Evidence map›Paper›PMID 35196359›Full record

ArticlePloS one2022

Increased dosage and treatment time of Epigallocatechin-3-gallate (EGCG) negatively affects skeletal parameters in normal mice and Down syndrome mouse models.

Raza Jamal, Jonathan LaCombe, Roshni Patel, Matthew Blackwell, Jared R Thomas, Kourtney Sloan, Joseph M Wallace, Randall J Roper

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  9. Article
  10. Sex specific emergence of trisomicbioRxiv : the preprint server for biology · 2024
    Article
  11. Article
  12. Skeletal health inFrontiers in neuroscience · 2024
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. 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

8 authors at 2 institutions in 1 country.

Raza JamalDepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana, United States of America.
Jonathan LaCombeDepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana, United States of America.
Roshni PatelDepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana, United States of America.
Matthew BlackwellDepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana, United States of America.
Jared R ThomasDepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana, United States of America.
Kourtney SloanDepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana, United States of America.
Joseph M WallaceDepartment of Biomedical Engineering, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana, United States of America.
Randall J RoperDepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana, United States of America.ORCID 0000-0002-9860-5037
Indiana University – Purdue University Indianapolis · USUniversity of Indianapolis · US

Funding

Development and treatment of skeletal deficits in a Down syndrome mouse modelR15HD090603 · NICHD · INDIANA UNIVERSITY INDIANAPOLIS · PI ROPER, RANDALL J · 2017 to 2020
$900k
NICHD NIH HHS R15 HD090603
6 · The paper itself

Abstract

Bone abnormalities affect all individuals with Down syndrome (DS) and are linked to abnormal expression of DYRK1A, a gene found in three copies in people with DS and Ts65Dn DS model mice. Previous work in Ts65Dn male mice demonstrated that both genetic normalization of Dyrk1a and treatment with ~9 mg/kg/day Epigallocatechin-3-gallate (EGCG), the main polyphenol found in green tea and putative DYRK1A inhibitor, improved some skeletal deficits. Because EGCG treatment improved mostly trabecular skeletal deficits, we hypothesized that increasing EGCG treatment dosage and length of administration would positively affect both trabecular and cortical bone in Ts65Dn mice. Treatment of individuals with DS with green tea extract (GTE) containing EGCG also showed some weight loss in individuals with DS, and we hypothesized that weights would be affected in Ts65Dn mice after EGCG treatment. Treatment with ~20 mg/kg/day EGCG for seven weeks showed no improvements in male Ts65Dn trabecular bone and only limited improvements in cortical measures. Comparing skeletal analyses after ~20mg/kg/day EGCG treatment with previously published treatments with ~9, 50, and 200 mg/kg/day EGCG showed that increased dosage and treatment time increased cortical structural deficits leading to weaker appendicular bones in male mice. Weight was not affected by treatment in mice, except for those given a high dose of EGCG by oral gavage. These data indicate that high doses of EGCG, similar to those reported in some treatment studies of DS and other disorders, may impair long bone structure and strength. Skeletal phenotypes should be monitored when high doses of EGCG are administered therapeutically.

Indexed as

AnimalsCatechinDown SyndromeDrug Administration ScheduleDyrk KinasesFemaleMaleMiceMuscle, SkeletalProtein Serine-Threonine KinasesProtein-Tyrosine KinasesCatechinDyrk Kinasesepigallocatechin gallateProtein Serine-Threonine KinasesProtein-Tyrosine Kinases

Identifiers

PMID35196359
PMCPMC8865638
OpenAlexW4212991432

What OpenQuestion holds

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LicenceCC BY
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.