Abstract
In persistent hyperinsulinemic hypoglycemia of infancy, ketone body concentrations are abnormally low at times of hypoglycemia, depriving the brain of its most important alternative fuel. The neuroprotective effect of endogenous ketone bodies is evidenced by animal and human studies, but knowledge about exogenous supply is limited. Assuming that exogenous ketone body compounds as a dietetic food might replace this alternative energy source for the brain, we have monitored the fate of orally supplemented dl sodium β-hydroxybutyrate (β-OHB) in two 6-mo-old infants with persistent hyperinsulinemic hypoglycemia for 5 and 7 mo, while on frequent tube-feedings and treatment with octreotide. Near total (95%) pancreatectomy had been ineffective in one patient and was refused in the other. In blood, concentrations of β-OHB increased to levels comparable to a 16- to 24-h fast while on dl sodium β-OHB 880 to 1000 mg/kg per day. In cerebrospinal fluid, concentrations of β-OHB increased to levels comparable to a 24- to 40-h fast, after single dosages of 4 and 8 g, respectively. High ratios of β-OHB to acetoacetate indicated exogenous origin of β-OHB. An increase of intracerebral concentrations of β-OHB could be demonstrated by repetitive single-voxel proton magnetic resonance spectroscopy by a clear doublet at 1.25 ppm. Oral dl sodium β-OHB was tolerated without side effects. This first report on oral supplementation of dl sodium β-OHB in two patients with persistent hyperinsulinemic hypoglycemia demonstrates effective uptake across the blood–brain barrier and could provide the basis for further evaluation of the neuroprotective effect of β-OHB in conditions with hypoketotic hypoglycemia.
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Abbreviations
- PHHI:
-
persistent hyperinsulinemic hypoglycemia of infancy
- MRS:
-
magnetic resonance spectroscopy
- CSF:
-
cerebrospinal fluid
- β-OHB:
-
β-hydroxybutyrate
- AA:
-
acetoacetate
References
Soltesz G, Aynsley-Green A 1984 Hyperinsulinism in infancy childhood. Ergeb Inn Med Kinderheilkd 51: 115–202
Aynsley-Green A, Polak JM, Bloom SR, Gough MH, Keeling J, Ashcroft SJ, Turner RC, Baum JD 1981 Nesidioblastosis of the pancreas: definition of the syndrome the management of the severe neonatal hyperinsulinaemic hypoglycaemia. Arch Dis Child 56: 496–508
Saudubray JM, de Lonlay P, Touati G, Martin D, Nassogne MC, Castelnau P, Sevin C, Laborde C, Baussan C, Brivet M, Vassault A, Rabier D, Bonnenfont JP, Kamoun P 2000 Genetic hypoglycaemia in infancy childhood: pathophysiology diagnosis. J Inherit Metab Dis 23: 197–214
Glaser B 2000 Hyperinsulinism of the newborn. Semin Perinatol 24: 150–163
DeLonlay P, Fournet JC, Rahier J, Gross-Morand MS, Poggi-Travert F, Foussier V, Bonnefont JP, Brusset MC, Brunelle F, Robert JJ, Nihoul-Fekete C, Saudubray JM, Junien C 1997 Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia endorses partial pancreatectomy. J Clin Invest 100: 802–4807
Stanley CA 1997 Hyperinsulinism in infants children. Pediatr Clin North Am 44: 363–374
Touati G, Poggi-Travert F, Ogier de Baulny H, Rahier J, Brunelle C, Nihoul-Fekete C, Czernichow P, Saudubray JM 1998 Long-term treatment of persistent hyperinsulinaemic hypoglycaemia of infancy with diazoxide: a retrospective review of 77 cases analysis of efficacy-predicting criteria. Eur J Pediatr 157: 628–633
Thornton PS, Craig A, Katz LE, Baker L, Stanley A 1993 Short- long-term use of octreotide in the treatment of congenital hyperinsulinism. J Pediatr 123: 637–643
Aynsley-Green A, Hussain K, Hall J, Saudubray JM, Nihoul-Fekete C, De Lonlay-Debeney, Brunelle F, Otonkoski T, Thornton P, Lindley KJ 2000 Practical management of hyperinsulinism in infancy. Arch Dis Child Fetal Neonatal Ed 82: F98–F107
Zuppinger K 1983 Disorders of the endocrine pancreas. Prog Pediatr Surg 16: 51–61
Owen OE, Morgan AP, Kemp HG, Sullivan JM, Herrera MG, Cahill GF 1967 Brain metabolism during fasting. J Clin Invest 46: 1589–1595
Mitchell GA, Kassovska-Bratinova S, Boukaftane Y, Robert MF, Wang SP, Ashmarina L, Lambert M, Lapierre P, Potier E 1995 Medical aspects of ketone body metabolism. Clin Invest Med 18: 193–216
Robinson AM, Williamson DH 1980 Physiological roles of ketone bodies as substrates signals in mammalian tissues. Physiol Rev 60: 143–187
Hawdon JM, Ward Platt MP, Aynsley-Green A 1992 Patterns of metabolic adaptation for preterm term infants in the first neonatal week. Arch Dis Child 67: 357–365
Aynsley-Green A 1996 Glucose, the brain the paediatric endocrinologist. Horm Res 46: 8–25
Meissner T, Brune W, Mayatepek E 1997 Persistent hyperinsulinaemic hypoglycaemia of infancy: therapy, clinical outcome mutational analysis. Eur J Pediatr 156: 754–757
Thurston JH, Hauhart RE, Schiro JA 1986 β-Hydroxybutyrate reverses insulin-induced hypoglycemic coma in suckling-weanling mice despite low blood brain glucose levels. Metab Brain Dis 1: 63–82
Drenick EJ, Alvarez LC, Tamasi GC, Brickman AS 1972 Resistance to symptomatic insulin reactions after fasting. J Clin Invest 51: 2757–2762
Bonham JR, Tanner MS, Pollitt RJ, Manning NJ, Olpin SE, Downing M, Robertson L, Pourfarzam M, Bartlett K 1999 Oral sodium 3-hydroxybutyrate, a novel adjunct to treatment for multiple acyl-CoA dehydrogenase deficiency (abstr). J Inherit Metab Dis 22 ( suppl): 101
Newsholme EA, Randle PJ 1964 Regulation of glucose uptake by muscle. 7. Effects of fatty acids, ketone bodies pyruvate, of alloxan-diabetes, starvation, hypophysectomy adrenalectomy, on the concentrations of hexose phosphates, nucleotides inorganic phosphate in perfused rat heart. Biochem J 93: 641–651
Liebich HM 1986 Gas chromatographic profiling of ketone bodies organic acids in diabetes. J Chromatogr 379: 347–366
Frahm J, Bruhn H, Gyngell ML, Merboldt KD, Hanicke W, Sauter R 1989 Localized high-resolution proton NMR spectroscopy using stimulated echoes: initial applications to human brain in vivo. Magn Reson Med 9: 79–93
Wolfsdorf JI, Sadeghi-Nejad A, Senior B 1982 Fat-derived fuels during a 24 hour fast in children. Eur J Pediatr 138: 141–144
Patel MS, Johnson CA, Rajan R, Owen OE 1975 The metabolism of ketone bodies in developing human brain: development of ketone-body-utilizing enzymes ketone bodies as precursors for lipid synthesis. J Neurochem 25: 905–908
Bonnefont JP, Specola NB, Vassault A, Lombes A, Ogier H, de Klerk JBC, Munnich A, Coude M, Paturneau-Jouas M, Saudubray JM 1990 The fasting test in paediatrics: application to the diagnosis of pathological hypo- hyperketotic states. Eur J Pediatr 150: 80–85
Saudubray JM, Marsac C, Limal JM, Dumurgier E, Charpentier CH, Ogier H, Coude FX 1981 Variation in plasma ketone bodies during a 24 hour fast in normal in hypoglycemic children: relationship to age. J Pediatr 98: 904–908
Lamers KJB, Doesburg WH, Gabreels FJM, Romsom AC, Lemmens WAJ, Wevers RA, Renier WO 1987 CSF concentrations CSF/blood ratio of fuel related components in children after prolonged fasting. Clin Chim Acta 167: 135–145
Kraus H, Schlenker S, Schwedesky D 1974 Developmental changes of cerebral ketone body utilization in human infants. Hoppe-Seyler‘s Z Physiol Chem 355: 164–170
Persson B, Settergren G, Dahlquist G 1972 Cerebral arteriovenous difference of acetoacetate β-hydroxybutyrate in children. Acta Paediatr Scand 61: 273–278
Settergren G, Persson B, Dahlquist G 1973 The effect of moderate hypocapnia on the cerebral arteriovenous difference of acetoacetate,d-β-hydroxybutyrate oxygen in children. Acta Paediatr Scand 62: 141–145
Pi-Sunyer FX, Campell RG, Hashim SA 1970 Experimentally induced hyperketonemia insulin secretion in the dog. Metabolism 19: 263–270
Langhans W, Pantel K, Scharrer E 1985 Ketone kineticsd-(-)-β-hydroxybutyrate-induced inhibition of feeding in rats. Physiol Behav 34: 579–582
Kahler A, Zimmermann M, Langhans W 1999 Suppression of hepatic fatty acid oxidation food intake in men. Nutrition 15: 819–828
Huttenlocher PR 1976 Ketonemia seizures: metabolic anticonvulsant effects of two ketogenic diets in childhood epilepsy. Pediatr Res 10: 536–540
Best TH, Franz DN, Gilbert DL, Nelson DP, Epstein MR 2000 Cardiac complications in pediatric patients on the ketogenic diet. Neurology 54: 2328–2330
Teijema HA, Van Gelderen HH, Giesbert MAH 1980 Hypoketosis as a cause of symptoms in childhood hypoglycaemia. Eur J Pediatr 134: 51–55
Koh TH, Aynsley-Green A, Tarbit M, et al 1988 Neuronal dysfunction during hypoglycaemia. Arch Dis Child 63: 1353–1358
Siesjo BK 1988 Hypoglycaemia, brain metabolism brain damage. Diabetes Metab Rev 4: 113–144
Acknowledgements
The authors thank Prof. Dr. H. Przyrembel (BGVV, Berlin) for fruitful discussion on dietetic food and food supplements.
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Supported in part by Invita-Gesellschaft zur Foerderung der Gesundheit unserer Kinder (B.P.), the Scientific Funds of the Austrian National Bank [OENB 7908 (B.P.); and OENB 7507 (H.S.)], and the Scientific Trust of the Major of Vienna [BM 1692 (V.M., S.G.)].
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Plecko, B., Stoeckler-Ipsiroglu, S., Schober, E. et al. Oral β-Hydroxybutyrate Supplementation in Two Patients with Hyperinsulinemic Hypoglycemia: Monitoring of β-Hydroxybutyrate Levels in Blood and Cerebrospinal Fluid, and in the Brain by In Vivo Magnetic Resonance Spectroscopy. Pediatr Res 52, 301–306 (2002). https://doi.org/10.1203/00006450-200208000-00025
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DOI: https://doi.org/10.1203/00006450-200208000-00025
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