ReviewFrontiers in endocrinology2026
Bone mineral density assessment by DXA in disease-associated osteoporosis: the limitations.
Review in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Is Follicle-Stimulating Hormone (FSH) Misnamed? Rethinking Its Role in Menopause as a Systemic Regulator of Bone, Brain, Metabolism, and Aging.Journal of clinical medicine · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Measuring bone density by DXA is a routine means of predicting fracture risk. These 2-dimensional images have limitations and may underestimate the risk of fracture due to inadequate evaluation of bone strength. The inclusion of clinical risk factors, calculating FRAX and adding TBS values all improve our ability in bone screening by DXA. However, secondary osteoporosis is not always associated with classical risk factors for bone loss. In addition, unrecognized underlying conditions may contribute to further bone loss and increased risk of low trauma fracture. Therefore, new technologies that assess bone microarchitecture, such as HR-pQCT, can improve our risk assessment for fragility fracture.
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Registered trials
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.