Evidence map›Paper›PMID 11704974›Full record

ReviewReviews in endocrine & metabolic disorders2001

Animal models for osteoporosis.

R T Turner, A Maran, S Lotinun, T Hefferan, G L Evans, M Zhang, J D Sibonga, New Collective Author

Abstract readReview
PubMed Publisher
In one paragraph

Review in Reviews in endocrine & metabolic disorders, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 2 pooled it
1.2field-weighted citation impact, top 24% of its field
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

67 citing papers in PubMed, 2 syntheses or guidelines pooled it, 193 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Administration of Young Coconut (Diseases (Basel, Switzerland) · 2024
    Article
  10. Article
  11. Direct Assessment of Rabbit Cortical Bone Basic Multicellular Unit Longitudinal Erosion Rate: A 4D Synchrotron-Based Approach.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  12. Dentoalveolar Defects of Hypophosphatasia are Recapitulated in a Sheep Knock-In Model.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  13. Article
  14. Ovariectomy Affects Acute Pancreatitis in Mice.Digestive diseases and sciences · 2022
    Article
  15. Review
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  17. Review
  18. Article
  19. Article
  20. Article

7 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

R T TurnerMayo Clinic, 200 First Street SW, Rochester, MN 55905, USA. turner.russell@mayo.edu
A Maran
S Lotinun
T Hefferan
G L Evans
M Zhang
J D Sibonga
New Collective Author
Mayo Clinic · USMayo Clinic in Florida · US

Funding

DOSE RESPONSE EFFECTS OF ALCOHOL ON BONE METABOLISMR01AA011140 · NIAAA · OREGON STATE UNIVERSITY · PI TURNER, RUSSELL THOMAS · 1996 to 2006
$1.8M
ESTROGEN METABOLITES EFFECTS ON BONER01AR045233 · NIAMS · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI TURNER, RUSSELL THOMAS · 1999 to 2002
$675k
NIAAA NIH HHS AA11140NIAMS NIH HHS AR45233
6 · The paper itself

Abstract

Animal models will continue to be important tools in the quest to understand the contribution of specific genes to establishment of peak bone mass and optimal bone architecture, as well as the genetic basis for a predisposition toward accelerated bone loss in the presence of co-morbidity factors such as estrogen deficiency. Existing animal models will continue to be useful for modeling changes in bone metabolism and architecture induced by well-defined local and systemic factors. However, there is a critical unfulfilled need to develop and validate better animal models to allow fruitful investigation of the interaction of the multitude of factors which precipitate senile osteoporosis. Well characterized and validated animal models that can be recommended for investigation of the etiology, prevention and treatment of several forms of osteoporosis have been listed in Table 1. Also listed are models which are provisionally recommended. These latter models have potential but are inadequately characterized, deviate significantly from the human response, require careful choice of strain or age, or are not practical for most investigators to adopt. It cannot be stressed strongly enough that the enormous potential of laboratory animals as models for osteoporosis can only be realized if great care is taken in the choice of an appropriate species, age, experimental design, and measurements. Poor choices will results in misinterpretation of results which ultimately can bring harm to patients who suffer from osteoporosis by delaying advancement of knowledge.

Indexed as

AnimalsBone and BonesDisease Models, AnimalDogsHaplorhiniHumansMiceOsteoporosisRatsNASA Discipline Regulatory PhysiologyNon-NASA Center

Identifiers

PMID11704974
OpenAlexW1583033333

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.