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Neurodevelopmental Reflex Testing in Neonatal Rat Pups
Published on: April 24, 2017
H-reflex and motor nerve conduction studies in growth retarded newborn babies
Narendra Reddy Dereddy1, Sunil Muthusami, B D Bhatia
1Department of Pediatrics, Unit of Neonatology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
Insights
Full-term intrauterine growth-retarded (IUGR) babies show faster postnatal neural maturation. By two months, their motor nerve conduction velocity matches that of appropriate-for-gestational-age (AGA) babies, compensating for early deficits.
Area of Science:
- Neonatal neurology
- Developmental pediatrics
- Neurophysiology
Background:
- Intrauterine growth restriction (IUGR) can lead to deficits in early development.
- Peripheral myelination is crucial for normal neurological function.
- Compensatory mechanisms may exist in growth-restricted infants.
Purpose of the Study:
- To investigate accelerated postnatal neural maturation in full-term IUGR infants.
- To compare peripheral nerve function between IUGR and appropriate-for-gestational-age (AGA) infants.
- To assess catch-up myelination in IUGR neonates.
Main Methods:
- Studied 16 full-term AGA and 10 full-term IUGR infants at birth and 2 months.
- Measured H-reflex latency (HRL), motor nerve conduction velocity (MNCV), and H-reflex excitability (H/M).
- Recorded anthropometric measurements and conducted clinical neurological evaluations.
Main Results:
- At birth, IUGR infants had significantly lower MNCV than AGA infants.
- At 2 months, MNCV was comparable between IUGR and AGA infants.
- HRL and H/M were similar between groups at both time points; IUGR infants remained smaller.
Conclusions:
- Full-term IUGR infants exhibit accelerated postnatal peripheral nerve maturation.
- Rapid postnatal myelination in IUGR infants leads to neurological equivalence with AGA peers by 2 months.
- Despite catch-up in nerve function, anthropometric deficits persist in IUGR infants.
Objective:
To demonstrate the accelerated postnatal maturation/myelination in growth retarded babies compensating the deficit suffered by them during intrauterine life.
Methods:
We studied 16 babies within the first 3 days of birth. These included 6 full term appropriate for gestational age babies (FT AGA) and 10 full term intrauterine growth retarded (FT IUGR). A separate group of 16 babies was examined at 2 months of age. In this group 7 were FT AGA and 9 were FT IUGR at the time of birth. H-reflex latency (HRL), motor nerve conduction velocity (MNCV) and H-reflex excitability (H/M) were measured in the right lower limb. Anthropometric measurements of the babies were also recorded meticulously. All the babies were neurologically normal on clinical evaluation.
Result:
At birth, MNCV was significantly lower in FT IUGR babies compared to FT AGA babies. However at the age of 2 months the MNCV of both FT AGA and FT IUGR was comparable. Other parameters (HRL and H/M) in the IUGR babies were comparable with normal babies both at birth and 2 months of age. In FT IUGR babies crown-heel length and weight was significantly lower than FT AGA babies both at the time of birth and at 2 months of age.
Conclusion And Significance:
The findings suggest that FT IUGR babies demonstrate accelerated postnatal peripheral neural maturation. At 2 months of age, the motor nerve conduction velocity of these growth retarded babies was comparable to that observed in normal AGA babies of similar age. This provides an insight into the functional aspect of the proven theories of decreased peripheral myelination in FT IUGR babies with subsequent rapid postnatal myelination that renders these babies neurologically equivalent to FT AGA babies despite not achieving comparable anthropometric parameters.
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