Literature DB >> 9606249

Magnetic resonance imaging and spectroscopy of regional brain structure in a 10-year-old boy with elevated blood lead levels.

I Trope1, D Lopez-Villegas, R E Lenkinski.   

Abstract

OBJECTIVE: The effects of elevated blood lead levels on the development of children have been examined only in the context of behavioral and neuropsychological evaluations. No studies have examined the effects of lead on brain metabolism in vivo or on structural and/or functional correlates of brain function in children. In the human brain, magnetic resonance spectroscopy (MRS) provides a noninvasive, risk-free method to monitor the biochemistry of acute and chronic stages of disease. The purpose of this study was to examine in vivo the use of MRS for the evaluation of the neurotoxic effects of lead on the nervous system, by detection of brain metabolism, especially N-acetylaspartate, a metabolite shown to decrease in processes that involve neuronal loss.
METHODOLOGY: Two male cousins who live in the same household and share the same socioeconomic background and home environment were studied. The subject, a 10-year-old boy, had elevated blood lead levels. His cousin, a 9-year-old boy, was not exposed to lead. Both underwent a comprehensive neuropsychological evaluation and both were evaluated using the magnetic resonance imaging (MRI) and MRS at the University of Pennsylvania Medical Center. High-resolution MRI and MRS were performed using a 3-in surface coil. Localized proton spectra were obtained from contiguous 6 x 6 x 10-mm voxels using one-dimensional phase encoding, with a 2000-millisecond repetition time and a 31-millisecond echo time.
RESULTS: Neuropsychological evaluation demonstrated areas of impairment in the lead-exposed child, including difficulties in academic skills of reading, writing, and arithmetic, as well as deficient linguistic skills and attentional mechanism. By contrast, studies of the cousin, who was not exposed to lead, showed overall neuropsychological functioning within normal limits. Although both children had a normal MRI examination of the brain, studies of the lead-exposed boy showed a significant alteration in brain metabolites, with a reduction in the N-acetylaspartate:creatine ratio for both gray and white matter on the MRS examination, compared with his cousin.
CONCLUSIONS: The present study is a first attempt to determine in vivo metabolic differences in the brain of a child exposed to lead compared with a healthy control subject. This is a unique case because these children were matched on a number of variables usually regarded as confounders in behavioral lead studies, and therefore can be regarded as matched controls. The present study demonstrates that MRS is a feasible, noninvasive technique for in vivo examination of the brains of children exposed to lead. We were able to obtain high-quality spectra from voxels as small as 0.36 cm at 1.5T. The spatial resolution used in the present study is sufficient to obtain spectra from voxels almost exclusively composed of gray matter. The one-dimensional phase-encoding approach used presents the advantage of obtaining several spectra simultaneously in a relatively short time. The present study has allowed us to examine the spectroscopic patterns of frontal gray and white matter after lead exposure relative to the normal pattern seen in healthy children and adults. The MRS study of the healthy, nonlead-exposed cousin demonstrated spectra entirely consistent with the spectral pattern reported in previous studies of healthy individuals. By contrast, the spectra obtained from the lead-exposed child deviated from the expected pattern in all metabolite ratios analyzed. Because N-acetylaspartate has been shown as a measure of neuronal viability, the level of N-acetylaspartate may enable us to evaluate the degree of neuronal loss in children exposed to lead. The MRI examination indicated no structural abnormalities or cortical thinning, and no abnormal findings in either case. By contrast, MRS indicated a significant change from normal values for the lead-exposed child. This supports the idea that lead neurodevelopmental toxicity may be related to inter

Entities:  

Mesh:

Year:  1998        PMID: 9606249     DOI: 10.1542/peds.101.6.e7

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  10 in total

1.  Evidence for altered hippocampal volume and brain metabolites in workers occupationally exposed to lead: a study by magnetic resonance imaging and (1)H magnetic resonance spectroscopy.

Authors:  Yue-Ming Jiang; Li-Ling Long; Xia-Yan Zhu; Hong Zheng; Xue Fu; Shi-Yan Ou; Dong-Lu Wei; Hai-Lin Zhou; Wei Zheng
Journal:  Toxicol Lett       Date:  2008-07-23       Impact factor: 4.372

2.  Brain proton magnetic resonance spectroscopy and imaging in children exposed to cocaine in utero.

Authors:  L M Smith; L Chang; M L Yonekura; K Gilbride; J Kuo; R E Poland; I Walot; T Ernst
Journal:  Pediatrics       Date:  2001-02       Impact factor: 7.124

Review 3.  Allelic variation and environmental lead exposure in urban children.

Authors:  Jacquelyn Long; Chandice Covington; Virginia Delaney-Black; Beth Nordstrom
Journal:  AACN Clin Issues       Date:  2002-11

Review 4.  Is lead exposure in early life an environmental risk factor for Schizophrenia? Neurobiological connections and testable hypotheses.

Authors:  Tomás R Guilarte; Mark Opler; Mikhail Pletnikov
Journal:  Neurotoxicology       Date:  2011-12-09       Impact factor: 4.294

5.  A proton magnetic resonance spectroscopy study of the chronic lead effect on the Basal ganglion and frontal and occipital lobes in middle-age adults.

Authors:  Tsyh-Jyi Hsieh; Yi-Chun Chen; Chun-Wei Li; Gin-Chang Liu; Yu-Wen Chiu; Hung-Yi Chuang
Journal:  Environ Health Perspect       Date:  2009-02-09       Impact factor: 9.031

Review 6.  Neurotoxic effects and biomarkers of lead exposure: a review.

Authors:  Talia Sanders; Yiming Liu; Virginia Buchner; Paul B Tchounwou
Journal:  Rev Environ Health       Date:  2009 Jan-Mar       Impact factor: 3.458

Review 7.  Neuroimaging is a novel tool to understand the impact of environmental chemicals on neurodevelopment.

Authors:  Megan K Horton; Amy E Margolis; Cheuk Tang; Robert Wright
Journal:  Curr Opin Pediatr       Date:  2014-04       Impact factor: 2.856

8.  Proton magnetic resonance spectroscopy in adults with childhood lead exposure.

Authors:  Kim M Cecil; Kim N Dietrich; Mekibib Altaye; John C Egelhoff; Diana M Lindquist; Christopher J Brubaker; Bruce P Lanphear
Journal:  Environ Health Perspect       Date:  2010-10-13       Impact factor: 9.031

9.  Proton magnetic resonance spectroscopic evidence of glial effects of cumulative lead exposure in the adult human hippocampus.

Authors:  Marc G Weisskopf; Howard Hu; David Sparrow; Robert E Lenkinski; Robert O Wright
Journal:  Environ Health Perspect       Date:  2007-01-03       Impact factor: 9.031

Review 10.  Pediatric Exposures to Neurotoxicants: A Review of Magnetic Resonance Imaging and Spectroscopy Findings.

Authors:  Kim M Cecil
Journal:  Diagnostics (Basel)       Date:  2022-03-05
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.