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The impact of long-term corticotherapy on bone health in children with idiopathic nephrotic syndrome


Authors: K. Kubejová 1;  L. Turoňová 2;  V. Vargová 1;  M. Čaprnda 3;  G. Koľvek 1;  Ľ. Podracká 4
Authors place of work: Klinika detí a dorastu LF UPJŠ a DFN Košice, Slovensko 1;  Klinika detí a dorastu JLF UK a UNM, Martin, Slovensko 2;  1. interná klinika LFUK a UNB, Bratislava, Slovensko 3;  Detská klinika (DK) LF UK a NÚDCH, Bratislava, Slovensko 4
Published in the journal: Čes-slov Pediat 2019; 74 (4): 224-232.
Category: Original Papers

Summary

Objective: The aim of the study was to assess the impact of prolonged corticotherapy on growth, bone metabolism and bone mineral density (BMD) parameters in children with idiopathic nephrotic syndrome (INS).

Methods: 39 patients with INS (24 boys, mean age 11.09±4.29 years) and 40 healthy controls of comparable age and gender were enrolled in the study. In the INS group, the mean daily dose of prednisone was 0.70±0.24 mg/kg/day (mean cumulative corticosteroid dose 367.13±268.45 mg/kg, mean duration of corticosteroid treatment was 551.15±343.10 days). The effect of corticotherapy on bone health was assessed by 1) anthropometric measurements 2) bone metabolism testing, taking into account laboratory deviations specific to INS 3) DXA (dual-energy X-ray absorptiometry).

Results: Compared with the control group of healthy children, we observed a significantly lower Z-score of body height (-0.81±1.34 vs 0.32±0.87; p<0.001) in the INS group, which correlated negatively with the cumulative dose of corticoids (p=0.03) and the length of corticotherapy (p=0.025). Patients taking prednisone at the time of measurement had a more pronounced decrease in body height Z-score compared to patients without steroids (-1.26±1.34 vs -0.33±1.2; p=0.002). BMD Z-scores in L1-L4 and TBLH (total body less head) in the INS group were also significantly lower compared to the control group (-0.29±1.30 vs 0.70±1.10; p˂0.001, 0.10±1.15 vs 0.99±1.10; p=0.001). In patients receiving corticoids, we found a statistically significant decrease in BMD Z-score of L1-L4 and TBLH compared with patients free of steroids (L1-L4: p=0.001; TBLH: p=0.003). BMD Z-score significantly correlated with the cumulative corticosteroid dose (L1-L4: p˂0.001, TBLH: p=0.002) and correlated with the length of corticotherapy (L1-L4: p=0.006; TBLH: p=0.043). We did not confirm statistically significant differences in serum concentrations of 25-OH-D, ALP, iPTH, calcium and phosphorus depending on the cumulative corticosteroid dose or the duration of corticosteroid therapy.

Conlusion: Linear growth and BMD Z-scores in the L1-L4 and TBLH regions are during long-term corticosteroid treatment in the comparison to the healthy control group significantly reduced and negatively correlate with the cumulative corticosteroid dose and the length of corticotherapy. The role of a first contact pediatrician (during the long-term corticotherapy) is to monitor the clinical and laboratory indicators (in cooperation with a specialist) of corticoid-induced bone damage and to monitor the effectiveness of preventive regimens.

Keywords:

idiopathic nephrotic syndrome – linear growth – DXA – aBMD


Zdroje

1. Fung BE, Sawyer AJ, Bachrach KL. Bone Health Assessment in Pediatrics – Guidelines for Clinical Practice. 2nd ed. Springer International Publishing, 2016: 1–347.

2. El-Mashad GM, El-Hawy MA, El-Hefnawy SM, Mohamed SM. Bone mineral density in children with idiopathic nephrotic syndrome. J Pediatr 2016; 93: 142–147.

3. Canalis E, Mazziotti G, Giustina A, Bilezikian JP. Glucocorticoid-induced osteoporosis: pathophysiology and therapy. Osteoporos Int 2007; 18: 1319.

4. Bayer M, Růžičková O, Pavelka K, Palička V. Doporučení pro prevenci a léčbu glukokortikoidy indukované osteoporózy u pacientů s revmatickým onemocněním (společné stanovisko České revmatologické společnosti a Společnosti pro metabolická onemocnění skeletu). Čes Revmatol 2004; 4: 163–174.

5. Gulati S, Godbole M, Singh U, et al. Are children with idiopathic nephrotic syndrome at risk for metabolic bone disease? Am J Kidney Dis 2003; 41: 1163–1169.

6. Waljee AK, Rogers MA, Lin P, et al. Short term use of oral corticosteroids and related harms among adults in the United States: population based cohort study. BMJ 2017; 357: 1415.

7. Aceto G, D’Addato O, Giovanni Messina G, et al. Bone health in children and adolescents with steroid-sensitive nephrotic syndrome assessed by DXA and QUS. Pediatr Nephrol 2014; 29: 2147–2155.

8. Jabor A. Vnitřní prostředí. Praha: Grada, 2008: 1–530.

9. Gordon CM, Leonard MB, Zemel BS. Pediatric Position Development Conference: executive summary and reflections. J Clin Densitom 2014; 17: 219–224.

10. Choudhary S, Agarwal I, Seshadri MS. Calcium and vitamin D for osteoprotection in children with new-onset nephrotic syndrome treated with steroids: a prospective, randomized, controlled, interventional study. Pediatr Nephrol 2014; 29: 1025–1032.

11. Leonard MB. Glucocorticoid-induced osteoporosis in children: impact of the underlying disease. Pediatrics 2007; 119 (3): 166–174.

12. Leonard MB, Feldman HI, Shults J, et al. Long-term, high-dose glucocorticoids and bone mineral content in childhood glucocorticoid-sensitive nephrotic syndrome. N Engl J Med 2004; 351 (8): 868–878.

13. Srivastava RN, Agarwal RK, Moudgil A, Bhuyan UN. Late resistance to corticosteroids in nephrotic syndrome. J Pediatr 1986; 108: 66.

14. Gulati S, Gulati K. Bone disease in nephrotic syndrome-prevention is better than cure. Pediatr Nephrol 2005; 20: 111–112.

15. Allen DB. Growth suppression by glucocorticoid therapy. Endocrinol Metab Clin North Am 1996; 25: 699.

16. Allen DB, Julius JR, Breen TJ, Attie KM. Treatment of glucocorticoid-induced growth suppression with growth hormone. National Cooperative Growth Study. J Clin Endocrinol Metab 1998; 83: 2824.

17. Lai HC, Fitz Simmons SC, Allen DB, et al. Risk of persistent growth impairment after alternate-day prednisone treatment in children with cystic fibrosis. N Engl J Med 2000; 342: 851.

18. Banerjee S, Basu S, Sen A, Sengupta J. Vitamin D in nephrotic syndrome remission: a case-control study. Pediatr Nephrol 2013; 28: 1983–1989.

19. Banerjee S, Basu S, Sen A, Sengupta J. The effect of vitamin D and calcium supplementation in pediatric steroid-sensitive nephrotic syndrome. Pediatr Nephrol 2017; 32: 2063–2070.

20. Tsampalieros A, Gupta P, Denburg MR, et al. Glucocorticoid effects on changes in bone mineral density and cortical structure in bone mineral density and cortical structure in childhood nephrotic syndrome. J Bone Miner Res 2013; 28: 480–488.

21. Hogler W, Blimkie CJ, Cowell CT, et al. A comparison of bone geometry and cortical density at the mid-femur between prepuberty and young adulthood using magnetic resonance imaging. Bone 2013; 33: 771–778.

22. Movsowitz C, Epstein S, Fallon M, et al. Cyclosporin-A in vivo produces severe osteopenia in the rat: effect of dose and duration of administration. Endocrinology 1988; 123: 2571.

23. Šašinka M, Furková K. „Slnečný“ vitamín. Bratislava: Herba, 2012: 1–184.

24. Gulati S, Sharma RK, Gulati K, et al. Longitudinal follow-up of bone mineral density in children with nephrotic syndrome and the role of calcium and vitamin D supplements. Nephrol Dial Transplant 2005; 20: 1598–1603.

25. Bak M, Serdaroglu E, Guclu R. Prophylactic calcium and vitamin D treatments in steroid-treated children with nephrotic syndrome. Pediatr Nephrol 2006; 21: 350–354.

Štítky
Neonatology Paediatrics General practitioner for children and adolescents

Článok vyšiel v časopise

Czech-Slovak Pediatrics

Číslo 4

2019 Číslo 4
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