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Triglyceride-rich LIPoproteins and INflammatory Cytokines After Oral FAT Loading as Potential Early Biomarkers of the Risk of Progression Towards DIABETES and Development of Complications. LIPINFAT Diabetes Study. (LIPINFAT)

14 maggio 2026 aggiornato da: Angelina Passaro

The aim of the study is to evaluate whether the Oral Fat Loading Test (OFLT) determines a different response in terms of the quantity, quality, and kinetics of triglyceride-rich lipoproteins in subjects with T2D, prediabetics, and control subjects, and whether triglyceride-rich lipoproteins and inflammatory cytokines after OFLT are potential early biomarkers of the risk of progression to diabetes and the development of complications in a general practice setting.

To address these questions, a hybrid cohort study was designed by identifying three groups of subjects: T2D and prediabetics (exposed and near-exposed) and control subjects (unexposed).

Panoramica dello studio

Stato

Reclutamento

Descrizione dettagliata

Diabetes is a serious chronic disease characterized by elevated blood glucose levels resulting from abnormal pancreatic β-cell biology in relation to insulin action.

According to estimates from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD), diabetes is the eighth leading cause of death and disability worldwide, affecting nearly 460 million people of all ages and in all countries in 2019. It is currently estimated that approximately 529 million people of all ages worldwide are living with diabetes, with a global age-standardized prevalence of 6.1%.

Estimates from the International Diabetes Federation (IDF) indicate that global health expenditure on diabetes reached 910 billion euros in 2021 and is projected to exceed 1,000 billion euros by 2045.

Diabetes is also a major risk factor for ischemic heart disease and stroke, which according to GBD estimates are the first and second leading causes of disease globally. Diabetes itself is associated with increased mortality compared with non-diabetic individuals, worsens prognosis for all other diseases, increases premature mortality (Years of Life Lost, YLL), years lived with disability (Years Lived with Disability, YLD), and loss of healthy life years (Disability-Adjusted Life Years, DALY). Globally, diabetes accounted for 37.8 million YLL due to premature death and 41.4 million YLD, for a total of 79.2 million DALYs in 2021. Type 2 diabetes accounted for the vast majority of YLL, YLD, and DALYs attributable to diabetes. The global age-standardized DALY rate for diabetes was 915 per 100,000, with YLL and YLD rates of 437 and 478 per 100,000, respectively. In Italy, age-standardized DALYs in 2021 were 521.1 thousand, representing an 11.5% reduction compared with 2010, whereas increases were observed in the rest of Western Europe, in high-income countries, and globally.

Type 1 diabetes (T1D) and type 2 diabetes (T2D) are the most common forms of the disease and are diagnosed according to well-defined criteria reported in the operational manual. T1D often develops during childhood, whereas T2D has a strong genetic component and is strongly associated with obesity and a sedentary lifestyle. Cases of T2D account for approximately 96% of all diabetes cases.

Between 20% and 25% of adults with diabetes meet laboratory criteria for the diagnosis but have not been formally diagnosed (undiagnosed diabetes). Several studies have shown that individuals may spend 5-6 years in an asymptomatic phase of prediabetes and T2D prior to diagnosis, during which microvascular and macrovascular complications may already develop.

Prediabetes refers to individuals whose glucose levels do not meet diagnostic criteria for diabetes but who exhibit abnormal carbohydrate metabolism. Prediabetes is defined by impaired fasting glucose (IFG), and/or impaired glucose tolerance (IGT) following an oral glucose load, and/or HbA1c values between 5.7% and 6.4%, as reported in the operational manual.

Prediabetes should not be considered a distinct clinical entity, but rather a risk factor for progression to diabetes and cardiovascular disease (CVD). Prediabetes is associated with obesity, particularly abdominal or visceral obesity, dyslipidemia characterized by elevated triglycerides and/or low HDL cholesterol, and hypertension. The presence of prediabetes should prompt comprehensive cardiovascular risk factor screening.

Although prevention and management strategies differ across diabetes types, established approaches exist to reduce disease burden, including control of risk factors for the development and progression of T2D and improvement of healthcare system infrastructure.

T2D and prediabetes are characterized by insulin resistance (IR) in multiple cellular systems, including hepatocytes, adipocytes, and myocytes, excessive hepatic glucose production, altered lipid metabolism, and progressive impairment of insulin secretion. IR represents a central mechanism not only in diabetes but also in obesity and metabolic syndrome, and is associated with an increased risk of microvascular and macrovascular complications. While hyperglycemia, hypertension, kidney disease, and dyslipidemia are considered traditional CVD risk factors in diabetes, an association between IR and CVD has been increasingly recognized even in the absence of overt diabetes. IR is linked to alterations in lipid and lipoprotein metabolism, resulting in atherogenic dyslipidemia. Atherogenic dyslipidemia is highly prevalent in patients with T2D.

IR plays a major role in the metabolism of triglyceride-rich lipoproteins of hepatic origin, particularly very low-density lipoproteins (VLDL), including increased hepatic VLDL triglyceride synthesis. A key mechanism underlying increased VLDL triglyceride production is the accelerated lipolysis of stored triglycerides in adipose tissue, leading to increased free fatty acid flux to the liver. In insulin-resistant adipocytes, lipolysis is dysregulated, resulting in continuous release of free fatty acids into circulation. In hepatocytes, this promotes increased triglyceride synthesis, contributing both to intracellular lipid accumulation and hepatic steatosis, as well as enhanced VLDL production. Increased VLDL triglyceride synthesis is variably associated with increased hepatic production of apolipoprotein B-100. Overall, this results in hypertriglyceridemia, increased numbers of apoB-100-containing particles, and reduced HDL cholesterol concentrations. IR is also associated with increased hepatic triglyceride lipase activity, which may accelerate HDL clearance and reduce HDL cholesterol levels. In addition to increased VLDL synthesis, IR is associated with impaired VLDL clearance in skeletal muscle and adipose tissue due to reduced activity of lipoprotein lipases.

The lipid abnormalities of atherogenic dyslipidemia are not only quantitative but also qualitative and kinetic. IR is associated with changes in the average particle size of lipoproteins and likely in the lipoprotein lipidome. Lipids constitute a major and heterogeneous family of biomolecules within the metabolome. Complex lipids can be classified into multiple classes and subclasses, including triacylglycerols, diacylglycerols, phosphatidylcholines, phosphatidylethanolamines, ceramides, sphingomyelins, and cholesterol esters. Abnormal lipid profiles are associated with several diseases, including metabolic syndrome, T2D, cancer, nephropathy, and cardiovascular and neurodegenerative diseases.

A key feature of atherogenic dyslipidemia in T2D and IR is postprandial hyperlipidemia, which plays a fundamental role in the development of cardiovascular disease. Postprandial serum triglyceride levels vary considerably depending on meal composition and time elapsed after food intake. Due to this variability, assessment of postprandial hyperlipidemia requires an oral fat loading test (OFLT). Elevated postprandial triglyceride levels reflect increased concentrations of triglyceride-rich lipoproteins, including chylomicrons, VLDL, and their remnants. Intestinally synthesized chylomicrons transport dietary triglycerides to peripheral tissues in the postprandial state. Reduced lipoprotein lipase activity associated with IR impairs triglyceride hydrolysis from chylomicrons, leading to altered postprandial chylomicron responses. Measurement of apolipoprotein B48, non-fasting triglycerides, non-HDL cholesterol, and remnant cholesterol is essential for identifying postprandial hyperlipidemia.

Multiple factors contribute to chylomicron production during the postprandial phase. Substantial evidence supports the physiological role of glucagon-like peptides, microsomal triglyceride transfer protein, and the central role of apolipoprotein B48 in chylomicron synthesis and postprandial kinetics.

Just as postprandial triglycerides are an independent predictor of coronary artery disease, remnant lipoproteins possess multiple atherogenic properties and are associated with increased all-cause mortality in patients with ischemic heart disease and with the development of coronary artery disease, even after adjustment for major risk factors.

Diagnosis of postprandial hyperlipidemia requires an OFLT; however, there is no consensus on the optimal timing of postprandial measurements or on meal standardization. The test is time-consuming and requires prolonged rest. Despite these limitations, the OFLT remains the only available test for assessing postprandial hyperlipidemia.

Dyslipidemia and chronic inflammation are considered the main drivers of atherosclerotic plaque formation in diabetes. Atherosclerosis is accompanied by local inflammation within the vascular wall due to endothelial dysfunction and vascular smooth muscle cell involvement. Components of the diabetic milieu, oxidative stress, and other factors are believed to damage vascular endothelial cells, leading to increased expression of adhesion molecules and secretion of chemokines, promoting monocyte adhesion. Adherent monocytes migrate into the subendothelial space and differentiate into macrophages, which release cytokines such as interleukin-1β, interleukin-18, tumor necrosis factor-α, and interferon-γ, amplifying the inflammatory process. Compared with chylomicrons and VLDL, remnant lipoproteins can penetrate the arterial wall and do not require oxidation for macrophage uptake. Remnants enhance monocyte rolling, adhesion, and transmigration on endothelial cells and are involved in inflammation, platelet activation, and endothelial dysfunction through activation of transcription factors such as NF-κB. Adipocyte dysfunction associated with obesity is an integral component of T2D pathogenesis and, together with atherogenic dyslipidemia, promotes chronic systemic inflammation that contributes to insulin resistance, β-cell dysfunction, and ultimately T2D. This chronic inflammatory state contributes to long-term diabetic complications.

Despite substantial evidence supporting a strong relationship among insulin resistance, inflammation, and dyslipidemia, the determinants of progression from isolated insulin resistance to prediabetes, overt T2D, and T2D with complications remain unclear. Moreover, investigation of the postprandial phase, which occupies a large portion of the day, may provide critical insights into whether postprandial metabolism differentiates prediabetes from clinically overt diabetes, thereby elucidating pathophysiological mechanisms and informing dietary and pharmacological strategies to reduce disease progression.

The aim of the study is to evaluate whether the Oral Fat Loading Test (OFLT) determines a different response in terms of the quantity, quality, and kinetics of triglyceride-rich lipoproteins in subjects with T2D, prediabetics, and control subjects, and whether triglyceride-rich lipoproteins and inflammatory cytokines after OFLT are potential early biomarkers of the risk of progression to diabetes and the development of complications in a general practice setting.

To address these questions, a hybrid cohort study was designed by identifying three groups of subjects: T2D and prediabetics (exposed and near-exposed) and control subjects (unexposed). The subjects were recruited from the patient datasets of the Poggio Renatico Primary Care Unit - Poggio Rete Salute Group Medicine, Ferrara Local Health Authority, with the support of a propensity score matching analysis. In an initial cross-sectional phase, the differential response to OFLT will be studied in the three groups (TRL, TRL remnants, lipidoma, inflammatory cytokines, etc.). The second prospective phase will observe up to 36 months whether the response to OFLT of triglyceride-rich lipoproteins and inflammatory cytokines are potential early biomarkers of the risk of progression to diabetes and the development of complications.

Main Objectives:

Primary (Cross-sectional phase) To evaluate the odds ratio (OR) that TG after OFLT is higher in T2D, in good glycemic control (A1c <7%) and treated with "standard of care" and in prediabetics compared to controls.

(Prospective phase) To evaluate whether TG after OFLT are early biomarkers of risk of progression to diabetes (ADA criteria) in prediabetic subjects treated with "standard of care" in a 36-month follow-up.

Secondary (Cross-sectional phase) To evaluate the odds ratio (OR) that TRLs after OFLT are higher in T2D, in good glycemic control (A1c <7%) and treated with "standard of care" and in prediabetics compared to controls.

To evaluate the odds ratio (OR) that remnant CM after OFLT are higher in T2D, in good glycemic control (A1c <7%) and treated with "standard of care" and in prediabetics compared to controls.

To evaluate whether the levels of interleukin-1β (IL-1β), interleukin-18 (IL-18), tumor necrosis factor-α (TNF-α), measured after 6 hours from OFLT, change from baseline.

To evaluate the odds ratio (OR) that cytokine levels after OFLT are higher in T2D, in good glycemic control (A1c <7%) and treated with "standard of care" and in prediabetics compared to controls.

(Prospective phase) To evaluate whether TG after OFLT are early biomarkers of risk of progression to nephropathy defined as a doubling of the urine albumin-creatinine ratio (uACR) >2 times compared to baseline and/or progression to a higher stage of renal disease; estimated glomerular filtration rate, eGFR <60 ml/min and uACR ≥30 mg/mmol for 3 months or more in diabetic subjects, in good glycemic control (A1c <7%), treated with "standard of care" over a 36-month follow-up.

To evaluate whether TG after OFLT are early biomarkers of risk of developing major cardiovascular events (Major Adverse Cardiac Events, five-point MACE: nonfatal stroke, nonfatal myocardial infarction, cardiovascular death, admission for unstable angina or heart failure) in diabetic subjects treated with "standard of care" in a 36-month follow-up.

To evaluate whether TRL after OFLT are early biomarkers of risk of progression to diabetes (ADA criteria[5]) in prediabetic subjects treated with "standard of care" in a 36-month follow up.

To evaluate whether TRL after OFLT are early biomarkers of risk of progression to nephropathy defined as uACR, >2 times compared to baseline and/or progression to a higher stage of renal disease (eGFR <60 ml/min and uACR ≥30 mg/mmol for 3 months or more) in diabetic subjects, in good glycemic control (A1c <7%), treated with "standard of care" in a 36-month follow-up.

To evaluate whether TRL after OFLT are early biomarkers of risk of developing major cardiovascular events (Major Adverse Cardiac Events, five-point MACE: nonfatal stroke, nonfatal myocardial infarction, cardiovascular death, admission for unstable angina or heart failure) in diabetic subjects, with good glycemic control (A1c <7%), treated with "standard of care" in a 36-month follow-up.

To evaluate whether remnant CM after OFLT are early biomarkers of risk of progression to diabetes (ADA criteria) in prediabetic subjects treated with "standard of care" in a 36-month follow-up.

To evaluate whether remnant CM after OFLT are early biomarkers of risk of progression to nephropathy defined as uACR, >2 times compared to baseline and/or progression to a higher stage of renal disease (eGFR <60 ml/min and uACR ≥30 mg/mmol for 3 months or more) in diabetic subjects, in good glycemic control (A1c <7%), treated with "standard of care" in a 36-month follow-up.

To evaluate whether remnant CM after OFLT are early biomarkers of risk of developing major cardiovascular events (Major Adverse Cardiac Events, five-point MACE: nonfatal stroke, nonfatal myocardial infarction, cardiovascular death, admission for unstable angina or heart failure) in diabetic subjects, with good glycemic control (A1c <7%), treated with "standard of care" in a 36-month follow-up.

To evaluate whether changes in cytokine levels predict the risk of progression to diabetes (ADA criteria) in diabetic subjects with good glycemic control (A1c <7%), treated with "standard of care" over a 36-month follow-up.

To evaluate whether changes in cytokine levels predict the risk of progression to uACR-defined nephropathy, >2 times compared to baseline, and/or progression to a higher stage of renal disease (eGFR <60 ml/min and uACR ≥30 mg/mmol for 3 months or more) in diabetic subjects with good glycemic control (A1c <7%), treated with "standard of care" over a 36-month follow-up.

To evaluate whether variations in cytokine levels predict the risk of developing major cardiovascular events (Major Adverse Cardiac Events, five-point MACE: nonfatal stroke, nonfatal myocardial infarction, cardiovascular death, admission for unstable angina or heart failure) in diabetic subjects with good glycemic control (A1c <7%), treated with "standard of care" in a 36-month follow-up.

Others (Cross sectional Phase) To evaluate whether circulating ceramide content is different in T2D, prediabetic, and control subjects.

To evaluate whether circulating ceramide content, measured 6 hours after OFLT, changes compared to baseline.

(Prospective Phase) To evaluate whether baseline circulating ceramide content predicts the risk of progression to diabetes (ADA criteria) in diabetic subjects with good glycemic control (A1c <7%), treated with "standard of care" over a 36-month follow-up.

To evaluate whether baseline circulating ceramide content predicts the risk of progression to nephropathy defined as uACR >2 times baseline and/or progression to a higher stage of renal disease (eGFR <60 ml/min and uACR ≥30 mg/mmol for 3 months or more) in diabetic subjects with good glycemic control (A1c <7%), treated with "standard of care" over a 36-month follow-up.

To evaluate whether baseline circulating ceramide content predicts the risk of developing major cardiovascular events (Major Adverse Cardiac Events, five-point MACE: nonfatal stroke, nonfatal myocardial infarction, cardiovascular death, admission for unstable angina or heart failure) in diabetic subjects with good glycemic control (A1c <7%), treated with "standard of care" over a 36-month follow-up.

Statistical analysis Variables will be expressed as mean ± standard deviation (SD) or median and 95% confidence intervals (95% CI), while categorical variables will be expressed as frequencies. The Shapiro-Wilk test will be used to assess the normality of continuous variables. Variables with symmetric distribution will be presented as mean ± standard deviation (SD), whereas non-normally distributed variables will be expressed as median and interquartile range [Q1-Q3]. Categorical data will be expressed as counts and percentages (%). Non-normally distributed variables will be log-transformed before parametric statistical analyses.

Percentages will be compared using the chi-square test, Fisher's exact test, or Yates' correction, as appropriate. Continuous variables will be compared using Student's t-test or Mann-Whitney/Kruskal-Wallis tests, as appropriate. Box plots will be used to compare continuous variables among groups.

Chi-square tests for risk estimates and one-vs-one analyses between the main endpoints will also be performed, with calculation of relative Odds Ratios (OR) and 95% confidence intervals (95% CI). ORs and 95% CIs will be estimated using unadjusted logistic regression models considering diabetes conversion and development of complications as dependent variables, and age, sex, 5-point MACE events, and other potential confounding variables as independent variables.

Overall survival curves will be generated using the Kaplan-Meier method and compared among subgroups using the log-rank test. A p-value <0.05 will be considered statistically significant.

Correlations between continuous variables will be assessed using Pearson correlation tests for normally distributed variables, whereas non-normally distributed variables will be analyzed after log-transformation or using non-parametric tests (Spearman correlation test). Results will be reported as correlation coefficient (r) and p-value.

For all variables of interest, absolute (Δ) and percentage (Δ%) changes between baseline, Time+6 months, Time+12 months, Time+24 months, and Time+36 months will be calculated. Changes over time will be analyzed using repeated-measures t-tests or general linear models (GLM) for repeated measures, including within-subject and between-subject analyses.

Statistical analyses will be performed using SPSS software version 29.0 (SPSS Inc., Chicago, IL, USA). When relevant, effect size measures will also be reported.

Study Team PI per AOUFe e UniFe - Prof. Angelina Passaro, MD, PhD PI per AUSLFe - Dott. Luca Catapano, MD CoPI per UniFe - Dott. Juana Maria Sanz Molina, MSc, PhD e CoPI per UniFe -- Prof. Domenico Sergi, MSc, PhD CoPI per AOUFe - Dott. Edoardo Dalla Nora, MD, PhD CoPI per AUSLFe - Dott.ssa Eleonora Petrucci, MD Researcher And Primary Study Coordinator - Fabiola Castaldo, MSc Researcher - Simona Colombari, MSc Researcher - Sharon Angelini, MSc

Tipo di studio

Osservativo

Iscrizione (Stimato)

150

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Ferrara
      • Ferrara, Ferrara, Italia, 44124
        • Reclutamento
        • University Hospital "Sant'Anna" of Ferrara
        • Contatto:
        • Sub-investigatore:
          • Juana Maria Sanz Molina, Chemistry Degree
        • Sub-investigatore:
          • Domenico Sergi, Nutritional science
        • Investigatore principale:
          • Angelina Passaro, Degree in Medicine and Surgery
        • Sub-investigatore:
          • Edoardo Dalla Nora, Degree in Medicine and Surgery
        • Sub-investigatore:
          • Simona Colombari, Degree in Dietetics
      • Poggio Renatico, Ferrara, Italia, 44023
        • Reclutamento
        • Nucleo di Cure Primarie di Poggio Renatico - Medicina di Gruppo Poggio Rete Salute Via Salvo D'Acquisto, 1/a
        • Contatto:
          • Luca Catapano, Medicine and Surgery
          • Numero di telefono: +39 3384838817
          • Email: l.catapano@gmail.com
        • Contatto:
          • Eleonora Petrucci, Medicine and Surgery
          • Numero di telefono: +39 3461812406
        • Investigatore principale:
          • Luca Catapano, Degree in Medicine and Surgery
        • Sub-investigatore:
          • Eleonora Petrucci, Degree in Medicine and Surgery

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Metodo di campionamento

Campione di probabilità

Popolazione di studio

All individuals attending the Poggio Renatico Primary Care Unit - Poggio Rete Salute Group Medicine, Ferrara Local Health Authority who have undergone at least two diagnostic tests for diabetes in the last 12 months will be contacted.

Descrizione

Inclusion Criteria:

  • Males and females aged 50-70 years
  • BMI between 25-30 kg/m2
  • HbA1c ≤7% for T2D
  • HbA1c ≤6.5% for prediabetes
  • HbA1c ≤5.7% for controls
  • Signed Project Information and Informed Consent Form
  • Signed Data Processing Consent Form

Exclusion Criteria:

  • Lipid-lowering therapy with ezetimibe, fenofibrate, omega-3 fatty acids, or other drugs that can interfere with lipoprotein absorption and metabolism
  • Chronic Kidney Disease (CKD) with estimated glomerular filtration rate (eGFR) <60 ml/min and renal impairment (e.g., uACR ≥30 mg/mmol) for 3 months or more
  • Secondary or syndromic forms of obesity
  • Patients on insulin therapy
  • All acute and chronic conditions that, in the opinion of the investigators, may cause bias.
  • Hospitalization for acute illness or major surgery in the last 6 months
  • Patients on stable therapy for less than 3 months
  • Allergy or intolerance to one or more components of the meal used in the protocol
  • Pregnancy or breastfeeding
  • Habitual consumption of alcoholic beverages (>20 g/day for females and >30 g/day for males) or unwillingness to abstain from alcoholic beverages during the study run-in period
  • All subjects who do not consent to participate in the study

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
Controlli

After a 12-hour overnight fast, each participant will be given a sugar-free mascarpone cream containing 75 g of fat.

Blood samples will be collected before (OFL Time -1 minute) and 1 (OFL Time +1 hour), 2 (OFL Time +2 hours), 3 (OFL Time +3 hours), 4 (OFL Time +4 hours), and 6 (OFL Time +6 hours) hours after the OFL.

Diabetici

After a 12-hour overnight fast, each participant will be given a sugar-free mascarpone cream containing 75 g of fat.

Blood samples will be collected before (OFL Time -1 minute) and 1 (OFL Time +1 hour), 2 (OFL Time +2 hours), 3 (OFL Time +3 hours), 4 (OFL Time +4 hours), and 6 (OFL Time +6 hours) hours after the OFL.

Prediabetics

After a 12-hour overnight fast, each participant will be given a sugar-free mascarpone cream containing 75 g of fat.

Blood samples will be collected before (OFL Time -1 minute) and 1 (OFL Time +1 hour), 2 (OFL Time +2 hours), 3 (OFL Time +3 hours), 4 (OFL Time +4 hours), and 6 (OFL Time +6 hours) hours after the OFL.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Triglyceride concentrations after oral fat loading test
Lasso di tempo: From enrollment after two years at the end of the enrollment
Serum triglyceride concentrations measured before and 6 hours after oral fat loading test in participants with type 2 diabetes, prediabetes, and controls.
From enrollment after two years at the end of the enrollment
Progression from prediabetes to type 2 diabetes
Lasso di tempo: At 36-month follow-up
Development of type 2 diabetes according to American Diabetes Association (ADA) diagnostic criteria during follow-up in participants with prediabetes.
At 36-month follow-up

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Triglyceride-rich lipoprotein concentrations after oral fat loading test
Lasso di tempo: From enrollment after two years at the end of the enrollment
Serum triglyceride-rich lipoprotein (TRL) concentrations measured before and 6 hours after oral fat loading test in participants with type 2 diabetes, prediabetes, and controls.
From enrollment after two years at the end of the enrollment
Chylomicron remnant concentrations after oral fat loading test
Lasso di tempo: From enrollment after two years at the end of the enrollment
Chylomicron remnant concentrations measured before and 6 hours after oral fat loading test.
From enrollment after two years at the end of the enrollment
Interleukin-1β concentration after oral fat loading test
Lasso di tempo: From enrollment after two years at the end of the enrollment
Plasma interleukin-1β (IL-1β) concentrations measured before and 6 hours after oral fat loading test.
From enrollment after two years at the end of the enrollment
Interleukin-18 (IL-18) concentration after oral fat loading test
Lasso di tempo: From enrollment after two years at the end of the enrollment
Plasma interleukin-1β interleukin-18 (IL-18) concentrations measured before and 6 hours after oral fat loading test.
From enrollment after two years at the end of the enrollment
Tumor necrosis factor-α (TNF-α) concentration after oral fat loading test
Lasso di tempo: From enrollment after two years at the end of the enrollment
Tumor necrosis factor-α (TNF-α) concentrations measured before and 6 hours after oral fat loading test.
From enrollment after two years at the end of the enrollment
Progression of diabetic nephropathy during follow-up
Lasso di tempo: 36-month follow-up
Progression of diabetic nephropathy defined as doubling of urine albumin-creatinine ratio compared to baseline, progression to a higher stage of renal disease, estimated glomerular filtration rate below 60 mL/min, and/or urine albumin-creatinine ratio ≥30 mg/mmol for at least 3 months.
36-month follow-up
Major adverse cardiovascular events (5-point MACE)
Lasso di tempo: 36-month follow-up
Occurrence of major adverse cardiovascular events defined as nonfatal stroke, nonfatal myocardial infarction, cardiovascular death, hospitalization for unstable angina, or hospitalization for heart failure during follow-up.
36-month follow-up

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Circulating ceramide content
Lasso di tempo: From enrollment after two years at the end of the enrollment
Plasma circulating ceramide concentrations measured in participants with type 2 diabetes, prediabetes, and controls.
From enrollment after two years at the end of the enrollment
Change in circulating ceramide concentrations after oral fat loading test
Lasso di tempo: From enrollment after two years at the end of the enrollment
Plasma circulating ceramide concentrations measured before and 6 hours after oral fat loading test.
From enrollment after two years at the end of the enrollment
Proteomic analyses
Lasso di tempo: From enrollment after two years at the end of the enrollment
To perform untargeted proteomic analyses on serum samples collected at baseline, T0 and postprandial peak, from subjects with diabetes, pre-diabetes, and controls, in order to identify differential protein patterns associated with the postprandial response. The aim is to identify early proteomic biomarkers of altered lipid metabolism and subclinical inflammatory signaling. Proteomic data will be integrated with bioinformatic pathway enrichment analyses to characterize the key biological processes involved, with particular focus on inflammation, oxidative stress, and lipoprotein metabolism.
From enrollment after two years at the end of the enrollment
Metabolomic analyses
Lasso di tempo: From enrollment after two years at the end of the enrollment
To conduct targeted and untargeted metabolomic analyses on the same serum samples previously analyzed by proteomics, collected at baseline (T0) and postprandial peak. Metabolic profiles will be compared among subjects with type 2 diabetes (T2D), pre-diabetes, and healthy controls. Metabolomic data will be integrated with proteomic datasets using a multi-omics approach to identify early metabolic signatures of postprandial dysfunction, predictors of altered lipid response, and metabolites with potential relevance as therapeutic or diagnostic targets.
From enrollment after two years at the end of the enrollment
In vitro model using VLDL
Lasso di tempo: From enrollment after two years at the end of the enrollment
To develop in vitro cellular models to investigate the pathophysiological mechanisms underlying postprandial metabolic dysfunction. Human endothelial cells (HUVEC) and human monocytic cells (U937) will be established and exposed to postprandial VLDL isolated from patient serum samples. Cells will be incubated for 4 hours with VLDL isolated from patient serum. Following incubation, total RNA will be extracted and real-time PCR analyses will be performed to assess the gene expression of selected target genes, including IL-6, IL-1β, VCAM-1, E-selectin (ELAM-1), ICAM-1, and P-SEL. The impact of postprandial VLDL will be evaluated in terms of endothelial activation, expression of adhesion molecules, monocytic inflammatory responses, and induction of oxidative stress-related signals. Cellular responses will be correlated with proteomic and metabolomic profiles, as well as with clinical parameters of the subjects, in order to identify causal mechanisms and targetable biological pathways.
From enrollment after two years at the end of the enrollment
Extracellullar vescicles content
Lasso di tempo: From enrollment after two years at the end of the enrollment
To evaluate whether the composition of extracellular vesicles differs among subjects with type 2 diabetes, prediabetes, and healthy controls.
From enrollment after two years at the end of the enrollment
Extracellular vescicles after OFL
Lasso di tempo: From enrollment after two years at the end of the enrollment
To assess whether circulating extracellular vesicle levels measured 6 hours after the Oral Fat Loading Test (OFLT) differ from baseline values.
From enrollment after two years at the end of the enrollment
Fast Protein Liquid Chromatography analysis
Lasso di tempo: From enrollment after two years at the end of the enrollment
Separation and characterization of the different protein and lipoprotein fractions in serum samples from enrolled subjects at baseline (T0) and at the triglyceride peak time point after OFL
From enrollment after two years at the end of the enrollment
RNA-seq analysis
Lasso di tempo: From enrollment after two years at the end of the enrollment
Total RNA will be extracted from buffy coat samples obtained from peripheral blood at T0 and at peak triglicerydes time and used for transcriptomic analyses
From enrollment after two years at the end of the enrollment
RNA-Seq on Huvec and VLDL
Lasso di tempo: From enrollment after two years at the end of the enrollment
Total RNA will be extracted from Huvec cells trated with VLDL extracted from serum at T0 and at peak truglicerydes time and used for transcriptomic analyses.
From enrollment after two years at the end of the enrollment

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Cattedra di studio: Angelina Passaro, Degree in Medicine and Surgery, University Hospital of Ferrara "Sant'Anna"
  • Investigatore principale: Luca Catapano, Degree in Medicine and Surgery, Azienda USL Ferrara
  • Investigatore principale: Angelina Passaro, Degree in Medicine and Surgery, University Hospital of Ferrara "Sant'Anna"
  • Direttore dello studio: Angelina Passaro, Degree in Medicine and Surgery, University Hospital of Ferrara "Sant'Anna"

Pubblicazioni e link utili

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Pubblicazioni generali

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

14 maggio 2024

Completamento primario (Stimato)

14 maggio 2026

Completamento dello studio (Stimato)

14 maggio 2028

Date di iscrizione allo studio

Primo inviato

2 gennaio 2026

Primo inviato che soddisfa i criteri di controllo qualità

14 maggio 2026

Primo Inserito (Effettivo)

22 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

22 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 maggio 2026

Ultimo verificato

1 ottobre 2025

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

Sensitive participant data will not be shared. However, the management and sharing of non-identifiable data will fully comply with the FAIR principles (Findable, Accessible, Interoperable, Reusable), ensuring traceability, interoperability, and reusability of the data for scientific research purposes, in accordance with applicable data protection regulations

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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