50 years ago in the journal of pediatrics

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24. Schwartz GJ, Abraham AG, Furth SL, Warady BA, Mu~ noz A. Optimizing iohexol plasma disappearance curves to measure the glomerular filtration rate in children with chronic kidney disease. Kidney Int 2010;77:65-71. 25. Schwartz GJ, Schneider MF, Maier PS, Moxey-Mims M, Dharnidharka VR, Warady BA, et al. Improved equations estimating GFR in children with chronic kidney disease using an immunonephelo- metric determination of cystatin C. Kidney Int 2012;82:445-53. 26. Hricak H, Lieto RP. Sonographic determination of renal volume. Radi- ology 1983;148:311-2. 27. Cohen HL, Cooper J, Eisenberg P, Mandel FS, Gross BR, Goldman MA, et al. Normal length of fetal kidneys: sonographic study in 397 obstetric patients. AJR Am J Roentgenol 1991;157:545-8. 28. Lee JH, Hahn WH, Ahn J, Chang JY, Bae CW. Serum cystatin C during 30 postnatal days is dependent on the postconceptional age in neonates. Pediatr Nephrol 2013;28:1073-8. 29. Filler G, Lepage N. Cystatin C adaptation in the first month of life. Pe- diatr Nephrol 2013;28:991-4. 30. Konopska B, Gburek J, Go1a ˛b K, Warwas M. Influence of aminoglyco- side antibiotics on chicken cystatin binding to renal brush-border mem- branes. J Pharm Pharmacol 2013;65:988-94. 31. Shlipak MG, Matsushita K, Arnlov J, Inker LA, Katz R, Polkinghorne KR, et al. CKD Prognosis Consortium. Cystatin C versus creatinine in deter- mining risk based on kidney function. N Engl J Med 2013;369:932-43. 32. Kandasamy Y, Smith R, Wright IM, Lumbers ER. Extra-uterine renal growth in preterm infants: oligonephropathy and prematurity. Pediatr Nephrol 2013;28:1791-6. 33. Singh GR, Hoy WE. Kidney volume, blood pressure, and albuminuria: findings in an Australian Aboriginal community. Am J Kidney Dis 2004;43:254-9. 34. Luyckx VA, Brenner BM. The clinical importance of nephron mass. J Am Soc Nephrol 2010;21:898-910. 35. Keijzer-Veen MG, Devos AS, Meradji M, Dekker FW, Nauta J, van der Heijden BJ. Reduced renal length and volume 20 years after very preterm birth. Pediatr Nephrol 2010;25:499-507. 50 Years Ago in THE JOURNAL OF PEDIATRICS The Route of Insulin Administration in the Management of Diabetes Mellitus Nora JJ, Smith DW, Cameron JR. J Pediatr 1964;64:547-51 N ora et al administered 131 I-labeled lente insulin to 10 children with diabetes and determined a faster clearance time for insulin administered in the upper arm compared with the thigh and no difference in the rate of insulin clearance between intramuscular and subcutaneous injections. This study was conducted a little over 30 years from the discovery of insulin and about a decade after protamine-free, lente insulin became available. In the early 1960s, the first synthetic insulin was produced, but it became commercially available only in 1982. In the decade that followed, the advent of insulin analogs, with various absorption profiles, provided more freedom in dosing and helped with a better diabetes control. What has changed in the past 50 years about diabetes management? We now have a detailed understanding of the pathologic processes that lead to type 1 or type 2 diabetes. We know that tight control of blood glucose levels decreases the long-term complications of diabetes, and we have a multitude of insulin formulations to ensure maximum freedom in management. Technological advances in insulin pens and insulin pumps allow ease of use and better qual- ity of life for children and adults living with diabetes. However, the route of delivery has remained the same, and the findings by Nora et al have stood the test of time and are accepted as undebatable truths. Subcutaneously administered insulin is the mainstay of therapy in diabetes for a simple reason—it is a very effective treatment with minimal adverse effects. Current efforts aimed at curing diabetes, through transdifferentiation of stem cell into insulin-producing beta cell or islet and pancreas transplants, are still far from being viable treatment options and have to raise to the effec- tiveness of insulin therapy. Diana E. Stanescu, MD Division of Endocrinology and Diabetes The Children’s Hospital of Philadelphia Philadelphia, Pennsylvania http://dx.doi.org/10.1016/j.jpeds.2013.10.078 May 2014 ORIGINAL ARTICLES Neonatal Kidney Size and Function in Preterm Infants: What Is a True Estimate of Glomerular Filtration Rate? 1031

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Page 1: 50 Years Ago in The Journal of Pediatrics

May 2014 ORIGINAL ARTICLES

24. Schwartz GJ, Abraham AG, Furth SL, Warady BA, Mu~noz A. Optimizing

iohexol plasma disappearance curves to measure the glomerular filtration

rate in children with chronic kidney disease. Kidney Int 2010;77:65-71.

25. Schwartz GJ, Schneider MF, Maier PS, Moxey-Mims M,

Dharnidharka VR, Warady BA, et al. Improved equations estimating

GFR in children with chronic kidney disease using an immunonephelo-

metric determination of cystatin C. Kidney Int 2012;82:445-53.

26. Hricak H, Lieto RP. Sonographic determination of renal volume. Radi-

ology 1983;148:311-2.

27. Cohen HL, Cooper J, Eisenberg P, Mandel FS, Gross BR, Goldman MA,

et al. Normal length of fetal kidneys: sonographic study in 397 obstetric

patients. AJR Am J Roentgenol 1991;157:545-8.

28. Lee JH, Hahn WH, Ahn J, Chang JY, Bae CW. Serum cystatin C during

30 postnatal days is dependent on the postconceptional age in neonates.

Pediatr Nephrol 2013;28:1073-8.

29. Filler G, Lepage N. Cystatin C adaptation in the first month of life. Pe-

diatr Nephrol 2013;28:991-4.

Neonatal Kidney Size and Function in Preterm Infants: What Is a

30. Konopska B, Gburek J, Go1ab K, Warwas M. Influence of aminoglyco-

side antibiotics on chicken cystatin binding to renal brush-border mem-

branes. J Pharm Pharmacol 2013;65:988-94.

31. ShlipakMG,Matsushita K, €Arnl€ov J, Inker LA, Katz R, Polkinghorne KR,

et al. CKD Prognosis Consortium. Cystatin C versus creatinine in deter-

mining risk based on kidney function. N Engl J Med 2013;369:932-43.

32. Kandasamy Y, Smith R, Wright IM, Lumbers ER. Extra-uterine renal

growth in preterm infants: oligonephropathy and prematurity. Pediatr

Nephrol 2013;28:1791-6.

33. Singh GR, Hoy WE. Kidney volume, blood pressure, and albuminuria:

findings in an Australian Aboriginal community. Am J Kidney Dis

2004;43:254-9.

34. Luyckx VA, Brenner BM. The clinical importance of nephronmass. J Am

Soc Nephrol 2010;21:898-910.

35. Keijzer-Veen MG, Devos AS, Meradji M, Dekker FW, Nauta J, van der

Heijden BJ. Reduced renal length and volume 20 years after very preterm

birth. Pediatr Nephrol 2010;25:499-507.

50 Years Ago in THE JOURNAL OF PEDIATRICS

The Route of Insulin Administration in the Management of Diabetes MellitusNora JJ, Smith DW, Cameron JR. J Pediatr 1964;64:547-51

Nora et al administered 131I-labeled lente insulin to 10 children with diabetes and determined a faster clearancetime for insulin administered in the upper arm compared with the thigh and no difference in the rate of insulin

clearance between intramuscular and subcutaneous injections. This study was conducted a little over 30 years from thediscovery of insulin and about a decade after protamine-free, lente insulin became available. In the early 1960s, the firstsynthetic insulin was produced, but it became commercially available only in 1982. In the decade that followed, theadvent of insulin analogs, with various absorption profiles, provided more freedom in dosing and helped with a betterdiabetes control.

What has changed in the past 50 years about diabetes management? We now have a detailed understanding of thepathologic processes that lead to type 1 or type 2 diabetes. We know that tight control of blood glucose levels decreasesthe long-term complications of diabetes, and we have a multitude of insulin formulations to ensure maximumfreedom in management. Technological advances in insulin pens and insulin pumps allow ease of use and better qual-ity of life for children and adults living with diabetes. However, the route of delivery has remained the same, and thefindings by Nora et al have stood the test of time and are accepted as undebatable truths. Subcutaneously administeredinsulin is the mainstay of therapy in diabetes for a simple reason—it is a very effective treatment with minimal adverseeffects. Current efforts aimed at curing diabetes, through transdifferentiation of stem cell into insulin-producing betacell or islet and pancreas transplants, are still far from being viable treatment options and have to raise to the effec-tiveness of insulin therapy.

Diana E. Stanescu, MDDivision of Endocrinology and DiabetesThe Children’s Hospital of Philadelphia

Philadelphia, Pennsylvaniahttp://dx.doi.org/10.1016/j.jpeds.2013.10.078

True Estimate of Glomerular Filtration Rate? 1031