Evidence map›Paper›PMID 20814769›Full record

ReviewCurrent osteoporosis reports2010

The skeletal subsystem as an integrative physiology paradigm.

Aaron J Weiss, Jameel Iqbal, Neeha Zaidi, Jeffrey I Mechanick

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current osteoporosis reports, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Recent advancement of HDAC inhibitors against breast cancer.Medical oncology (Northwood, London, England) · 2023
    Review
  2. The NO-cGMP-PKG pathway in skeletal remodeling.Annals of the New York Academy of Sciences · 2021
    Review
  3. Review
  4. Review
  5. 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

4 authors.

Aaron J WeissDepartment of Medicine, Mount Sinai School of Medicine, New York, NY 10029, USA.
Jameel Iqbal
Neeha Zaidi
Jeffrey I Mechanick

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Homeostatic bone remodeling depends on precise regulation of osteoblast-osteoclast coupling through intricate endocrine, immune, neuronal, and mechanical factors. The osteoblast-osteoclast model of bone physiology with layers of regulatory complexity can be investigated as a component of a local skeletal subsystem or as a part of a complete whole-body system. In this review, we flip the traditional investigative paradigm of scientific experimentation ("bottom-top research") to a "top-bottom" approach using systems biology. We first establish the intricacies of the two-cell model at the molecular signaling level. We then provide, on a systems level, an integrative physiologic approach involving many recognized organ-level subsystems having direct and/or indirect effects on bone remodeling. Lastly, a hypothetical model of bone remodeling based on frequency and amplitude regulatory mechanisms is presented. It is hoped that by providing a thorough model of skeletal homeostasis, future progress can be made in researching and treating skeletal morbidities.

Indexed as

Adipose TissueAnimalsBone RemodelingBone ResorptionCytokinesHomeostasisHumansOsteoblastsOsteoclastsOsteocytesParathyroid HormoneRANK LigandThyrotropinCytokinesParathyroid HormoneRANK LigandThyrotropinTNFSF11 protein, human

Identifiers

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.