Evidence map›Paper›PMID 32934756›Full record

ArticleDisease markers2020

Pharmacogenomics Study for Raloxifene in Postmenopausal Female with Osteoporosis.

Hsing-Fang Lu, Po-Hsin Chou, Gan-Hong Lin, Wan-Hsuan Chou, Shih-Tien Wang, Wirawan Adikusuma, Eko Mugiyanto, Kuo-Sheng Hung, Wei-Chiao Chang

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

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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

9 authors at 4 institutions in 2 countries.

Hsing-Fang LuDepartment of Clinical Pharmacy, School of Pharmacy, Taipei Medical University, Taipei, Taiwan.
Po-Hsin ChouSchool of Medicine, National Yang-Ming University, Taipei, Taiwan.
Gan-Hong LinClinical Pharmacogenomics and Pharmacoproteomics, School of Pharmacy, Taipei Medical University, Taipei, Taiwan.
Wan-Hsuan ChouDepartment of Clinical Pharmacy, School of Pharmacy, Taipei Medical University, Taipei, Taiwan.
Shih-Tien WangSchool of Medicine, National Yang-Ming University, Taipei, Taiwan.
Wirawan AdikusumaDepartment of Clinical Pharmacy, School of Pharmacy, Taipei Medical University, Taipei, Taiwan.ORCID https://orcid.org/0000-0001-9165-690X
Eko MugiyantoClinical Drug Development of Chinese Herbal Medicine, School of Pharmacy, Taipei Medical University, Taipei, Taiwan.
Kuo-Sheng HungClinical Pharmacogenomics and Pharmacoproteomics, School of Pharmacy, Taipei Medical University, Taipei, Taiwan.ORCID https://orcid.org/0000-0002-4147-0960
Wei-Chiao ChangDepartment of Clinical Pharmacy, School of Pharmacy, Taipei Medical University, Taipei, Taiwan.ORCID https://orcid.org/0000-0002-8573-5924
Taipei Medical University · TWNational Yang Ming Chiao Tung University · TWWan Fang Hospital · TWUniversity of Muhammadiyah Mataram · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoporosis is characterized by decreased bone mineral density and increased risk of fracture. Raloxifene is one of the treatments of osteoporosis. However, the responses were variable among patients. Previous studies revealed that the genetic variants are involved in the regulation of treatment outcomes. To date, studies that evaluate the influence of genes across all genome on the raloxifene treatment response are still limited. In this study, a total of 41 postmenopausal osteoporosis patients under regular raloxifene treatment were included. Gene-based analysis using MAGMA was applied to investigate the genetic association with the bone mineral density response to raloxifene at the lumbar spine or femoral neck site. Results from gene-based analysis indicated several genes (

Indexed as

Pharmacogenomic VariantsAgedAged, 80 and overAnimalsBone Density Conservation AgentsDisease Models, AnimalEpoxide HydrolasesFemaleGenotyping TechniquesHumansMembrane ProteinsMiceMiddle AgedOsteoporosis, PostmenopausalRaloxifene HydrochlorideReceptors, NeuropeptideBone Density Conservation AgentsEpoxide HydrolasesGHRHR protein, humanMembrane ProteinsRaloxifene HydrochlorideReceptors, NeuropeptideReceptors, Pituitary Hormone-Regulating HormoneSerine EndopeptidasesTMPRSS6 protein, human

Identifiers

PMID32934756
PMCPMC7479487
OpenAlexW3082566593

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Registered trials

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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.