Evidence map›Paper›PMID 42081927›Full record

ArticleBone2026

Sex- and site-specific associations between hemoglobin levels and cortical bone structure and microarchitecture in older adults.

Nicole M Sekel, Mita Lovalekar, Kelly H Mroz, Lauren S Roe, Nina Z Heilmann, Kerri S Freeland, Kristen J Koltun, Katelyn Guerriere Aaron, Nancy E Lane, Anne B Newman and 4 more

Abstract read
In one paragraph

Article in Bone, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Nicole M SekelNeuromuscular Research Laboratory/ Warrior Human Performance Research Center, Department of Sports Medicine and Nutrition, University of Pittsburgh, Pittsburgh, PA, USA.
Mita LovalekarNeuromuscular Research Laboratory/ Warrior Human Performance Research Center, Department of Sports Medicine and Nutrition, University of Pittsburgh, Pittsburgh, PA, USA.
Kelly H MrozNeuromuscular Research Laboratory/ Warrior Human Performance Research Center, Department of Sports Medicine and Nutrition, University of Pittsburgh, Pittsburgh, PA, USA.
Lauren S RoeEpidemiology, School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Nina Z HeilmannEpidemiology, School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Kerri S FreelandEpidemiology, School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Kristen J KoltunNeuromuscular Research Laboratory/ Warrior Human Performance Research Center, Department of Sports Medicine and Nutrition, University of Pittsburgh, Pittsburgh, PA, USA.
Katelyn Guerriere AaronMilitary Performance Division, U.S. Army Research Institute of Environmental Medicine, Natick, MA, USA.
Nancy E LaneMusculoskeletal Health, U.C. Davis Health, Sacramento, CA, USA.
Anne B NewmanEpidemiology, School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Julie M HughesDepartment of Orthopedic Surgery, School of Medicine, University of South Carolina, Columbia, SC, USA.
Elsa S StrotmeyerEpidemiology, School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Bradley C NindlNeuromuscular Research Laboratory/ Warrior Human Performance Research Center, Department of Sports Medicine and Nutrition, University of Pittsburgh, Pittsburgh, PA, USA. Electronic address: bnindl@pitt.edu.
Jane A CauleyEpidemiology, School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.

Funding

Study of Muscle, Mobility and Aging: SOMMA2R01AG059416 · NIA · CALIFORNIA PACIFIC MED CTR RES INSTITUTE · PI STEVEN RON CUMMINGS, Peggy Mannen Cawthon · 2018 to 2026
$70.3M
Wake Forest Claude D. Pepper OAIC - RenewalP30AG021332 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LEON LENCHIK · 2002 to 2026
$36.4M
Wake Forest Clinical and Translational Science AwardUL1TR001420 · NCATS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ARD, JAMY D, FOLEY, KRISTIE L · 2015 to 2023
$32.3M
VARIABILITY, STABILITY & SMOOTHNESS OF WALKINGP30AG024827 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JENNIFER S BRACH · 2004 to 2026
$28.6M
Bone microarchitecture and bone strength relationships to muscle quantity, quality and function in older adultsR01AR076752 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CAULEY, JANE ANN, STROTMEYER, ELSA S. · 2019 to 2023
$1.5M
NCATS NIH HHS UL1 TR001420NIAMS NIH HHS R01 AR076752NIA NIH HHS P30 AG021332NIA NIH HHS P30 AG024827NIA NIH HHS R01 AG059416
6 · The paper itself

Abstract

Anemia is prevalent among older adults and is associated with increased fracture risk, yet its relationship with bone microarchitecture remains poorly understood. We examined associations between hemoglobin (Hgb) concentrations and compartment-specific bone density, microarchitecture, structure and strength in older males and females.

methodsThis cross-sectional analysis included 126 males and 185 females aged ≥70 years. Hgb quartiles and anemia status (Males: <13 g/dL; Females: <12 g/dL) were measured at baseline. High-resolution peripheral quantitative computed tomography (HR-pQCT) assessed bone parameters at the tibial (T) and radial (R) metaphysis (M) and diaphysis (D). Multiple linear regression models evaluated associations between Hgb quartile and anemia with sex-standardized bone parameters.

resultsAt the RM, females in higher quartiles of Hgb tended to have the lowest total area (p trend = 0.034) and the highest cortical porosity (p trend = 0.006). In males, higher Hgb was associated with greater TD total volumetric bone mineral density (Tt.vBMD; Q4 vs. Q2: β = 0.67, p = 0.005), but anemia status showed no significant associations. In females, lower Hgb was linked to greater cortical perimeter (Q1 vs. Q2: β = 0.66, p = 0.003) at the TM and greater total area (Q1 vs. Q2: β = 0.71, p = 0.002) at the TM and RD (Q1 vs. Q2: β = 0.59, p = 0.018). Anemic females exhibited greater total area (β = 0.80, p = 0.018) and cortical perimeter (β = 0.75, p = 0.014) but lower Tt.vBMD (β = -0.56, p = 0.022, vs. non-anemic) at the RD.

conclusionsHgb levels and anemia status exhibited sex- and site-specific associations with cortical bone structure with more pronounced effects in females. Higher Hgb in males correlated with increased bone density, while in females, it was related to smaller bone areas and more pronounced porosity. These findings suggest cortical bone is more sensitive to Hgb variations than trabecular bone, potentially due to differences in vascularization and oxygen supply.

Indexed as

Cortical BoneHemoglobinsSex CharacteristicsAgedAnemiaBone DensityCross-Sectional StudiesFemaleHumansMaleTomography, X-Ray ComputedHemoglobinsanemia statusBoneHemoglobin quartilesHigh-resolution imagingHR-pQCT

Identifiers

PMID42081927
PMCPMC13499963

What Socratic 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 Socratic graph.