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Scientists Map Five Life Stages of the Human Brain — Including a Long Adolescence (Ages 9–32)

Researchers analysed MRI tractography from about 3,800 neurologically typical participants (birth–90) and identified five major phases of brain wiring. Key turning points occur near ages 9, 32, 66 and 83, with an extended adolescent reorganisation lasting roughly from 9 to 32. The results emphasise discrete developmental shifts rather than steady change and may help explain individual differences in development and vulnerability to neurodegenerative disease.

Scientists Map Five Life Stages of the Human Brain — Including a Long Adolescence (Ages 9–32)

New research maps five distinct phases of brain wiring across the lifespan, revealing that the brain’s “adolescent” reorganisation lasts far longer than previously thought — roughly from age 9 into the early 30s. The findings come from MRI tractography data that trace how white-matter pathways change from birth through advanced age, and they highlight major turning points rather than a steady, uniform progression.

Study and method
The team analysed MRI tractography from about 3,800 neurologically typical participants aged from birth to 90. Using tractography to track the direction and integrity of white-matter fibres, researchers identified ages at which brain wiring shows clear shifts in organisation and connectivity. The project was led by Dr Alexa Mousley, with senior author Professor Duncan Astle.

Five life stages of brain wiring

1. Rapid growth (birth–~9)

Early childhood is dominated by rapid formation of connections. Billions of synapses are created, followed by intense synaptic pruning and consolidation: frequently used connections strengthen while weaker ones are eliminated to refine brain networks.

2. Prolonged adolescence (≈9–32)

Rather than a brief teenage blip, adolescence appears to be a multi-decade phase of structural refinement. During these years the brain improves communication within and between regions, becoming more efficient and integrated. As Dr Mousley notes, this does not mean adults in their late 20s behave like teenagers — it means adolescent-like structural changes and gains in neural efficiency continue into the early 30s.

3. Adult plateau (≈32–66)

By about 32 the brain reaches a more stable adult configuration: personality and many cognitive skills stabilise, neural efficiency nears its peak, and the brain shifts toward a more compartmentalised, less plastic organisation that can persist for several decades.

4. Early aging (≈66–83)

Around the mid-60s the study finds the first signs of noticeable age-related decline. White-matter integrity and interregional connectivity begin a gradual decline, and reduced cerebral blood flow and other age-related changes increase vulnerability to disease.

5. Advanced decline (≈83+)

By the early 80s the decline in connectivity becomes more pronounced: previously abundant white matter thins, and the brain increasingly relies on a smaller set of regions to support cognitive function.

Implications
The researchers say identifying a small number of major turning points in brain wiring can help scientists pinpoint when development is most vulnerable to disruption and may shed light on individual differences in development and the emergence of neurodegenerative conditions such as dementia.

"This study is the first to identify major phases of brain wiring across a human lifespan," said Dr Alexa Mousley. "Understanding these turning points can help us identify when and how wiring is vulnerable to disruption."

Professor Tara Spires-Jones, who was not involved in the study, described the findings as "a very cool study" that aligns with established knowledge about brain ageing, while cautioning that not everyone will experience these network changes at the exact same ages.

Takeaway: The brain’s structural journey is marked by distinct phases — rapid childhood growth, an extended adolescent refinement, a long adult plateau, and two stages of aging — and recognising those phases offers a clearer framework for studying development, resilience and disease risk across life.

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