1 Psychology and human development1.11 Underlying concepts in human development

1.11.5 Neuroimaging and its role in understanding development

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Written by Resident Doctor Committee · Published

What each modality measures

Modality

What it measures

Main limitation

Structural magnetic resonance imaging (MRI)

Volume, cortical thickness, surface area

Does not measure cells; movement and scanner differences

Diffusion MRI

Water diffusion (anisotropy, diffusivity); tractography

Not a direct myelin measure; crossing fibres

Functional MRI

Blood oxygen level dependent signal, task or resting

Indirect; movement and task performance confound

Positron emission tomography (PET)

Metabolism, blood flow or molecular binding

Radiotracer exposure limits research in healthy children

MRI dominates developmental research because it uses no ionising radiation, so children can be scanned repeatedly.

Study designs

  • Cross-sectional studies compare age groups once; they are quick but confound age with cohort and individual differences.

  • Longitudinal studies rescan the same people and show that development varies between individuals and is often non-linear.

  • Longitudinal studies suffer attrition, scanner changes, practice effects and measurement error.

Shape of brain development

  • Brain volume is about a quarter of adult size at birth, three quarters by age two and 90 to 95% by about six.

  • Later, white matter volume increases while many cortical grey matter measures decline.

  • Synaptogenesis peaks earlier in visual than in prefrontal cortex.

  • Sensory and motor systems mature before association regions, which go on changing into adulthood.

  • Timing varies by region, measure and person, so no scan places an individual on a universal maturity scale.

Compare the two curves: frontal cortical grey matter volume peaks at about 11 to 12 years and then declines, while cerebral white matter volume keeps rising into adult life (schematic, after longitudinal MRI studies). Drawn for MRCPsychiatrist

Cortical thinning

  • MRI measures thickness between tissue contrast boundaries, so it does not directly measure synaptic pruning.

  • Apparent thinning can reflect changes in synapses, dendrites, glia, water, folding or analysis method.

  • Increasing myelination can shift the grey-white matter boundary without any tissue loss.

White matter and networks

  • White matter develops into early adulthood, including long-range frontal connections.

  • Rising fractional anisotropy and falling diffusivity may reflect myelination and axonal organisation, but fibre geometry also affects both.

  • Functional networks become more differentiated from one another and more integrated internally.

  • Head movement can mimic the reported childhood pattern of stronger short-range and weaker long-range connectivity.

Adolescence

  • Dual systems accounts propose that reward responses and cognitive control mature on different schedules, contributing to context-dependent risk-taking.

  • Adolescents may reason about risk like adults when calm, yet behave differently under arousal or peer influence.

  • Group findings cannot establish an individual young person's maturity, intent or capacity for control.

In the left panel, the Dual Systems Model, the socioemotional (reward) system peaks early while cognitive control matures steadily into the mid twenties, opening a gap in adolescence. Stash85, CC BY-SA 4.0, via Wikimedia Commons

Ageing

  • HAROLD (hemispheric asymmetry reduction in older adults) describes more bilateral recruitment.

  • The posterior-anterior shift in ageing describes greater frontal than posterior recruitment.

Account

Claim

Supporting finding

Compensation (scaffolding)

Extra recruitment helps performance

More recruitment with better performance

Dedifferentiation

Activity becomes less specialised

Broader activation with poorer performance

Both accounts may apply in different tasks.

Interpreting findings

  • Group-level brain-behaviour associations do not show direction, because experience changes the brain and shared causes affect both.

  • Reverse inference wrongly concludes that a process occurred because a region linked to it activated; most regions serve several functions.

Limitation

Consequence

Participant movement

Correlates with age or symptoms, creating bias

Selected samples

Children who tolerate scanning may not represent clinical populations

Multiple comparisons

Inadequate correction produces false positives

Small studies

Overestimate effects and fail to replicate

Group to individual inference

Overlapping distributions limit individual conclusions

  • Research scans cannot determine maturity, verify symptoms or diagnose most psychiatric disorders.

  • Clinical imaging answers specific questions, such as suspected lesions, malformations, hydrocephalus or neurological disease.