Evolution of Nutritional Status and Intestinal Function in Patients With MNGIE

This is a drug-free observational study, both retrospective and prospective, single-center carried out on adult patients with MNGIE, followed at the Regional Reference Center for Benign Chronic Intestinal Insufficiency-Pironi of the IRCCS-AOUBo based on data collected during clinical follow-up at the same centre. The data will be collected in a structured manner using the information present in the medical records obtained in the past as part of normal clinical practice for patients already in the care of the Center at the time of inclusion in the study and that obtained at the time of taking charge of the Center and during clinical follow-up, for new patients.

The study is an observational study without drug and does not involve any study-specific treatment or visit, but exclusively the structured collection of information obtained in the past as part of normal practice (clinical records and related documents) for the retrospective phase and the registration of clinical data collected during the normal care process (follow-up), for the prospective phase. The study does not include any study-specific visits The data will be collected at quarterly intervals starting from the moment the Center takes charge of the patients (time T0).

The following data relating to the history of the disease will also be collected: age at onset of symptoms, age at diagnosis, symptoms and signs at onset, symptoms and signs at diagnosis, symptoms and signs during clinical follow-up. The study population consists of patients with MNGIE followed at the SSD-Clinical Nutrition and Metabolism - Regional Reference Center for Benign Chronic Intestinal Insufficiency-Pironi of the AOU-Policlinico di Sant'Orsola.

MNGIE is a rare syndrome for which a prevalence of 1-9 cases per million inhabitants is described. In Italy there are about ten confirmed cases. To date, the Center has followed 8 patients with MNGIE, of which 6 are currently still in the care of the center and two have died.

It will also be necessary to use the data of patients who did not give consent because they had died or were no longer associated with our center, since failure to involve this population would reduce the eligible sample, producing negative consequences for the study in terms of the significance of the results. Therefore, in the case of deceased or untraceable patients following every reasonable effort made to contact them (via postal address, contact with the general practitioner or via telephone call but only in cases in which the patient had previously expressed consent to telephone contact ), on the basis of General Authorization no. 9 to the processing of personal data carried out for scientific research purposes, issued by the Guarantor on 11/12/2014, the processing of personal data will be carried out in the absence of consent.

For each patient meeting the inclusion criteria, the following parameters will be recorded in a structured way at time T0 (time of taking charge of the patient by the Centre) and at subsequent quarterly intervals:

• Personal data: Age, gender
• Vital parameters: Blood pressure (BP) and heart rate (HR)
• Laboratory tests. Hemoglobin (Hb) and MCV, serum iron (Fe), ferritin, albumin, prealbumin, glycemia, triglycerides, total cholesterol, HDL cholesterol, uric acid, lactic acid, serum bicarbonates, lipase, electrolytes and serum mineral salts (Nas, Ks, Cls, Cas, Ps, Mgs), trace elements (Cu, Zn, Sel), ceruloplasmin, parathyroid hormone (PTH), osteocalcin, cross laps; Urine: chemical-physical examination, electrolytes and urinary mineral salts ([Nau, Ku, Clu, Cau, Pu, Mgu]), thymidine and deoxyuridine dosage;
• Nutrition status. Weight history: healthy weight, weight at diagnosis, current weight), height, body mass index (BMI kg/h (m)2); body composition: with impedance measurement [body cell mass (BCM), fat mass (FM), total water (TBW), extracellular water (ECW), phase angle] and with total body bone densitometry (DEXA) [lean mass (FFM), fat mass (FM)]; bone mineral density (MBD): L1-L4 and femoral neck: MBD (g/cm3), T-score, Z-score; vitamins: folate, vitamin B12, vitamin 25D, vitamin A, vitamin E, vitE/(TGL+Col) ratio; hand grip strength (kg)
• Energy balance: food intake (diary/survey), evaluation of appetite (absent, low, preserved, increased), type of diet (water, liquid, creamy, free of waste and lactose, low-lipid, free); Basal energy expenditure (BEE) calculated according to the Harris-Benedict equation and measured with indirect calorimetry; Total energy expenditure (TEE): calculated (BEEx Physical Activity Level [LAF]) and measured with Sensewear-Armband slide.
• Intestinal absorption: lipid absorption (Wandekamer micromethod), energy absorption (energy absorption % = 100-lipid excretion+10).
• Intestinal protein dispersion: clearance of fecal alpha-1 antitrypsin
• Intestinal motility: bowel characteristics, clinical evaluation and instrumental evaluation through direct abdominal x-ray, gastrointestinal manometry; investigation for the presence of intestinal bacterial hyperproliferation syndrome (SIBO) with breath test-lactulose or glucose and/or; Fecal calprotectin. • Endoscopic investigations: esophagogastroduodenoscopies (EGDS), rectoscopies (RCS)
• Complete abdominal ultrasound with study of the loops and hepatic elastometry
• Nutritional therapies

• Home Parenteral Nutrition (NPD). Characteristics of the nutritional mixture [volume (mL/day), caloric intake (Kcal/day); bromatological composition (amino acids, carbohydrates, lipids (g/day and Kcal/day), vitamins and trace elements]; number of weekly infusions;
• Oral nutritional supplements (type and quantity/day)
• Transplant therapy if carried out Marrow transplant or liver transplant (date and clinical progress). The following data relating to the history of the disease will also be collected: age at onset of symptoms, age at diagnosis, symptoms and signs at onset, symptoms and signs at diagnosis, symptoms and signs during clinical follow-up.

Inclusion criteria

• Diagnosis of MNGIE (positive genetic investigation for the presence of mutation of the nuclear TYMP gene).
• Obtaining informed consent

Exclusion criteria

• none