Magnetic Resonance Imaging Outcomes From a Comprehensive Magnetic Resonance Study of Children With Fetal Alcohol Spectrum Disorders

Background:  Magnetic resonance (MR) technology offers noninvasive methods for in vivo assessment of neuroabnormalities. Methods:  A comprehensive neuropsychological/psychiatric battery, coupled with MR imaging, (MRI), MR spectroscopy (MRS), and functional MRI (fMRI) assessments, were administered t...

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Veröffentlicht in:Alcoholism, clinical and experimental research clinical and experimental research, 2009-10, Vol.33 (10), p.1671-1689
Hauptverfasser: Astley, Susan J., Aylward, Elizabeth H., Olson, Heather Carmichael, Kerns, Kimberly, Brooks, Allison, Coggins, Truman E., Davies, Julian, Dorn, Susan, Gendler, Beth, Jirikowic, Tracy, Kraegel, Paul, Maravilla, Kenneth, Richards, Todd
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container_end_page 1689
container_issue 10
container_start_page 1671
container_title Alcoholism, clinical and experimental research
container_volume 33
creator Astley, Susan J.
Aylward, Elizabeth H.
Olson, Heather Carmichael
Kerns, Kimberly
Brooks, Allison
Coggins, Truman E.
Davies, Julian
Dorn, Susan
Gendler, Beth
Jirikowic, Tracy
Kraegel, Paul
Maravilla, Kenneth
Richards, Todd
description Background:  Magnetic resonance (MR) technology offers noninvasive methods for in vivo assessment of neuroabnormalities. Methods:  A comprehensive neuropsychological/psychiatric battery, coupled with MR imaging, (MRI), MR spectroscopy (MRS), and functional MRI (fMRI) assessments, were administered to children with fetal alcohol spectrum disorders (FASD) to determine if global and/or focal abnormalities could be identified, and distinguish diagnostic subclassifications across the spectrum. The 4 study groups included: (i) fetal alcohol syndrome (FAS)/partial FAS (PFAS); (ii) static encephalopathy/alcohol exposed (SE/AE); (iii) neurobehavioral disorder/alcohol exposed (ND/AE) as diagnosed with the FASD 4‐Digit Code; and (iv) healthy peers with no prenatal alcohol exposure. Presented here are the MRI assessments that were used to compare the sizes of brain regions between the 4 groups. The neuropsychological/behavioral, MRS, and fMRI outcomes are reported separately. Results:  Progressing across the 4 study groups from Controls to ND/AE to SE/AE to FAS/PFAS, the mean absolute size of the total brain, frontal lobe, caudate, putamen, hippocampus, cerebellar vermis, and corpus callosum length decreased incrementally and significantly. The FAS/PFAS group (the only group with the 4‐Digit FAS facial phenotype) had disproportionately smaller frontal lobes relative to all other groups. The FAS/PFAS and SE/AE groups [the 2 groups with the most severe central nervous system (CNS) dysfunction] had disproportionately smaller caudate regions relative to the ND/AE and Control groups. The prevalence of subjects in the FAS/PFAS, SE/AE, and ND/AE groups that had 1 or more brain regions, 2 or more SDs below the mean size observed in the Control group was 78, 58, and 43%, respectively. Significant correlations were observed between size of brain regions and level of prenatal alcohol exposure, magnitude of FAS facial phenotype, and level of CNS dysfunction. Conclusions:  Magnetic resonance imaging provided further validation that ND/AE, SE/AE, and FAS/PFAS as defined by the FASD 4‐Digit Code are 3 clinically distinct and increasingly more affected diagnostic subclassifications under the umbrella of FASD. Neurostructural abnormalities are present across the spectrum. MRI could importantly augment diagnosis of conditions under the umbrella of FASD, once population‐based norms for structural development of the human brain are established.
doi_str_mv 10.1111/j.1530-0277.2009.01004.x
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Methods:  A comprehensive neuropsychological/psychiatric battery, coupled with MR imaging, (MRI), MR spectroscopy (MRS), and functional MRI (fMRI) assessments, were administered to children with fetal alcohol spectrum disorders (FASD) to determine if global and/or focal abnormalities could be identified, and distinguish diagnostic subclassifications across the spectrum. The 4 study groups included: (i) fetal alcohol syndrome (FAS)/partial FAS (PFAS); (ii) static encephalopathy/alcohol exposed (SE/AE); (iii) neurobehavioral disorder/alcohol exposed (ND/AE) as diagnosed with the FASD 4‐Digit Code; and (iv) healthy peers with no prenatal alcohol exposure. Presented here are the MRI assessments that were used to compare the sizes of brain regions between the 4 groups. The neuropsychological/behavioral, MRS, and fMRI outcomes are reported separately. Results:  Progressing across the 4 study groups from Controls to ND/AE to SE/AE to FAS/PFAS, the mean absolute size of the total brain, frontal lobe, caudate, putamen, hippocampus, cerebellar vermis, and corpus callosum length decreased incrementally and significantly. The FAS/PFAS group (the only group with the 4‐Digit FAS facial phenotype) had disproportionately smaller frontal lobes relative to all other groups. The FAS/PFAS and SE/AE groups [the 2 groups with the most severe central nervous system (CNS) dysfunction] had disproportionately smaller caudate regions relative to the ND/AE and Control groups. The prevalence of subjects in the FAS/PFAS, SE/AE, and ND/AE groups that had 1 or more brain regions, 2 or more SDs below the mean size observed in the Control group was 78, 58, and 43%, respectively. Significant correlations were observed between size of brain regions and level of prenatal alcohol exposure, magnitude of FAS facial phenotype, and level of CNS dysfunction. Conclusions:  Magnetic resonance imaging provided further validation that ND/AE, SE/AE, and FAS/PFAS as defined by the FASD 4‐Digit Code are 3 clinically distinct and increasingly more affected diagnostic subclassifications under the umbrella of FASD. Neurostructural abnormalities are present across the spectrum. 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Methods:  A comprehensive neuropsychological/psychiatric battery, coupled with MR imaging, (MRI), MR spectroscopy (MRS), and functional MRI (fMRI) assessments, were administered to children with fetal alcohol spectrum disorders (FASD) to determine if global and/or focal abnormalities could be identified, and distinguish diagnostic subclassifications across the spectrum. The 4 study groups included: (i) fetal alcohol syndrome (FAS)/partial FAS (PFAS); (ii) static encephalopathy/alcohol exposed (SE/AE); (iii) neurobehavioral disorder/alcohol exposed (ND/AE) as diagnosed with the FASD 4‐Digit Code; and (iv) healthy peers with no prenatal alcohol exposure. Presented here are the MRI assessments that were used to compare the sizes of brain regions between the 4 groups. The neuropsychological/behavioral, MRS, and fMRI outcomes are reported separately. Results:  Progressing across the 4 study groups from Controls to ND/AE to SE/AE to FAS/PFAS, the mean absolute size of the total brain, frontal lobe, caudate, putamen, hippocampus, cerebellar vermis, and corpus callosum length decreased incrementally and significantly. The FAS/PFAS group (the only group with the 4‐Digit FAS facial phenotype) had disproportionately smaller frontal lobes relative to all other groups. The FAS/PFAS and SE/AE groups [the 2 groups with the most severe central nervous system (CNS) dysfunction] had disproportionately smaller caudate regions relative to the ND/AE and Control groups. The prevalence of subjects in the FAS/PFAS, SE/AE, and ND/AE groups that had 1 or more brain regions, 2 or more SDs below the mean size observed in the Control group was 78, 58, and 43%, respectively. Significant correlations were observed between size of brain regions and level of prenatal alcohol exposure, magnitude of FAS facial phenotype, and level of CNS dysfunction. Conclusions:  Magnetic resonance imaging provided further validation that ND/AE, SE/AE, and FAS/PFAS as defined by the FASD 4‐Digit Code are 3 clinically distinct and increasingly more affected diagnostic subclassifications under the umbrella of FASD. Neurostructural abnormalities are present across the spectrum. MRI could importantly augment diagnosis of conditions under the umbrella of FASD, once population‐based norms for structural development of the human brain are established.</description><subject>Abnormalities, Drug-Induced - pathology</subject><subject>Alcohol Drinking</subject><subject>Alcoholism and acute alcohol poisoning</subject><subject>Analysis of Variance</subject><subject>Basal Ganglia - pathology</subject><subject>Biological and medical sciences</subject><subject>Brain - pathology</subject><subject>Cerebellum - pathology</subject><subject>Child</subject><subject>Corpus Callosum - pathology</subject><subject>FASD 4-Digit Diagnostic Code</subject><subject>Female</subject><subject>Fetal Alcohol Spectrum Disorder</subject><subject>Fetal Alcohol Spectrum Disorders - diagnosis</subject><subject>Fetal Alcohol Spectrum Disorders - pathology</subject><subject>Frontal Lobe - pathology</subject><subject>Hippocampus - pathology</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>Magnetic Resonance Imaging</subject><subject>Medical sciences</subject><subject>Neuropsychological Tests</subject><subject>Pregnancy</subject><subject>Psychiatric Status Rating Scales</subject><subject>Sample Size</subject><subject>Socioeconomic Factors</subject><subject>Toxicology</subject><issn>0145-6008</issn><issn>1530-0277</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcFv0zAUxiMEYmXwLyBf4JZgx46dXJCqsJZJG0PbUI-W47w0Lknc2cloz_zjJLTqQOKAL7b0vu_3nt8XBIjgiIznwyYiCcUhjoWIYoyzCBOMWbR7FsxOhefBDBOWhBzj9Cx45f0Gj5qU85fBGckSEWcpnwU_r9W6g95odAvedqrTgC5btTbdGt0MvbYteLRwtkUK5bbdOqih8-YR0D-Md_1Q7pGtUF6bpnTQoZXpa7SAXjVo3mhb2wbdbUH3bmjRJ-OtK8H518GLSjUe3hzv8-Db4uI-_xxe3Swv8_lVqBNBWVgQCpgWZVUyRiFJGZCyZAA0iVWaQQWCFbxIEsaISDnDaUZoqXkpADhTjNDz4OOBux2KFkoNXe9UI7fOtMrtpVVG_l3pTC3X9lGOQJyKdAS8PwKcfRjA97I1XkPTqA7s4GVMMB83nI3C9CDUznrvoDo1IVhOCcqNnIKSU1BySlD-TlDuRuvbP4d8Mh4jGwXvjgLltWoqN67e-JMuJlkmYsqffvvDNLD_7wHkPL-4nZ4jIDwAjO9hdwIo911yQUUiV1-WcrFaXt-Tr0xS-guMtsj6</recordid><startdate>200910</startdate><enddate>200910</enddate><creator>Astley, Susan J.</creator><creator>Aylward, Elizabeth H.</creator><creator>Olson, Heather Carmichael</creator><creator>Kerns, Kimberly</creator><creator>Brooks, Allison</creator><creator>Coggins, Truman E.</creator><creator>Davies, Julian</creator><creator>Dorn, Susan</creator><creator>Gendler, Beth</creator><creator>Jirikowic, Tracy</creator><creator>Kraegel, Paul</creator><creator>Maravilla, Kenneth</creator><creator>Richards, Todd</creator><general>Blackwell Publishing Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>200910</creationdate><title>Magnetic Resonance Imaging Outcomes From a Comprehensive Magnetic Resonance Study of Children With Fetal Alcohol Spectrum Disorders</title><author>Astley, Susan J. ; 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Methods:  A comprehensive neuropsychological/psychiatric battery, coupled with MR imaging, (MRI), MR spectroscopy (MRS), and functional MRI (fMRI) assessments, were administered to children with fetal alcohol spectrum disorders (FASD) to determine if global and/or focal abnormalities could be identified, and distinguish diagnostic subclassifications across the spectrum. The 4 study groups included: (i) fetal alcohol syndrome (FAS)/partial FAS (PFAS); (ii) static encephalopathy/alcohol exposed (SE/AE); (iii) neurobehavioral disorder/alcohol exposed (ND/AE) as diagnosed with the FASD 4‐Digit Code; and (iv) healthy peers with no prenatal alcohol exposure. Presented here are the MRI assessments that were used to compare the sizes of brain regions between the 4 groups. The neuropsychological/behavioral, MRS, and fMRI outcomes are reported separately. Results:  Progressing across the 4 study groups from Controls to ND/AE to SE/AE to FAS/PFAS, the mean absolute size of the total brain, frontal lobe, caudate, putamen, hippocampus, cerebellar vermis, and corpus callosum length decreased incrementally and significantly. The FAS/PFAS group (the only group with the 4‐Digit FAS facial phenotype) had disproportionately smaller frontal lobes relative to all other groups. The FAS/PFAS and SE/AE groups [the 2 groups with the most severe central nervous system (CNS) dysfunction] had disproportionately smaller caudate regions relative to the ND/AE and Control groups. The prevalence of subjects in the FAS/PFAS, SE/AE, and ND/AE groups that had 1 or more brain regions, 2 or more SDs below the mean size observed in the Control group was 78, 58, and 43%, respectively. Significant correlations were observed between size of brain regions and level of prenatal alcohol exposure, magnitude of FAS facial phenotype, and level of CNS dysfunction. Conclusions:  Magnetic resonance imaging provided further validation that ND/AE, SE/AE, and FAS/PFAS as defined by the FASD 4‐Digit Code are 3 clinically distinct and increasingly more affected diagnostic subclassifications under the umbrella of FASD. Neurostructural abnormalities are present across the spectrum. MRI could importantly augment diagnosis of conditions under the umbrella of FASD, once population‐based norms for structural development of the human brain are established.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>19572986</pmid><doi>10.1111/j.1530-0277.2009.01004.x</doi><tpages>19</tpages><oa>free_for_read</oa></addata></record>
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ispartof Alcoholism, clinical and experimental research, 2009-10, Vol.33 (10), p.1671-1689
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Journals@Ovid Complete
subjects Abnormalities, Drug-Induced - pathology
Alcohol Drinking
Alcoholism and acute alcohol poisoning
Analysis of Variance
Basal Ganglia - pathology
Biological and medical sciences
Brain - pathology
Cerebellum - pathology
Child
Corpus Callosum - pathology
FASD 4-Digit Diagnostic Code
Female
Fetal Alcohol Spectrum Disorder
Fetal Alcohol Spectrum Disorders - diagnosis
Fetal Alcohol Spectrum Disorders - pathology
Frontal Lobe - pathology
Hippocampus - pathology
Humans
Image Processing, Computer-Assisted
Magnetic Resonance Imaging
Medical sciences
Neuropsychological Tests
Pregnancy
Psychiatric Status Rating Scales
Sample Size
Socioeconomic Factors
Toxicology
title Magnetic Resonance Imaging Outcomes From a Comprehensive Magnetic Resonance Study of Children With Fetal Alcohol Spectrum Disorders
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