1) Cerebral Phosphorus Nuclear Magnetic Resonance Spectroscopy in Perinatal Asphyxia: Our preliminary studies with in vivo 31-phosphorus nuclear magnetic resonance spectroscopy (MRS) in asphyxiated newborns suggest that there are three patterns of phosphorus metabolite changes following severe perinatal asphyxia (see report), and that these patterns correlate with neurologic prognosis. During the next year, we plan to continue our studies of asphyxiated babies by enrolling an additional 10-15 infants. MRS will be performed daily for the first 7 days. All babies will be followed with neurologic and developmental examinations at 6 months, 1 year and 2 years. With increased experience using the MRS technique and more sophisticated monitoring capabilities, we are able to study more critically ill infants. Hopefully, we will be able to add the most severely asphyxiated babies to our study group during the next year. 2) Effect of Seizures on Cerebral MRS: We have demonstrated dramatic, reversible changes in the phosphorus spectra during neonatal seizures (see report). During the coming year, we will study a more diverse group of babies with seizures. When the NIH Regional Resource Spectrometer is installed and approved for human studies, we plan to study older children with seizure disorders. 3) MRS in Pediatric Neuromuscular Disorders: Our recent study (see report) suggests that MRS may be helpful in evaluating and following children with muscular dystrophy. During the next year, we plan to continue our preliminary work by studying additional patients with Duchenne Dystrophy (n=10), Becker Dystrophy (n=10), carriers for these disorders (n=10), and repeating studies on the patients already evaluated. We have also made arrangements to study a few patients with Duchenne Dystrophy who are being treated with penicillamine. 4) Animal Model of Perinatal Asphyxia: Despite the importance of perinatal asphyxia, a good animal model of this disorder is not available. As mentioned in Section 1 and in the report, our studies in asphyxiated infants suggest that there are 3 distinct patterns of metabolic changes following perinatal asphyxia. During the next year, we will try to create these patterns in newborn puppies. If we are successful, they will be correlated with neuropathologic change.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Academic/Teacher Award (ATA) (K07)
Project #
5K07NS000774-04
Application #
3078131
Study Section
Neurological Disorders Program Project Review B Committee (NSPB)
Project Start
1983-01-01
Project End
1987-12-31
Budget Start
1986-01-01
Budget End
1986-12-31
Support Year
4
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Younkin, D; Delivoria-Papadopoulos, M; Reivich, M et al. (1988) Regional variations in human newborn cerebral blood flow. J Pediatr 112:104-8
Younkin, D; Medoff-Cooper, B; Guillet, R et al. (1988) In vivo 31P nuclear magnetic resonance measurement of chronic changes in cerebral metabolites following neonatal intraventricular hemorrhage. Pediatrics 82:331-6
Younkin, D P; Berman, P; Sladky, J et al. (1987) 31P NMR studies in Duchenne muscular dystrophy: age-related metabolic changes. Neurology 37:165-9
Younkin, D P (1987) Phosphorus nuclear magnetic resonance spectroscopy in neonatal disorders. Mead Johnson Symp Perinat Dev Med :19-25
Younkin, D P; Reivich, M; Jaggi, J L et al. (1987) The effect of hematocrit and systolic blood pressure on cerebral blood flow in newborn infants. J Cereb Blood Flow Metab 7:295-9
Younkin, D P; Delivoria-Papadopoulos, M; Maris, J et al. (1986) Cerebral metabolic effects of neonatal seizures measured with in vivo 31P NMR spectroscopy. Ann Neurol 20:513-9
Younkin, D; Hungerbuhler, J P; O'Connor, M et al. (1985) Superficial temporal-middle cerebral artery anastomosis: effects on vascular, neurologic, and neuropsychological functions. Neurology 35:462-9