Evidence map›Paper›PMID 17565272›Full record

ReviewCurrent opinion in nephrology and hypertension2007

Mineral metabolism and aging: the fibroblast growth factor 23 enigma.

Beate Lanske, M Shawkat Razzaque

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in nephrology and hypertension, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. FGF-23/Klotho signaling is not essential for the phosphaturic and anabolic functions of PTH.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2011
    Article
  10. Review
  11. Article
  12. Article
  13. In vivo genetic evidence for klotho-dependent, fibroblast growth factor 23 (Fgf23) -mediated regulation of systemic phosphate homeostasis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2009
    Article
  14. Article
  15. Review
  16. Article
  17. Klotho and Na+,K+-ATPase activity: solving the calcium metabolism dilemma?Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2008
    Article
  18. Review
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

2 authors at 1 institution in 1 country.

Beate LanskeDepartment of Developmental Biology, Harvard School of Dental Medicine, Boston, Massachusetts 02115, USA. beate_lanske@hsdm.harvard.edu
M Shawkat Razzaque
Harvard University · US

Funding

Pathophysiologic Regulation of Fgf-23 in Phosphate Homeostasis: Role of Vitamin DR01DK073944 · NIDDK · HARVARD MEDICAL SCHOOL · PI MANNSTADT, BEATE · 2007 to 2010
$1.7M
NIDDK NIH HHS R01 DK073944
6 · The paper itself

Abstract

purpose of reviewThe regulation of phosphate homeostasis was thought to be passively mediated by the calciotrophic hormones parathyroid hormone and 1,25(OH)2D3. This article summarizes the emerging trends that show an active regulation of phosphate homeostasis by fibroblast growth factor 23 (FGF-23) - a process fairly independent of calcium homeostasis - and how altered mineral ion metabolism may affect the aging process. RECENT

findingsA major breakthrough in FGF-23 biology has been achieved by the demonstration of strikingly similar physical/biochemical phenotypes of Fgf-23(-/-) and klotho hypomorph mice, which eventually led to the identification of klotho as a cofactor in FGF-23 and its receptor interactions. Furthermore, FGF-23 has emerged as a counter regulator of the renal 1alpha(OH)ase and sodium-phosphate cotransporter activities to modulate phosphate homeostasis. Finally, studies point towards a role of dentine matrix protein 1 in affecting phosphate homeostasis, in coordination with FGF-23. SUMMARY: Recent mouse genetic studies have broadened our understanding of biochemical/molecular pathways involved in phosphate homeostasis, and linked FGF-23 to such regulation. Understanding the molecular interactions of essential calcium and phosphate regulators will enhance our knowledge of the coordinated regulation of mineral ion metabolism, and will help to redefine the molecular pathology of age-associated lesions accompanied by abnormal mineral ion metabolism such as vascular calcifications and osteoporosis.

Indexed as

25-Hydroxyvitamin D3 1-alpha-HydroxylaseAgedAgingAnimalsCalcinosisCalcitriolCalciumFemaleFibroblast Growth Factor-23Fibroblast Growth FactorsGlucuronidaseHomeostasisHumansKlotho ProteinsMiceMice, Knockout25-Hydroxyvitamin D3 1-alpha-HydroxylaseCalcitriolCalciumFGF23 protein, humanFgf23 protein, mouseFibroblast Growth Factor-23Fibroblast Growth FactorsGlucuronidaseKlotho ProteinsPhosphatesSodium-Phosphate Cotransporter Proteins, Type IIa

Identifiers

PMID17565272
PMCPMC2901548
OpenAlexW2120945659

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.