Paul Balanescu

Dr. Paul Balanescu


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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1 March 2015 in Romanian Journal of Internal Medicine
Verified
Journal Article
Open access
PDF file
PBPaul Balanescu
Paul Balanescu
ALAnca Lădaru
Anca Lădaru
EBEugenia Bălănescu
Eugenia Bălănescu
ANAdriana Nicolau
Adriana Nicolau
Cristian BaicusCristian Baicus
Cristian Baicus
GDGh.A. Dan
Gh.A. Dan
Background. Systemic sclerosis (Ssc) is an autoimmune disease characterized by cutaneous and visceral fibrosis and its pathogenesis is incompletely understood. T helper cells are key regulators of the immune response and they seem to be involved in Ssc clinical manifestations. The aim of the study is to determine key cytokines secreted by Th1 (IFN-γ), Th2 (IL-6) and Th17 (IL-17) in Ssc patients and correlate them with specific manifestations of Ssc patients. Material and methods. 35 consecutive Ssc patients and 20 age and sex matched controls were recruited. Serum IL-17, IFN-γ and IL-6 were determined using ELISA method. Results. Serum IL-17 and IL-6 levels were not significantly different in Ssc patients and controls. Serum IFN-γ levels were higher in Ssc patients when compared to controls. Higher serum IFN-γ levels associated with pulmonary hypertension. After adjusting for gender and age, IL-17 levels remained independently associated with some clinical manifestations of Ssc patients (telangiectasia and high activity score of Ssc). Conclusion. Th17 and Th1 cell responses are active in Ssc patients as their cytokines associated with higher disease activity scores and pulmonary manifestations. Th17 and Th1 specific activity and homing within Ssc patients still needs to be defined and determined in order to target them as potential future therapeutic targets in Ssc patients.

3 December 2019 in Disease Markers
Verified
Journal Article
Open access
PDF file
Anca BalanescuAnca Balanescu
Anca Balanescu
ISIustina Stan
Iustina Stan
ICIoana Codreanu
Ioana Codreanu
VCValentina Comănici
Valentina Comănici
EBEugenia Bălănescu
Eugenia Bălănescu
PBPaul Balanescu
Paul Balanescu
Background. Obesity prevalence is increasing in children. It is associated with various comorbidities including nonalcoholic fatty liver disease (NAFLD). Hsp90 isoforms were identified in previous proteomic studies as potential biomarkers for NAFLD. The aim of the study was to analyze circulating levels of Hsp90α and Hsp90β in overweight and obese children. In addition, Hsp90α and Hsp90β were evaluated as biomarkers for NAFLD in overweight and obese children. Methods. 68 overweight and obese children and ten age- and gender-matched controls were recruited. Hsp90α and Hsp90β levels were analyzed from serum in both controls and overweight and obese children by ELISA. Results. Serum Hsp90β and total Hsp90 levels were statistically significantly higher in overweight and obese children compared to controls. On the contrary, there was no difference in Hsp90α levels between overweight and obese children and healthy controls. Hsp90 isoforms had different expression in NAFLD patients. Hsp90β levels were higher in overweight and obese NAFLD patients while Hsp90α levels were lower. Hsp90α to Hsp90β ratio had better accuracy for NAFLD diagnosis in obese and overweight patients compared to individual biomarkers. Conclusion. Hsp90 isoforms were confirmed on an independent cohort as biomarkers for NAFLD in overweight and obese children. In these patients, it seems to be more useful to separately analyze Hsp90 isoforms rather than total Hsp90 as the isoforms have greater discriminative capacity.

15 November 2017 in Romanian Journal of Internal Medicine
Verified
Journal Article
Open access
PDF file
PBPaul Balanescu
Paul Balanescu
EBEugenia Bălănescu
Eugenia Bălănescu
Anca BalanescuAnca Balanescu
Anca Balanescu
T cells (especially T helper cells) seem to be strongly associated with systemic sclerosis pathogenesis. Th17-IL-17 axis was proved to be involved in the pathogenesis of multiple autoimmune diseases. By performing a comprehensive research of the literature indexed in PubMed database, the current review summarizes current knowledge related to Th17 and IL-17 in systemic sclerosis. While there is promising data suggesting inhibition of Tregulatory and Th1 signals on one hand and promotion of Th17 and Th2 signals on the other, studies that include prospective and integrated analysis of Tregulatory, Th17, Th1, Th2 (cells and derived cytokines) on the same cohort of Ssc patients are warranted.

1 September 2015 in Journal of Clinical Laboratory Analysis
Verified
Journal Article
Closed access
PBPaul Balanescu
Paul Balanescu
ALAnca Lădaru
Anca Lădaru
EBEugenia Bălănescu
Eugenia Bălănescu
Theodor VoiosuTheodor Voiosu
Theodor Voiosu
Cristian BaicusCristian Baicus
Cristian Baicus
GDGheorghe Andrei Dan
Gheorghe Andrei Dan

30 July 2024 in Clinical Endoscopy
Verified
Journal Article
Open access
AVAndrei Voiosu
Andrei Voiosu
MSMonica State
Monica State
VDVictor Drăgan
Victor Drăgan
SVSergiu Văduva
Sergiu Văduva
PBPaul Balanescu
Paul Balanescu
Theodor VoiosuTheodor Voiosu
Theodor Voiosu
Background/Aims: Gastrointestinal bleeding is a significant and potentially lethal event. We aimed to review the efficiency and safety of self-assembling peptides for the treatment and prevention of gastrointestinal tract bleeding.Methods: We conducted a systematic search for studies describing the endoscopic use of self-assembling peptides for treatment or prevention of bleeding in the gastrointestinal tract in a parallel, independent fashion. The primary outcomes were rates of successful initial hemostasis, delayed bleeding, and rebleeding. The secondary outcomes were adverse events and ease and volume of gel used.Results: Seventeen studies were analyzed. Overall success rate of self-assembling peptides in gastrointestinal bleeding was 87.7% (38%–100%), regardless of etiology or associated treatments. Rebleeding rate ranged from 0% to 16.2%, with a mean of 4.7%, and overall delayed bleeding rate was 5% (range, 0%–15.9%). Only three adverse events were reported in a pooled number of 815 patients. The volume of gel used varied (0.43 to 3.7 mL) according to indication and type of bleeding.Conclusions: The limited available data on the use of self-assembling peptides in gastrointestinal endoscopy suggest a high efficiency and good safety profile.

16 May 2014 in Biomarkers
Verified
Journal Article
Open access
PBPaul Balanescu
Paul Balanescu
ALAnca Lădaru
Anca Lădaru
EBEugenia Bălănescu
Eugenia Bălănescu
Cristian BaicusCristian Baicus
Cristian Baicus
GDGheorghe Andrei Dan
Gheorghe Andrei Dan
Systemic sclerosis (SSc) is an autoimmune disease with incompletely known physiopathology. There is a great challenge to predict its course and therapeutic response using biomarkers. To critically review proteomic biomarkers discovered from biological specimens from systemic sclerosis patients using mass spectrometry technologies. Medline and Embase databases were searched in February 2014. Out of the 199 records retrieved, a total of 20 records were included, identifying 116 candidate proteomic biomarkers. Research in SSc proteomic biomarkers should focus on biomarker validation, as there are valuable mass-spectrometry proteomics studies in the literature.