Ipovitaminosi D e metabolismo calcio-fosforo in dialisi peritoneale. Maurizio Gallieni Università degli Studi di Milano

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Ipovitaminosi D e metabolismo calcio-fosforo in dialisi peritoneale Maurizio Gallieni Università degli Studi di Milano

G Ital Nefrol 2018 - ISSN 1724-5990

Nutrients 2017, 9, 328

Vitamin D deficiency (<20 ng/ml) and insufficiency (20 29 ng/ml) are common among patients with CKD or undergoing dialysis.

Wang Am J Clin Nutr 2008;87:1631

Vitamin D 3 biotransformation pathway Michaud, JASN 2010; 21: 1488 1497

Physiological disturbances reported in children at different serum 25(OH)D levels <4 ng/ml >16 ng/ml >30 ng/ml >48 ng/ml >100 ng/ml Shtoff, NDT 2017; 32: 1098 1113

Causes and risk factors for 25(OH)D deficiency or insufficiency in CKD and dialysis patients. - Age, - Female sex - Adiposity - Proteinuria - Low physical activity - Peritoneal dialysis - Diabetes mellitus - Impaired 25(OH)D tubular reabsorption - Reduced skin synthesis of vitamin D - Calcineurin inhibitor prescriptions - Reduced hepatic synthesis of Calcidiol (secondary to a PTH-mediated reduction in liver CYP450 isoforms) Nutrients 2017, 9, 328

ng/ml Transpl. Proc. 2015, 47, 1405 1407.

J Hum Nutr Diet. 2014; 28, 209 218

Prognosis of CKD, by categories of GFR and albuminuria.

JASN 2010; 21: 1488 1497 Uremic rats had 52% lower concentrations of serum calcidiol. Uremic rats produced 71% less calcidiol and 48% less calcitriol after the administration of vitamin D3 or 1alfa(OH)vitamin D3, respectively, suggesting impaired C-25-hydroxylation of vitamin D3. Uremia associated with a reduction of liver CYP450 isoforms Parathyroidectomy prevented the uremia-associated decreases in calcidiol and liver CYP450 isoforms.

Association between vitamin D deficiency or insufficiency and outcomes for CKD and dialysis populations - Secondary HPT and high bone turnover markers - Low bone mineral density - Muscle weakness and risk of falls - Metabolic syndrome and obesity, insulin resistance - Left ventricular hypertrophy and atherosclerosis - Vascular calcification and arterial stiffness - Cognitive impairment - Progression of kidney disease - Mortality Nutrients 2017, 9, 328

Cardiovascular event-free survival probability of patients in relation to serum 25(OH)D Wang Am J Clin Nutr 2008;87:1631

Overall survival probability of patients in relation to serum 25(OH)D Wang Am J Clin Nutr 2008;87:1631

Reported effects of vitamin D supplementation on CKD and dialysis patients. - Serum PTH level decrease - Serum 1,25(OH)2D level increase - Reduced proteinuria - Endothelial cardiovascular markers improvement - Inflammation markers decrease Nutrients 2017, 9, 328

Studies on the therapeutic effects of vitamin D in PD are limited and describe small population samples. Vitamin D compounds reduce PTH levels, but not consistently. The administration of active vitamin D in PD may have interesting pleiotropic effects. According to these effects, vitamin D could help to preserve residual renal function and ensure efficient peritoneal membrane dialysance Russo R et al. J Nephrol (2014) 27:483 494

Potential pleiotropic effects of vitamin D in PD patients Russo R et al. J Nephrol (2014) 27:483 494

2018;168:422-430 KDOQI and KDIGO experts have recognized that vitamin D insufficiency and deficiency should be avoided in CKD and dialysis patients by using supplementation to prevent SHPT.

KDIGO 2017 guideline 3.1.3: In patients with CKD G3a to G5D, we suggest that 25-(OH)D (calcidiol) levels might be measured, and repeated testing determined by baseline values and therapeutic interventions. (Grade 2C recommendation) We suggest that vitamin D deficiency and insufficiency be corrected using treatment strategies recommended for the general population. (Grade 2C recommendation) Ann Intern Med. 2018;168:422-430

Shroff et al. NDT 2017; 32: 1098 1113

Shroff et al. NDT 2017; 32: 1098 1113

Shroff et al. NDT 2017; 32: 1098 1113

Shroff et al. NDT 2017; 32: 1098 1113

Why use supplements for vitamin D deficiency or insufficiency for CKD and dialysis patients? - Low serum 25(OH)D level is reported in approximatively 90% of CKD and dialysis patients - 25(OH)D is the fuel for endocrine renal and cellular 1,25(OH)2D synthesis - 25(OH)D interacts with VDR in various target organs - Low vitamin D status leads to SHPT - 25(OH)D deficiency and insufficiency are associated with progression of renal disease, morbidity and mortality in CKD and dialysis patients - Nutritional compounds are inexpensive, not harmful, and are effective for preventing SHPT - Pleiotropic effects such as improvements in proteinuria and cardiovascular disease have been reported Nutrients 2017, 9, 328

Unanswered questions on vitamin D in CKD and dialysis patients - What is the optimal serum 25(OH)D target level according to different CKD stages and severity of SHPT? - Should we supplement patients with low serum PTH level? - What is the optimal 25(OH)D level for different outcomes (proteinuria, fractures, cancer, cardiovascular and immune disease)? - Is it necessary to maintain native vitamin D supplements in patients treated with VDRAs? - Other than hypercalcemia, is there long-term toxicity associated with maintaining high serum 25(OH)D levels? - Are daily vitamin D doses better than weekly or monthly bolus doses? - Large RCTs with clinically meaningful endpoints (fractures, hospitalization, parathyroidectomy, death) are still required to assess the usefulness of different vitamin D compounds for CKD and dialysis patients Nutrients 2017, 9, 328