Evidence map›Paper›PMID 31242815›Full record

ArticleJournal of the American Heart Association2019

Identification of Differential Roles of MicroRNA-33a and -33b During Atherosclerosis Progression With Genetically Modified Mice.

Satoshi Koyama, Takahiro Horie, Tomohiro Nishino, Osamu Baba, Naoya Sowa, Yui Miyasaka, Yasuhide Kuwabara, Tetsushi Nakao, Masataka Nishiga, Hitoo Nishi and 14 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 31% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. MicroRNAs Regulate Function in Atherosclerosis and Clinical Implications.Oxidative medicine and cellular longevity · 2023
    Review
  9. Article
  10. Article
  11. Genomic Variants and Multilevel Regulation ofJournal of cardiovascular development and disease · 2021
    Review
  12. Review
  13. Article
  14. MicroRNA regulation of cholesterol metabolism.Annals of the New York Academy of Sciences · 2021
    Review
  15. MicroRNAs and Circular RNAs in Lipoprotein Metabolism.Current atherosclerosis reports · 2021
    Review
  16. Review
  17. Article
  18. Review
  19. 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

24 authors at 3 institutions in 1 country.

Satoshi Koyama1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Takahiro Horie1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Tomohiro Nishino1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Osamu Baba1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Naoya Sowa1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Yui Miyasaka1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Yasuhide Kuwabara1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Tetsushi Nakao1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Masataka Nishiga1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Hitoo Nishi1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Yasuhiro Nakashima1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Fumiko Nakazeki1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Yuya Ide1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Masahiro Kimura1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Shuhei Tsuji1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Randolph Ruiz Rodriguez1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Sijia Xu1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Tomohiro Yamasaki1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Chiharu Otani1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Toshimitsu Watanabe1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Tomoyuki Nakamura2 Department of Pharmacology Kansai Medical University Hirakata Japan.
Koji Hasegawa3 Division of Translational Research Clinical Research Institute National Hospital Organization Kyoto Medical Center Kyoto Japan.
Takeshi Kimura1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Koh Ono1 Department of Cardiovascular Medicine Graduate School of Medicine Kyoto University Kyoto Japan.
Kyoto University · JPKansai Medical University · JPKyoto Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Micro RNA (miR)-33 targets cholesterol transporter ATP -binding cassette protein A1 and other antiatherogenic targets and contributes to atherogenic progression. Its inhibition or deletion is known to result in the amelioration of atherosclerosis in mice. However, mice lack the other member of the miR-33 family, miR-33b, which exists in humans and other large mammals. Thus, precise evaluation and comparison of the responsibilities of these 2 miRs during the progression of atherosclerosis has not been reported, although they are essential. Methods and Results In this study, we performed a comprehensive analysis of the difference between the function of miR-33a and miR-33b using genetically modified mice. We generated 4 strains with or without miR-33a and miR-33b. Comparison between mice with only miR-33a (wild-type mice) and mice with only miR-33b (miR-33a

Indexed as

AnimalsApolipoproteins BAtherosclerosisBone Marrow TransplantationCholesterolCholesterol, DietaryDiet, High-FatDisease ProgressionGene Expression ProfilingGene Knock-In TechniquesHepatocytesLiverMacrophages, PeritonealMiceMice, KnockoutMice, Knockout, ApoEApolipoproteins BCholesterolCholesterol, DietaryMicroRNAsMIRN33b microRNA, humanMirn33 microRNA, mouseTriglyceridesatherosclerosishumanized mouse modellipid metabolismmicroRNA

Identifiers

PMID31242815
PMCPMC6662357
OpenAlexW2954469793

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.