Anatomic magnetic resonance imaging of the developing child and adolescent brain and effects of genetic variation.
- Authors
- Giedd, Jay N; Stockman, Michael; Weddle, Catherine; Liverpool, Maria; Alexander-Bloch, Aaron; Wallace, Gregory L; Lee, Nancy R; Lalonde, Francois; Lenroot, Rhoshel K
- Year
- 2010
- Journal
- Neuropsychology review
- PMID
- 21069466
- DOI
- 10.1007/s11065-010-9151-9
- PMCID
- PMC3268519
Magnetic resonance imaging studies have begun to map effects of genetic variation on trajectories of brain development. Longitudinal studies of children and adolescents demonstrate a general pattern of childhood peaks of gray matter followed by adolescent declines, functional and structural increases in connectivity and integrative processing, and a changing balance between limbic/subcortical and frontal lobe functions, which extends well into young adulthood. Twin studies have demonstrated that genetic factors are responsible for a significant amount of variation in pediatric brain morphometry. Longitudinal studies have shown specific genetic polymorphisms affect rates of cortical changes associated with maturation. Although over-interpretation and premature application of neuroimaging findings for diagnostic purposes remains a risk, converging data from multiple imaging modalities is beginning to elucidate the influences of genetic factors on brain development and implications of maturational changes for cognition, emotion, and behavior.
Scatterplot of longitudinal measurements of total brain volume for males (N=475 scans, shown in dark gray) and females (N=354 scans, shown in light gray) (Lenroot et al. 2007)
LLM interpretation
This scatterplot shows longitudinal measurements of total brain volume (cc³) across age (years) for males (dark gray) and females (light gray). The x-axis ranges from 0 to 30 years, and the y-axis ranges from 500 to 1500 cc³. Data points are connected by lines for individual subjects, showing a general trend of volume increase during childhood followed by stabilization or slight decline in adolescence and early adulthood, with males generally exhibiting higher volumes than females.
Mean volume by age in years for males (N=475 scans) and females (N=354 scans). Middle lines in each set of three lines represent mean values, and upper and lower lines represent upper and lower 95% confidence intervals. a Total brain volume, b Gray matter volume, c White matter volume, d Lateral ventricle volume, e Mid-sagittal area of the corpus callosum, f Caudate volume (Lenroot et al. 2007)
LLM interpretation
This figure consists of six line graphs (a-f) showing the mean volume or area of various brain structures across ages 7 to 19 years for males and females. Each plot displays two sets of lines representing the mean and 95% confidence intervals for each sex, with the x-axis representing age in years and the y-axis representing volume in cubic centimeters (cc) or area in $\text{cc}^2$. Trends vary by structure: total brain, gray matter, and caudate volumes generally peak in early adolescence before plateauing or declining, while white matter, lateral ventricle, and corpus callosum measurements show a steady increase with age.
Right lateral and top views of the dynamic sequence of GM maturation over the cortical surface. The side bar shows a color representation in units of GM volume (Gogtay et al. 2004)
LLM interpretation
This figure presents a dynamic sequence of brain surface maps showing gray matter (GM) maturation from age 5 to 20. The visualization includes right lateral and top views of the cortex, with a color scale indicating GM volume. A clear trend of decreasing GM volume is visible over time, as the colors shift from warm (red/yellow) to cool (blue/purple) tones across the cortical surface.
Graphic representation of structural equation modeling with genetically informative data
LLM interpretation
This is a structural equation modeling diagram of an ACE model comparing two individuals (Phenotype Twin 1 and Phenotype Twin 2). The model shows that each phenotype is influenced by three latent variables: additive genetic effects (A), common environmental effects (C), and unique environmental effects (E). Double-headed arrows indicate correlational relationships between the twins' latent variables, with specified coefficients of 1 for C and either 0.5 or 1 for A.
Heritability at ages 5, 12, and 18 years for superior, inferior, right and left cortical surfaces. Colorbar shows scale of heritability values from 0.0 to 1.0 (Lenroot et al. 2009)
LLM interpretation
This figure consists of a series of brain surface maps showing heritability values across three age groups: 5 years (column a), 12 years (column b), and 18 years (column c). The maps display superior, inferior, right, and left cortical surfaces, with a colorbar indicating heritability values ranging from 0.0 (purple) to 1.0 (red). Visually, heritability appears lowest at age 12 and highest at age 18, with the most intense colors (higher heritability) concentrated in the 18-year-old group.
Vertex maps of areas showing statistically significant differences in the rate of cortical thinning between genotype groups. Pheu607Leu top panel, Ser704Cys bottom panel. Phe carriers (PheCar) showed a significant attenuation of cortical thinning relative to Leu homozygotes (LeuLeu) in the colored regions shown. The inset plot illustrates estimated genotype group trajectories for the left superior frontal focus. Ser homozygotes (SerSer) showed a significant acceleration of cortical thinning in the colored regions shown. The inset plot illustrates estimated genotype group trajectories for the left posterior superior temporal focus. In all instances ‘Warmer’ colors indicate thickness trajectory differences of greater statistical significance (Raznahan et al. 2010)
LLM interpretation
This figure consists of two panels of cortical vertex maps paired with line graphs showing cortical thickness trajectories over age (7 to 22 years). The top panel shows regions where Phe carriers (PheCar) have attenuated cortical thinning compared to Leu homozygotes (LeuLeu), while the bottom panel shows regions where Ser homozygotes (SerSer) have accelerated thinning compared to Cys carriers (CysCar). Colored regions on the brain maps indicate statistical significance, with warmer colors representing higher significance levels.
| # | Section | Preview |
|---|---|---|
| 0 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence | Data taken from the Child Psychiatry Branch (CPB) cohort has shown several striking findings. One is… |
| 1 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence | childhood and adolescence in this sample the group average brain size for males is approximately 10%… |
| 2 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence | These findings highlight one of the most important principles emerging from neuroimaging research,… |
| 3 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Trajectories of Brain Volumes | Brain volume follows an inverted U shape trajectory, which peaks at approximately age 10.5 in girls… |
| 4 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Trajectories of Brain Volumes | White matter volumes instead increase throughout childhood and adolescence (Fig. 2c). At lobar… |
| 5 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Trajectories of Brain Volumes | The corpus callosum (CC) is the most prominent white matter structure and easily visualized on mid… |
| 6 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Trajectories of Brain Volumes | Increasing white matter during childhood and adolescence allows for greater integration of disparate… |
| 7 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Trajectories of Brain Volumes | Recognition of the importance of white matter development for brain function has stimulated the… |
| 8 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Subcortical Structures — Basal Ganglia | The basal ganglia are a collection of subcortical nuclei (caudate, putamen, globus pallidus,… |
| 9 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Subcortical Structures — Amygdala and Hippocampus | The temporal lobes, amygdala, and hippocampus are integral players in the arenas of emotion,… |
| 10 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Subcortical Structures — Amygdala and Hippocampus | Description of the amygdala and hippocampus has been performed using manual tracing by expert… |
| 11 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Lateral Ventricles | The lateral ventricles are distinctive as a brain morphometry measure, as they are compartments… |
| 12 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Cerebellum | Although only about 1/9 the volume of the cerebrum, the cerebellum (Latin for “little brain”)… |
| 13 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Cerebellum | peak size occurring at 11.3 in girls and 15.6 in boys, similar to the cerebrum. However, these… |
| 14 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Regional Differences in Cortical Thickness | Although some functional implications may be gleaned by examining GM at the lobar level, a… |
| 15 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Regional Differences in Cortical Thickness | We have created movies of changes in cortical thickness over development by analyzing scans acquired… |
| 16 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Regional Differences in Cortical Thickness | The thinning associated with cortical maturation appears to occur first in primary sensorimotor… |
| 17 | Mapping Developmental Anatomic Trajectories During Typical Childhood and Adolescence — Regional Differences in Cortical Thickness | Another potential contributor to decreased GM volume and cortical thickness is the ongoing… |
| 18 | Genetic and Environmental Influences on Brain Development: Quantitative Genetics | Individual variation in the trajectory of brain development arises from the interaction of genetic… |
| 19 | Genetic and Environmental Influences on Brain Development: Quantitative Genetics | In the classical twin model, it is assumed that the amount of genetic material shared by a pair of… |
No entities extracted from this document yet.
No uploaded files.
In this knowledge base
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| A longitudinal DNA methylation atlas and its link to brain structure and mental health. | Chen D et al. | — | 2026 | → |
| Polygenic architecture of brain structure and function, behaviors, and psychopathologies in children. | Joo YY et al. | — | 2025 | → |
| Longitudinal change of inhibitory control functional connectivity associated with the development of heavy alcohol drinking. | Antón-Toro LF et al. | — | 2023 | → |
| Do aggregate, multimodal structural neuroimaging measures replicate regional developmental differences observed in highly cited cellular histological studies? | Hagler DJ et al. | — | 2022 | → |
| Design Fluency in Children with ADHD and Comorbid Disorders. | Fournier A et al. | — | 2020 | → |
| Cortical surface architecture endophenotype and correlates of clinical diagnosis of autism spectrum disorder | Yamagata B et al. | — | 2019 | — |
| Cortical surface architecture endophenotype and correlates of clinical diagnosis of autism spectrum disorder. | Yamagata B et al. | — | 2019 | → |
| Gender differences in brain processes during inhibition of manual movements programs. | Korzhyk O et al. | — | 2019 | → |
| Genetic Influences on the Development of Cerebral Cortical Thickness During Childhood and Adolescence in a Dutch Longitudinal Twin Sample: The Brainscale Study. | Teeuw J et al. | — | 2019 | → |
| Outdoor Air Pollution and Brain Structure and Function From Across Childhood to Young Adulthood: A Methodological Review of Brain MRI Studies. | Herting MM et al. | — | 2019 | → |
| The association between under-nutrition, school performance and perceptual motor functioning in first-grade South African learners: The North-West Child Health Integrated with Learning and Development study. | Pienaar AE | — | 2019 | → |
| Evaluation of non-negative matrix factorization of grey matter in age prediction. | Varikuti DP et al. | — | 2018 | → |
| Pediatric Brain Development in Down Syndrome: A Field in Its Infancy. | Hamner T et al. | — | 2018 | → |
| Psychotic-spectrum symptoms, cumulative adversity exposure and substance use among high-risk girls. | Lansing AE et al. | — | 2018 | → |
| The association between caries related treatment needs and socio-demographic variables among young Israeli adults: a record based cross sectional study. | Levy DH et al. | — | 2018 | → |
| Total brain, cortical, and white matter volumes in children previously treated with glucocorticoids. | Holm SK et al. | — | 2018 | → |
| Brain structure, working memory and response inhibition in childhood leukemia survivors. | van der Plas E et al. | — | 2017 | → |
| Genetic correlates of the development of theta event related oscillations in adolescents and young adults. | Chorlian DB et al. | — | 2017 | → |
| Paired-Associative Stimulation-Induced Long-term Potentiation-Like Motor Cortex Plasticity in Healthy Adolescents. | Lee JC et al. | — | 2017 | → |
| Shared atypical brain anatomy and intrinsic functional architecture in male youth with autism spectrum disorder and their unaffected brothers. | Lin HY et al. | — | 2017 | → |
| Abnormal spindle-like microcephaly-associated (ASPM) mutations strongly disrupt neocortical structure but spare the hippocampus and long-term memory. | Passemard S et al. | — | 2016 | → |
| Acute brain trauma. | Martin GT | — | 2016 | → |
| Adolescent Development of Cortical and White Matter Structure in the NCANDA Sample: Role of Sex, Ethnicity, Puberty, and Alcohol Drinking. | Pfefferbaum A et al. | — | 2016 | → |
| Age-Related Differences in Sleep Architecture and Electroencephalogram in Adolescents in the National Consortium on Alcohol and Neurodevelopment in Adolescence Sample. | Baker FC et al. | — | 2016 | → |
| A Systematic Review and Meta-analysis of Neuroimaging in Oppositional Defiant Disorder (ODD) and Conduct Disorder (CD) Taking Attention-Deficit Hyperactivity Disorder (ADHD) Into Account. | Noordermeer SD et al. | — | 2016 | → |
| Cortical thickness change in autism during early childhood. | Smith E et al. | — | 2016 | → |
| Cumulative trauma, adversity and grief symptoms associated with fronto-temporal regions in life-course persistent delinquent boys. | Lansing AE et al. | — | 2016 | → |
| Development of brain networks and relevance of environmental and genetic factors: A systematic review. | Richmond S et al. | — | 2016 | → |
| Development of the Cell Population in the Brain White Matter of Young Children. | Sigaard RK et al. | — | 2016 | → |
| Nutritional quality of diet and academic performance in Chilean students. | Correa-Burrows P et al. | — | 2016 | → |
| Sleep disturbances in adolescents with ADHD: A systematic review and framework for future research. | Lunsford-Avery JR et al. | — | 2016 | → |
| The contributions of resting state and task-based functional connectivity studies to our understanding of adolescent brain network maturation. | Stevens MC | — | 2016 | → |
| A new template to study callosal growth shows specific growth in anterior and posterior regions of the corpus callosum in early childhood. | Ansado J et al. | — | 2015 | → |
| Cross-sectional versus longitudinal estimates of age-related changes in the adult brain: overlaps and discrepancies. | Pfefferbaum A et al. | — | 2015 | → |
| Fusion analysis of first episode depression: where brain shape deformations meet local composition of tissue. | Ramezani M et al. | — | 2015 | → |
| Gender modulates the development of theta event related oscillations in adolescents and young adults. | Chorlian DB et al. | — | 2015 | → |
| Preschool externalizing behavior predicts gender-specific variation in adolescent neural structure. | Caldwell JZ et al. | — | 2015 | → |
| The pediatric template of brain perfusion. | Avants BB et al. | — | 2015 | → |
| The Relationship between Nutrition in Infancy and Cognitive Performance during Adolescence. | Nyaradi A et al. | — | 2015 | → |
| Development and heritability of subcortical brain volumes at ages 9 and 12. | Swagerman SC et al. | — | 2014 | → |
| Dissociation of preparatory attention and response monitoring maturation during adolescence. | Padilla ML et al. | — | 2014 | → |
| Postnatal development of the hippocampus in the Rhesus macaque (Macaca mulatta): a longitudinal magnetic resonance imaging study. | Hunsaker MR et al. | — | 2014 | → |
| Age, sex, and performance influence the visuospatial working memory network in childhood. | Spencer-Smith M et al. | — | 2013 | → |
| Brain white matter microstructure alterations in adolescent rhesus monkeys exposed to early life stress: associations with high cortisol during infancy. | Howell BR et al. | — | 2013 | → |
| Developmental differences in diffusion tensor imaging parameters in borderline personality disorder. | New AS et al. | — | 2013 | → |
| Edited magnetic resonance spectroscopy detects an age-related decline in brain GABA levels. | Gao F et al. | — | 2013 | → |
| Effects of age and gender on neural networks of motor response inhibition: from adolescence to mid-adulthood. | Rubia K et al. | — | 2013 | → |
| Effects of repeated adolescent stress and serotonin transporter gene partial knockout in mice on behaviors and brain structures relevant to major depression. | Spinelli S et al. | — | 2013 | → |
| Functional connectivity between parietal and frontal brain regions and intelligence in young children: the Generation R study. | Langeslag SJ et al. | — | 2013 | → |
| Puberty and adolescent sexuality. | Fortenberry JD | — | 2013 | → |
| The role of nutrition in children's neurocognitive development, from pregnancy through childhood. | Nyaradi A et al. | — | 2013 | → |
| Variation in longitudinal trajectories of regional brain volumes of healthy men and women (ages 10 to 85 years) measured with atlas-based parcellation of MRI. | Pfefferbaum A et al. | — | 2013 | → |
| Adolescent social cognitive and affective neuroscience: past, present, and future. | Pfeifer JH et al. | — | 2012 | → |
| Assessment of intelligence in the preschool period. | Baron IS et al. | — | 2012 | → |
| Elevated amygdala activity to negative faces in young adults with early onset major depressive disorder. | Mingtian Z et al. | — | 2012 | → |
| Emotional modulation of the ability to inhibit a prepotent response during childhood. | Urben S et al. | — | 2012 | → |
| Executive function in early- and adult onset schizophrenia. | Holmén A et al. | — | 2012 | → |
| Frontal lobe morphometry with MRI in a normal age group of 6-17 year-olds. | Ilkay Koşar M et al. | — | 2012 | → |
| Prenatal stress and peripubertal stimulation of the endocannabinoid system differentially regulate emotional responses and brain metabolism in mice. | Macrì S et al. | — | 2012 | → |
| Recovery from medial prefrontal cortex injury during adolescence: implications for age-dependent plasticity. | Nemati F et al. | — | 2012 | → |
| The NKI-Rockland Sample: A Model for Accelerating the Pace of Discovery Science in Psychiatry. | Nooner KB et al. | — | 2012 | → |
| Changes in sleep as a function of adolescent development. | Colrain IM et al. | — | 2011 | → |
| Developmental change in regional brain structure over 7 months in early adolescence: comparison of approaches for longitudinal atlas-based parcellation. | Sullivan EV et al. | — | 2011 | → |
| Prematurity affects cortical maturation in early childhood. | Phillips JP et al. | — | 2011 | → |
| Sleep EEG, the clearest window through which to view adolescent brain development. | Colrain IM et al. | — | 2011 | → |
| The contribution of imaging genetics to the development of predictive markers for addictions. | Loth E et al. | — | 2011 | → |