Publications by authors named "Iancu Mihaela"

: Heart failure (HF) is one of the most common initial presentations of cardiovascular disease (CVD) in patients with type 2 diabetes mellitus (T2DM). There are different cardiac biomarkers related to the pathophysiological mechanisms of HF in T2DM. The current research aims to identify additional biomarkers that could improve the diagnosis and prognosis of HFpEF, which is currently assessed using NT pro-BNP levels.

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  • * The study examined the relationship between certain gene variations (polymorphisms) of IL17 and TLR4 and their impact on the likelihood of developing metabolic associated fatty liver disease (MASLD), using genetic testing and serum level analysis.
  • * Findings revealed that individuals with specific genetic variants of IL17 and TLR4 had significantly higher odds of developing conditions like metabolic associated steatotic liver disease (MASH) and metabolic associated fatty liver (MAFL); notably, certain alleles were strongly correlated with these increased risks.
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The HLA profile is essential in cell and tissue transplantation, particularly in patients with autoimmune conditions and infections. Due to the extreme polymorphism in certain HLA loci, it also serves as a key tool for population genetic analysis. This study aimed to identify the allele and haplotype distributions of HLA class I (A, B, and C) and class II (DRB1) genotypes in unrelated hematopoietic stem cell donors.

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  • The study examines the relationship between Type 2 diabetes mellitus (T2DM) and cardiovascular disease (CVD) in Romanian patients, highlighting the effectiveness of antidiabetic drugs like GLP-1 Ras and SGLT-2 inhibitors.
  • Conducted with 405 T2DM patients, the study found that while many achieved satisfactory blood sugar levels, they struggled to meet overall health targets including blood pressure and cholesterol management.
  • Results indicated a high prevalence of comorbidities, particularly hypertension and obesity, and revealed a low usage of advanced treatments like GLP-1 Ras and SGLT-2 inhibitors, along with statins.
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  • Polycystic ovary syndrome (PCOS) is a complex condition, and this study aimed to explore how genetic variations in the vitamin D receptor (VDR) are linked to skin issues, hormone levels, and oxidative stress in women with PCOS.
  • The research involved 46 women with PCOS and 39 healthy controls, examining skin conditions like acne and hirsutism, as well as assessing hormone levels and specific VDR gene polymorphisms (FokI, TaqI, and ApaI).
  • Key findings show that the FokI CC genotype may protect against acne and seborrhea, while the TaqI dominant genotype is linked to lower oxidative stress levels in women with PCOS.
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: The pathogenesis of MASLD (metabolic dysfunction-associated steatotic liver disease) is driven by environmental, genetic, metabolic, immune, and inflammatory factors. IL-17 and TLR4 determine hepatic steatosis, inflammation, and finally fibrosis. : To explore the associations between the plasma levels of inflammatory markers, TLR4, and the cytokines IL17A/F, as well as their connections with the degree of hepatic steatosis and the risk of hepatic fibrosis (defined by the FIB-4 score) in MASLD patients.

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Cytopenias or coagulation deficiencies can occur in people living with HIV (PLWH). The severity of these disorders is influenced by the low levels of CD4+ lymphocytes, viral load, and the stage of viral infection. The aim of our retrospective observational study was to determine the frequency of cytopenias and coagulation deficiencies in PLWH as well as the need for replacement therapy with blood products.

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Multiple myeloma, the disease characterized by the malignant proliferation of plasma cells that invades the bone marrow, produces osteolytic lesions and secretes monoclonal proteins. Several biomarkers have been shown to represent important tools in the pathogenesis of myeloma and offer insights into bone degradation and formation. The objectives of this current study were to assess the associations of modern biomarkers (TNF-α: tumor necrosis factor; IFN: Interferon; FreeRANKL: Free Receptor Activator for Nuclear Factor kappa B Ligand; RANKL: Receptor Activator for Nuclear Factor kappa B Ligand, Beta crosslaps, IL-6: Interleukin 6) with osteolytic lesions status after first-line treatment and to evaluate the correlations between modern and classical biomarkers (LDH: Lactate Dehydrogenase; VSH: Erythrocyte Sedimentation Rate; Hgb: Hemoglobin, Calcium, Albumin, B2microglobulin) stratified by osteolytic lesions status.

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One of the most prominent symptoms in multiple sclerosis is pathological fatigue, often described by sufferers as one of the most debilitating symptoms, affecting quality of life and employment. However, the mechanisms of both, physical and cognitive fatigue in multiple sclerosis remain elusive. Here, we use behavioural tasks and quantitative MRI to investigate the neural correlates of interoception (the ability to sense internal bodily signals) and metacognition (the ability of the brain to assess its own performance), in modulating cognitive fatigue.

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As the population ages, promoting healthy aging through targeted interventions becomes increasingly crucial. Growing evidence suggests that dietary interventions can significantly impact this process by modulating fundamental molecular pathways. This review focuses on the potential of targeted dietary strategies in promoting healthy aging and the mechanisms by which specific nutrients and dietary patterns influence key pathways involved in cellular repair, inflammation, and metabolic regulation.

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Schizophrenia poses significant challenges for individuals and caregivers, often leading to recurrent hospitalizations. Limited information on patients with schizophrenia and multiple hospitalizations in Romania is available in the scientific literature. Our study aimed to evaluate the characteristics of patients with schizophrenia with multiple hospitalizations in a single center in Cluj-Napoca, analyzing if specific patterns exist between patients with two or more hospitalizations or between men and women.

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An adequate vitamin D level is essential for optimal bone mass formation during growth. The present study aimed to assess (i) the sex-specific, age-specific, and potential seasonal (spring, summer, winter) influences on the pediatric circulating levels of 25-hydroxyvitamin D (25(OH)D); (ii) determine the frequency of pediatric patients with vitamin D deficiency (VDD) or insufficiency (VDI); and (iii) quantify the association between age category, sex, and season types and susceptibility to VDD and VDI, respectively. Laboratory data were collected on serum 25(OH)D levels in children aged between 2 and 18 years (n = 1674) who underwent blood sampling following admission to a university pediatric hospital in Cluj-Napoca (Romania) between January and June 2023.

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  • Maldevelopment of the fetal bowel can lead to intestinal atresia, a rare condition causing congenital bowel obstruction; this report focuses on a case detected during a routine ultrasound at 22 weeks of gestation.
  • A 24-year-old woman with gestational diabetes underwent ultrasound and was diagnosed with bowel issues, prompting counseling about potential complications; by 33 weeks, the condition worsened and surgery was performed after birth.
  • The case underscores the significance of prenatal ultrasounds in identifying fetal abnormalities, demonstrates effective management of intestinal atresia, and highlights the challenges of coexisting conditions like gestational diabetes.
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Hepatocellular carcinoma (HCC) is the most frequently found primary malignancy of the liver, showing an accelerated upward trend over the past few years and exhibiting an increasing relationship with metabolic syndrome, obesity, dyslipidemia and type 2 diabetes mellitus. The connection between these risk factors and the occurrence of HCC is represented by the occurrence of non-alcoholic fatty liver disease (NAFLD) which later, based on genetic predisposition and various triggers (including the presence of chronic inflammation and changes in the intestinal microbiome), may evolve into HCC. HCC in many cases is diagnosed at an advanced stage and can be an incidental finding.

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Background And Objectives: The purpose of our study was to obtain and characterize carrier systems in different sizes that can affect oral absorption, since the mechanisms of liposome absorption are not yet fully understood. From stomach to the small intestine, liposomes can be gradually destroyed. Understanding the factors that affect oral absorption leads to developing safe and effective nanosystems to improve the oral delivery of therapeutics.

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  • Cardiac arrhythmias are common in patients with congenital heart disease, especially after corrective surgery, and are influenced by various patient-related factors.
  • The risk is higher in young, low-weight patients, and factors like heart geometry changes, hemodynamic stress, and surgical scars contribute to arrhythmia development.
  • Accurate diagnosis and tailored management are crucial for reducing morbidity and mortality, making it vital to identify risk factors for each patient to improve their life expectancy and quality of life.
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  • Idiopathic recurrent pericarditis (IRP) is a condition marked by chest pain episodes and symptom-free periods, particularly common in children, with a recurrence rate of about 35%.
  • IRP may appear alone or as part of systemic autoinflammatory diseases, and conditions like Familial Mediterranean Fever and others need to be ruled out in IRP patients.
  • A unique case is reported of an adolescent with relapsing pericarditis linked to a mutation in the NLRP12 gene, suggesting a potential connection between this genetic alteration and increased inflammation in the heart.
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The gut microbiota represents a community of microorganisms (bacteria, fungi, archaea, viruses, and protozoa) that colonize the gut and are responsible for gut mucosal structural integrity and immune and metabolic homeostasis. The relationship between the gut microbiome and human health has been intensively researched in the past years. It is now widely recognized that gut microbial composition is highly responsible for the general health of the host.

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Background: interleukin 23 (IL-23) is an important factor involved in the survival and proliferation of T helper 17 cells (Th17), known for their implication in multiple sclerosis (MS). By contrast, IL-27 regulates and modulates the function of T lymphocytes, in particular as a suppressor of Th17 differentiation. The aims of the study were i) to test the association of cytokines with the clinical and genetic characteristics in each of the multiple sclerosis groups (CIS - clinically isolated syndrome, RRMS - relapsing-remitting MS and SPMS - Secondary progressive MS) and ii) to evaluate the association between serum levels of IL-23 and IL-27 with (IL-27), (IL-27) and (IL-23) gene polymorphisms in RRMS patients.

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The transposition of great arteries (TGA) is one of the most frequent and severe congenital heart diseases. After newborn stabilization and while pending surgical correction, echocardiographic monitoring with a careful evaluation of left ventricle (LV) performance is warranted. In this study, our objectives were (i) to compare myocardial function, assessed via speckle-tracking echocardiography, between neonates with TGA and neonates without TGA and (ii) to identify a strain parameter with a good discriminatory ability for TGA.

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Isolated right ventricle hypoplasia (IRVH) is a disease characterized by an underdeveloped right ventricle. It is a congenital heart disease than can associate heterogeneous structural defects and nonspecific clinical features, which can often present a challenging therapeutic management. In this article, there are presented diagnostic methods and treatment options for right ventricle hypoplasia (RVH) according to clinical features, patients age and associated structural heart defects.

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Data regarding reference intervals for strain parameters derived from 2D speckle-tracking echocardiography in full-term newborns are limited and still under development. Our objectives were to establish the level of reproducibility and reference intervals in assessing myocardial function using 2D speckle-tracking echocardiography for longitudinal and regional strain measurements. A total of 127 full-term newborns were examined to be included in the study, of which 103 were analyzed.

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Childhood obesity progresses to metabolic disturbances via low-grade inflammation. Identifying novel molecules that reflect the activity of the immune responses is critical in understanding its underlying pathogenesis. Our exploratory study aimed to evaluate the change of chitotriosidase (CHIT1) plasma activity according to Body Mass Index (BMI)-for-age z score in pediatric patients.

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(1) Background: Near-infrared spectroscopy (NIRS) is a non-invasive, easily performed method of monitoring brain oxygenation. The regional cerebral oxygen saturation (crSaO2) and the cerebral fractional tissue oxygen extraction (cFTOE) evaluated by NIRS provide more accurate information on brain oxygenation than the blood oxygen saturation. We investigated the effect of perinatal factors on cerebral oxygenation of preterm newborns.

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Toll-like receptors (TLRs) have an important role in innate immunity, and single nucleotide polymorphisms (SNPs) of genes influence the risk of developing hematological malignancies. We aimed to evaluate the effect of (rs5743708), (rs11536889, rs4986790, rs4986791), (rs187084, rs352140, rs5743836) on AML risk, the relation between investigated SNPs and somatic mutations, clinical features, and the overall survival of adult AML patients. All mentioned SNPs were genotyped in 511 AML cases and 503 healthy controls.

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