Minimizing Growth Suppression in Children with Steroid-sensitive Nephrotic Syndrome

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Minimizing Growth Suppression in Children with Steroid-sensitive Nephrotic Syndrome Alex Constantinescu, MD Director, Pediatric Nephrology Joe DiMaggio Children s Hospital Hollywood, Florida

Outline Define steroid-sensitive nephrotic syndrome Disease course relapse pattern Side effects of steroids Growth suppression data Strategies to prevent growth-suppression

Definition Nephrotic Syndrome = clinical entity having multiple causes, characterized by high glomerular membrane permeability, manifested by massive proteinuria and lipiduria, in the absence of depressed GFR. (G. Schreiner, 1963) Upr excretion rates are usually >40 mg/m 2 /hr in children, or >1 g protein/g creatinine (random sample)

Childhood Nephrotic Syndrome (NS) Most common cause: minimal change disease (MCD) First line of therapy: corticosteroids daily followed by alternate day Many protocols ISKDC 1978, 1981

Types of Nephrotic Syndrome Based on steroid sensitivity: steroid-responsive (protein-free) Infrequent relapsers (<2 in a year) Frequent relapsers (2 in 6 months, or >3 in a year) Steroid-dependent (within 1 month after steroids stopped or while on alternate day therapy) steroid-resistant (no response after 4-6 weeks)

Systems Affected by Steroid Therapy Gastro-intestinal (gastritis) Cardio-vascular (hypertension) Hematological (leukocytosis, immunosuppression) Neuro-psychological (psychosis, depression) Bone metabolism (osteoporosis) Skin and Eye (striae, cataracts) Glucose metabolism (diabetes, cushingoid body habitus) Growth suppression, leading to short stature

Steroid-induced Growth Suppression - Mechanisms - Hypothalamus GHRH + + - Somatostatin Steroids - Pituitary Pulsatile GH secretion + Liver IGF-1 Growth plate Connective tissue + - GH receptor expression and binding; IGF-1 activity Adrenal gland -

Impact of Short Stature Body image Psychosocial adaptation Bone metabolism Pubertal development

Growth in Children with Nephrotic Syndrome Single center - Robert Wood Johnson Medical School, New Brunswick, NJ We sought to identify: Degree of growth suppression caused by steroid therapy in children with NS, presumed to have MCD Moment of maximum impact Frequency of this adverse effect Is this long-lasting? Patients with focal segmental sclerosis on biopsy, as well as those with other steroid-resistant forms of NS were excluded Data entered in GrowTrack v 1.0.6 Software (Genentech, Inc.) Standard deviation scores (SDS) for Ht (HtSDS) and GR (GRSDS), were calculated and compared with normal values for age and gender Cederbaum N, Constantinescu A. J Investigative Medicine 50:187, 2002.

Results 69 children with complete growth data 44 boys, 25 girls, M:F=1.8:1 Age range 1-17.8 years Younger than 6 yrs of age 75.4% Older than 6 yrs of age 24.6%

Ht SDS in Children with Nephrotic Syndrome 4 3 2 Ht SDS S 1 0-1 -2-3 -4 3m 6m 1y 2y 3y 4y 5y 6y 7y 8y 9y 10y 11y Time -1.8 SD

HtSDS in Children with Nephrotic Syndrome HtSD DS 6 5 4 3 2-1 01-2 -3 3 mos 6 mos 12 mos HtSDS in M<6y (n=31) HtSDS in F<6y (n=21) HtSDS in M>6y (n=13) HtSDS in F>6y (n=4)

Growth Rate SDS in Children with Nephrotic Syndrome Growth Rate SDS 12 10 8 6 4 2 0-2 -4-6 -8 3m 6m 1y 2y 3y 4y 5y 6y 7y 8y 9y 10y 11y 12y Time

Growth Velocity Rate (GVR) in Children with NS 20.0 GVR for 3-6-12 mo. 15.0 p=0.029 10.0 5.0 20.0 GVR - M vs. F >6 yrs. 0.0 3 m 6 m 12 m 15.0 10.0 20.0 15.0 GVR - M vs. F <6 yrs. p=0.019 5.0 0.0 M M M F F 3 m 6 m 12 m 10.0 5.0 0.0 M F M F M F 3 m 6 m 12 m

Long-term Linear Growth in Children with SD or FR Nephrotic Syndrome 56 children (37 M, 19 F) followed-up for 10.5±3.1 yrs SD = 42, FR = 14 Average growth loss was 0.66±0.89 SD 2 patients fell below -2SD 23 reached final height with loss of: 0.92±0.8 HtSDS from the onset of disease (p=0.001) 0.68±0.7 HtSDS from predicted target height (p=0.001) Correlated with steroid dose higher risk if more than 6 months Growth velocity rate lower in younger children, <4 yrs Emma F, et al. Pediatr Nephrol 18:783-8, 2003

So far Reviewed the impact of steroids on growth How can we minimize exposure to steroids? Lower the frequency of relapse Lower the initial dose of steroids Can we tailor the therapy?

Tailor Therapy Arbeitsgemanschaft für Pädiatrische Nephrologie published in 1998, in Lancet, the finding that 6 weeks of daily steroids + 6 weeks of alternate day steroids appear to reduce the relapse rate larger cumulative steroid dose Niaudet and Habib in 1994 introduced cyclosporine in the treatment of NS, as steroid-sparing agent. No sustained remission, additional side effects Segregate according to days to remission?

Predictors of Frequent Relapses in NS Mishra et al. J Trop Pediatr 2013; 59:343-349 60% relapse (150 1 year) young age and longer time to remission predicts frequent relapsing course Harambat et al. Pediatr Nephrol 2013; 28:631-638 70% FR/SD (120 6.7 years) longer time to remission predicts use of steroid-sparing agents Sureshkumar et al. Pediatr Nephrol 2014; 29:1039 1046 66% relapse (129 1 year) male, young age, short time to first relapse predicts FR

Distribution Based on Days to Remission No. of Patien nts 20 18 16 14 12 10 8 6 4 2 0 1 wk 2 wks 4 wks >4 wks Days to Remission IR FR+SD Constantinescu et al, Pediatrics 2000; 105:492-495

Disease Course in Patients with Hematuria Relapse pattern vs. Days to remission Nr. patients with hematuria 10 5 0 0-7 >7 IR FR+SD Constantinescu et al, Pediatrics 2000; 105:492-495

Disease Course in Patients without Hematuria Relapse Pattern vs. Days to remission Nr. Patients without hematuria 16 14 12 10 8 6 4 2 0 0-7 * >7 IR FR+SD Predicts infrequent relapsing course * p<0.05 Constantinescu et al, Pediatrics 2000; 105:492-495

MDR-1 Gene Polymorphism MDR-1 encodes for P-glycoprotein-170, a biological barrier Up-regulated MDR-1 gene expression correlates with a poor response to steroids MDR-1 polymorphism studies in NS, TT genotype associated with a delayed response to steroids and a FR course Wasilewska, A, et al. Pediatr Nephrol 22:44-51, 2007

Our Approach to Minimize Exposure to Steroids Establish the diagnosis of nephrotic syndrome Determine if hematuria is present at the onset Start steroid therapy Parents call first day urine is protein-free With hematuria, steroids 6 wks QD + 6 wks QOD Without hematuria AND response in >1 wk, therapy for 6 wks QD + 6 wks QOD Without hematuria AND response in <1 wk, therapy only for 4 wks QD + 4 wks QOD No response in 4 wks - kidney biopsy

Our Data 2006 present: 60 children with steroid-sensitive NS 26 with complete growth records 34 either recently diagnosed, incomplete records, or lost to follow-up Relapse pattern noted (IR, FR/SD) Initial steroid course (4+4 or 6+6) Ht SDS at the last visit

Ht SDS - A Function of Relapse Pattern and Steroid Dose Ht SDS in Children with NS Ht SDS 0.4 0.2 0-0.2-0.4-0.6-0.8-1 -1.2-1.4-1.6 IR 4+4 IR 6+6 FR/SD 6+6 (pre-ssa) 5 11 10 * FR/SD 6+6 (on SSA, last) 10 #, SSA = patient receiving steroid-sparing agent (tacrolimus or cyclosporine) * p = 0.039 between IR 4+4 and pre-ssa # p = 0.0000133 between pre-ssa and last visit on SSA p = 0.29 between IR 4+4 and FR/SD 6+6 at last visit on SSA

Conclusions Steroids have growth-suppression potential Attempts needed to minimize the exposure Change in daily dose is not recommended Cumulative dose can be decreased by predicting the infrequent relapsing pattern based on: response within one week and, the absence of hematuria. Prospective studies needed