Cristiana-Elena Vlad

Dr. Cristiana-Elena Vlad

Department of Nephrology-Internal Medicine, “Dr.C.I. Parhon” Clinical Hospital, Iasi, Romania
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Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

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

Representative Publications

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7 March 2023 in Antioxidants
Verified
Journal Article
Open access
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KCKarina Alexandra Cojocaru
Karina Alexandra Cojocaru
Ionut LuchianIonut Luchian
Ionut Luchian
Ancuta GoriucAncuta Goriuc
Ancuta Goriuc
LALucian-Mihai Antoci
Lucian-Mihai Antoci
CCCristian-Gabriel Ciobanu
Cristian-Gabriel Ciobanu
Liliana Georgeta FoiaLiliana Georgeta Foia
Liliana Georgeta Foia
Mitochondria are subcellular organelles involved in essential cellular functions, including cytosolic calcium regulation, cell apoptosis, and reactive oxygen species production. They are the site of important biochemical pathways, including the tricarboxylic acid cycle, parts of the ureagenesis cycle, or haem synthesis. Mitochondria are responsible for the majority of cellular ATP production through OXPHOS. Mitochondrial dysfunction has been associated with metabolic pathologies such as diabetes, obesity, hypertension, neurodegenerative diseases, cellular aging, and cancer. In this article, we describe the pathophysiological changes in, and mitochondrial role of, metabolic disorders (diabetes, obesity, and cardiovascular disease) and their correlation with oxidative stress. We highlight the genetic changes identified at the mtDNA level. Additionally, we selected several representative biomarkers involved in oxidative stress and summarize the progress of therapeutic strategies.

1 January 2020 in BioMed Research International
Verified
Journal Article
Open access
Alexandru BurlacuAlexandru Burlacu
Alexandru Burlacu
AIAdrian Iftene
Adrian Iftene
Daniel JugrinDaniel Jugrin
Daniel Jugrin
IPIolanda Valentina Popa
Iolanda Valentina Popa
PLPaula Madalina Lupu
Paula Madalina Lupu
ACAdrian Constantin Covic
Adrian Constantin Covic
Background. The purpose of this review is to depict current research and impact of artificial intelligence/machine learning (AI/ML) algorithms on dialysis and kidney transplantation. Published studies were presented from two points of view: What medical aspects were covered? What AI/ML algorithms have been used? Methods. We searched four electronic databases or studies that used AI/ML in hemodialysis (HD), peritoneal dialysis (PD), and kidney transplantation (KT). Sixty‐nine studies were split into three categories: AI/ML and HD, PD, and KT, respectively. We identified 43 trials in the first group, 8 in the second, and 18 in the third. Then, studies were classified according to the type of algorithm. Results. AI and HD trials covered: (a) dialysis service management, (b) dialysis procedure, (c) anemia management, (d) hormonal/dietary issues, and (e) arteriovenous fistula assessment. PD studies were divided into (a) peritoneal technique issues, (b) infections, and (c) cardiovascular event prediction. AI in transplantation studies were allocated into (a) management systems (ML used as pretransplant organ‐matching tools), (b) predicting graft rejection, (c) tacrolimus therapy modulation, and (d) dietary issues. Conclusions. Although guidelines are reluctant to recommend AI implementation in daily practice, there is plenty of evidence that AI/ML algorithms can predict better than nephrologists: volumes, Kt/V, and hypotension or cardiovascular events during dialysis. Altogether, these trials report a robust impact of AI/ML on quality of life and survival in G5D/T patients. In the coming years, one would probably witness the emergence of AI/ML devices that facilitate the management of dialysis patients, thus increasing the quality of life and survival.

12 December 2022 in International Urology and Nephrology
Verified
Journal Article
Closed access
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SVSimona Volovat
Simona Volovat
MAMugurel Apetrii
Mugurel Apetrii
ASAnca Elena Stefan
Anca Elena Stefan
CVCristiana-Elena Vlad
Cristiana-Elena Vlad
LVLuminita Voroneanu
Luminita Voroneanu
SHSimona Hogas
Simona Hogas

14 December 2019 in Journal of Diabetes Research
Verified
Journal Article
Open access
PDF file
CVCristiana-Elena Vlad
Cristiana-Elena Vlad
Liliana Georgeta FoiaLiliana Georgeta Foia
Liliana Georgeta Foia
RPRoxana Popescu
Roxana Popescu
IIIuliu Ivanov
Iuliu Ivanov
MLMihaela Catalina Luca
Mihaela Catalina Luca
LFLaura Florea
Laura Florea
Purpose. Nontraditional cardiovascular risk factors as apolipoprotein A (ApoA), apolipoprotein B (ApoB), and the proprotein convertase subtilisin/kexin type 9 (PCSK9) increase the prevalence of cardiovascular mortality in chronic kidney disease (CKD) or in end-stage renal disease (ESRD) through quantitative alterations. This review is aimed at establishing the biomarker (ApoA, ApoB, and PCSK9) level variations in uremic patients, to identify the studies showing the association between these biomarkers and the development of cardiovascular events and to depict the therapeutic options to reduce cardiovascular risk in CKD and ESRD patients.Methods. We searched the electronic database of PubMed, Scopus, EBSCO, and Cochrane CENTRAL for studies evaluating apolipoproteins and PCSK9 in CKD and ESRD. Randomized controlled trials, observational studies (including case-control, prospective or retrospective cohort), and reviews/meta-analysis were included if reference was made to those keys and cardiovascular outcomes in CKD/ESRD.Results. 18 studies met inclusion criteria. Serum ApoA-I has been significantly associated with the development of new cardiovascular event and with cardiovascular mortality in ESRD patients. ApoA-IV level was independently associated with maximum carotid intima-media thickness (cIMT) and was a predictor for sudden cardiac death. The ApoB/ApoA-I ratio represents a strong predictor for coronary artery calcifications, cardiovascular mortality, and myocardial infarction in CKD/ESRD. Plasma levels of PCSK9 were not associated with cardiovascular events in CKD patients.Conclusions. Although the “dyslipidemic status” in CKD/ESRD is not clearly depicted, due to different research findings, ApoA-I, ApoA-IV, and ApoB/ApoA-I ratio could be predictors of cardiovascular risk. Serum PCSK9 levels were not associated with the cardiovascular events in patients with CKD/ESRD. Probably in the future, the treatment of dyslipidemia in CKD/ESRD will be aimed at discovering new effective therapies on the action of these biomarkers.

20 February 2020 in Nutrients
Verified
Journal Article
Open access
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MBMaria Bogdan
Maria Bogdan
Andreea Daniela MecaAndreea Daniela Meca
Andreea Daniela Meca
Mihail Virgil BoldeanuMihail Virgil Boldeanu
Mihail Virgil Boldeanu
Dorin GheorgheDorin Gheorghe
Dorin Gheorghe
Adina Turcu-StiolicaAdina Turcu-Stiolica
Adina Turcu-Stiolica
PSPetra Surlin
Petra Surlin
Ascorbic acid (vitamin C) is an important water-soluble vitamin found in many fruits and vegetables. It has well-documented beneficial effects on the human body and is used as a supplement, alone or in combination with other vitamins and minerals. Over recent years, research has focused on possible new therapeutic actions in chronic conditions including periodontal disease (PD). We conducted a systematic review on clinical trials from four databases (PubMed, Clinical Trials, Cochrane, Web of Science) which measured plasmatic/salivary levels of ascorbic acid in PD–diabetes mellitus (DM) association. Six studies were included in our review, three of them analyzing patients with different grades of PD and DM who received vitamin C as a treatment (500 mg vitamin C/day for 2 months and 450 mg/day for 2 weeks) or as part of their alimentation (guava fruits), in combination with standard therapies and procedures. Decreased levels of vitamin C were observed in PD patients with DM but data about efficacy of vitamin C administration are inconclusive. Given the important bidirectional relationship between PD and DM, there is a strong need for more research to assess the positive effects of ascorbic acid supplementation in individuals suffering from both diseases and also its proper regimen for these patients.

11 January 2021 in Lipids in Health and Disease
Verified
Journal Article
Open access
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CVCristiana-Elena Vlad
Cristiana-Elena Vlad
Liliana Georgeta FoiaLiliana Georgeta Foia
Liliana Georgeta Foia
LFLaura Florea
Laura Florea
ICIrina-Iuliana Costache
Irina-Iuliana Costache
ACAndreea Covic
Andreea Covic
ACAdrian Covic
Adrian Covic
Background: Familial hypercholesterolemia(FH) is one of the most frequent and important monogenic cholesterol pathologies. Traditional and non-traditional cardiovascular risk factors increase the prevalence of atherosclerotic cardiovascular disease(ASCVD) in this population. The aims of the study were: (a) to identify FH patients in the North-Eastern part of Romania and to analyze demographic, clinical and paraclinical data (b) to evaluate the risk of new cardiovascular events at follow-up in FH patients stratified by lipid-lowering agents. Methods: This first prospective study in the North-Eastern part of Romania was carried out between October 2017 and October 2019; out of 980 patients with dyslipidemia evaluated with the Dutch Lipid Network(DLCN) and Simon Broome(SM) scores, 61 patients with DLCN score above 3 and possible/probable FH(SM score) were included. Results: Nine hundred-eighty patients were examined and 61 (6.2%) were received the clinical diagnosis of FH. The mean age was 48.5±12.5 years, with more female patients than male patients (63.9% versus 36%). Hypertension was the main cardiovascular risk factor for both genders, followed by physical inactivity and obesity for the female group and active smoking for the male group. The measured DLCN score recorded: “possible” FH identified in 39.4%, “probable” FH in 45.9% and “definite” FH in 14.7%. The effective lipid-lowering drugs used were statin alone and statin in association with fenofibrate, which improved both the lipid profile values and the subclinical atherosclerosis markers (ankle-brachial index, carotid intima-media thickness and high-sensitivity C-reactive protein). New ASCVDs that emerged during the study were most commonly represented by coronary heart disease and stroke. At the same time, the new cardiovascular events were delayed in patients receiving the lipid-lowering drugs, without significant differences between them. Conclusions: In patients with suspected FH, the lipid-lowering agents during the follow-up period delayed the new cardiovascular events, yet failed to reach the goals proposed by the guidelines.