Diabetes and Lipid Accumulationand Heart Transplant

BACKGROUND Heart failure (HF) is an increasing disease, with a prevalence and incidence of about 1% and 0.15% of the general population respectively, affecting at least 300,000 patients in the USA. However, in cases of advanced heart failure, refractory to maximal medical therapy, and to devices supporting the heart rhythm and cardio-circulatory function, the only valid therapeutic option remains the cardiac transplant. Diabetic patients with advanced heart failure seem to benefit from this therapy not differently as compared to non-diabetics. On other hand, in patients with advanced heart failure and selected for heart transplantation, the diabetes may condition a different degree of structural and molecular pathology that is not present, or present at least in a different way in non-diabetics selected for same HF etiology, clinical features, and HF stage. Therefore, in this study authors will study the anatomical-pathological, cellular, and molecular characteristics, as the pathways of inflammatory, oxidative, apoptotic and epigenetic expression in diabetics vs. non diabetics affected by idiopathic dilated cardiomyopathy (IDCM) and therefore in the absence of ischemic heart disease, and referred to Heart Center for cardiac transplantation. Authors' study hypothesis is that diabetes can condition a different degree of structural, cellular, and molecular pathology in patients with IDCM Vs. non-diabetic patients, due to excessive metabolic activity, with increased synthesis and release of inflammatory, oxidative, and apoptotic molecules. These investigations will be focused on microscopic, histological and functional analysis of the cellular metabolism of cardiac tissue extracted from diabetics vs. non diabetics IDCM patients, and removed during cardiac transplantation. However, in a subsequent ex vivo phase authors will evaluate cellular, molecular, inflammatory and epigenetic effectors related to the different microscopic tissue pattern obtained from myocardial tissue samples. From authors' investigations, these new identified targets of the HF molecular and cellular processes in diabetics vs. non diabetics, may be used in the future as specific therapeutic targets to improve clinical outcomes in IDCM diabetics with advanced heart failure.

MATERIALS AND METHODS Study population Authors will enroll a population of IDCM diabetics and non diabetics selected to receive a heart transplant. This study will be conducted at the Department of Medical Sciences, at the Department of Cardiac Surgery, and at the Department of Biochemistry of the University of Campania "Luigi Vanvitelli". Selection, randomization and enrollment of patients will be carried out at the Department of Medical Sciences, followed by clinical follow up; Cardiac transplantation and cardiac tissue sampling will be performed at the Cardiosurgery Department; Molecular and cellular studies will be conducted at the biochemistry department. The follow-up will be 12 months. The diabetic pathology will be diagnosed according to the international guidelines of the American Heart Association.

Inclusion criteria: patients aged > 18, <75 years, with indication to receive a heart transplant (survival score for accepted heart failure accepted (HFSS) at high risk, peak VO2 <10 ml / kg / min after reaching the anaerobic threshold; arrhythmias recurrent symptomatic ventricles refractory to medical treatment, ICD and surgical), affected by IDCM with heart failure in NYHA class III / IV refractory to maximal medical therapy; diabetic and non-diabetic patients Exclusion criteria: contraindication to receiving cardiac transplantation; non-idiopathic dilated cardiopathy (valvulopathies, ischemic-infarct cardiopathy, etc.), acute myocardial infarction, acute heart failure, neoplastic disease, and chronic diseases that may influence the inflammatory profile both systemic and cardiac (cancer, chronic intestinal inflammation, hepatitis, AIDS) , and a life expectancy <6 months. All patients will be included in the study after signing informed consent to participate in the study. Routine analysis will be performed upon enrollment in the study, before cardiac transplantation and follow-up. During the follow-up (figure 1) clinical examinations, routine ecg and echocardiography will be performed regularly. Molecular study and cell study will be performed on myocardial tissue from explanted hearts. The study will be performed according to the Helsinki declaration.

Intervention In this observational study, authors will evaluate a cohort of consecutive patients (diabetic vs. non-diabetic) affected by IDCM and heart failure in class III / IV NYHA refractory to maximal medical therapy and treated at the Division of Cardiac Surgery of the University of Campania "Luigi Vanvitelli "by cardiac transplantation. The study will be conducted in three different parts: human study, ex vivo cell study, molecular study.

Human study: conducted in the Department of Medical Sciences and Cardiac Surgery, the enrolled patient will be treated by heart transplant, according to the international guidelines governing cardiac transplantation. After cardiac transplantation, a biopsy of myocardial tissue of the removed heart will be performed. The intervention will be conducted at the Cardiosurgery Division of the "Luigi Vanvitelli" University of Campania.

Cardiac tissue analysis A portion of muscle tissue (50 grams) will be removed from the explanted heart, from which 3 portions will be obtained: a portion will be incorporated in the OCT compound and frozen in liquid nitrogen for immunohistochemical analysis, a second portion will be immediately frozen in nitrogen liquid and stored at -70 ° C for the isolation of RNA, and a third portion will be weighed, cut into small pieces (2 mm3) and transferred to a 12-well plate. Based on the weight of the tissue, serum-free DMEM (2 ml / g) will be added to the well and incubated at 37 ° C in a mild-fluctuated CO2 incubator. At 3 hours, the conditioned soils will be collected and centrifuged at 4 ° C for 10 minutes. The supernatants from cultures of epiphonic and subcutaneous adipose tissue will be stored in aliquots at -70 ° C for the measurement of inflammation mediators released by ELISA.

Blood samples

Blood collection will be carried out on the morning of surgery and during the follow-up phases by peripheral venous blood taken in tubes without pyrogen with or without EDTA as anticoagulant. For plasma, the EDTA tubes will be placed on melted ice, then centrifuged within 20 minutes at 1500 g for 10 minutes at 4 ° C. The plasma will be stored in aliquots at 80 ° C for all ELISA tests. Serum glucose, lipid panels and inflammatory markers will be analyzed in the University of Campania's Biochemistry Laboratory.

Inflammatory markers

The authors will analyze the mediators of plasma and cardiac inflammation with ELISA (R \& D systems) according to the procedure recommended by the manufacturer. ELISA standard kit they will be used for IL-6 measurements, and highly sensitive ELISA kits for TNF-alpha and IL-1 measurements. Intra-assay variability will be set at 10%, while inter-assay variability will be 15%.

RNA analysis and Real-Time Reverse Transcription

Samples of myocardial tissue will be minced in a TriZol reagent (Invitrogen) and homogenized completely on ice. The total RNA will be extracted from the chloroform and purified twice through the mini RNAasy columns. After the DNase treatment on a column, the RNA will be eluted with RNase-free water. Transcripts encoding various inflammatory mediators will be measured by the TaqMan real-time reverse-polymerase-RT (PCR) chain reaction with the TaqMan Gold RT-PCR and the PRISM 7700 Sequence Detection System (Applied Biosystems). PCR primers and TaqMan probes will be obtained from Applied Biosystems and optimized according to the manufacturer's protocol. The PCR reaction conditions will be at 48 ° C for 30 minutes, at 95 ° C for 10 minutes, followed by 40 cycles of 95 ° C for 15 seconds and 60 ° C for 1 minute. The GAPDH transcripts will be amplified in a separate tube to normalize the variance in the input RNA. The mRNA in various samples will be estimated by the relative standard method with a series of dilutions of RNA from human vascular cells or from leukocytes.

Immunohistochemistry The authors will obtain frozen sections (10 m), which will be air-dried for 15 minutes and immersed in xylene for 10 minutes to remove the fat. The sections will then be hydrated in decreasing degrees of alcohol and stained with hematoxylin and eosin. The selected serial sections will be immunosimochemical with the Universal Elite ABC (Vector Laboratories) kit according to the manufacturer's protocol. Briefly, the sections will be incubated with 0.3% H2O2 in methanol for 30 minutes, followed by a block with horse serum or 5% goat. After washing in PBS, the sections will be incubated with primary antibodies for 1 hour in a wet chamber. Subsequently, the slides will be incubated with secondary antibodies for 30 minutes followed by avidin-biotin for 30 minutes. The sections will then be exposed to DAB and counterstained with hematoxylin. The following antibodies will be used: CD3 (Tlymphocyte, 1:50, Novocastra), CD68 (monocytes / macrophages, 1: 100, Dako) and triptases (mast cells, 1:50, Novocastra).

Follow-up After being discharged from the hospital, all patients will be required to carry out control visits, as indicated by the authors on the management of patients post-transplant cardiac, at the Division of Cardiac Surgery of the University of Campania "Luigi Vanvitelli "and the sixth division of Internal Medicine of the University of Campania" Luigi Vanvitelli ". All patients will be monitored for 12 months after follow-up, by clinical evaluation (ECG, stress test, echocardiogram) to maintain HbA1c levels <7%, fasting glycemia between 90 and 140 mg / dl and post-prandial glycemia <180 mg / dl, as indicated in the guidelines for the management of diabetic and post-CABG patients. In the 12 months of follow-up, patient management will be conducted by telephone interview, physical examination (at discharge and 3, 6 and 12 after cardiac transplantation), ecg and echocardiography (at discharge and 3, 6 and 12 after cardiac transplantation); CMRI will be conducted at baseline and 12 months after CABG. Similarly, the bio-humoral evaluation will be conducted during all the follow-up phases.

Statistical Analysis The study population groups (diabetics vs. non-diabetics) will be compared using the Pearson test for categorical variables and the Kruskal-Wallis test for continuous variables. Candidates for admission to the multivariate model will be identified by focusing on factors that will differ significantly (P value <0.05) in the univariate analysis between diabetics vs. non-diabetics. Cox regression will be used to construct the predictive model of mortality. The risk ratio for mortality will be adjusted for age, BMI, cholesterol, LDL, triglycerides and aspirin, ticlopidine, anti-aggregating agents, beta-blockers, ACE inhibitors or sartans, antidiabetic drugs, statins, etc. present at the time of hospitalization for cardiac transplantation. Analysis of survival after cardiac transplantation will be performed using the Kaplan-Meier curve and Cox regression method. Mortality curves will be obtained separately for diabetic patients compared to non-diabetic patients, and then compared using the log-rank test. All tests will be considered significant if with a value of p <0.05. All analyzes will be conducted in 2 populations: diabetic vs non-diabetic patients after cardiac transplantation. For all analyzes the SPSS program will be used (version 21, IBM SPSS).