Publications by authors named "Gian P Fadini"

Managing Inherited Metabolic Disorders (IMDs) at risk for hypoglycemia, such as Glycogen Storage Diseases (GSDs), Hereditary Fructose Metabolism Disorders (HFMDs) and Congenital Hyperinsulinism (CH), poses challenges in dietary treatments and blood glucose monitoring. The effectiveness of Continuous Glucose Monitoring (CGM) remains a subject of ongoing debate, with IMD guidelines maintaining caution. Therefore, a systematic evaluation is needed to understand the potential benefits of CGM during dietary interventions.

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Aims/hypothesis: We compared the effects of sodium-glucose cotransporter 2 (SGLT2) inhibitors (SGLT2i) and glucagon-like peptide-1 receptor agonists (GLP-1RA) on renal outcomes in individuals with type 2 diabetes, focusing on the changes in eGFR and albuminuria.

Methods: This was a multicentre retrospective observational study on new users of diabetes medications. Participant characteristics were assessed before and after propensity score matching.

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Article Synopsis
  • * The report aims to provide current insights into the causes, symptoms, and management strategies for diabetic ketoacidosis (DKA) and hyperglycemic hyperosmolar state (HHS).
  • * New recommendations were developed based on an examination of studies published since the last update, targeting diabetes health care professionals and individuals living with diabetes.
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  • - From clinical trials and observational studies, oral semaglutide has emerged as the top option for second-line oral treatment in type 2 diabetes management, highlighting its effectiveness in both controlled and real-world settings.
  • - An expert panel in Italy discussed the practical challenges of using oral semaglutide in everyday clinical care, covering topics like its effectiveness, flexible dosing, communication with patients, and handling side effects.
  • - The panel also analyzed available data, debated fixed versus flexible dosing schedules, and offered recommendations to help clinicians effectively prescribe and monitor patients using oral semaglutide.
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  • MODY (maturity-onset diabetes of the young) includes genetic forms of diabetes often misdiagnosed as type 1 or type 2 diabetes, with diagnosis relying primarily on genetic testing due to varying clinical features.
  • ABCC8-MODY is a subtype caused by mutations in the ABCC8 gene, affecting insulin secretion, and presenting a complex range of symptoms with unclear genotype-phenotype links.
  • Effective treatment primarily involves sulfonylureas targeting the defective gene product, but their effectiveness can vary; more research is needed to better understand ABCC8-MODY and the implications of different genetic variants.
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  • A collaboration of major diabetes organizations met to update guidelines on managing hyperglycaemic crises in adults, focusing on diabetic ketoacidosis (DKA) and hyperglycaemic hyperosmolar state (HHS).
  • The updated consensus report provides current insights on the causes, symptoms, and best practices for diagnosing, treating, and preventing these conditions.
  • This effort aims to inform diabetes healthcare professionals and individuals living with diabetes about the latest evidence-based strategies since the previous guidelines were published in 2009.
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  • The study aimed to compare the effectiveness of injectable versus oral semaglutide in managing type 2 diabetes by examining real-world clinical outcomes, including changes in HbA1c and body weight.
  • Researchers analyzed data from two matched groups of 107 participants each, finding that both formulations led to similar reductions in HbA1c and comparable weight loss after 18 months, although injectable users showed greater persistence with the medication.
  • The findings suggest that, in practical settings, both forms of semaglutide are effective for T2D management, but results may not apply universally to all patient populations due to specific characteristics of the cohorts studied.
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  • Glomerular hyperfiltration is an early sign of diabetic nephropathy and can lead to serious kidney and heart issues, which researchers aimed to study in a large group of individuals with type 2 diabetes (T2D).
  • In a study of over 202,000 T2D patients in Italy, only 0.6% showed unequivocal glomerular hyperfiltration, with significant variability in prevalence between different clinics.
  • Factors such as age, body mass index (BMI), and overall metabolic control were linked to higher rates of hyperfiltration, emphasizing the need for better management of diabetes to prevent its negative health effects.
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  • Dapagliflozin, a medication for type 2 diabetes (T2D), was found to better preserve kidney function and reduce albuminuria compared to other diabetes treatments over a 2.5-year follow-up.
  • In a study involving nearly 12,000 matched patients, those using dapagliflozin experienced less decline in estimated glomerular filtration rate (eGFR) and showed significant reductions in albumin levels within 6 months.
  • The findings suggest dapagliflozin may lower the risk of developing chronic kidney disease (CKD) in T2D patients with low initial kidney risk, making it a beneficial treatment option.
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Aim: The study was designed to generate real-world evidence on IDegLira in the Italian clinical practice in two groups of patients with type 2 diabetes (T2D), switching to IDegLira either from a basal only (basal group) or basal-bolus insulin regimen (BB group).

Materials And Methods: This was a non-interventional, multicentre, single-cohort, prospective study assessing the long-term glycaemic control in patients with T2D, who switched to IDegLira from a basal insulin ± glucose-lowering medication regimen with or without a bolus insulin component for approximately 18 months, conducted in 28 Italian diabetes centres. The primary endpoint was the change in glycated haemoglobin (HbA1c) levels from baseline to 6 months after IDegLira initiation.

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Background: Revascularization is the primary treatment modality for chronic limb-threatening ischaemia (CLTI), but is not feasible in all patients. PLX-PAD is an off-the-shelf, placental-derived, mesenchymal stromal cell-like cell therapy. This study aimed to evaluate whether PLX-PAD would increase amputation-free survival in people with CLTI who were not candidates for revascularization.

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Background And Aims: An acute depletion of circulating haematopoietic stem/progenitor cells (HSPCs) occurs during COVID-19, especially among patients with a poorer disease course. We herein examined whether HSPCs levels at hospital admission for COVID-19 predict 1-year mortality and the long-COVID syndrome.

Materials And Methods: Patients hospitalized for COVID-19 in an infectious disease ward were consecutively enrolled.

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The Ser-Thr kinase CK2 plays important roles in sustaining cell survival and resistance to stress and these functions are exploited by different types of blood tumors. Yet, the physiological involvement of CK2 in normal blood cell development is poorly known. Here, we discovered that the β regulatory subunit of CK2 is critical for normal hematopoiesis in the mouse.

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Writing notes is the most widespread method to report clinical events. Therefore, most of the information about the disease history of a patient remains locked behind free-form text. Natural language processing (NLP) provides a solution to automatically transform free-form text into structured data.

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Introduction: This study aimed to address therapeutic inertia in the management of type 2 diabetes (T2D) by investigating the potential of early treatment with oral semaglutide.

Methods: A cross-sectional survey was conducted between October 2021 and April 2022 among specialists treating individuals with T2D. A scientific committee designed a data collection form covering demographics, cardiovascular risk, glucose control metrics, ongoing therapies, and physician judgments on treatment appropriateness.

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Aim/hypothesis: We examined whether prediction of long-term kidney outcomes in individuals with type 2 diabetes can be improved by measuring circulating levels of haematopoietic stem/progenitor cells (HSPCs), which are reduced in diabetes and are associated with cardiovascular risk.

Methods: We included individuals with type 2 diabetes who had a baseline determination of circulating HSPCs in 2004-2019 at the diabetes centre of the University Hospital of Padua and divided them into two groups based on their median value per ml of blood. We collected updated data on eGFR and albuminuria up to December 2022.

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Article Synopsis
  • * Current treatments focus on surgical revascularisation, but many patients can't undergo surgery, and surgical success is variable; research is exploring new medical targets to treat ischaemia.
  • * Recent studies identify various biological pathways and novel therapies that may enhance blood flow recovery and healing in ischaemic limbs, but translating these findings into effective clinical treatments remains a challenge.
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Type 2 diabetes (T2D), cardiovascular disease (CVD) and chronic kidney disease (CKD), are recognized among the most disruptive public health issues of the current century. A large body of evidence from epidemiological and clinical research supports the existence of a strong interconnection between these conditions, such that the unifying term cardio-metabolic-renal (CMR) disease has been defined. This coexistence has remarkable epidemiological, pathophysiologic, and prognostic implications.

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Aim: Sodium-glucose cotransporter 2 inhibitors (SGLT2is) are particularly effective in preventing adverse outcomes of heart failure and chronic kidney disease, which are highly prevalent in the elderly. Here, we aimed to access the safety of SGLT2i in elderly patients with type 2 diabetes.

Materials And Methods: We performed a meta-analysis of randomized controlled trials (RCTs) reporting safety outcomes of the elderly (≥65 years) patients with type 2 diabetes, randomized to an SGLT2i or placebo.

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Objective: Long noncoding RNAs (lncRNAs) are involved in diabetogenesis in experimental models, yet their role in humans is unclear. We investigated whether circulating lncRNAs associate with incident type 2 diabetes in older adults.

Research Design And Methods: A preselected panel of lncRNAs was measured in serum of individuals without diabetes (n = 296) from the Vienna Transdanube Aging study, a prospective community-based cohort study.

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Alström syndrome (AS) is a rare genetic disease caused by ALMS1 mutations, characterized by short stature, and vision and hearing loss. Patients with AS develop the metabolic syndrome, long-term organ complications, and die prematurely. We explored the association between AS and a shortage of hematopoietic stem/progenitor cells (HSPCs), which is linked to metabolic diseases and predicts diabetic complications.

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Innate immune cells infiltrate growing adipose tissue and propagate inflammatory clues to metabolically distant tissues, thereby promoting glucose intolerance and insulin resistance. Cytokines of the IL-6 family and gp130 ligands are among such signals. The role played by oncostatin M (OSM) in the metabolic consequences of overfeeding is debated, at least in part, because prior studies did not distinguish OSM sources and dynamics.

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