Three-dimensional surface deformation-based shape analysis of hippocampus and caudate nucleus in children with fetal alcohol spectrum disorders
Surface deformation‐based analysis was used to assess local shape variations in the hippocampi and caudate nuclei of children with fetal alcohol spectrum disorders. High‐resolution structural magnetic resonance imaging images were acquired for 31 children (19 controls and 12 children diagnosed with...
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Published in | Human brain mapping Vol. 35; no. 2; pp. 659 - 672 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Blackwell Publishing Ltd
01.02.2014
Wiley-Liss John Wiley & Sons, Inc John Wiley and Sons Inc |
Subjects | |
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Abstract | Surface deformation‐based analysis was used to assess local shape variations in the hippocampi and caudate nuclei of children with fetal alcohol spectrum disorders. High‐resolution structural magnetic resonance imaging images were acquired for 31 children (19 controls and 12 children diagnosed with fetal alcohol syndrome/partial FAS). Hippocampi and caudate nuclei were manually segmented, and surface meshes were reconstructed. An iterative closest point algorithm was used to register the template of one control subject to all other shapes in order to capture the true geometry of the shape with a fixed number of landmark points. A point distribution model was used to quantify the shape variations in terms of a change in co‐ordinate positions. Using the localized Hotelling T2 method, regions of significant shape variations between the control and exposed subjects were identified and mapped onto the mean shapes. Binary masks of hippocampi and caudate nuclei were generated from the segmented volumes of each brain. These were used to compute the volumes and for further statistical analysis. The Mann–Whitney test was performed to predict volume differences between the groups. Although the exposed and control subjects did not differ significantly in their volumes, the shape analysis showed the hippocampus to be more deformed at the head and tail regions in the alcohol‐exposed children. Between‐group differences in caudate nucleus morphology were dispersed across the tail and head regions. Correlation analysis showed associations between the degree of compression and the level of alcohol exposure. These findings demonstrate that shape analysis using three‐dimensional surface measures is sensitive to fetal alcohol exposure and provides additional information than volumetric measures alone. Hum Brain Mapp 35:659–672, 2014. © 2012 Wiley Periodicals, Inc. |
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AbstractList | Surface deformation-based analysis was used to assess local shape variations in the hippocampi and caudate nuclei of children with fetal alcohol spectrum disorders. High-resolution structural magnetic resonance imaging images were acquired for 31 children (19 controls and 12 children diagnosed with fetal alcohol syndrome/partial FAS). Hippocampi and caudate nuclei were manually segmented, and surface meshes were reconstructed. An iterative closest point algorithm was used to register the template of one control subject to all other shapes in order to capture the true geometry of the shape with a fixed number of landmark points. A point distribution model was used to quantify the shape variations in terms of a change in co-ordinate positions. Using the localized Hotelling T(2) method, regions of significant shape variations between the control and exposed subjects were identified and mapped onto the mean shapes. Binary masks of hippocampi and caudate nuclei were generated from the segmented volumes of each brain. These were used to compute the volumes and for further statistical analysis. The Mann-Whitney test was performed to predict volume differences between the groups. Although the exposed and control subjects did not differ significantly in their volumes, the shape analysis showed the hippocampus to be more deformed at the head and tail regions in the alcohol-exposed children. Between-group differences in caudate nucleus morphology were dispersed across the tail and head regions. Correlation analysis showed associations between the degree of compression and the level of alcohol exposure. These findings demonstrate that shape analysis using three-dimensional surface measures is sensitive to fetal alcohol exposure and provides additional information than volumetric measures alone. Surface deformation‐based analysis was used to assess local shape variations in the hippocampi and caudate nuclei of children with fetal alcohol spectrum disorders. High‐resolution structural magnetic resonance imaging images were acquired for 31 children (19 controls and 12 children diagnosed with fetal alcohol syndrome/partial FAS). Hippocampi and caudate nuclei were manually segmented, and surface meshes were reconstructed. An iterative closest point algorithm was used to register the template of one control subject to all other shapes in order to capture the true geometry of the shape with a fixed number of landmark points. A point distribution model was used to quantify the shape variations in terms of a change in co‐ordinate positions. Using the localized Hotelling T 2 method, regions of significant shape variations between the control and exposed subjects were identified and mapped onto the mean shapes. Binary masks of hippocampi and caudate nuclei were generated from the segmented volumes of each brain. These were used to compute the volumes and for further statistical analysis. The Mann–Whitney test was performed to predict volume differences between the groups. Although the exposed and control subjects did not differ significantly in their volumes, the shape analysis showed the hippocampus to be more deformed at the head and tail regions in the alcohol‐exposed children. Between‐group differences in caudate nucleus morphology were dispersed across the tail and head regions. Correlation analysis showed associations between the degree of compression and the level of alcohol exposure. These findings demonstrate that shape analysis using three‐dimensional surface measures is sensitive to fetal alcohol exposure and provides additional information than volumetric measures alone. Hum Brain Mapp 35:659–672, 2014. © 2012 Wiley Periodicals, Inc. Surface deformation‐based analysis was used to assess local shape variations in the hippocampi and caudate nuclei of children with fetal alcohol spectrum disorders. High‐resolution structural magnetic resonance imaging images were acquired for 31 children (19 controls and 12 children diagnosed with fetal alcohol syndrome/partial FAS). Hippocampi and caudate nuclei were manually segmented, and surface meshes were reconstructed. An iterative closest point algorithm was used to register the template of one control subject to all other shapes in order to capture the true geometry of the shape with a fixed number of landmark points. A point distribution model was used to quantify the shape variations in terms of a change in co‐ordinate positions. Using the localized Hotelling T 2 method, regions of significant shape variations between the control and exposed subjects were identified and mapped onto the mean shapes. Binary masks of hippocampi and caudate nuclei were generated from the segmented volumes of each brain. These were used to compute the volumes and for further statistical analysis. The Mann–Whitney test was performed to predict volume differences between the groups. Although the exposed and control subjects did not differ significantly in their volumes, the shape analysis showed the hippocampus to be more deformed at the head and tail regions in the alcohol‐exposed children. Between‐group differences in caudate nucleus morphology were dispersed across the tail and head regions. Correlation analysis showed associations between the degree of compression and the level of alcohol exposure. These findings demonstrate that shape analysis using three‐dimensional surface measures is sensitive to fetal alcohol exposure and provides additional information than volumetric measures alone. Hum Brain Mapp 35:659–672, 2014. © 2012 Wiley Periodicals, Inc. Surface deformation-based analysis was used to assess local shape variations in the hippocampi and caudate nuclei of children with fetal alcohol spectrum disorders. High-resolution structural magnetic resonance imaging images were acquired for 31 children (19 controls and 12 children diagnosed with fetal alcohol syndrome/partial FAS). Hippocampi and caudate nuclei were manually segmented, and surface meshes were reconstructed. An iterative closest point algorithm was used to register the template of one control subject to all other shapes in order to capture the true geometry of the shape with a fixed number of landmark points. A point distribution model was used to quantify the shape variations in terms of a change in co-ordinate positions. Using the localized Hotelling T2 method, regions of significant shape variations between the control and exposed subjects were identified and mapped onto the mean shapes. Binary masks of hippocampi and caudate nuclei were generated from the segmented volumes of each brain. These were used to compute the volumes and for further statistical analysis. The Mann-Whitney test was performed to predict volume differences between the groups. Although the exposed and control subjects did not differ significantly in their volumes, the shape analysis showed the hippocampus to be more deformed at the head and tail regions in the alcohol-exposed children. Between-group differences in caudate nucleus morphology were dispersed across the tail and head regions. Correlation analysis showed associations between the degree of compression and the level of alcohol exposure. These findings demonstrate that shape analysis using three-dimensional surface measures is sensitive to fetal alcohol exposure and provides additional information than volumetric measures alone. Hum Brain Mapp 35:659-672, 2014. © 2012 Wiley Periodicals, Inc. [PUBLICATION ABSTRACT] Surface deformation-based analysis was used to assess local shape variations in the hippocampi and caudate nuclei of children with fetal alcohol spectrum disorders. High-resolution structural magnetic resonance imaging images were acquired for 31 children (19 controls and 12 children diagnosed with fetal alcohol syndrome/partial FAS). Hippocampi and caudate nuclei were manually segmented, and surface meshes were reconstructed. An iterative closest point algorithm was used to register the template of one control subject to all other shapes in order to capture the true geometry of the shape with a fixed number of landmark points. A point distribution model was used to quantify the shape variations in terms of a change in co-ordinate positions. Using the localized Hotelling T(2) method, regions of significant shape variations between the control and exposed subjects were identified and mapped onto the mean shapes. Binary masks of hippocampi and caudate nuclei were generated from the segmented volumes of each brain. These were used to compute the volumes and for further statistical analysis. The Mann-Whitney test was performed to predict volume differences between the groups. Although the exposed and control subjects did not differ significantly in their volumes, the shape analysis showed the hippocampus to be more deformed at the head and tail regions in the alcohol-exposed children. Between-group differences in caudate nucleus morphology were dispersed across the tail and head regions. Correlation analysis showed associations between the degree of compression and the level of alcohol exposure. These findings demonstrate that shape analysis using three-dimensional surface measures is sensitive to fetal alcohol exposure and provides additional information than volumetric measures alone.Surface deformation-based analysis was used to assess local shape variations in the hippocampi and caudate nuclei of children with fetal alcohol spectrum disorders. High-resolution structural magnetic resonance imaging images were acquired for 31 children (19 controls and 12 children diagnosed with fetal alcohol syndrome/partial FAS). Hippocampi and caudate nuclei were manually segmented, and surface meshes were reconstructed. An iterative closest point algorithm was used to register the template of one control subject to all other shapes in order to capture the true geometry of the shape with a fixed number of landmark points. A point distribution model was used to quantify the shape variations in terms of a change in co-ordinate positions. Using the localized Hotelling T(2) method, regions of significant shape variations between the control and exposed subjects were identified and mapped onto the mean shapes. Binary masks of hippocampi and caudate nuclei were generated from the segmented volumes of each brain. These were used to compute the volumes and for further statistical analysis. The Mann-Whitney test was performed to predict volume differences between the groups. Although the exposed and control subjects did not differ significantly in their volumes, the shape analysis showed the hippocampus to be more deformed at the head and tail regions in the alcohol-exposed children. Between-group differences in caudate nucleus morphology were dispersed across the tail and head regions. Correlation analysis showed associations between the degree of compression and the level of alcohol exposure. These findings demonstrate that shape analysis using three-dimensional surface measures is sensitive to fetal alcohol exposure and provides additional information than volumetric measures alone. Surface deformation‐based analysis was used to assess local shape variations in the hippocampi and caudate nuclei of children with fetal alcohol spectrum disorders. High‐resolution structural magnetic resonance imaging images were acquired for 31 children (19 controls and 12 children diagnosed with fetal alcohol syndrome/partial FAS). Hippocampi and caudate nuclei were manually segmented, and surface meshes were reconstructed. An iterative closest point algorithm was used to register the template of one control subject to all other shapes in order to capture the true geometry of the shape with a fixed number of landmark points. A point distribution model was used to quantify the shape variations in terms of a change in co‐ordinate positions. Using the localized Hotelling T2 method, regions of significant shape variations between the control and exposed subjects were identified and mapped onto the mean shapes. Binary masks of hippocampi and caudate nuclei were generated from the segmented volumes of each brain. These were used to compute the volumes and for further statistical analysis. The Mann–Whitney test was performed to predict volume differences between the groups. Although the exposed and control subjects did not differ significantly in their volumes, the shape analysis showed the hippocampus to be more deformed at the head and tail regions in the alcohol‐exposed children. Between‐group differences in caudate nucleus morphology were dispersed across the tail and head regions. Correlation analysis showed associations between the degree of compression and the level of alcohol exposure. These findings demonstrate that shape analysis using three‐dimensional surface measures is sensitive to fetal alcohol exposure and provides additional information than volumetric measures alone. Hum Brain Mapp 35:659–672, 2014. © 2012 Wiley Periodicals, Inc. |
Author | Warton, Christopher Phillips, Owen R. Molteno, Chris D. Eicher, Anton Joseph, Jesuchristopher Marais, Patrick Meintjes, Ernesta M. Narr, Katherine L. Jacobson, Sandra W. Jacobson, Joseph L. |
AuthorAffiliation | 6 Laboratory of Neuro Imaging Department of Neurology Geffen School of Medicine at UCLA Los Angeles 3 Psychiatry and Behavioral Neurosciences Wayne State University School of Medicine Detroit 4 Department of Psychiatry and Mental Health Faculty of Health Sciences University of Cape Town South Africa 5 Department of Computer Science University of Cape Town South Africa 2 Department of Human Biology Faculty of Health Sciences University of Cape Town South Africa 1 MRC/UCT Medical Imaging Research Unit Faculty of Health Sciences University of Cape Town South Africa |
AuthorAffiliation_xml | – name: 4 Department of Psychiatry and Mental Health Faculty of Health Sciences University of Cape Town South Africa – name: 1 MRC/UCT Medical Imaging Research Unit Faculty of Health Sciences University of Cape Town South Africa – name: 3 Psychiatry and Behavioral Neurosciences Wayne State University School of Medicine Detroit – name: 5 Department of Computer Science University of Cape Town South Africa – name: 2 Department of Human Biology Faculty of Health Sciences University of Cape Town South Africa – name: 6 Laboratory of Neuro Imaging Department of Neurology Geffen School of Medicine at UCLA Los Angeles |
Author_xml | – sequence: 1 givenname: Jesuchristopher surname: Joseph fullname: Joseph, Jesuchristopher email: jesuinmit@gmail.com organization: MRC/UCT Medical Imaging Research Unit, Faculty of Health Sciences, University of Cape Town, South Africa – sequence: 2 givenname: Christopher surname: Warton fullname: Warton, Christopher organization: Department of Human Biology, Faculty of Health Sciences, University of Cape Town, South Africa – sequence: 3 givenname: Sandra W. surname: Jacobson fullname: Jacobson, Sandra W. organization: Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit – sequence: 4 givenname: Joseph L. surname: Jacobson fullname: Jacobson, Joseph L. organization: Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit – sequence: 5 givenname: Chris D. surname: Molteno fullname: Molteno, Chris D. organization: Department of Psychiatry and Mental Health, Faculty of Health Sciences, University of Cape Town, South Africa – sequence: 6 givenname: Anton surname: Eicher fullname: Eicher, Anton organization: Department of Computer Science, University of Cape Town, South Africa – sequence: 7 givenname: Patrick surname: Marais fullname: Marais, Patrick organization: Department of Computer Science, University of Cape Town, South Africa – sequence: 8 givenname: Owen R. surname: Phillips fullname: Phillips, Owen R. organization: Laboratory of Neuro Imaging, Department of Neurology, Geffen School of Medicine at UCLA, Los Angeles – sequence: 9 givenname: Katherine L. surname: Narr fullname: Narr, Katherine L. organization: Laboratory of Neuro Imaging, Department of Neurology, Geffen School of Medicine at UCLA, Los Angeles – sequence: 10 givenname: Ernesta M. surname: Meintjes fullname: Meintjes, Ernesta M. organization: MRC/UCT Medical Imaging Research Unit, Faculty of Health Sciences, University of Cape Town, South Africa |
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Keywords | Human Fetal alcohol syndrome Nervous system diseases Deformation Ethanol Radiodiagnosis Central nervous system Alcohol Basal ganglion shape analysis Three dimensional shape Surface analysis surface deformation Encephalon Newborn diseases Caudate nucleus Child Hippocampus caudate nucleus fetal alcohol syndrome hippocampus |
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PublicationTitleAlternate | Hum. Brain Mapp |
PublicationYear | 2014 |
Publisher | Blackwell Publishing Ltd Wiley-Liss John Wiley & Sons, Inc John Wiley and Sons Inc |
Publisher_xml | – name: Blackwell Publishing Ltd – name: Wiley-Liss – name: John Wiley & Sons, Inc – name: John Wiley and Sons Inc |
References | Gonzalo SB, Beatriz GA, Aitor S, Yolanda V, Manuel D, Jordi PC (2010): Manual validation of FreeSurfer's automated hippocampal segmentation in normal aging, mild cognitive impairment, and Alzheimer Disease subjects. Psychiatry Research: Neuroimaging 181:219-225. Narr KL, Thompson PM, Sharma T, Moussai J, Cannestra AF, Toga AW (2000): Mapping morphology of the corpus callosum in schizophrenia. Cereb Cortex 10:40-49. Rueckert D, Frangi A, Schnabel JA (2003): Automatic construction of 3-D statistical deformation models of the brain using nonrigid registration. IEEE Trans Med Imag 22:1014-1025. Mattson SN, Riley EP, Sowell ER, Jernigan TL, Sobel DF, Jones KL (1996): A decrease in the size of the basal ganglia in children with fetal alcohol syndrome. Alcohol Clin Exp Res 20:1088-1093. Sowell ER, Mattson SN, Thompson PM, Jernigan TL, Riley EP, Toga AW (2001a): Mapping callosal morphology and cognitive correlates: Effects of heavy prenatal alcohol exposure. Neurology 57:235-244. Archibald SL, Fennema-Notestine C, Gamst A, Riley EP, Mattson SN, Jernigan TL (2001): Brain dysmorphology in individuals with severe prenatal alcohol exposure. Dev Med Child Neurol 43:148-154. Kelemen A, Szekely G, Gerig G (1997): Three-dimensional model-based segmentation of brain MRI. Proc IEEE Int Workshop Model Based 3D Image Anal 178:828-839. Wright IC, McGuire PK, Poline JB, Travere JM, Murray RM, Frith CD, Frackowiak RS, Friston KJ (1995): A voxel-based method for the statistical analysis of gray and white matter density applied to schizophrenia. Neuroimage 2:244-252. Sullivan EV, Deshmukh A, Desmond JE, Lim KO, Pfefferbaum A (2000): Cerebellar volume decline in normal aging, alcoholism, and Korsakoff's syndrome: Relation to ataxia. Neuropsychology 14:341-352. Styner M, Lieberman JA, Pantazis D, Gerig G (2004): Boundary and medial shape analysis of the hippocampus in schizophrenia. Med Image Anal 8:197-203. Juergen M, George P, Thomas V (2007):Atlas of the Human Brain, Third Edition.Academic Press,280 p. Pfefferbaum A, Lim KO, Desmond JE, Sullivan EV (1996): Thinning of the corpus callosum in older alcoholic men: A magnetic resonance imaging study. Alcohol Clin Exp Res 20:752-757. Sullivan EV, Marsh L, Pfefferbaum A (2005): Preservation of hippocampal volume throughout adulthood in healthy men and women. Neurobiol Aging 26:1093-1098. May PA, Brooke L, Gossage JP, Croxford J, Adnams C, Jones KL, Robinson L, Viljoen D (2000): Epidemiology of fetal alcohol syndrome in a South African community in the Western Cape Province. Am J Publ Health 90:1905-1912. Fleute M, Lavallee S, Julliard R (1999): Incorporating a statistically based shape model into a system for computer-assisted anterior cruciate ligament surgery. Med Image Anal 3:209-222. Sullivan EV, Rosenbloom MJ, Serventi KL, Deshmukh A, Pfefferbaum A (2003): Effects of alcohol dependence comorbidity and antipsychotic medication on volumes of the thalamus and pons in schizophrenia. Am J Psychiatry 160,1110-1116. Meintjes EM, Jacobson JL, Molteno CD, Gatenby JC, Warton C, Cannistraci CJ, Hoyme HE, Robinson LK, Khaole N, Gore JC, Jacobson SW (2010): An FMRI study of number processing in children with fetal alcohol syndrome. Alcohol Clin Exp Res 34:1450-1464. Bookstein FL (1997): Landmark methods for forms without landmarks: Morphometrics of group differences in outline shape. Med Image Anal 1:225-243. Gerig G, Styner M, Shenton ME, Lieberman JA (2001): Shape versus size: Improved understanding of the morphology of brain structures. Med Image Comput Computer-Assist Interv 2208:24-32. Narr KL, Thompson PM, Szeszko P, Robinson D, Jang S, Woods RP, Kim S, Hayashi KM, Asunction D, Toga AW, Bilder RM (2004): Regional specificity of hippocampal volume reductions in first-episode schizophrenia. Neuroimage 21:1563-1575. Bookstein FL, Sampson PD, Connor PD, Streissguth AP (2002): Midline corpus callosum is a neuroanatomical focus of fetal alcohol damage. Anat Rec 269:162-174. Machado AMC, Gee JC (1998): Atlas warping for brain morphometry. Proc SPIE Med Imag Image Process 3338:642-651. Raz N, Gunning-Dixon F, Head D, Rodrigue KM, Williamson A, Acker JD (2004): Aging, sexual dimorphism, and hemispheric asymmetry of the cerebral cortex: Replicability of regional differences in volume. Neurobiol Aging 25:377-396. Astley SJ (2004):Diagnostic Guide for Fetal Alcohol Spectrum Disorders: The 4-Digit Diagnostic Code, 3rd ed.Seattle WA:University of Washington Publication Services. pp1-114. Duta N, Sonka M (1997): Segmentation and interpretation of MR brain images: An improved active shape model. IEEE Trans Med Imag 17:1049-1062. Jacobson SW, Warton C, Dodge NC, De Guio F, Molteno CD, Jacobson JL, Meintjes EM (2010): Differential vulnerability of three brain structures to fetal alcohol exposure: An MRI study of school-age children in Cape Town. Alcohol Clin Exp Res A 34:93. Shen L, Ford J, Makedon F, Saykin A (2004): A surface-based approach for classification of 3D neuroanatomical structures. Intell Data Anal 8:519-542. Sowell ER, Thompson PM, Mattson SN, Tessner KD, Jernigan TL, Riley EP, Toga AW (2001b): Voxel-based morphometric analyses of the brain in children and adolescents prenatally exposed to alcohol. Neuroreport 12:515-523. May PA, Gossage JP, Marais AS, Adnams CM, Hoyme HE, Jones KL, Robinson LK, Khaole NC, Snell C, Kalberg WO, Hendricks L, Brooke L, Stellavato C, Viljoen DL (2007): The epidemiology of fetal alcohol syndrome and partial FAS in a South African community. Drug Alcohol Depend 88:259-271. Cootes TF, Taylor CJ, Cooper DH, Graham J (1995): Active shape models-Their training and application. Computer Vis Image Understand 61:38-59. Yonggang S, Paul MT, Greig IZ, Stephen ER, Zhuowen T, Ivo D, Arthur WT (2007): Direct mapping of hippocampal surfaces with intrinsic shape context. Neuroimage 37:792-807. Besl PJ, McKay ND (1992): A method for registration of 3-d shapes. IEEE Trans Pattern Anal Mach Intell 14:239-256. Golland P, Grimson WEL, Kikinis R (1999): Statistical shape analysis using fixed topology skeletons: Corpus callosum Study. Inform Process Med Imag 1613:382-387. Mai J, Paxinos G, Voss T.2007.Atlas of the Human Brain, 3rd ed.New York:Academic Press. Kaus MR, Pekar V, Lorenz C, Truyen R, Lobregt S, Weese J (2003): Automated 3-D PDM construction from segmented images using deformable models. IEEE Trans Med Imag 22:1005-1013. Jacobson SW, Stanton ME, Dodge NC, Pienaar M, Fuller DS, Molteno CD, Meintjes EM, Hoyme HE, Robinson LK, Khaole N, Jacobson JL (2011): Impaired delay and trace eyeblink conditioning in school-age children with fetal alcohol syndrome. Alcohol Clin Exp Res 35:250-264. Manning MA, Hoyme HE (2007): Fetal alcohol spectrum disorders: A practical clinical approach to diagnosis. Neurosci Biobehav Rev 31:230-238. Bookstein FL, Sampson PD, Streissguth AP, Connor PD (2001): Geometric morphometrics of corpus callosum and subcortical structures in the fetal alcohol affected brain. Teratology 64:4-32. Woods RP (2003): Multitracer: A java-based tool for anatomic delineation of grayscale volumetric images. Neuroimage 19:1829-1834. Basso M, Yang J, Warren L, MacAvoy MG, Varma P, Bronen RA, Van Dyck CH (2006): Volumetry of amygdala and hippocampus and memory performance in Alzheimer's disease. Psychiatry Res 146:251-261. Styner M, Oguz I, Xu S, Brechbuhler C, Pantazis D, Levitt JJ, Shenton ME, Gerig G (2006): Framework for the statistical shape analysis of brain structures using spharm-pdm. Insight J 1701:242-250. Jacobson SW, Stanton ME, Molteno CD, Burden MJ, Fuller DS, Hoyme HE, Robinson LK, Khaole N, Jacobson JL (2008): Impaired eyeblink conditioning in children with fetal alcohol syndrome. Alcohol Clin Exp Res 32:365-372. 2010; 34 2004; 21 1998; 3338 2004; 25 2004; 8 2006; 1701 1997; 178 2009 2007 1997; 1 2008; 32 2011; 35 2000; 90 2004 1992; 14 1999; 3 2010; 181 2003; 19 2007; 31 2005; 26 1995; 2 2001; 64 2007; 37 2001; 43 1995; 61 2000; 14 2000; 1935/2000 2000; 10 1999; 1613 2002; 269 1997; 17 2003; 160 2001; 2208 2001b; 12 2001a; 57 2007; 88 1996; 20 2003; 22 2006; 146 Astley SJ (e_1_2_6_3_1) 2004 e_1_2_6_32_1 e_1_2_6_10_1 e_1_2_6_31_1 e_1_2_6_30_1 Gerig G (e_1_2_6_13_1) 2001; 2208 e_1_2_6_19_1 Mai J (e_1_2_6_24_1) 2007 e_1_2_6_36_1 e_1_2_6_14_1 e_1_2_6_11_1 e_1_2_6_34_1 e_1_2_6_12_1 e_1_2_6_33_1 e_1_2_6_17_1 Jacobson SW (e_1_2_6_18_1) 2010; 34 e_1_2_6_38_1 e_1_2_6_16_1 Juergen M (e_1_2_6_20_1) 2007 Machado AMC (e_1_2_6_23_1) 1998; 3338 e_1_2_6_37_1 e_1_2_6_42_1 e_1_2_6_43_1 e_1_2_6_21_1 e_1_2_6_41_1 e_1_2_6_40_1 Kelemen A (e_1_2_6_22_1) 1997; 178 Shen L (e_1_2_6_35_1) 2004; 8 e_1_2_6_9_1 e_1_2_6_8_1 e_1_2_6_5_1 e_1_2_6_4_1 e_1_2_6_7_1 Golland P (e_1_2_6_15_1) 2000 e_1_2_6_6_1 e_1_2_6_25_1 e_1_2_6_2_1 e_1_2_6_29_1 e_1_2_6_44_1 e_1_2_6_28_1 Styner M (e_1_2_6_39_1) 2006; 1701 e_1_2_6_45_1 e_1_2_6_27_1 e_1_2_6_26_1 |
References_xml | – reference: Duta N, Sonka M (1997): Segmentation and interpretation of MR brain images: An improved active shape model. IEEE Trans Med Imag 17:1049-1062. – reference: Basso M, Yang J, Warren L, MacAvoy MG, Varma P, Bronen RA, Van Dyck CH (2006): Volumetry of amygdala and hippocampus and memory performance in Alzheimer's disease. Psychiatry Res 146:251-261. – reference: Jacobson SW, Stanton ME, Molteno CD, Burden MJ, Fuller DS, Hoyme HE, Robinson LK, Khaole N, Jacobson JL (2008): Impaired eyeblink conditioning in children with fetal alcohol syndrome. Alcohol Clin Exp Res 32:365-372. – reference: Narr KL, Thompson PM, Sharma T, Moussai J, Cannestra AF, Toga AW (2000): Mapping morphology of the corpus callosum in schizophrenia. Cereb Cortex 10:40-49. – reference: Rueckert D, Frangi A, Schnabel JA (2003): Automatic construction of 3-D statistical deformation models of the brain using nonrigid registration. IEEE Trans Med Imag 22:1014-1025. – reference: Sowell ER, Mattson SN, Thompson PM, Jernigan TL, Riley EP, Toga AW (2001a): Mapping callosal morphology and cognitive correlates: Effects of heavy prenatal alcohol exposure. Neurology 57:235-244. – reference: Narr KL, Thompson PM, Szeszko P, Robinson D, Jang S, Woods RP, Kim S, Hayashi KM, Asunction D, Toga AW, Bilder RM (2004): Regional specificity of hippocampal volume reductions in first-episode schizophrenia. Neuroimage 21:1563-1575. – reference: Jacobson SW, Warton C, Dodge NC, De Guio F, Molteno CD, Jacobson JL, Meintjes EM (2010): Differential vulnerability of three brain structures to fetal alcohol exposure: An MRI study of school-age children in Cape Town. Alcohol Clin Exp Res A 34:93. – reference: Archibald SL, Fennema-Notestine C, Gamst A, Riley EP, Mattson SN, Jernigan TL (2001): Brain dysmorphology in individuals with severe prenatal alcohol exposure. Dev Med Child Neurol 43:148-154. – reference: Sullivan EV, Rosenbloom MJ, Serventi KL, Deshmukh A, Pfefferbaum A (2003): Effects of alcohol dependence comorbidity and antipsychotic medication on volumes of the thalamus and pons in schizophrenia. Am J Psychiatry 160,1110-1116. – reference: Yonggang S, Paul MT, Greig IZ, Stephen ER, Zhuowen T, Ivo D, Arthur WT (2007): Direct mapping of hippocampal surfaces with intrinsic shape context. Neuroimage 37:792-807. – reference: Gonzalo SB, Beatriz GA, Aitor S, Yolanda V, Manuel D, Jordi PC (2010): Manual validation of FreeSurfer's automated hippocampal segmentation in normal aging, mild cognitive impairment, and Alzheimer Disease subjects. Psychiatry Research: Neuroimaging 181:219-225. – reference: Bookstein FL, Sampson PD, Connor PD, Streissguth AP (2002): Midline corpus callosum is a neuroanatomical focus of fetal alcohol damage. Anat Rec 269:162-174. – reference: Styner M, Lieberman JA, Pantazis D, Gerig G (2004): Boundary and medial shape analysis of the hippocampus in schizophrenia. Med Image Anal 8:197-203. – reference: Fleute M, Lavallee S, Julliard R (1999): Incorporating a statistically based shape model into a system for computer-assisted anterior cruciate ligament surgery. Med Image Anal 3:209-222. – reference: Cootes TF, Taylor CJ, Cooper DH, Graham J (1995): Active shape models-Their training and application. Computer Vis Image Understand 61:38-59. – reference: Juergen M, George P, Thomas V (2007):Atlas of the Human Brain, Third Edition.Academic Press,280 p. – reference: Sullivan EV, Marsh L, Pfefferbaum A (2005): Preservation of hippocampal volume throughout adulthood in healthy men and women. Neurobiol Aging 26:1093-1098. – reference: Jacobson SW, Stanton ME, Dodge NC, Pienaar M, Fuller DS, Molteno CD, Meintjes EM, Hoyme HE, Robinson LK, Khaole N, Jacobson JL (2011): Impaired delay and trace eyeblink conditioning in school-age children with fetal alcohol syndrome. Alcohol Clin Exp Res 35:250-264. – reference: Mattson SN, Riley EP, Sowell ER, Jernigan TL, Sobel DF, Jones KL (1996): A decrease in the size of the basal ganglia in children with fetal alcohol syndrome. Alcohol Clin Exp Res 20:1088-1093. – reference: Sowell ER, Thompson PM, Mattson SN, Tessner KD, Jernigan TL, Riley EP, Toga AW (2001b): Voxel-based morphometric analyses of the brain in children and adolescents prenatally exposed to alcohol. Neuroreport 12:515-523. – reference: Gerig G, Styner M, Shenton ME, Lieberman JA (2001): Shape versus size: Improved understanding of the morphology of brain structures. Med Image Comput Computer-Assist Interv 2208:24-32. – reference: May PA, Brooke L, Gossage JP, Croxford J, Adnams C, Jones KL, Robinson L, Viljoen D (2000): Epidemiology of fetal alcohol syndrome in a South African community in the Western Cape Province. Am J Publ Health 90:1905-1912. – reference: Mai J, Paxinos G, Voss T.2007.Atlas of the Human Brain, 3rd ed.New York:Academic Press. – reference: Besl PJ, McKay ND (1992): A method for registration of 3-d shapes. IEEE Trans Pattern Anal Mach Intell 14:239-256. – reference: Woods RP (2003): Multitracer: A java-based tool for anatomic delineation of grayscale volumetric images. Neuroimage 19:1829-1834. – reference: Styner M, Oguz I, Xu S, Brechbuhler C, Pantazis D, Levitt JJ, Shenton ME, Gerig G (2006): Framework for the statistical shape analysis of brain structures using spharm-pdm. Insight J 1701:242-250. – reference: Manning MA, Hoyme HE (2007): Fetal alcohol spectrum disorders: A practical clinical approach to diagnosis. Neurosci Biobehav Rev 31:230-238. – reference: Astley SJ (2004):Diagnostic Guide for Fetal Alcohol Spectrum Disorders: The 4-Digit Diagnostic Code, 3rd ed.Seattle WA:University of Washington Publication Services. pp1-114. – reference: Machado AMC, Gee JC (1998): Atlas warping for brain morphometry. Proc SPIE Med Imag Image Process 3338:642-651. – reference: Bookstein FL (1997): Landmark methods for forms without landmarks: Morphometrics of group differences in outline shape. Med Image Anal 1:225-243. – reference: Raz N, Gunning-Dixon F, Head D, Rodrigue KM, Williamson A, Acker JD (2004): Aging, sexual dimorphism, and hemispheric asymmetry of the cerebral cortex: Replicability of regional differences in volume. Neurobiol Aging 25:377-396. – reference: Shen L, Ford J, Makedon F, Saykin A (2004): A surface-based approach for classification of 3D neuroanatomical structures. Intell Data Anal 8:519-542. – reference: Bookstein FL, Sampson PD, Streissguth AP, Connor PD (2001): Geometric morphometrics of corpus callosum and subcortical structures in the fetal alcohol affected brain. Teratology 64:4-32. – reference: Golland P, Grimson WEL, Kikinis R (1999): Statistical shape analysis using fixed topology skeletons: Corpus callosum Study. Inform Process Med Imag 1613:382-387. – reference: Meintjes EM, Jacobson JL, Molteno CD, Gatenby JC, Warton C, Cannistraci CJ, Hoyme HE, Robinson LK, Khaole N, Gore JC, Jacobson SW (2010): An FMRI study of number processing in children with fetal alcohol syndrome. Alcohol Clin Exp Res 34:1450-1464. – reference: Kelemen A, Szekely G, Gerig G (1997): Three-dimensional model-based segmentation of brain MRI. Proc IEEE Int Workshop Model Based 3D Image Anal 178:828-839. – reference: Kaus MR, Pekar V, Lorenz C, Truyen R, Lobregt S, Weese J (2003): Automated 3-D PDM construction from segmented images using deformable models. IEEE Trans Med Imag 22:1005-1013. – reference: May PA, Gossage JP, Marais AS, Adnams CM, Hoyme HE, Jones KL, Robinson LK, Khaole NC, Snell C, Kalberg WO, Hendricks L, Brooke L, Stellavato C, Viljoen DL (2007): The epidemiology of fetal alcohol syndrome and partial FAS in a South African community. Drug Alcohol Depend 88:259-271. – reference: Wright IC, McGuire PK, Poline JB, Travere JM, Murray RM, Frith CD, Frackowiak RS, Friston KJ (1995): A voxel-based method for the statistical analysis of gray and white matter density applied to schizophrenia. Neuroimage 2:244-252. – reference: Pfefferbaum A, Lim KO, Desmond JE, Sullivan EV (1996): Thinning of the corpus callosum in older alcoholic men: A magnetic resonance imaging study. Alcohol Clin Exp Res 20:752-757. – reference: Sullivan EV, Deshmukh A, Desmond JE, Lim KO, Pfefferbaum A (2000): Cerebellar volume decline in normal aging, alcoholism, and Korsakoff's syndrome: Relation to ataxia. 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in older alcoholic men: A magnetic resonance imaging study publication-title: Alcohol Clin Exp Res – volume: 2 start-page: 244 year: 1995 end-page: 252 article-title: A voxel‐based method for the statistical analysis of gray and white matter density applied to schizophrenia publication-title: Neuroimage – volume: 26 start-page: 1093 year: 2005 end-page: 1098 article-title: Preservation of hippocampal volume throughout adulthood in healthy men and women publication-title: Neurobiol Aging – volume: 1 start-page: 225 year: 1997 end-page: 243 article-title: Landmark methods for forms without landmarks: Morphometrics of group differences in outline shape publication-title: Med Image Anal – volume: 181 start-page: 219 year: 2010 end-page: 225 article-title: Manual validation of FreeSurfer's automated hippocampal segmentation in normal aging, mild cognitive impairment, and Alzheimer Disease subjects publication-title: Psychiatry Research: Neuroimaging – volume: 12 start-page: 515 year: 2001b end-page: 523 article-title: Voxel‐based morphometric analyses of the brain in children and adolescents prenatally exposed to alcohol publication-title: Neuroreport – volume: 25 start-page: 377 year: 2004 end-page: 396 article-title: Aging, sexual dimorphism, and hemispheric asymmetry of the cerebral cortex: Replicability of regional differences in volume publication-title: Neurobiol Aging – volume: 8 start-page: 197 year: 2004 end-page: 203 article-title: Boundary and medial shape analysis of the hippocampus in schizophrenia publication-title: Med Image Anal – volume: 22 start-page: 1014 year: 2003 end-page: 1025 article-title: Automatic construction of 3‐D statistical deformation models of the brain using nonrigid registration publication-title: IEEE Trans Med Imag – volume: 35 start-page: 250 year: 2011 end-page: 264 article-title: Impaired delay and trace eyeblink conditioning in school‐age children with fetal alcohol syndrome publication-title: Alcohol Clin Exp Res – start-page: 1 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Snippet | Surface deformation‐based analysis was used to assess local shape variations in the hippocampi and caudate nuclei of children with fetal alcohol spectrum... Surface deformation-based analysis was used to assess local shape variations in the hippocampi and caudate nuclei of children with fetal alcohol spectrum... |
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SubjectTerms | Adolescent Biological and medical sciences Brain Mapping caudate nucleus Caudate Nucleus - pathology Child Female Fetal Alcohol Spectrum Disorders - pathology fetal alcohol syndrome hippocampus Hippocampus - pathology Humans Imaging, Three-Dimensional Investigative techniques, diagnostic techniques (general aspects) Magnetic Resonance Imaging Male Medical sciences Nervous system Nervous system involvement in other diseases. Miscellaneous Neurology Radiodiagnosis. Nmr imagery. Nmr spectrometry shape analysis Statistics, Nonparametric surface deformation |
Title | Three-dimensional surface deformation-based shape analysis of hippocampus and caudate nucleus in children with fetal alcohol spectrum disorders |
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