Evidence map›Paper›PMID 31079351›Full record

ArticleThe journal of physiological sciences : JPS2019

Renal involvement in the pathogenesis of mineral and bone disorder in dystrophin-deficient mdx mouse.

Eiji Wada, Takayuki Hamano, Isao Matsui, Mizuko Yoshida, Yukiko K Hayashi, Ryoichi Matsuda

Open access · goldAbstract read
In one paragraph

Article in The journal of physiological sciences : JPS, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Bone quality in Duchenne muscular dystrophy.Journal of endocrinological investigation · 2022
    Article
  6. 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

6 authors at 4 institutions in 1 country.

Eiji WadaDepartment of Pathophysiology, Tokyo Medical University, 6-1-1 Shinjuku, Shinjuku, Tokyo, 160-8402, Japan. ewada@tokyo-med.ac.jp.ORCID http://orcid.org/0000-0002-9139-9621
Takayuki HamanoDepartment of Comprehensive Kidney Disease Research, Osaka University Graduate of School Medicine, B6-2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Isao MatsuiDepartment of Comprehensive Kidney Disease Research, Osaka University Graduate of School Medicine, B6-2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Mizuko YoshidaGraduate School of Arts and Sciences, The University of Tokyo, 3-8-1 Komaba, Meguro, Tokyo, 153-8902, Japan.
Yukiko K HayashiDepartment of Pathophysiology, Tokyo Medical University, 6-1-1 Shinjuku, Shinjuku, Tokyo, 160-8402, Japan.
Ryoichi MatsudaGraduate School of Arts and Sciences, The University of Tokyo, 3-8-1 Komaba, Meguro, Tokyo, 153-8902, Japan.
The University of Osaka · JPTokyo Medical University · JPThe University of Tokyo · JPTokyo University of Science · JP

Funding

Grant-in aid from the Ministry of Education, Culture, Sports, Science and Technology of Japan 25650106Health and Labour Sciences Research Grant for Comprehensive Research on Disability Health and Welfare H22-016Intramural Research Grant for Neurological and Psychiatric Disorders from the National Center of Neurology and Psychiatry 29-4Neurological and Psychiatric Disorders of NCNP ・MEXT-Supported Program for the Strategic Research Foundation at Private Universities 29-4Research Grant from Tokyo Medical University H30
6 · The paper itself

Abstract

Duchenne muscular dystrophy is a severe muscular disorder, often complicated with osteoporosis, and impaired renal function has recently been featured. We aimed to clarify the involvement of renal function in the pathogenesis of mineral and bone disorder in mdx mice, a murine model of the disease. We clearly revealed renal dysfunction in adult mdx mice, in which dehydration and hypercalcemia were contributed. We also examined the effects of dietary phosphorus (P) overload on phosphate metabolism. Serum phosphate and parathyroid hormone (PTH) levels were significantly increased in mdx mice by dietary P in a dose-dependent manner; however, bone alkaline phosphatase levels were significantly lower in mdx mice. Additionally, bone mineral density in mdx mice were even worsened by increased dietary P in a dose-dependent manner. These results suggested that the uncoupling of bone formation and resorption was enhanced by skeletal resistance to PTH due to renal failure in mdx mice.

Indexed as

AnimalsBone DensityBone DiseasesDisease Models, AnimalDystrophinKidneyMaleMiceMice, Inbred C57BLMice, Inbred mdxMineralsMuscle, SkeletalMuscular Dystrophy, DuchenneDystrophinMineralsDuchenne muscular dystrophyMineral and bone disorderOsteoporosisPhosphate overloadingRenal dysfunction

Identifiers

PMID31079351
PMCPMC10717053
OpenAlexW2944195082

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.