Cited by 266Hypothalamic control of reproductive hormonesSexual Differentiation and DisordersNeural and Behavioral Psychology Studies

The DOI matches its Crossref record; 75 of the 75 references it cites were found in a registry or an index; none of the 38 sources its claims cite is checked for support yet.

Puberty Influences Medial Temporal Lobe and Cortical Gray Matter Maturation Differently in Boys Than Girls Matched for Sexual Maturity

Open access

Abstract

Sex differences in age- and puberty-related maturation of human brain structure have been observed in typically developing age-matched boys and girls. Because girls mature 1-2 years earlier than boys, the present study aimed at assessing sex differences in brain structure by studying 80 adolescent boys and girls matched on sexual maturity, rather than age. We evaluated pubertal influences on medial temporal lobe (MTL), thalamic, caudate, and cortical gray matter volumes utilizing structural magnetic resonance imaging and 2 measures of pubertal status: physical sexual maturity and circulating testosterone. As predicted, significant interactions between sex and the effect of puberty were observed in regions with high sex steroid hormone receptor densities; sex differences in the right hippocampus, bilateral amygdala, and cortical gray matter were greater in more sexually mature adolescents. Within sex, we found larger volumes in MTL structures in more sexually mature boys, whereas smaller volumes were observed in more sexually mature girls. Our results demonstrate puberty-related maturation of the hippocampus, amygdala, and cortical gray matter that is not confounded by age, and is different for girls and boys, which may contribute to differences in social and cognitive development during adolescence, and lasting sexual dimorphisms in the adult brain.

Overview

AI snapshot

Written from the paper’s full text.

TL;DR

In 80 adolescents matched on sexual maturity rather than age, puberty-related gray matter maturation differed by sex: more sexually mature boys showed larger medial temporal lobe volumes, while more sexually mature girls showed smaller amygdala and cortical gray matter volumes. These sex-by-puberty interactions were significant for the right hippocampus, bilateral amygdala, and cortical gray matter, independent of age in several analyses.

Key findings

  • Significant sex-by-pubertal-status interactions were found for the right hippocampus (b = −0.540, P = 0.013) and bilateral amygdala (right: b = −0.572, P = 0.010; left: b = −0.470, P = 0.035) using Tanner stage, with sex differences larger in mid/late puberty than pre/early puberty.
  • Boys in mid/late puberty had larger left amygdala volumes than boys in pre/early puberty (z = 1.82, P = 0.034), with trends for right amygdala (z = 1.55, P = 0.060) and right hippocampus (z = 1.61, P = 0.053); however, these effects could not be dissociated from age.
  • Girls in mid/late puberty had smaller bilateral cortical gray matter volumes than girls in pre/early puberty (right: z = −2.60, P = 0.005; left: z = −2.88, P = 0.002), and advanced Tanner stage predicted declining bilateral amygdala (right: b = −0.363, P = 0.018; left: b = −0.090, P = 0.568) and cortical gray matter (right: b = −0.379, P = 0.013; left: b = −0.415, P = 0.006) independent of age.
  • In girls, circulating testosterone correlated inversely with right amygdala volume (r = −0.289, P = 0.046) and bilateral cortical gray matter (right: r = −0.355, P = 0.014; left: r = −0.380, P = 0.008); no significant sex-by-puberty interactions were detected for thalamus or caudate.

Methods

  • Cross-sectional study of 80 healthy adolescents (48 girls, 32 boys) with complete data; girls’ age range 10.75–13.48 years, boys’ 11.73–13.98 years. Pubertal status was measured by physical exam using Tanner stages and by circulating testosterone from finger-stick blood samples.
  • Structural MRI was acquired on a 3-T Siemens Allegra scanner; FreeSurfer was used for automated segmentation of amygdala, hippocampus, thalamus, caudate, and cortical gray matter, with manual editing of hippocampal and amygdala delineations.
  • Analyses included t-tests, simultaneous multiple regression for sex, age, whole-brain volume, and sex-by-puberty interactions, Wilcoxon–Mann–Whitney tests for Tanner-stage group differences, and Pearson correlations for testosterone; boys and girls were also analyzed separately.

Limitations

  • Stated: in boys, effects of sexual maturity on amygdala volume could not be dissociated from concomitant age effects; in girls, testosterone effects on right MTL volume did not remain significant when age was added.
  • Stated: the study was cross-sectional, and the authors note future longitudinal studies are needed to parse hormonal versus age-related influences; results were not corrected for multiple comparisons because a relatively small number of hypothesis-driven tests were conducted.
  • Stated/evident: FreeSurfer validity varies by region, with amygdala and hippocampus less valid than some other regions, though manual editing and reliability checks were performed; the restricted age range and sampling difference in pre/early versus mid/late puberty proportions between boys and girls may limit generalization.

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Integrity signals

Registry

Crossref · 10.1093/cercor/bhq137

Cites

75 of 75 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

57 Own result · 27 Not checked yet · 10 Own interpretation · 6 Own method

Verify all 38 references — free account
  • It may state two separate claims as one. 29
  • Probably not a substantial claim. 17
  • The quote only partly states this claim. 1
41 of 41
  • The paper relies on this without support.

    MRI-derived volume changes in the hippocampus, amygdala, and cortical gray matter reflect underlying maturational changes in these structures.

    “The cellular etiology of human brain maturational change is not well understood given the paucity of postmortem material in the childhood to adolescent age range.”
    “Our results demonstrate puberty-related maturation of the hippocampus, amygdala, and cortical gray matter that is not confounded by age, and is different for girls and boys”
  • The paper relies on this without support.

    Circulating testosterone level is a valid measure of pubertal status in both boys and girls.

    “We focus on TES in our report of hormonal effects on brain maturation because TES was collected in both boys and girls.”
  • The paper relies on this without support.

    Tanner staging (TS) is a valid measure of pubertal status.

    “Experiment 1: pubertal status determined by TS”
  • The paper relies on this without support.

    Circulating testosterone (TES) levels reflect brain-relevant pubertal hormone exposure.

    “Experiment 2: pubertal status determined by TES”
  • The paper relies on this without support.

    Cross-sectional differences in brain volume across pubertal stages reflect developmental changes (maturation) rather than cohort effects.

    “Future longitudinal studies will be ideal in parsing hormonal or other age-related influences on changes in the trajectories of gray matter volumes.”
  • The paper relies on this without support.

    Age is an adequate covariate to dissociate pubertal from age-related effects.

    “All these effects were significant even when age was used as an additional predictor”
6 of 6

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Statistics recomputed

Every reported test result, recomputed from its test statistic and degrees of freedom. A result shows as not adding up only once an independent check has confirmed it.

  • Consistentz = 1.82reported p = .034 · recomputed p = .069

    “(z = 1.82,p = .034”

    The paper states a one-tailed test

  • Consistentz = 1.55reported p = .06 · recomputed p = .121

    “(z = 1.55,p = .060”

    The paper states a one-tailed test

  • Consistentz = 1.61reported p = .053 · recomputed p = .107

    “(z = 1.61,p = .053”

    The paper states a one-tailed test

  • Consistentz = -2.6reported p = .005 · recomputed p = .009

    “(z = -2.60,p = .005”

    The paper states a one-tailed test

  • Consistentz = -2.88reported p = .002 · recomputed p = .004

    “z = -2.88,p = .002”

    The paper states a one-tailed test

  • Consistentz = 2.51reported p = .006 · recomputed p = .012

    “(z = 2.51, p = .006”

    The paper states a one-tailed test

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Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

Each contradiction between two passages listed here was confirmed by an independent check.

3 of 3

Citations

Cites

Show all 75 references

Research works printed but not linked: 6

  1. 2009, 30, 1
  2. 2006, 138, 997
  3. 2006, STAT COMPUT GRAPHICS, 17, 11
  4. 2009, FRONT NEUROINFORMAT, 3, 22
  5. 2002, 33, 341
  6. 2009, 34, 332

Cited by

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Metadata

Authors
Bramen, J. E., Hranilovich, J. A., Dahl, R. E., Forbes, E. E., Chen, J., Toga, A. W., Dinov, I. D., Worthman, C. M., & Sowell, E. R.
Affiliations
  • University of California, Los Angeles (US)
  • University of Pittsburgh (US)
  • Emory University (US)
Venue
Cerebral Cortex
Published
2010-08-16
Volume
21
Issue
3
Pages
636-646
ISSN
  • 1047-3211 (ISSN-L)
  • 1460-2199
OpenAlex
W2169286936
Cited by
266
References
75
Citations by year
2026: 6 · 2025: 8 · 2024: 8 · 2023: 20 · 2022: 7 · 2021: 17 · 2020: 24 · 2019: 13 · 2018: 17 · 2017: 14 · 2016: 24 · 2015: 25 · 2014: 18 · 2013: 27 · 2012: 28
FWCI
24.66
Type
journal article
Language
en
Open access
Locations
  • Cerebral Cortex (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institute on Drug Abuse (R01DA018910, R01 DA 017831)
  • National Center for Research Resources (P41RR013642, U54RR021813)
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD053893)
Topics
  • Health Sciences › Medicine › Reproductive Medicine › Hypothalamic control of reproductive hormones
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Sexual Differentiation and Disorders
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Keywords
puberty, brain maturation, sex differences, medial temporal lobe, hippocampus, amygdala, cortical gray matter, sexual maturity, testosterone, thalamus, caudate nucleus, adolescent brain development, sexual dimorphism
MeSH terms
Adolescent, Cerebral Cortex, Child, Female, Humans, Image Interpretation, Computer-Assisted, Magnetic Resonance Imaging, Male, Puberty, Sex Characteristics

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