVD) in overall survival after radiotherapy.

1 August 2006 in Human Pathology
Verified
Journal Article
Closed access
VLVaiva Lesauskaite
Vaiva Lesauskaite
MEM Epistolato
M Epistolato
MCM Castagnini
M Castagnini
SUSigitas Urbonavicius
Sigitas Urbonavicius
PTP Tanganelli
P Tanganelli

2 December 2018 in Clinical Pharmacology & Therapeutics
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Journal Article
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EDElisa Danese
Elisa Danese
SRSara Raimondi
Sara Raimondi
MMMartina Montagnana
Martina Montagnana
ATAngela Tagetti
Angela Tagetti
TLTaimour Langaee
Taimour Langaee
Cristiano FavaCristiano Fava
Cristiano Fava

29 March 2017 in Oncotarget
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Journal Article
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UGUgne Gyvyte
Ugne Gyvyte
SJSimonas Juzenas
Simonas Juzenas
VSVioleta Salteniene
Violeta Salteniene
JKJuozas Kupcinskas
Juozas Kupcinskas
LPLina Poskiene
Lina Poskiene
JSJurgita Skieceviciene
Jurgita Skieceviciene
MiRNA profiling of gastrointestinal stromal tumors by next-generation sequencing

23 July 2012 in PLOS ONE
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JPJanina Petkeviciene
Janina Petkeviciene
ASAlina Smalinskienė
Alina Smalinskienė
DLDalia Ieva Luksiene
Dalia Ieva Luksiene
KJKristina Jureniene
Kristina Jureniene
VRVitalija Ramazauskiene
Vitalija Ramazauskiene
VLVaiva Lesauskaite
Vaiva Lesauskaite
Apolipoprotein E (APOE) polymorphism is associated with lipid levels. Some studies have reported that blood lipid response to diet or obesity varies depending on APOE genotypes. The aim of this study was to assess the effect of APOE genotypes, the intake of saturated fatty acids (SFA), and obesity on serum lipid levels in Lithuanian adult population. A cross-sectional health survey was carried out in five municipalities of Lithuania. The random sample was obtained from lists of 25–64 year-old inhabitants registered at primary health care centres. The data from 996 subjects (416 men and 580 women) were analysed in this study. Two single-nucleotide polymorphisms (rs429358 and rs7412) were assessed using a real-time polymerase chain reaction. 24-hour recall and food frequency questionnaire were used for evaluation of dietary habits. Serum lipids were determined using enzymatic methods. Men and women with the APOE2 genotype had the lowest level of total cholesterol (TC) (p = 0.002 for men, and p = 0.02 for women) and low-density lipoprotein cholesterol (LDL-C) (p0.05). However, the predictive power of the regression model for LDL-C improved when gene-BMI interaction and gene-BMI interaction plus gene-nutrient interaction were added (p = 0.04 and p = 0.032 for R2 change, respectively). APOE genotypes, SFA intake, and obesity were found to be associated with blood lipid levels in Lithuanian adult population. Analysis of gene-diet and gene-obesity interactions did not confirm that the effects of diet and obesity on TC and LDL-C level significantly depended on APOE genotype.

21 June 2021 in Genes
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Journal Article
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Asta RaskilienėAsta Raskilienė
Asta Raskilienė
ASAlina Smalinskienė
Alina Smalinskienė
Vilma KriaucionieneVilma Kriaucioniene
Vilma Kriaucioniene
VLVaiva Lesauskaite
Vaiva Lesauskaite
Janina PetkevičienėJanina Petkevičienė
Janina Petkevičienė
MC4R, LEP, and LEPR genes are involved in the hypothalamic leptin-melanocortin regulation pathway, which is important for energy homeostasis. Our study aimed to evaluate the associations between the MC4R rs17782313, LEP rs7799039, and LEPR rs1137101 polymorphisms with obesity-related parameters in childhood and adulthood. The data were obtained from the Kaunas Cardiovascular Risk Cohort study, which started in 1977 with 1082 participants aged 12–13 years. In 2012–2014, the follow-up survey was carried out. Genotype analysis of all respondents (n = 509) aged 48–49 years was performed for the gene polymorphisms using Real-Time Polymerase Chain Reaction. Anthropometric measurements were performed in childhood and adulthood. In childhood, only skinfold thicknesses were associated with gene variants being the lowest in children with MC4R TT genotype and LEP AG genotype. In adulthood, odds of obesity and metabolic syndrome was higher in MC4R CT/CC genotype than TT genotype carriers (OR 1.8; 95% CI 1.2–2.8 and OR 1.6; 95% CI 1.1–2.4, respectively). In men, physical activity attenuated the effect of the MC4R rs17782313 on obesity. The LEP GG genotype was associated with higher BMI, waist circumference, and visceral fat level only in men. No associations of the LEPR rs1137101 polymorphisms with anthropometric measurements and leptin level were found. In conclusion, the associations of the MC4R and LEP gene polymorphisms with obesity-related parameters strengthened with age.