Evidence map›Paper›PMID 36320019›Full record

ArticleBMC cancer2022

Muscle strength is associated with fracture risk obtained by fracture risk assessment tool (FRAX) in women with breast cancer.

Rayne de Almeida Marques Bernabé, Mariana de Souza Vieira, Vanusa Felício de Souza, Luana Gomes Fontana, Ben-Hur Albergaria, José Luiz Marques-Rocha, Valdete Regina Guandalini

Abstract read
In one paragraph

Article in BMC cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Observational
  5. Article
  6. Article
  7. Frontiers in genetics · 2023
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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

7 authors.

Rayne de Almeida Marques BernabéPostgraduate Program in Nutrition and Health, Health Science Center, Federal University of Espírito Santo, Marechal Campos Avenue, 1468 - Maruípe, Vitória, CEP: 29040-090, Espírito Santo, Brazil.
Mariana de Souza VieiraPostgraduate Program in Nutrition and Health, Health Science Center, Federal University of Espírito Santo, Marechal Campos Avenue, 1468 - Maruípe, Vitória, CEP: 29040-090, Espírito Santo, Brazil.
Vanusa Felício de SouzaPostgraduate Program in Nutrition and Health, Health Science Center, Federal University of Espírito Santo, Marechal Campos Avenue, 1468 - Maruípe, Vitória, CEP: 29040-090, Espírito Santo, Brazil.
Luana Gomes FontanaDepartment of Integrated Health Education, Health Science Center, Federal University of Espírito Santo, Marechal Campos Avenue, 1468 - Maruípe, Espírito Santo, Vitória, CEP: 29040-090, Brazil.
Ben-Hur AlbergariaDepartment of Social Medicine, Health Science Center, Federal University of Espírito Santo, Marechal Campos Avenue, 1468 - Maruípe, Espírito Santo, Vitória, CEP: 29040-090, Brazil.
José Luiz Marques-RochaPostgraduate Program in Nutrition and Health, Health Science Center, Federal University of Espírito Santo, Marechal Campos Avenue, 1468 - Maruípe, Vitória, CEP: 29040-090, Espírito Santo, Brazil.
Valdete Regina GuandaliniPostgraduate Program in Nutrition and Health, Health Science Center, Federal University of Espírito Santo, Marechal Campos Avenue, 1468 - Maruípe, Vitória, CEP: 29040-090, Espírito Santo, Brazil. valdete.guandalini@ufes.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWomen with breast cancer are at risk for the development of sarcopenia and occurrence of fractures. The initial and periodic screening of these conditions can prevent the risks of disability, poor quality of life, and death. The present study investigated the association between sarcopenia phenotypes and fracture risk, assessed by the Fracture Risk Assessment Tool (FRAX) in women with breast cancer.

methodsCross-sectional study. It included women aged between 40 and 80 years, diagnosed with Luminal subtype breast cancer, with time of diagnosis ≤ 12 months, who had not started endocrine therapy, did not have metastasis, had not been treated for another malignancy, and had no recurrences. Sociodemographic, habits and lifestyle, clinical, anthropometric, and body composition variables were considered. Muscle strength, skeletal muscle mass, and physical performance were investigated using handgrip strength (HGS), appendicular skeletal muscle mass index (ASMI), and Timed Up and Go test (TUGT), respectively. Fracture risk was assessed using FRAX. Multiple linear regression models were conducted to verify the association between exposure variables and sarcopenia phenotypes. A significance level of p < 0.05 was adopted for all tests using the SPPS 25.0 program.

resultsSixty-two women with a mean age of 58.1 ± 10.4 years were evaluated. Of these, 66.1% self-declared to be non-white, 41.9% and 71.0% did not consume alcohol or smoke, respectively, and 61.3% were insufficiently active. A total of 45.2% had clinical stage II carcinoma and 65.5% had the invasive breast carcinoma histological subtype. There was a predominance of adequacy of HGS (88.7%), ASMI (94.5%), and TUGT (96.8%), as well as low risk of hip fractures (85.5%) and major fractures (82.3%). HGS remained associated with FRAX hip fractures (p = 0.007) and FRAX major fractures (p = 0.007) in the adjusted models, while ASMI was associated with body mass (p < 0.001).

conclusionsLow muscle strength was the sarcopenia phenotype that remained associated with fracture risk in women with breast cancer, independently of sociodemographic factors, level of physical activity, and clinical factors. In addition to the assessment of probable sarcopenia, this measurement may point out the risk of fractures.

Indexed as

Hip FracturesNeoplasmsSarcopeniaBone DensityCross-Sectional StudiesFemaleHand StrengthHumansMuscle StrengthPostural BalanceQuality of LifeRisk AssessmentRisk FactorsTime and Motion StudiesFractureMuscle strengthNeoplasmOsteoporosisSarcopenia

Identifiers

PMID36320019
PMCPMC9623985

What OpenQuestion holds

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LicenceCC BY
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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.