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Research article summary (published 18 Feb 2007):

Abnormal flash visual evoked potentials in malnourished infants: an evaluation using principal component analysis.

Full Abstract

OBJECTIVE:
To characterize the morphology of flash visual evoked potentials (fVEPs) obtained from infants hospitalized with severe, chronic malnutrition (marasmus).

METHODS:
A covariance-based principal component analysis with Promax factor rotation was applied to fVEPs obtained from malnourished infants and age-matched control subjects.

RESULTS:
The analysis suggests the presence of a late positive complex in the fVEP, with at least one of its components being significantly diminished in marasmic infants. The N3 component was also diminished in marasmic infants. Following remediation, the marasmic group no longer differed with respect to these components. However, an abnormally large late, positive deflection was evident at discharge.

CONCLUSIONS:
The fVEP morphology of infants hospitalized with severe malnutrition was found to be significantly different from age-matched controls. Moreover, although there was evidence of recovery following remediation, fVEPs continued to show abnormality at discharge, suggesting the possibility that nutritional rehabilitation did not fully eliminate the physiological deficit.

SIGNIFICANCE:
Malnourishment during early infancy results in altered neurophysiological functioning, possibly in cortical areas responsible for higher order visual processing.

 

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Author information

Author/s: McDonald, Craig G (CG); Joffe, Cora L (CL); Barnet, Ann B (AB); Flinn, Jane M (JM);

Affiliation: Department of Psychology, George Mason University, Fairfax, VA, USA. cmcdona3(-atsign-)gmu.edu

Journal and publication information

Publication Type: Journal Article

Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology (Clin Neurophysiol), published in Netherlands. (Language: eng)

Reference: 2007-Apr; vol 118 (issue 4) : pp 896-900

Dates: Created 2007/03/12; Completed 2007/05/15; Revised 2008/09/10;

PMID: 17317298, status: MEDLINE (last retrieval date: 12/26/2008)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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