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ESPN 2014 Porto, September 19, 2014 CKD-MBD in children/adults Markus Ketteler [email protected] Pathogenesis of secondary hyperparathyroidism CaR Ca2+ VDR PTH PTH secretion PTH synthesis Normal kidney function Cell proliferation Normal Ca2+- levels keep PTH secretion/synthesis under control Silver J et al. Am J Physiol Renal Physiol 2002;283:F367–76 Brown EM. In: The Parathyroids – Basic and Clinical Concepts 2nd edn. 2001. Bilezikian JP et al. (eds) Pathogenesis of secondary hyperparathyroidism Calcitriol CaR Ca2+ VDR PTH secretion PTH synthesis Phosphate Slatopolsky E et al. Kidney Int 1999;73:S14–9 Cell proliferation PTH Pathogenesis of secondary hyperparathyroidism solitary nodes Gland volume VDR CaR Early nodules secretory Normal cells Nodular transformation Diffuse VDR CaR Normal PTH Ref: Tominaga Y et al. Curr Opin Nephrol Hypertens 1996;5:336–41 very high Kidney Int Suppl 2009: S1-S130 Kidney Int Suppl 2009: S1-S130 Kidney Int Suppl 2009: S1-S130 Kidney Int Suppl 2009: S1-S130 Kidney Int Suppl 2009: S1-S130 CKD-MBD: children vs. adults – a few differences… During growth, children require a (moderately) positive calcium balance Alkaline phosphatase and phosphate serum concentrations are increased vs. the normal laboratory range in adults Interpretation of bone density may differ from adults (?) How about glucocorticoid therapies (?) Minimal Change GN: Glucocorticoids and bone metabolism Leonard MB et al. NEJM 2004; 351:868 Minimal Change GN: Glucocorticoids and bone metabolism Leonard MB et al. NEJM 2004; 351:868 Bone density and structure: Influence of age and CKD stage Wetzsteon RJ et al. JBMR 2011; 26:2235 Bone density and structure: Influence of age and CKD stage Wetzsteon RJ et al. JBMR 2011; 26:2235 Vitamin D and • • • • • • • Bone metabolism Diabetes CV disorders Multiple sclerosis Rheumatoid arthritis Cancer Infections Adapted from: Time Magazine, US Edition 2007 (December 24);26:170 Vitamin D – deficiency / insufficiency UVB Skin: 7-Dehydrocholesterol CH2 LIVER HO OH Vitamin D3 Liver or fatty fish: D3 (Cholecalciferol) (Cholecalciferol) CH2 Nutrition HO OH NIERE CH2 HO OH 1α,25(OH)2 Vitamin D3 (Calcitriol, endogenous VDRactivator, 1,25D) 24-Hydroxylase 25(OH) Vitamin D3 (Calcidiol, 25D) 24-Hydroxylase Plants: Ergosterol D2 (Ergocalciferol) 24,25(OH)2D3 and 1α,24,25(OH)2D3 Inactivation Vitamin D – deficiency / insufficiency Vitamin D – deficiency / insufficiency Institute of Medicine (IOM), Report November 2010 Grant WB, Holick MF. Altern Med Rev 2005; 10:94-111 / Rosen CJ. N Engl J Med 2011; 364:248-54 Vitamin D – deficiency / insufficiency 20 – 60 ng/ml 600 – 4.000 IU per day Institute of Medicine (IOM), Report November 2010 Grant WB, Holick MF. Altern Med Rev 2011; 2005; 364:248-54 10:94-111 / Rosen CJ. N Engl J Med Serum phosphate vs. mortality risk in hemodialysis patients Relative mortality risk 3.2 40538 Patients 3.0 Fresenius Medical Care North America Patient Statitics 2.8 Multivariate analysis 2.6 Block GA et al., JASN 2004 3.2 14435 Patients 3.0 QiN-Register 3 different analyses 2.8 2.6 2.4 2.4 2.2 2.2 2 2 1.8 1.8 1.6 1.6 1.4 1.4 1.2 1.2 1 1 0.8 <3 3-4 4-5 5-6 6-7 7-8 8-9 >9 0.8 unadjusted multivariate limited multivariate adjusted Stoffels et al., unpublished QiN Daten <3 3-4 4-5 5-6 6-7 7-8 8-9 >9 S-Phosphate [mg/dl] (mmol :3,1) Atherosclerosis • Inflammatory • Lipid deposition • ischemia-related, occlusion Mediasclerosis • Non-inflammatory • No lipid deposition • Usually asymptomatic • pseudohypertension Pathomechanisms of extraosseous calcification Giachelli C. Kidney Int 2009 Coronary artery calcifications are observed in childhoodonset dialysis patients CAC Goodman et al., NEJM (2000) 342:1478-83 Alter (Jahre) Chronic dialysis patients 60 controls (20-30-y-old) Coronary artery calcifications are observed in childhoodonset dialysis patients Circulation 2002 Calcium and the bone-vascular-axis J Am Soc Nephrol 2010; 21:103-12 Calcium and the bone-vascular-axis J Am Soc Nephrol 2010; 21:103-12 Calcium and the bone-vascular-axis J Am Soc Nephrol 2010; 21:103-12 Phosphate balance in normal kidney function Berndt T, Kumar R, Physiology 2009; 24:17-25 Prie et al., Kidney Int 2009; 75:882-9 FGF23, PTH and Phosphate in CKD Isakova T et al., Kidney Int 2011 FGF23 and other bone biomarkers in CKD: Stage dependency in children Wan et al. NDT 2013; 28:153 Dtsch Arztebl Int. 2012 Jan;109(4):49-55. o Phosphate additives (mostly phosphate salts) are intestinally absorbed in up to 100% o Absorption of natural phosphates (phosphate esters, phytates, phospholipids, phosphoproteins) is estimated in a range of 30 – 60 % o Restriction of phosphate additives would be feasible without a reduction of the dietary protein content of the ingested food o Some natural polyphosphates possess protective properties (e.g. pyrophosphate, phytate) o USA – RDA: 700 mg/day, EAR: 580 mg/day, UL: 4.200 mg/day * P = GRAS („generally regarded as safe“) From dietary phosphate restriction to dietary phosphate additive restriction ? http://ec.europa.eu/food/food/fAEF/additives/index_en.htm Food additives are: o Sweeteners to sweeten foods or in table-top sweeteners; o Colours adding or restoring colour in a food; o Preservatives prolonging shelf-life of foods by protecting them against deterioration by micro-organisms; o Antioxidants prolonging shelf-life of foods by protecting them against oxidation e.g. fat rancidity, colour changes; o Stabilisers to maintain the physico-chemical state of a foodstuff; o Emulsifiers to maintain the mixture of oil and water in a foodstuff. From dietary phosphate restriction to dietary phosphate additive restriction ? Sehgal AR, ASN Philadelphia 2011 „LookForPhos“: Dialysis patients received a magnifying glass and instructions concerning better choices in fastfood-restaurants and supermarkets = Net phosphate lowering: 0.6 mg/dl From dietary phosphate restriction to dietary phosphate additive restriction ? Sehgal AR, ASN Philadelphia 2011 LookForPhos: Flow of Participants Through the Trial Sullivan, C. et al. JAMA 2009;301:629-635 Copyright restrictions may apply. LookForPhos: Primary and Secondary Outcomes Among 145 Intervention and 134 Control Participants. Sullivan, C. et al. JAMA 2009;301:629-635 Copyright restrictions may apply. Chairpersons: Mary Leonard, Philadelphia, and Markus Ketteler, Coburg Ketteler M et al., Kidney Int 2014 (in press) VC: The group also believed that there were insufficient data to support special considerations for CKD subgroups including predialysis CKD, transplant recipients, children, and the elderly. Bone quality: The working group noted that none of the studies addressing bone therapies or DXA BMD fracture prediction included children but given the unique characteristics of the growing skeleton, the future updating Work Group may elect to examine this issue more closely with the hope to provide some pediatric guidance. Ca + P: Studies of the impact of calcium and non-calcium containing phosphate binders, and other therapies that impact calcium balance should consider the special needs of the growing skeleton. Vitamin D + PTH: Target PTH levels may also differ during growth and development; however, there are insufficient data to provide pediatric-specific recommendations. CKD-MBD GL Update 2015 CKD-MBD Controversies Conference | 2014 October│ 25-27, 2013 | Madrid, Spain JSDT Congress │ June 15, Kobe, Japan Sausage is so expensive, boy! Just be so kind to eat your phosphate pure today…