33 results on '"Botteron K"'
Search Results
2. Increased Extra-axial Cerebrospinal Fluid in High-Risk Infants Who Later Develop Autism.
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Emerson, Robert, Shaw, Dennis, Elison, Jed, Swanson, Meghan, Fonov, Vladimir, Gerig, Guido, Dager, Stephen, Botteron, Kelly, Paterson, Sarah, Schultz, Robert, Evans, Alan, Estes, Annette, Zwaigenbaum, Lonnie, Styner, Martin, Amaral, David, Piven, J, Hazlett, H, Chappell, C, Dager, S, Estes, A, Shaw, D, Botteron, K, McKinstry, R, Constantino, J, Pruett, J, Schultz, R, Zwaigenbaum, L, Elison, J, Evans, A, Collins, D, Pike, G, Fonov, V, Kostopoulos, P, Das, S, Gerig, G, Styner, M, Gu, H, Piven, Joseph, Shen, Mark, Kim, Sun, McKinstry, Robert, Gu, Hongbin, Hazlett, Heather, and Nordahl, Christine
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Autism ,Brain development ,CSF ,Extra-axial fluid ,Infancy ,MRI ,Autism Spectrum Disorder ,Axis ,Cervical Vertebra ,Cerebral Ventricles ,Cerebrospinal Fluid ,Child ,Preschool ,Female ,Genetic Predisposition to Disease ,Humans ,Image Processing ,Computer-Assisted ,Infant ,Longitudinal Studies ,Magnetic Resonance Imaging ,Male ,Motor Skills ,Organ Size ,Pattern Recognition ,Automated ,Prodromal Symptoms ,Prognosis ,Sensitivity and Specificity ,Severity of Illness Index ,Siblings ,Subarachnoid Space - Abstract
BACKGROUND: We previously reported that infants who developed autism spectrum disorder (ASD) had increased cerebrospinal fluid (CSF) in the subarachnoid space (i.e., extra-axial CSF) from 6 to 24 months of age. We attempted to confirm and extend this finding in a larger independent sample. METHODS: A longitudinal magnetic resonance imaging study of infants at risk for ASD was carried out on 343 infants, who underwent neuroimaging at 6, 12, and 24 months. Of these infants, 221 were at high risk for ASD because of an older sibling with ASD, and 122 were at low risk with no family history of ASD. A total of 47 infants were diagnosed with ASD at 24 months and were compared with 174 high-risk and 122 low-risk infants without ASD. RESULTS: Infants who developed ASD had significantly greater extra-axial CSF volume at 6 months compared with both comparison groups without ASD (18% greater than high-risk infants without ASD; Cohens d = 0.54). Extra-axial CSF volume remained elevated through 24 months (d = 0.46). Infants with more severe autism symptoms had an even greater volume of extra-axial CSF from 6 to 24 months (24% greater at 6 months, d = 0.70; 15% greater at 24 months, d = 0.70). Extra-axial CSF volume at 6 months predicted which high-risk infants would be diagnosed with ASD at 24 months with an overall accuracy of 69% and corresponding 66% sensitivity and 68% specificity, which was fully cross-validated in a separate sample. CONCLUSIONS: This study confirms and extends previous findings that increased extra-axial CSF is detectable at 6 months in high-risk infants who develop ASD. Future studies will address whether this anomaly is a contributing factor to the etiology of ASD or an early risk marker for ASD.
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- 2017
3. Analysis of Cortical Morphometric Variability Using Labeled Cortical Distance Maps
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Ceyhan, E., Nishino, T., Botteron, K. N., Miller, M. I., and Ratnanather, J. T.
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Statistics - Applications ,Statistics - Methodology ,62F03, 62G10, 62P10, 92C50, 62H35 - Abstract
Morphometric differences in the anatomy of cortical structures are associated with neuro-developmental and neuropsychiatric disorders. Such differences can be quantized and detected by a powerful tool called Labeled Cortical Distance Map (LCDM). The LCDM method pro-vides distances of labeled gray matter (GM) voxels from the GM/white matter (WM) surface for specific cortical structures (or tissues). Here we describe a method to analyze morphometric variability in the particular tissue using LCDM distances. To extract more of the information provided by LCDM distances, we perform pooling and censoring of LCDM distances. In particular, we employ Brown-Forsythe (BF) test of homogeneity of variance (HOV) on the LCDM distances. HOV analysis of pooled distances provides an overall analysis of morphometric variability of the LCDMs due to the disease in question, while the HOV analysis of censored distances suggests the location(s) of significant variation in these differences (i.e., at which distance from the GM/WM surface the morphometric variability starts to be significant). We also check for the influence of assumption violations on the HOV analysis of LCDM distances. In particular, we demonstrate that BF HOV test is robust to assumption violations such as the non-normality and within sample dependence of the residuals from the median for pooled and censored distances and are robust to data aggregation which occurs in analysis of censored distances. We illustrate the methodology on a real data example, namely, LCDM distances of GM voxels in ventral medial prefrontal cortices (VMPFCs) to see the effects of depression or being of high risk to depression on the morphometry of VMPFCs. The methodology used here is also valid for morphometric analysis of other cortical structures., Comment: 40 pages, 16 figures, 12 tables
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- 2015
4. The Importance of Temperament for Understanding Early Manifestations of Autism Spectrum Disorder in High-Risk Infants
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Paterson, Sarah J., Wolff, Jason J., Elison, Jed T., Winder-Patel, Breanna, Zwaigenbaum, Lonnie, Estes, Annette, Pandey, Juhi, Schultz, Robert T., Botteron, Kelly, Dager, Stephen R., Hazlett, Heather C., Piven, Joseph, Piven, J., Hazlett, H. C., Chappell, C., Dager, S., Estes, A., Shaw, D., Botteron, K. N., McKinstry, R. C., Constantino, J., Pruett, J., Schultz, R. T., Paterson, S., Zwaigenbaum, L., Elison, J., Evans, A. C., Collins, D. L., Pike, G. B., Fonov, V., Kostopoulos, P., Das, S., Gerig, G., Styner, M., and Gu, H.
- Abstract
The present study investigated the relationship between infant temperament characteristics and autism spectrum disorder (ASD) risk status. Temperament was examined at 6, 12, and 24 months in 282 infants at high familial risk for ASD and 114 low-risk controls using the Infant Behavior Questionnaire-Revised and Early Childhood Behavior Questionnaire. Infants were divided into three groups at 24 months: High-Risk Positive--classified as ASD (HR Pos), High-Risk Negative (HR Neg), and Low-Risk Negative (LR Neg). At 6 and 12 months HR Pos infants exhibited lower Surgency and Regulatory Capacity than LR Neg infants. By 12 months they also demonstrated increased Negative Affect. Group differences remained, when early signs of ASD were controlled for, suggesting that temperament differences could be useful targets for understanding the development of ASD.
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- 2019
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5. Subcortical Brain and Behavior Phenotypes Differentiate Infants With Autism Versus Language Delay
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Piven, J., Hazlett, H.C., Chappell, C., Dager, S., Estes, A.M., Shaw, D., Botteron, K., McKinstry, R., Constantino, J., Pruett, J., Schultz, R.T., Pandey, J., Paterson, S., Zwaigenbaum, L., Elison, J.T., Wolff, J.J., Evans, A.C., Collins, D.L., Pike, G.B., Fonov, V., Kostopoulos, P., Das, S., Gerig, G., Styner, M., Gu, H., Swanson, Meghan R., Shen, Mark D., Wolff, Jason J., Elison, Jed T., Emerson, Robert W., Styner, Martin A., Hazlett, Heather C., Truong, Kinh, Watson, Linda R., Paterson, Sarah, Marrus, Natasha, Botteron, Kelly N., Pandey, Juhi, Schultz, Robert T., Dager, Stephen R., Zwaigenbaum, Lonnie, Estes, Annette M., and Piven, Joseph
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- 2017
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6. Increased Extra-axial Cerebrospinal Fluid in High-Risk Infants Who Later Develop Autism
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Shen, Mark D., Kim, Sun Hyung, McKinstry, Robert C., Gu, Hongbin, Hazlett, Heather C., Nordahl, Christine W., Emerson, Robert W., Shaw, Dennis, Elison, Jed T., Swanson, Meghan R., Fonov, Vladimir S., Gerig, Guido, Dager, Stephen R., Botteron, Kelly N., Paterson, Sarah, Schultz, Robert T., Evans, Alan C., Estes, Annette M., Zwaigenbaum, Lonnie, Styner, Martin A., Amaral, David G., Piven, Joseph, Piven, J., Hazlett, H.C., Chappell, C., Dager, S., Estes, A., Shaw, D., Botteron, K., McKinstry, R., Constantino, J., Pruett, J., Schultz, R., Zwaigenbaum, L., Elison, J., Evans, A.C., Collins, D.L., Pike, G.B., Fonov, V., Kostopoulos, P., Das, S., Gerig, G., Styner, M., and Gu, H.
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- 2017
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7. Infants who develop autism show smaller inventories of deictic and symbolic gestures at 12 months of age.
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Wu, Dennis, Wolff, Jason J., Ravi, Shruthi, Elison, Jed T., Estes, Annette, Paterson, Sarah, St. John, Tanya, Abdi, Hervé, Moraglia, Luke E., Piven, Joseph, Swanson, Meghan R., Hazlett, H. C., Chappell, C., Dager, S., Estes, A., Shaw, D., Botteron, K., McKinstry, R., Constantino, J., and Pruett, J.
- Abstract
Gestures are an important social communication skill that infants and toddlers use to convey their thoughts, ideas, and intentions. Research suggests that early gesture use has important downstream impacts on developmental processes, such as language learning. However, autistic children are more likely to have challenges in their gestural development. The current study expands upon previous literature on the differences in gesture use between young autistic and non‐autistic toddlers by collecting data using a parent‐report questionnaire called the MCDI–Words and Gestures at three time points, 12, 18, and 24 months of age. Results (N = 467) showed that high‐likelihood infants who later met diagnostic criteria for ASD (n = 73 HL‐ASD) have attenuated gesture growth from 12 to 24 months for both deictic gestures and symbolic gestures when compared to high‐likelihood infants who later did not meet criteria for ASD (n = 249 HL‐Neg) and low‐likelihood infants who did not meet criteria for ASD (n = 145 LL‐Neg). Other social communicative skills, like play behaviors and imitation, were also found to be impacted in young autistic children when compared to their non‐autistic peers. Understanding early differences in social communication growth before a formal autism diagnosis can provide important insights for early intervention. Lay Summary: As infants learn to talk, they use gestures to communicate. In this study, we used a parent‐report questionnaire to look at the group level differences of gestures in the first 2 years of life by comparing infants who later developed autism to infants who did not develop autism. We found that infants who later developed autism have fewer gestures and a slower rate of gesture growth compared to infants who did not develop autism. Play behaviors and imitation skills were also impacted in young autistic children when compared to their non‐autistic peers. [ABSTRACT FROM AUTHOR]
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- 2024
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8. Early brain development in infants at high risk for autism spectrum disorder
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Hazlett, Heather Cody, Gu, Hongbin, Munsell, Brent C., Kim, Sun Hyung, Styner, Martin, Wolff, Jason J., Elison, Jed T., Swanson, Meghan R., Zhu, Hongtu, Botteron, Kelly N., Collins, D. Louis, Constantino, John N., Dager, Stephen R., Estes, Annette M., Evans, Alan C., Fonov, Vladimir S., Gerig, Guido, Kostopoulos, Penelope, McKinstry, Robert C., Pandey, Juhi, Paterson, Sarah, Pruett, John R., Schultz, Robert T., Shaw, Dennis W., Zwaigenbaum, Lonnie, Piven, Joseph, Piven, J., Hazlett, H. C., Chappell, C., Dager, S. R., Estes, A. M., Shaw, D. W., Botteron, K. N., McKinstry, R. C., Constantino, J. N., Pruett Jr, J. R., Schultz, R. T., Paterson, S., Zwaigenbaum, L., Elison, J. T., Wolff, J. J., Evans, A. C., Collins, D. L., Pike, G. B., Fonov, V. S., Kostopoulos, P., Das, S., Gerig, G., Styner, M., and Gu, Core H.
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Risk factors ,Health aspects ,Autism -- Risk factors ,Infant development -- Health aspects - Abstract
Author(s): Heather Cody Hazlett (corresponding author) [1, 2]; Hongbin Gu [1]; Brent C. Munsell [3]; Sun Hyung Kim [1]; Martin Styner [1]; Jason J. Wolff [4]; Jed T. Elison [5]; [...]
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- 2017
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9. Language delay aggregates in toddler siblings of children with autism spectrum disorder
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Marrus, N, Hall, L P, Paterson, S J, Elison, J T, Wolff, J J, Swanson, M R, Parish-Morris, J, Eggebrecht, A T, Pruett, Jr., J R, Hazlett, H C, Zwaigenbaum, L, Dager, S, Estes, A M, Schultz, R T, Botteron, K N, Piven, J, Constantino, J N, and for the IBIS Network
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- 2018
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10. Additional file 1 of Infants later diagnosed with autism have lower canonical babbling ratios in the first year of life
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Yankowitz, L. D., Petrulla, V., Plate, S., Tunc, B., Guthrie, W., Meera, S. S., Tena, K., Pandey, J., Swanson, M. R., Pruett, J. R., Cola, M., Russell, A., Marrus, N., Hazlett, H. C., Botteron, K., Constantino, J. N., Dager, S. R., Estes, A., Zwaigenbaum, L., Piven, J., Schultz, R. T., and Parish-Morris, J.
- Abstract
Additional file 1: Supplementary Material. Supplementary figure, tables, and text.
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- 2022
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11. Examining the factor structure and discriminative utility of the Infant Behavior Questionnaire–Revised in infant siblings of autistic children.
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Sung, Sooyeon, Fenoglio, Angela, Wolff, Jason J., Schultz, Robert T., Botteron, Kelly N., Dager, Stephen R., Estes, Annette M., Hazlett, Heather C., Zwaigenbaum, Lonnie, Piven, Joseph, Elison, Jed T., Piven, J., Hazlett, H. C., Chappell, C., Dager, S., Estes, A., Shaw, D., Botteron, K., McKinstry, R., and Constantino, J.
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AUTISM risk factors ,SIBLINGS ,QUESTIONNAIRES ,AUTISTIC children ,TEMPERAMENT in infants ,TEST validity ,EMOTIONS - Abstract
Using the Infant Behavior Questionnaire–Revised in a longitudinal sample of infant siblings of autistic children (HR; n = 427, 171 female, 83.4% White) and a comparison group of low‐risk controls (LR, n = 200, 86 female, 81.5% White), collected between 2007 and 2017, this study identified an invariant factor structure of temperament traits across groups at 6 and 12 months. Second, after partitioning the groups by familial risk and diagnostic outcome at 24 months, results reveal an endophenotypic pattern of Positive Emotionality at both 6 and 12 months, (HR‐autism spectrum disorder [ASD] < HR‐no‐ASD < LR). Third, increased 'Duration of Orienting' at 12 months was associated with lower scores on the 24‐month developmental outcomes in HR infants. These findings may augment efforts for early identification of ASD. [ABSTRACT FROM AUTHOR]
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- 2022
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12. Resting-state fMRI in sleeping infants more closely resembles adult sleep than adult wakefulness
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Mitra, Anish, Snyder, Abraham Z., Tagliazucchi, Enzo Rodolfo, Laufs, Helmut, Elison, Jed, Emerson, Robert W., Shen, Mark D., Wolff, Jason J., Botteron, Kelly N., Dager, Stephen, Estes, Annette M., Evans, A.C., Gerig, Guido, Hazlett, Heather C., Paterson, Sarah J., Schultz, Robert T., Styner, Martin A., Zwaigenbaum, Lonnie, Chappell, C., Estes, A., Shaw, D., Botteron, K., McKinstry, R., Constantino, J., Pruett, J., Schultz, R., Paterson, S., Collins, D.L., Pike, G.B., Fonov, V., Kostopoulos, P., Dasso, Sergio Alberto, Styner, M., Gu, H., Schlaggar, Bradley L., Piven, Joseph, Pruett, John R., and Raichle, Marcus
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Physiology ,Ciencias Físicas ,lcsh:Medicine ,Audiology ,Electroencephalography ,Pediatrics ,Diagnostic Radiology ,purl.org/becyt/ford/1 [https] ,Families ,0302 clinical medicine ,Mathematical and Statistical Techniques ,Thalamus ,Functional Magnetic Resonance Imaging ,Medicine and Health Sciences ,lcsh:Science ,Children ,Default mode network ,Brain Mapping ,Principal Component Analysis ,Multidisciplinary ,medicine.diagnostic_test ,Radiology and Imaging ,05 social sciences ,Brain ,Software Engineering ,Sleep in non-human animals ,Magnetic Resonance Imaging ,3. Good health ,Child, Preschool ,Physical Sciences ,Engineering and Technology ,Wakefulness ,Anatomy ,Psychology ,Infants ,psychological phenomena and processes ,Statistics (Mathematics) ,CIENCIAS NATURALES Y EXACTAS ,Research Article ,Adult ,medicine.medical_specialty ,Computer and Information Sciences ,Imaging Techniques ,NEUROIMAGING ,Otras Ciencias Biológicas ,Neuroimaging ,Research and Analysis Methods ,Non-rapid eye movement sleep ,050105 experimental psychology ,Ciencias Biológicas ,03 medical and health sciences ,DEVELOPMENT ,Diagnostic Medicine ,medicine ,Connectome ,Humans ,0501 psychology and cognitive sciences ,Statistical Methods ,purl.org/becyt/ford/1.6 [https] ,Preprocessing ,Resting state fMRI ,lcsh:R ,Biology and Life Sciences ,Infant ,purl.org/becyt/ford/1.3 [https] ,SLEEP ,Astronomía ,Age Groups ,People and Places ,Multivariate Analysis ,lcsh:Q ,Population Groupings ,Functional magnetic resonance imaging ,Physiological Processes ,Sleep ,030217 neurology & neurosurgery ,Mathematics ,Neuroscience - Abstract
Resting state functional magnetic resonance imaging (rs-fMRI) in infants enables important studies of functional brain organization early in human development. However, rs-fMRI in infants has universally been obtained during sleep to reduce participant motion artifact, raising the question of whether differences in functional organization between awake adults and sleeping infants that are commonly attributed to development may instead derive, at least in part, from sleep. This question is especially important as rs-fMRI differences in adult wake vs. sleep are well documented. To investigate this question, we compared functional connectivity and BOLD signal propagation patterns in 6, 12, and 24 month old sleeping infants with patterns in adult wakefulness and non-REM sleep. We find that important functional connectivity features seen during infant sleep closely resemble those seen during adult sleep, including reduced default mode network functional connectivity. However, we also find differences between infant and adult sleep, especially in thalamic BOLD signal propagation patterns. These findings highlight the importance of considering sleep state when drawing developmental inferences in infant rs-fMRI. Fil: Mitra, Anish. Washington University School Of Medicine In St. Louis; Estados Unidos Fil: Snyder, Abraham Z.. Washington University School Of Medicine In St. Louis; Estados Unidos Fil: Tagliazucchi, Enzo Rodolfo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Física de Buenos Aires. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Física de Buenos Aires; Argentina Fil: Laufs, Helmut. Christian-albrechts-universitat Zu Kiel; Alemania Fil: Elison, Jed. University of Minnesota; Estados Unidos Fil: Emerson, Robert W.. University of North Carolina; Estados Unidos Fil: Shen, Mark D.. University of North Carolina; Estados Unidos Fil: Wolff, Jason J.. University of Minnesota; Estados Unidos Fil: Botteron, Kelly N.. Washington University School Of Medicine In St. Louis; Estados Unidos Fil: Dager, Stephen. University Of Washington, Seattle; Estados Unidos Fil: Estes, Annette M.. University Of Washington, Seattle; Estados Unidos Fil: Evans, A.C.. McGill University. Montreal Neurological Institute and Hospital; Canadá Fil: Gerig, Guido. University of New York; Estados Unidos Fil: Hazlett, Heather C.. University of North Carolina; Estados Unidos Fil: Paterson, Sarah J.. University of Pennsylvania; Estados Unidos Fil: Schultz, Robert T.. University of Pennsylvania; Estados Unidos Fil: Styner, Martin A.. University of North Carolina; Estados Unidos Fil: Zwaigenbaum, Lonnie. University of Alberta; Canadá Fil: Chappell, C.. Ibis Network Pi; Estados Unidos Fil: Estes, A.. University Of Washington, Seattle; Estados Unidos Fil: Shaw, D.. University Of Washington, Seattle; Estados Unidos Fil: Botteron, K.. University Of Washington, Seattle; Estados Unidos Fil: McKinstry, R.. University Of Washington, Seattle; Estados Unidos Fil: Constantino, J.. University Of Washington, Seattle; Estados Unidos Fil: Pruett, J.. University Of Washington, Seattle; Estados Unidos Fil: Schultz, R.. The Children?s Hospital Of Philadelphia; Estados Unidos Fil: Paterson, S.. The Children?s Hospital Of Philadelphia; Estados Unidos Fil: Collins, D.L.. McGill University. Montreal Neurological Institute and Hospital; Canadá Fil: Pike, G.B.. McGill University. Montreal Neurological Institute and Hospital; Canadá Fil: Fonov, V.. McGill University. Montreal Neurological Institute and Hospital; Canadá Fil: Kostopoulos, P.. McGill University. Montreal Neurological Institute and Hospital; Canadá Fil: Dasso, Sergio Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Física de Buenos Aires. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Física de Buenos Aires; Argentina Fil: Styner, M.. The University Of North Carolina System; Estados Unidos Fil: Gu, H.. Statistical Analysis Core; Estados Unidos Fil: Schlaggar, Bradley L.. Washington University School Of Medicine In St. Louis; Estados Unidos Fil: Piven, Joseph. University of North Carolina; Estados Unidos Fil: Pruett, John R.. Washington University School Of Medicine In St. Louis; Estados Unidos Fil: Raichle, Marcus. Washington University School Of Medicine In St. Louis; Estados Unidos
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- 2017
13. Increased Extra-axial Cerebrospinal Fluid in High-Risk Infants Who Later Develop Autism
- Author
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McKinstry, R.C., Constantino, J., Schultz, R.T., Styner, M.A., Kostopoulos, P., Emerson, R.W., Zwaigenbaum, L., Botteron, K., Dager, S.R., Gu, H., Styner, M., Swanson, M.R., Kim, S.H., Nordahl, C.W., Schultz, R., Infant Brain Imaging Study Network, Pike, G.B., Collins, D.L., Fonov, V.S., Shaw, D., Das, S., Gerig, G., Paterson, S., Amaral, D.G., Shen, M.D., Piven, J., Elison, J.T., Hazlett, H.C., Chappell, C., Estes, A.M., McKinstry, R., Elison, J., Pruett, J., Evans, A.C., and Botteron, K.N.
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mental disorders ,behavioral disciplines and activities - Abstract
Background We previously reported that infants who developed autism spectrum disorder (ASD) had increased cerebrospinal fluid (CSF) in the subarachnoid space (i.e., extra-axial CSF) from 6 to 24 months of age. We attempted to confirm and extend this finding in a larger independent sample. Methods A longitudinal magnetic resonance imaging study of infants at risk for ASD was carried out on 343 infants, who underwent neuroimaging at 6, 12, and 24 months. Of these infants, 221 were at high risk for ASD because of an older sibling with ASD, and 122 were at low risk with no family history of ASD. A total of 47 infants were diagnosed with ASD at 24 months and were compared with 174 high-risk and 122 low-risk infants without ASD. Results Infants who developed ASD had significantly greater extra-axial CSF volume at 6 months compared with both comparison groups without ASD (18% greater than high-risk infants without ASD; Cohen's d = 0.54). Extra-axial CSF volume remained elevated through 24 months (d = 0.46). Infants with more severe autism symptoms had an even greater volume of extra-axial CSF from 6 to 24 months (24% greater at 6 months, d = 0.70; 15% greater at 24 months, d = 0.70). Extra-axial CSF volume at 6 months predicted which high-risk infants would be diagnosed with ASD at 24 months with an overall accuracy of 69% and corresponding 66% sensitivity and 68% specificity, which was fully cross-validated in a separate sample. Conclusions This study confirms and extends previous findings that increased extra-axial CSF is detectable at 6 months in high-risk infants who develop ASD. Future studies will address whether this anomaly is a contributing factor to the etiology of ASD or an early risk marker for ASD.
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- 2017
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14. Subcortical Brain and Behavior Phenotypes Differentiate Infants With Autism Versus Language Delay
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Swanson, Meghan R., primary, Shen, Mark D., additional, Wolff, Jason J., additional, Elison, Jed T., additional, Emerson, Robert W., additional, Styner, Martin A., additional, Hazlett, Heather C., additional, Truong, Kinh, additional, Watson, Linda R., additional, Paterson, Sarah, additional, Marrus, Natasha, additional, Botteron, Kelly N., additional, Pandey, Juhi, additional, Schultz, Robert T., additional, Dager, Stephen R., additional, Zwaigenbaum, Lonnie, additional, Estes, Annette M., additional, Piven, Joseph, additional, Piven, J., additional, Hazlett, H.C., additional, Chappell, C., additional, Dager, S., additional, Estes, A.M., additional, Shaw, D., additional, Botteron, K., additional, McKinstry, R., additional, Constantino, J., additional, Pruett, J., additional, Schultz, R.T., additional, Pandey, J., additional, Paterson, S., additional, Zwaigenbaum, L., additional, Elison, J.T., additional, Wolff, J.J., additional, Evans, A.C., additional, Collins, D.L., additional, Pike, G.B., additional, Fonov, V., additional, Kostopoulos, P., additional, Das, S., additional, Gerig, G., additional, Styner, M., additional, and Gu, H., additional
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- 2017
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15. Analysis of cortical morphometric variability using labeled cortical distance maps
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Ceyhan, E., primary, Nishino, T., additional, Botteron, K. N., additional, Miller, M. I., additional, and Ratnanather, J. T., additional
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- 2017
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16. Brain volumes, cognitive, and adaptive skills in school-age children with Down syndrome.
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Grzadzinski R, Mata K, Bhatt AS, Jatkar A, Garic D, Shen MD, Girault JB, St John T, Pandey J, Zwaigenbaum L, Estes A, Shen AM, Dager S, Schultz R, Botteron K, Marrus N, Styner M, Evans A, Kim SH, McKinstry R, Gerig G, Piven J, and Hazlett H
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- Humans, Male, Female, Child, Brain diagnostic imaging, Brain pathology, Brain physiopathology, Autism Spectrum Disorder diagnostic imaging, Autism Spectrum Disorder physiopathology, Autism Spectrum Disorder pathology, Organ Size, Cerebellum diagnostic imaging, Cerebellum pathology, Cerebellum physiopathology, Down Syndrome diagnostic imaging, Down Syndrome physiopathology, Down Syndrome pathology, Magnetic Resonance Imaging, Adaptation, Psychological physiology, Cognition physiology
- Abstract
Background: Down syndrome (DS) is the most common congenital neurodevelopmental disorder, present in about 1 in every 700 live births. Despite its prevalence, literature exploring the neurobiology underlying DS and how this neurobiology is related to behavior is limited. This study fills this gap by examining cortical volumes and behavioral correlates in school-age children with DS., Methods: School-age children (mean = 9.7 years ± 1.1) underwent comprehensive assessments, including cognitive and adaptive assessments, as well as an MRI scan without the use of sedation. Children with DS (n = 35) were compared to available samples of typically developing (TD; n = 80) and ASD children (n = 29). ANOVAs were conducted to compare groups on cognitive and adaptive assessments. ANCOVAs (covarying for age, sex, and total cerebral volume; TCV) compared cortical brain volumes between groups. Correlations between behavioral metrics and cortical and cerebellar volumes (separately for gray (GM) and white matter (WM)) were conducted separately by group., Results: As expected, children with DS had significantly lower cognitive skills compared to ASD and TD children. Daily Living adaptive skills were comparable between ASD children and children with DS, and both groups scored lower than TD children. Children with DS exhibited a smaller TCV compared to ASD and TD children. Additionally, when controlling for TCV, age, and sex, children with DS had significantly smaller total GM and tissue volumes. Cerebellum volumes were significantly correlated with Daily Living adaptive behaviors in the DS group only., Conclusions: Despite children with DS exhibiting lower cognitive skills and smaller brain volume overall than children with ASD, their deficits in Socialization and Daily Living adaptive skills are comparable. Differences in lobar volumes (e.g., Right Frontal GM/WM, Left Frontal WM, and Left and Right Temporal WM) were observed above and beyond overall differences in total volume. The correlation between cerebellum volumes and Daily Living adaptive behaviors in the DS group provides a novel area to explore in future research., Competing Interests: Declarations. Ethics approval and consent to participate: The research described in this work was approved by the local Institutional Review Board. Consent for publication: All authors have reviewed the manuscript and approved it for publication. Competing interests: The authors declare no competing interests., (© 2024. The Author(s).)
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- 2024
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17. White matter development and language abilities during infancy in autism spectrum disorder.
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McFayden TC, Rutsohn J, Cetin G, Forsen E, Swanson MR, Meera SS, Wolff JJ, Elison JT, Shen MD, Botteron K, Dager SR, Estes A, Gerig G, McKinstry RC, Pandey J, Schultz R, St John T, Styner M, Truong Y, Zwaigenbaum L, Hazlett HC, Piven J, and Girault JB
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- Humans, Male, Female, Infant, Child, Preschool, Siblings, Language, Autism Spectrum Disorder physiopathology, Autism Spectrum Disorder pathology, White Matter pathology, White Matter diagnostic imaging, Diffusion Tensor Imaging methods, Language Development, Brain pathology, Brain diagnostic imaging
- Abstract
White matter (WM) fiber tract differences are present in autism spectrum disorder (ASD) and could be important markers of behavior. One of the earliest phenotypic differences in ASD are language atypicalities. Although language has been linked to WM in typical development, no work has evaluated this association in early ASD. Participants came from the Infant Brain Imaging Study and included 321 infant siblings of children with ASD at high likelihood (HL) for developing ASD; 70 HL infants were later diagnosed with ASD (HL-ASD), and 251 HL infants were not diagnosed with ASD (HL-Neg). A control sample of 140 low likelihood infants not diagnosed with ASD (LL-Neg) were also included. Infants contributed expressive language, receptive language, and diffusion tensor imaging data at 6-, 12-, and 24 months. Mixed effects regression models were conducted to evaluate associations between WM and language trajectories. Trajectories of microstructural changes in the right arcuate fasciculus were associated with expressive language development. HL-ASD infants demonstrated a different developmental pattern compared to the HL-Neg and LL-Neg groups, wherein the HL-ASD group exhibited a positive association between WM fractional anisotropy and language whereas HL-Neg and LL-Neg groups showed weak or no association. No other fiber tracts demonstrated significant associations with language. In conclusion, results indicated arcuate fasciculus WM is linked to language in early toddlerhood for autistic toddlers, with the strongest associations emerging around 24 months. To our knowledge, this is the first study to evaluate associations between language and WM development during the pre-symptomatic period in ASD., (© 2024. The Author(s), under exclusive licence to Springer Nature Limited.)
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- 2024
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18. A global multicohort study to map subcortical brain development and cognition in infancy and early childhood.
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Alex AM, Aguate F, Botteron K, Buss C, Chong YS, Dager SR, Donald KA, Entringer S, Fair DA, Fortier MV, Gaab N, Gilmore JH, Girault JB, Graham AM, Groenewold NA, Hazlett H, Lin W, Meaney MJ, Piven J, Qiu A, Rasmussen JM, Roos A, Schultz RT, Skeide MA, Stein DJ, Styner M, Thompson PM, Turesky TK, Wadhwa PD, Zar HJ, Zöllei L, de Los Campos G, and Knickmeyer RC
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- Male, Female, Humans, Infant, Newborn, Child, Preschool, Child, Cognition, Brain diagnostic imaging, Neuroimaging, Magnetic Resonance Imaging, Premature Birth
- Abstract
The human brain grows quickly during infancy and early childhood, but factors influencing brain maturation in this period remain poorly understood. To address this gap, we harmonized data from eight diverse cohorts, creating one of the largest pediatric neuroimaging datasets to date focused on birth to 6 years of age. We mapped the developmental trajectory of intracranial and subcortical volumes in ∼2,000 children and studied how sociodemographic factors and adverse birth outcomes influence brain structure and cognition. The amygdala was the first subcortical volume to mature, whereas the thalamus exhibited protracted development. Males had larger brain volumes than females, and children born preterm or with low birthweight showed catch-up growth with age. Socioeconomic factors exerted region- and time-specific effects. Regarding cognition, males scored lower than females; preterm birth affected all developmental areas tested, and socioeconomic factors affected visual reception and receptive language. Brain-cognition correlations revealed region-specific associations., (© 2023. The Author(s).)
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- 2024
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19. Quantifying latent social motivation and its associations with joint attention and language in infants at high and low likelihood for autism spectrum disorder.
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Stallworthy IC, Berry D, Davis S, Wolff JJ, Burrows CA, Swanson MR, Grzadzinski RL, Botteron K, Dager SR, Estes AM, Schultz RT, Piven J, Elison JT, Pruett JR Jr, and Marrus N
- Subjects
- Humans, Infant, Motivation, Language, Communication, Attention, Autism Spectrum Disorder
- Abstract
Social motivation-the psychobiological predisposition for social orienting, seeking social contact, and maintaining social interaction-manifests in early infancy and is hypothesized to be foundational for social communication development in typical and atypical populations. However, the lack of infant social-motivation measures has hindered delineation of associations between infant social motivation, other early-arising social abilities such as joint attention, and language outcomes. To investigate how infant social motivation contributes to joint attention and language, this study utilizes a mixed longitudinal sample of 741 infants at high (HL = 515) and low (LL = 226) likelihood for ASD. Using moderated nonlinear factor analysis (MNLFA), we incorporated items from parent-report measures to establish a novel latent factor model of infant social motivation that exhibits measurement invariance by age, sex, and familial ASD likelihood. We then examined developmental associations between 6- and 12-month social motivation, joint attention at 12-15 months, and language at 24 months of age. On average, greater social-motivation growth from 6-12 months was associated with greater initiating joint attention (IJA) and trend-level increases in sophistication of responding to joint attention (RJA). IJA and RJA were both positively associated with 24-month language abilities. There were no additional associations between social motivation and future language in our path model. These findings substantiate a novel, theoretically driven approach to modeling social motivation and suggest a developmental cascade through which social motivation impacts other foundational skills. These findings have implications for the timing and nature of intervention targets to support social communication development in infancy. HIGHLIGHTS: We describe a novel, theoretically based model of infant social motivation wherein multiple parent-reported indicators contribute to a unitary latent social-motivation factor. Analyses revealed social-motivation factor scores exhibited measurement invariance for a longitudinal sample of infants at high and low familial ASD likelihood. Social-motivation growth from ages 6-12 months is associated with better 12-15-month joint attention abilities, which in turn are associated with greater 24-month language skills. Findings inform timing and targets of potential interventions to support healthy social communication in the first year of life., (© 2022 The Authors. Developmental Science published by John Wiley & Sons Ltd.)
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- 2023
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20. Infant vocalizing and phenotypic outcomes in autism: Evidence from the first 2 years.
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Plate S, Yankowitz L, Resorla L, Swanson MR, Meera SS, Estes A, Marrus N, Cola M, Petrulla V, Faggen A, Pandey J, Paterson S, Pruett JR Jr, Hazlett H, Dager S, St John T, Botteron K, Zwaigenbaum L, Piven J, Schultz RT, and Parish-Morris J
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- Biomarkers, Communication, Female, Humans, Infant, Phenotype, Prospective Studies, Siblings, Autism Spectrum Disorder diagnosis, Autistic Disorder
- Abstract
Infant vocalizations are early-emerging communicative markers shown to be atypical in autism spectrum disorder (ASD), but few longitudinal, prospective studies exist. In this study, 23,850 infant vocalizations from infants at low (LR)- and high (HR)-risk for ASD (HR-ASD = 23, female = 3; HR-Neg = 35, female = 13; LR = 32, female = 10; 80% White; collected from 2007 to 2017 near Philadelphia) were analyzed at 6, 12, and 24 months. At 12 months, HR-ASD infants produced fewer vocalizations than HR-Neg infants. From 6 to 24 months, HR-Neg infants demonstrated steeper vocalization growth compared to HR-ASD and LR infants. Finally, among HR infants, vocalizing at 12 months was associated with language, social phenotype, and diagnosis at age 2. Infant vocalizing is an objective behavioral marker that could facilitate earlier detection of ASD., (© 2021 The Authors. Child Development © 2021 Society for Research in Child Development.)
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- 2022
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21. A Prospective Evaluation of Infant Cerebellar-Cerebral Functional Connectivity in Relation to Behavioral Development in Autism Spectrum Disorder.
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Hawks ZW, Todorov A, Marrus N, Nishino T, Talovic M, Nebel MB, Girault JB, Davis S, Marek S, Seitzman BA, Eggebrecht AT, Elison J, Dager S, Mosconi MW, Tychsen L, Snyder AZ, Botteron K, Estes A, Evans A, Gerig G, Hazlett HC, McKinstry RC, Pandey J, Schultz RT, Styner M, Wolff JJ, Zwaigenbaum L, Markson L, Petersen SE, Constantino JN, White DA, Piven J, and Pruett JR Jr
- Abstract
Background: Autism spectrum disorder (ASD) is a neurodevelopmental disorder diagnosed based on social impairment, restricted interests, and repetitive behaviors. Contemporary theories posit that cerebellar pathology contributes causally to ASD by disrupting error-based learning (EBL) during infancy. The present study represents the first test of this theory in a prospective infant sample, with potential implications for ASD detection., Methods: Data from the Infant Brain Imaging Study ( n = 94, 68 male) were used to examine 6-month cerebellar functional connectivity magnetic resonance imaging in relation to later (12/24-month) ASD-associated behaviors and outcomes. Hypothesis-driven univariate analyses and machine learning-based predictive tests examined cerebellar-frontoparietal network (FPN; subserves error signaling in support of EBL) and cerebellar-default mode network (DMN; broadly implicated in ASD) connections. Cerebellar-FPN functional connectivity was used as a proxy for EBL, and cerebellar-DMN functional connectivity provided a comparative foil. Data-driven functional connectivity magnetic resonance imaging enrichment examined brain-wide behavioral associations, with post hoc tests of cerebellar connections., Results: Cerebellar-FPN and cerebellar-DMN connections did not demonstrate associations with ASD. Functional connectivity magnetic resonance imaging enrichment identified 6-month correlates of later ASD-associated behaviors in networks of a priori interest (FPN, DMN), as well as in cingulo-opercular (also implicated in error signaling) and medial visual networks. Post hoc tests did not suggest a role for cerebellar connections., Conclusions: We failed to identify cerebellar functional connectivity-based contributions to ASD. However, we observed prospective correlates of ASD-associated behaviors in networks that support EBL. Future studies may replicate and extend network-level positive results, and tests of the cerebellum may investigate brain-behavior associations at different developmental stages and/or using different neuroimaging modalities., (© 2021 The Authors.)
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- 2021
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22. Social and non-social sensory responsivity in toddlers at high-risk for autism spectrum disorder.
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Gunderson J, Worthley E, Grzadzinski R, Burrows C, Estes A, Zwaigenbaum L, Botteron K, Dager S, Hazlett H, Schultz R, Piven J, and Wolff J
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- Child, Preschool, Female, Humans, Infant, Male, Surveys and Questionnaires, Autism Spectrum Disorder
- Abstract
Empirical evidence concerning sensory responsivity in young children who later develop autism spectrum disorder (ASD) remains relatively limited. It is unclear whether specific patterns or aspects of sensory responsivity underlay the emergence of the disorder. The goals of this study were to (a) examine whether social versus non-social context impacted the expression of sensory responsivity in infants at high risk for ASD, and (b) examine if sensory responsivity in social or non-social contexts was associated with severity of ASD symptoms. The Sensory Experiences Questionnaire 2.1 was collected for 338 infants (131 females, 207 males) at high-risk for ASD at 12 and/or 24 months of age. High-risk toddlers meeting diagnostic criteria for ASD (n = 75) showed elevated sensory responsivity in both social and non-social contexts at 12 months of age and differences widened over the second year of life. Individuals with ASD demonstrate higher responsivity in both contexts suggestive of generalized atypical sensory responsivity in ASD. LAY SUMMARY: Behaviors such as avoiding or noticing sensory input (e.g., sounds, touches) are often different in individuals with autism spectrum disorder (ASD) than those without. The reason for this is widely unknown. The findings from this study show that in toddlers, sensory responsivity increased in both social and non-social situations. Therefore, the setting of sensory input does not explain these differences., (© 2021 International Society for Autism Research and Wiley Periodicals LLC.)
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- 2021
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23. Distributional Properties and Criterion Validity of a Shortened Version of the Social Responsiveness Scale: Results from the ECHO Program and Implications for Social Communication Research.
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Lyall K, Hosseini M, Ladd-Acosta C, Ning X, Catellier D, Constantino JN, Croen LA, Kaat AJ, Botteron K, Bush NR, Dager SR, Duarte CS, Fallin MD, Hazlett H, Hertz-Picciotto I, Joseph RM, Karagas MR, Korrick S, Landa R, Messinger D, Oken E, Ozonoff S, Piven J, Pandey J, Sathyanarayana S, Schultz RT, St John T, Schmidt R, Volk H, and Newschaffer CJ
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- Adolescent, Area Under Curve, Child, Child, Preschool, Female, Humans, Male, Psychometrics, Reproducibility of Results, Autism Spectrum Disorder diagnosis, Communication, Psychiatric Status Rating Scales standards, Social Behavior
- Abstract
Prior work proposed a shortened version of the Social Responsiveness Scale (SRS), a commonly used quantitative measure of social communication traits. We used data from 3031 participants (including 190 ASD cases) from the Environmental Influences on Child Health Outcomes (ECHO) Program to compare distributional properties and criterion validity of 16-item "short" to 65-item "full" SRS scores. Results demonstrated highly overlapping distributions of short and full scores. Both scores separated case from non-case individuals by approximately two standard deviations. ASD prediction was nearly identical for short and full scores (area under the curve values of 0.87, 0.86 respectively). Findings support comparability of shortened and full scores, suggesting opportunities to increase efficiency. Future work should confirm additional psychometric properties of short scores.
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- 2021
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24. A voxel-wise assessment of growth differences in infants developing autism spectrum disorder.
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Cárdenas-de-la-Parra A, Lewis JD, Fonov VS, Botteron KN, McKinstry RC, Gerig G, Pruett JR Jr, Dager SR, Elison JT, Styner MA, Evans AC, Piven J, and Collins DL
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- Brain diagnostic imaging, Gray Matter diagnostic imaging, Humans, Infant, Magnetic Resonance Imaging, Autism Spectrum Disorder diagnostic imaging, White Matter diagnostic imaging
- Abstract
Autism Spectrum Disorder (ASD) is a phenotypically and etiologically heterogeneous developmental disorder typically diagnosed around 4 years of age. The development of biomarkers to help in earlier, presymptomatic diagnosis could facilitate earlier identification and therefore earlier intervention and may lead to better outcomes, as well as providing information to help better understand the underlying mechanisms of ASD. In this study, magnetic resonance imaging (MRI) scans of infants at high familial risk, from the Infant Brain Imaging Study (IBIS), at 6, 12 and 24 months of age were included in a morphological analysis, fitting a mixed-effects model to Tensor Based Morphometry (TBM) results to obtain voxel-wise growth trajectories. Subjects were grouped by familial risk and clinical diagnosis at 2 years of age. Several regions, including the posterior cingulate gyrus, the cingulum, the fusiform gyrus, and the precentral gyrus, showed a significant effect for the interaction of group and age associated with ASD, either as an increased or a decreased growth rate of the cerebrum. In general, our results showed increased growth rate within white matter with decreased growth rate found mostly in grey matter. Overall, the regions showing increased growth rate were larger and more numerous than those with decreased growth rate. These results detail, at the voxel level, differences in brain growth trajectories in ASD during the first years of life, previously reported in terms of overall brain volume and surface area., (Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.)
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- 2021
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25. Hierarchical geodesic modeling on the diffusion orientation distribution function for longitudinal DW-MRI analysis.
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Kim H, Hong S, Styner M, Piven J, Botteron K, and Gerig G
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The analysis of anatomy that undergoes rapid changes, such as neuroimaging of the early developing brain, greatly benefits from spatio-temporal statistical analysis methods to represent population variations but also subject-wise characteristics over time. Methods for spatio-temporal modeling and for analysis of longitudinal shape and image data have been presented before, but, to our knowledge, not for diffusion weighted MR images (DW-MRI) fitted with higher-order diffusion models. To bridge the gap between rapidly evolving DW-MRI methods in longitudinal studies and the existing frameworks, which are often limited to the analysis of derived measures like fractional anisotropy (FA), we propose a new framework to estimate a population trajectory of longitudinal diffusion orientation distribution functions (dODFs) along with subject-specific changes by using hierarchical geodesic modeling. The dODF is an angular profile of the diffusion probability density function derived from high angular resolution diffusion imaging (HARDI) and we consider the dODF with the square-root representation to lie on the unit sphere in a Hilbert space, which is a well-known Riemannian manifold, to respect the nonlinear characteristics of dODFs. The proposed method is validated on synthetic longitudinal dODF data and tested on a longitudinal set of 60 HARDI images from 25 healthy infants to characterize dODF changes associated with early brain development., Competing Interests: Conflict of Interest Statement The authors declare that there are no conflicts or commercial interest related to this article.
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- 2020
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26. The Association Between Parental Age and Autism-Related Outcomes in Children at High Familial Risk for Autism.
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Lyall K, Song L, Botteron K, Croen LA, Dager SR, Fallin MD, Hazlett HC, Kauffman E, Landa R, Ladd-Acosta C, Messinger DS, Ozonoff S, Pandey J, Piven J, Schmidt RJ, Schultz RT, Stone WL, Newschaffer CJ, and Volk HE
- Subjects
- Adult, Autistic Disorder epidemiology, Autistic Disorder genetics, Child, Preschool, Female, Humans, Infant, Male, Prospective Studies, Autism Spectrum Disorder epidemiology, Autism Spectrum Disorder genetics, Genetic Predisposition to Disease, Maternal Age, Paternal Age
- Abstract
Advanced parental age is a well-replicated risk factor for autism spectrum disorder (ASD), a neurodevelopmental condition with a complex and not well-defined etiology. We sought to determine parental age associations with ASD-related outcomes in subjects at high familial risk for ASD. A total of 397 younger siblings of a child with ASD, drawn from existing prospective high familial risk cohorts, were included in these analyses. Overall, we did not observe significant associations of advanced parental age with clinical ASD diagnosis, Social Responsiveness Scale, or Vineland Adaptive Behavior Scales scores. Instead, increased odds of ASD were found with paternal age < 30 years (adjusted odds ratio [AOR] = 2.83 and 95% confidence intervals [CI] = 1.14-7.02). Likewise, younger age (<30 years) for both parents was associated with decreases in Mullen Scales of Early Learning early learning composite (MSEL-ELC) scores (adjusted β = -9.62, 95% CI = -17.1 to -2.15). We also found significant increases in cognitive functioning based on MSEL-ELC scores with increasing paternal age (adjusted β associated with a 10-year increase in paternal age = 5.51, 95% CI = 0.70-10.3). Results suggest the potential for a different relationship between parental age and ASD-related outcomes in families with elevated ASD risk than has been observed in general population samples. Autism Res 2020, 13: 998-1010. © 2020 International Society for Autism Research, Wiley Periodicals, Inc. LAY SUMMARY: Previous work suggests that older parents have a greater likelihood of having a child with autism. We investigated this relationship in the younger siblings of families who already had a child with autism. In this setting, we found a higher likelihood of autism, as well as poorer cognitive scores, in the siblings with younger fathers, and higher cognitive scores in the siblings with older parents. These results suggest that parental age associations may differ based on children's familial risk for autism., (© 2020 International Society for Autism Research, Wiley Periodicals, Inc.)
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- 2020
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27. Early language exposure supports later language skills in infants with and without autism.
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Swanson MR, Donovan K, Paterson S, Wolff JJ, Parish-Morris J, Meera SS, Watson LR, Estes AM, Marrus N, Elison JT, Shen MD, McNeilly HB, MacIntyre L, Zwaigenbaum L, St John T, Botteron K, Dager S, and Piven J
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- Child, Preschool, Female, Humans, Infant, Longitudinal Studies, Male, Risk, Autism Spectrum Disorder physiopathology, Child Language, Parent-Child Relations
- Abstract
The way that parents communicate with their typically developing infants is associated with later infant language development. Here we aim to show that these associations are observed in infants subsequently diagnosed with autism spectrum disorder (ASD). This study had three groups: high-familial-risk infants who did not have ASD (n = 46); high-familial-risk infants who had ASD (n = 14); and low-familial-risk infants who exhibited typical development (n = 36). All-day home language recordings were collected at 9 and 15 months, and language skills were assessed at 24 months. Across all infants in the study, including those with ASD, a richer home language environment (e.g., hearing more adult words and experiencing more conversational turns) at 9 and 15 months was associated with better language skills. Higher parental educational attainment was associated with a richer home language environment. Mediation analyses showed that the effect of education on child language skills was explained by the richness of the home language environment. Exploratory analyses revealed that typically developing infants experience an increase in caregiver-child conversational turns across 9-15 months, a pattern not seen in children with ASD. The current study shows that parent behavior during the earliest stages of life can have a significant impact on later development, highlighting the home language environment as means to support development in infants with ASD. Autism Res 2019, 12: 1784-1795. © 2019 International Society for Autism Research, Wiley Periodicals, Inc. LAY SUMMARY: It has long been understood that caregiver speech supports language skills in typically developing infants. In this study, parents of infants who were later diagnosed with ASD and parents of infants in the control groups completed all-day home language recordings. We found that for all infants in our study, those who heard more caregiver speech had better language skills later in life. Parental education level was also related to how much caregiver speech an infant experienced., (© 2019 International Society for Autism Research, Wiley Periodicals, Inc.)
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- 2019
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28. Parent Support of Preschool Peer Relationships in Younger Siblings of Children with Autism Spectrum Disorder.
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Estes A, Munson J, John TS, Dager SR, Rodda A, Botteron K, Hazlett H, Schultz RT, Zwaigenbaum L, Piven J, and Guralnick MJ
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- Adaptation, Psychological, Adult, Child, Child, Preschool, Female, Humans, Male, Parents psychology, Resilience, Psychological, Siblings psychology, Autism Spectrum Disorder psychology, Parent-Child Relations, Sibling Relations
- Abstract
Preschool-aged siblings of children with ASD are at high-risk (HR) for ASD and related challenges, but little is known about their emerging peer competence and friendships. Parents are the main providers of peer-relationship opportunities during preschool. Understanding parental challenges supporting early peer relationships is needed for optimal peer competence and friendships in children with ASD. We describe differences in peer relationships among three groups of preschool-aged children (15 HR-ASD, 53 HR-NonASD, 40 low-risk, LR), and examine parent support activities at home and arranging community-based peer activities. Children with ASD demonstrated precursors to poor peer competence and friendship outcomes. Parents in the HR group showed resilience in many areas, but providing peer opportunities for preschool-age children with ASD demanded significant adaptations.
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- 2018
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29. Naturalistic Language Recordings Reveal "Hypervocal" Infants at High Familial Risk for Autism.
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Swanson MR, Shen MD, Wolff JJ, Boyd B, Clements M, Rehg J, Elison JT, Paterson S, Parish-Morris J, Chappell JC, Hazlett HC, Emerson RW, Botteron K, Pandey J, Schultz RT, Dager SR, Zwaigenbaum L, Estes AM, and Piven J
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- Female, Humans, Infant, Male, Risk, Signal Processing, Computer-Assisted, Autism Spectrum Disorder physiopathology, Child Development physiology, Infant Behavior physiology, Siblings, Social Behavior, Verbal Behavior physiology
- Abstract
Children's early language environments are related to later development. Little is known about this association in siblings of children with autism spectrum disorder (ASD), who often experience language delays or have ASD. Fifty-nine 9-month-old infants at high or low familial risk for ASD contributed full-day in-home language recordings. High-risk infants produced more vocalizations than low-risk peers; conversational turns and adult words did not differ by group. Vocalization differences were driven by a subgroup of "hypervocal" infants. Despite more vocalizations overall, these infants engaged in less social babbling during a standardized clinic assessment, and they experienced fewer conversational turns relative to their rate of vocalizations. Two ways in which these individual and environmental differences may relate to subsequent development are discussed., (© 2017 The Authors. Child Development © 2017 Society for Research in Child Development, Inc.)
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- 2018
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30. Splenium development and early spoken language in human infants.
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Swanson MR, Wolff JJ, Elison JT, Gu H, Hazlett HC, Botteron K, Styner M, Paterson S, Gerig G, Constantino J, Dager S, Estes A, Vachet C, and Piven J
- Subjects
- Child Development, Corpus Callosum, Diffusion Magnetic Resonance Imaging, Humans, Infant, Nerve Fibers, Myelinated, Language, Language Development, Neural Pathways physiology, Speech Intelligibility physiology
- Abstract
The association between developmental trajectories of language-related white matter fiber pathways from 6 to 24 months of age and individual differences in language production at 24 months of age was investigated. The splenium of the corpus callosum, a fiber pathway projecting through the posterior hub of the default mode network to occipital visual areas, was examined as well as pathways implicated in language function in the mature brain, including the arcuate fasciculi, uncinate fasciculi, and inferior longitudinal fasciculi. The hypothesis that the development of neural circuitry supporting domain-general orienting skills would relate to later language performance was tested in a large sample of typically developing infants. The present study included 77 infants with diffusion weighted MRI scans at 6, 12 and 24 months and language assessment at 24 months. The rate of change in splenium development varied significantly as a function of language production, such that children with greater change in fractional anisotropy (FA) from 6 to 24 months produced more words at 24 months. Contrary to findings from older children and adults, significant associations between language production and FA in the arcuate, uncinate, or left inferior longitudinal fasciculi were not observed. The current study highlights the importance of tracing brain development trajectories from infancy to fully elucidate emerging brain-behavior associations while also emphasizing the role of the splenium as a key node in the structural network that supports the acquisition of spoken language., (© 2015 John Wiley & Sons Ltd.)
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- 2017
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31. Emerging Executive Functioning and Motor Development in Infants at High and Low Risk for Autism Spectrum Disorder.
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St John T, Estes AM, Dager SR, Kostopoulos P, Wolff JJ, Pandey J, Elison JT, Paterson SJ, Schultz RT, Botteron K, Hazlett H, and Piven J
- Abstract
Existing evidence suggests executive functioning (EF) deficits may be present in children with autism spectrum disorder (ASD) by 3 years of age. It is less clear when, prior to 3 years, EF deficits may emerge and how EF unfold over time. The contribution of motor skill difficulties to poorer EF in children with ASD has not been systematically studied. We investigated the developmental trajectory of EF in infants at high and low familial risk for ASD (HR and LR) and the potential associations between motor skills, diagnostic group, and EF performance. Participants included 186 HR and 76 LR infants. EF (A-not-B), motor skills (Fine and Gross Motor), and cognitive ability were directly assessed at 12 months and 24 months of age. Participants were directly evaluated for ASD at 24 months using DSM-IV-TR criteria and categorized as HR-ASD, HR-Negative, and LR-Negative. HR-ASD and HR-Negative siblings demonstrated less improvement in EF over time compared to the LR-Negative group. Motor skills were associated with group and EF performance at 12 months. No group differences were found at 12 months, but at 24 months, the HR-ASD and HR-Negative groups performed worse than the LR-Negative group overall after controlling for visual reception and maternal education. On reversal trials, the HR-ASD group performed worse than the LR-Negative group. Motor skills were associated with group and EF performance on reversal trials at 24 months. Findings suggest that HR siblings demonstrate altered EF development and that motor skills may play an important role in this process.
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- 2016
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32. Early Childhood Depression and Alterations in the Trajectory of Gray Matter Maturation in Middle Childhood and Early Adolescence.
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Luby JL, Belden AC, Jackson JJ, Lessov-Schlaggar CN, Harms MP, Tillman R, Botteron K, Whalen D, and Barch DM
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- Adolescent, Cerebral Cortex pathology, Child, Child, Preschool, Depressive Disorder pathology, Female, Gray Matter pathology, Humans, Longitudinal Studies, Magnetic Resonance Imaging, Male, Organ Size, Prospective Studies, Cerebral Cortex growth & development, Depressive Disorder, Major pathology, Gray Matter growth & development
- Abstract
Importance: The trajectory of cortical gray matter development in childhood has been characterized by early neurogenesis and volume increase, peaking at puberty followed by selective elimination and myelination, resulting in volume loss and thinning. This inverted U-shaped trajectory, as well as cortical thickness, has been associated with cognitive and emotional function. Synaptic pruning-based volume decline has been related to experience-dependent plasticity in animals. To date, there have been no data to inform whether and how childhood depression might be associated with this trajectory., Objective: To examine the effects of early childhood depression, from the preschool age to the school age period, on cortical gray matter development measured across 3 waves of neuroimaging from late school age to early adolescence., Design, Setting, and Participants: Data were collected in an academic research setting from September 22, 2003, to December 13, 2014, on 193 children aged 3 to 6 years from the St Louis, Missouri, metropolitan area who were observed for up to 11 years in a longitudinal behavioral and neuroimaging study of childhood depression. Multilevel modeling was applied to explore the association between the number of childhood depression symptoms and prior diagnosis of major depressive disorder and the trajectory of gray matter change across 3 scan waves. Data analysis was conducted from October 29, 2014, to September 28, 2015., Main Outcomes and Measures: Volume, thickness, and surface area of cortical gray matter measured using structural magnetic resonance imaging at 3 scan waves., Results: Of the 193 children, 90 had a diagnosis of major depressive disorder; 116 children had 3 full waves of neuroimaging scans. Findings demonstrated marked alterations in cortical gray matter volume loss (slope estimate, -0.93 cm³; 95% CI, -1.75 to -0.10 cm³ per scan wave) and thinning (slope estimate, -0.0044 mm; 95% CI, -0.0077 to -0.0012 mm per scan wave) associated with experiencing an episode of major depressive disorder before the first magnetic resonance imaging scan. In contrast, no significant associations were found between development of gray matter and family history of depression or experiences of traumatic or stressful life events during this period., Conclusions and Relevance: This study demonstrates an association between early childhood depression and the trajectory of cortical gray matter development in late school age and early adolescence. These findings underscore the significance of early childhood depression on alterations in neural development., Competing Interests: Dr. Luby declares no conflict of interest. Dr. Belden declares no conflict of interest. Dr. Harms declares no conflict of interest. Dr. Botteron declares no conflict of interest. Dr. Jackson declares no conflict of interest. Dr. Lessov-Schlaggar declares no conflict of interest. Ms. Tillman declares no conflict of interest. Dr. Whalen declares no conflict of interest.
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- 2016
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33. Ventromedial prefrontal cortex thinning in preschool-onset depression.
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Marrus N, Belden A, Nishino T, Handler T, Ratnanather JT, Miller M, Barch D, Luby J, and Botteron K
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- Age of Onset, Anxiety Disorders complications, Anxiety Disorders pathology, Case-Control Studies, Child, Depressive Disorder, Major complications, Depressive Disorder, Major psychology, Female, Humans, Image Processing, Computer-Assisted methods, Magnetic Resonance Imaging methods, Male, Neuroimaging, Depressive Disorder, Major pathology, Prefrontal Cortex pathology
- Abstract
Background: The ventromedial prefrontal cortex (VMPFC) is a key center of affect regulation and processing, fundamental aspects of emotional competence which are disrupted in mood disorders. Structural alterations of VMPFC have consistently been observed in adult major depression and are associated with depression severity, yet it is unknown whether young children with depression demonstrate similar abnormalities. We investigated cortical thickness differences in the VMPFC of children with a history of preschool-onset depression (PO-MDD)., Methods: Participants in a longitudinal study of PO-MDD underwent structural brain imaging between the ages of 7 and 12 years. Using local cortical distance metrics, cortical thickness of the VMPFC was compared in children with and without a history of PO-MDD., Results: Children previously diagnosed with PO-MDD (n=34) had significantly thinner right VMPFC vs. children without a history of PO-MDD [(n=95); F(1,126)=5.97, (p=.016)]. This effect was specific to children with a history of PO-MDD vs. other psychiatric conditions and was independent of comorbid anxiety or externalizing disorders. Decreases in right VMPFC thickness were predicted by preschool depressive symptoms independent of depressive symptoms in school age., Limitations: Results are cross-sectional and cannot distinguish whether thinner right VMPFC represents a vulnerability marker of MDD, consequence of MDD, or marker of remitted MDD. Longitudinal imaging is needed to contextualize how this difference relates to normative VMPFC structural development., Conclusions: Onset of depression at preschool age was associated with decreased cortical thickness of right VMPFC. This finding implicates the VMPFC in depression from very early stages of brain development., (Copyright © 2015 Elsevier B.V. All rights reserved.)
- Published
- 2015
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