Joanna Oswiecimska

Prof. Joanna Oswiecimska


Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

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

Representative Publications

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1 March 2017 in Advances in Medical Sciences
Verified
Journal Article
Closed access
JOJoanna Oswiecimska
Joanna Oswiecimska
ASAgnieszka Szymlak
Agnieszka Szymlak
WRWojciech Roczniak
Wojciech Roczniak
KGKatarzyna Girczys-Połedniok
Katarzyna Girczys-Połedniok
JKJarosław Kwiecień
Jarosław Kwiecień

16 October 2015 in Physiological Research
Verified
Journal Article
Closed access
JOJoanna Oswiecimska
Joanna Oswiecimska
ASA. Suwała
A. Suwała
EŚElżbieta Świętochowska
Elżbieta Świętochowska
ZOZ. Ostrowska
Z. Ostrowska
PGP. Gorczyca
P. Gorczyca
KZK. Ziora
K. Ziora
It is believed that omentin is secreted by stromal cells of adipose tissue and modulates insulin sensitivity. Data from a few studies have shown lower serum omentin in obese children and higher in anorexia nervosa. However, to date, there is lack of research on serum omentin concentrations in adolescent patients in a wide range of body mass index (BMI) and insulin resistance. In this cross-sectional study omentin-1 serum concentrations were evaluated using commercially available ELISA kit in 47 Polish girls with restrictive anorexia nervosa (AN), 50 with simple obesity (OB) and 39 healthy controls (C). The mean serum omentin-1 concentration in girls with AN was statistically significantly higher than that of C and OB girls. Statistically significant (P<0.0001) negative correlations between the serum concentrations of omentin-1 and body weight (r=−0.73), BMI (r=−0.75), standard deviation score for body mass index (BMI-SDS) (r=−0.75), insulin (r=−0.81) and HOMA-IR index (r=−0.82) were seen in the entire examined population. We conclude, that omentin-1 is the nutritional marker reflecting body weight and insulin resistance. Our findings support the hypothesized role of omentin in maintenance of body weight and regulation of appetite and suggest the adaptation of its secretion to body weight and glucose metabolism.

1 July 2007 in Bone
Verified
Journal Article
Closed access
JOJoanna Oswiecimska
Joanna Oswiecimska
KZKatarzyna Ziora
Katarzyna Ziora
WPWojciech Pluskiewicz
Wojciech Pluskiewicz
GGGabriela Geisler
Gabriela Geisler
KBKatarzyna Broll-Waśka
Katarzyna Broll-Waśka
ADAntoni Dyduch
Antoni Dyduch

22 January 2022 in Nutrients
Verified
Journal Article
Open access
PDF file
MCMarcin Chyra
Marcin Chyra
WRWojciech Roczniak
Wojciech Roczniak
EŚElżbieta Świętochowska
Elżbieta Świętochowska
MDMagdalena Dudzińska
Magdalena Dudzińska
JOJoanna Oswiecimska
Joanna Oswiecimska
Background: Changes in adipokine secretion may be involved in the anti-epileptic effect of a ketogenic diet (KD) in drug-resistant epilepsy (DRE). Objectives: The assessment of the influence of KD on serum adiponectin, omentin-1, and vaspin in children with DRE. Methods: Anthropometric measurements (weight, height, BMI, and waist-to-hip circumference ratio) were performed in 72 children aged 3–9 years, divided into 3 groups: 24 children with DRE treated with KD, 26—treated with valproic acid (VPA), and a control group of 22 children. Biochemical tests included fasting glucose, insulin, beta-hydroxybutyric acid, lipid profile, aminotransferases activities, and blood gasometry. Serum levels of adiponectin, omentin-1 and vaspin were assayed using commercially available ELISA tests. Results: Serum levels of adiponectin and omentin-1 in the KD group were significantly higher and vaspin—lower in comparison to patients receiving VPA and the control group. In all examined children, serum adiponectin and omentin-1 correlated negatively with WHR and serum triglycerides, insulin, fasting glucose, and HOMA-IR. Vaspin levels correlated negatively with serum triglycerides and positively with body weight, BMI, fasting glucose, insulin, and HOMA-IR. Conclusion: One of the potential mechanisms of KD in children with drug-resistant epilepsy may be a modulation of metabolically beneficial and anti-inflammatory adipokine levels.

7 March 2012 in Clinical Endocrinology
Verified
Journal Article
Closed access
PDF file
KZKatarzyna Ziora
Katarzyna Ziora
JOJoanna Oswiecimska
Joanna Oswiecimska
EŚElżbieta Świętochowska
Elżbieta Świętochowska
DZDariusz Ziora
Dariusz Ziora
MSMałgorzata Stojewska
Małgorzata Stojewska
BBBarbara Błońska-Fajfrowska
Barbara Błońska-Fajfrowska

15 March 2019 in The World Journal of Biological Psychiatry
Verified
Journal Article
Closed access
WRWojciech Roczniak
Wojciech Roczniak
AMAgata Mikołajczak-Będkowska
Agata Mikołajczak-Będkowska
EŚElżbieta Świętochowska
Elżbieta Świętochowska
ZOZofia Ostrowska
Zofia Ostrowska
KZKatarzyna Ziora
Katarzyna Ziora
JOJoanna Oswiecimska
Joanna Oswiecimska
Background: IL-15 plays a key role in the muscle-fat interaction, reducing adipose tissue mass without changes in the lean body mass and reduction of food intake. Here we assess serum IL-15 levels in girls with anorexia nervosa relative to obese and normal weight female adolescents. Material and Methods: Serum IL-15 concentrations were evaluated using a commercially available ELISA kit in 32 Polish girls with restrictive AN, 29 girls with obesity (O), and 21 healthy controls (C). Anthropometric measurements (weight, height, BMI) and laboratory assays (serum fasting glucose, insulin, HOMA-IR, total cholesterol, HDL, LDL, triglycerides, and C-reactive protein) were performed. Results: Mean serum IL-15 in the AN group was significantly higher than in C, but lower than in O. In all examined girls, significant positive correlations between IL-15 and body weight, BMI, insulin, HOMA, LDL, triglycerides, and CRP were noted. We also observed an inverse relationship between IL-15 and HDL. Conclusion: Our study demonstrated that serum IL-15 concentrations in adolescent girls with anorexia nervosa and obesity are significantly elevated in comparison to normal weight controls. However, the role of IL-15 in the pathogenesis of anorexia nervosa and obesity remains still unclear.