Effect of prematurity and intrauterine growth restriction on H-reflex recovery cycle in neonates

B D Bhatia1, Ayan Kumar, Deepshikha

  • 1Department of Pediatrics, Unit of Neonatology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India. baldev bhatia@rediffmail.com

Neuroscience Letters
|September 7, 2010
PubMed

Insights

Preterm infants show delayed spinal cord synapse function compared to full-term babies, impacting H-reflex recovery. This suggests potential neurotransmitter depletion in preterm neonates, affecting neural development.

Area of Science:

  • Neuroscience
  • Developmental Biology
  • Pediatrics

Background:

  • Spinal cord synapse development is crucial for motor function.
  • Prematurity and intrauterine growth restriction can impact neurological development.
  • The H-reflex is a valuable tool for assessing spinal cord reflex pathways.

Purpose of the Study:

  • To evaluate the impact of prematurity and intrauterine growth restriction on spinal cord synapses.
  • To compare H-reflex parameters in full-term appropriate for gestational age (FT AGA), full-term intrauterine growth restricted (FT IUGR), and preterm appropriate for gestational age (PT AGA) neonates.

Main Methods:

  • Investigated 33 neonates: 14 FT AGA, 10 FT IUGR, and 9 PT AGA.
  • Recorded H-reflex parameters including Hmax, HRL, H/M ratio, HRCV, and HRRC.
  • Utilized double stimuli technique to assess H-reflex recovery cycle in the soleus muscle.

Main Results:

  • H-reflex recovery was significantly lower in PT AGA neonates compared to FT AGA and FT IUGR groups.
  • No significant differences in H-reflex parameters were found between FT AGA and FT IUGR groups.
  • H-reflex latency (HRL) and H-reflex conduction velocity (HRCV) were significantly affected in the PT AGA group.

Conclusions:

  • Delayed H-reflex recovery in preterm infants may indicate prolonged neurotransmitter delay at Ia terminals.
  • This delay could stem from reduced neurotransmitter stores in synaptic vesicles within the preterm spinal cord.
  • Findings highlight potential synaptic functional deficits in preterm neonates.
Abstract