Evidence map›Paper›PMID 41211774›Full record

ArticleAnatomical record (Hoboken, N.J. : 2007)2026

Tracking adolescent bone remodeling through sex-specific femoral cross-sectional changes.

Julia Muñoz-Guarinos, Laura Rodríguez, José Miguel Carretero, Miguel Del Nogal Sánchez, Ana María Casas-Ferreira, José Luis Pérez Pavón, Rebeca García-González

Abstract read
In one paragraph

Article in Anatomical record (Hoboken, N.J. : 2007), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Julia Muñoz-GuarinosLaboratorio de Evolución Humana, Universidad de Burgos, Burgos, Spain.ORCID https://orcid.org/0000-0002-5260-1751
Laura RodríguezLaboratorio de Evolución Humana, Universidad de Burgos, Burgos, Spain.ORCID https://orcid.org/0000-0002-5090-1582
José Miguel CarreteroLaboratorio de Evolución Humana, Universidad de Burgos, Burgos, Spain.ORCID https://orcid.org/0000-0003-0409-8087
Miguel Del Nogal SánchezDepartamento de Química Analítica, Nutrición y Bromatología, Facultad de Ciencias Químicas, Universidad de Salamanca, Salamanca, Spain.
Ana María Casas-FerreiraDepartamento de Química Analítica, Nutrición y Bromatología, Facultad de Ciencias Químicas, Universidad de Salamanca, Salamanca, Spain.
José Luis Pérez PavónDepartamento de Química Analítica, Nutrición y Bromatología, Facultad de Ciencias Químicas, Universidad de Salamanca, Salamanca, Spain.
Rebeca García-GonzálezLaboratorio de Evolución Humana, Universidad de Burgos, Burgos, Spain.ORCID https://orcid.org/0000-0002-1035-6655

Funding

Junta de Castilla y LeónMinisterio de Ciencia, Innovación y Universidades
6 · The paper itself

Abstract

This study investigated the presence and expression of medullary contractions-defined as reductions in the medullary area (MA)-during adolescence, with particular focus on sex-specific patterns and regional variability within the femur. We assessed changes in cortical area (CA) and MA both in absolute terms and relative to total cross-sectional area (TA) at two anatomical locations: the femoral midshaft and midneck. By integrating developmental and structural indicators, we aim to explore how the hormonal surge associated with pubertal maturation influences femoral cross-sectional geometry, providing novel insights into life-history processes as recorded in skeletal remains. The study sample included 75 femora (46 non-adults and 29 adults) from the medieval population of San Pablo Monastery (Burgos, Spain, 14th-18th centuries). Individuals were assigned to one of four maturity groups based on dental and skeletal indicators. Sex estimation was performed macroscopically for adults and late adolescents, and via enamel peptide analysis (amelogenin) for younger individuals. Cross-sectional properties (including TA, CA, and MA) were extracted from CT scans at the midshaft and midneck. Multiple linear regression models (log-transformed variables) were used to assess the relationship between MA/CA and TA, testing to evaluate the effects of sex and skeletal maturity. At the midneck, both CA and MA increased with TA, with medullary expansion being more pronounced in females with larger bones, likely reflecting the influence of pelvic morphology and femoral neck orientation. In contrast, at the midshaft, TA was not generally associated with MA; however, interactions revealed that females and adults exhibited steeper increases in MA relative to TA, despite having smaller medullary cavities. Although CA was generally higher in adult females, its proportional increase with TA was attenuated, especially at the midshaft. These patterns reflect a shared trend toward medullary contraction, differentially modulated by anatomical region and biomechanical context. Our findings provide evidence for medullary contractions during late adolescence, particularly in females; however, their expression varies by anatomical region. The midneck shows more morphological plasticity, likely reflecting regional loading asymmetries, whereas the midshaft displays canalization with modulated trajectories in larger bones. Proximity to peak bone mass appears critical for detecting this process, which may be transient and obscured in cross-sectional studies. Future studies should increase the sampling of late-adolescent females and integrate pelvic proxies and other bones to better understand the timing and biomechanics of medullary contractions.

Indexed as

Bone RemodelingFemurSex CharacteristicsAdolescentAdultFemaleHumansMaleYoung Adultadolescent skeletal developmentbioarchaeologybone growth plasticitycortical bone distributionendosteal modelingpeak bone mass

Identifiers

PMID41211774
PMCPMC13549260

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.