Evidence map›Paper›PMID 37722854›Full record

ArticleJournal of cachexia, sarcopenia and muscle2023

Computed tomography-determined skeletal muscle density predicts 3-year mortality in initial-dialysis patients in China.

Ming-Jie Sheng, Jing-Yuan Cao, Shi-Mei Hou, Min Li, Yao Wang, Qiang Fang, A-Feng Miao, Min Yang, Shu-Su Liu, Chun-Hong Hu and 8 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.0field-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

15 citing papers in PubMed, 15 citations in OpenAlex.

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  13. The gut microbiome, chronic kidney disease, and sarcopenia.Cell communication and signaling : CCS · 2024
    Review
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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

18 authors at 7 institutions in 3 countries.

Ming-Jie ShengDepartment of Nephrology, Zhong Da Hospital, Southeast University School of Medicine, Nanjing, China.ORCID 0000-0003-1348-0501
Jing-Yuan CaoDepartment of Nephrology, Zhong Da Hospital, Southeast University School of Medicine, Nanjing, China.
Shi-Mei HouDepartment of Nephrology, Zhong Da Hospital, Southeast University School of Medicine, Nanjing, China.
Min LiDepartment of Nephrology, The First People's Hospital of Changzhou, Changzhou, China.
Yao WangDepartment of Nephrology, The Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou, China.
Qiang FangDepartment of Nephrology, The Affiliated Taizhou People's Hospital of Nanjing Medical University, Taizhou School of Clinical Medicine, Nanjing Medical University, Taizhou, China.
A-Feng MiaoDepartment of Nephrology, The Affiliated Taizhou People's Hospital of Nanjing Medical University, Taizhou School of Clinical Medicine, Nanjing Medical University, Taizhou, China.
Min YangDepartment of Nephrology, The First People's Hospital of Changzhou, Changzhou, China.
Shu-Su LiuDepartment of Nephrology, The First People's Hospital of Changzhou, Changzhou, China.
Chun-Hong HuDepartment of Nephrology, The Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou, China.
Cui-Lan LiuDepartment of Nephrology, The Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou, China.
Shi-Yuan WangDepartment of Epidemiology and Health Statistics, Southeast University School of Public Health, Nanjing, China.
Jing ZhengDepartment of Geriatrics, Zhong Da Hospital, Southeast University School of Medicine, Nanjing, China.
Jing-Jie XiaoCovenant Health Palliative Institute, Edmonton, Canada.
Xiao-Liang ZhangDepartment of Nephrology, Zhong Da Hospital, Southeast University School of Medicine, Nanjing, China.
Hong LiuDepartment of Nephrology, Zhong Da Hospital, Southeast University School of Medicine, Nanjing, China.
Bi-Cheng LiuDepartment of Nephrology, Zhong Da Hospital, Southeast University School of Medicine, Nanjing, China.
Bin WangDepartment of Nephrology, Zhong Da Hospital, Southeast University School of Medicine, Nanjing, China.
Zhongda Hospital Southeast University · CNNantong University · CNThe First People's Hospital of Changzhou · CNYangzhou University · CNCovenant Health · CAJiangsu University · CNSoutheast University · BD

Funding

333 Personnel Training Project of Jiangsu Province BRA2020156China Postdoctoral Science Foundation 2022M710686Foundation of Jiangsu Commission of Health M2021048National Natural Science Foundation of China 82070735National Natural Science Foundation of China 82100721National Natural Science Foundation of China 82230022National Natural Science Foundation of China 82241047Project of Taizhou Clinical Medical School of Nanjing Medical University TZKY20220209Science and Technology Support (Social Development) Project of Bureau of Science and Technology of Changzhou CE20215024Young Talent Development Plan of Changzhou Health Commission 2020-028'Zhishan Young Scholar' grants from the Southeast University
6 · The paper itself

Abstract

backgroundSkeletal muscle mass and quality assessed by computed tomography (CT) images of the third lumbar vertebra (L3) level have been established as risk factors for poor clinical outcomes in several illnesses, but the relevance for dialysis patients is unclear. A few studies have suggested a correlation between CT-determined skeletal muscle mass and quality at the first lumbar vertebra (L1) level and adverse outcomes. Generally, chest CT does not reach beyond L1. We aimed to determine whether opportunistic CT scan (chest CT)-determined skeletal muscle mass and quality at L1 are associated with mortality in initial-dialysis patients.

methodsThis 3-year multicentric retrospective study included initial-dialysis patients from four centres between 2014 and 2017 in China. Unenhanced CT images of the L1 and L3 levels were obtained to assess skeletal muscle mass [by skeletal muscle index, (SMI), cm

resultsA total of 485 patients were enrolled, of whom 257 had both L1 and L3 images. Pearson's correlation coefficient between L1 and L3 SMI was 0.84 (P < 0.001), and that between L1 and L3 SMD was 0.90 (P < 0.001). No significant association between L1 SMI and mortality was observed (P > 0.05). Low L1 SMD (n = 280, 57.73%) was diagnosed based on the optimal cutoff value (<39.56 HU for males and <33.06 HU for females). Multivariate regression analysis revealed that the low L1 SMD group had higher risks of all-cause death (hazard ratio 1.80; 95% confidence interval 1.05-3.11, P = 0.034) and cardiac death (hazard ratio 3.74; 95% confidence interval 1.43-9.79, P = 0.007).

conclusionsIn initial-dialysis patients, there is high agreement between the L1 and L3 measures for SMI and SMD. Low SMD measured at L1, but not low SMI, is an independent predictor of both all-cause death and cardiac death.

Indexed as

Muscle, SkeletalRenal DialysisDeathFemaleHumansMalePrognosisRetrospective StudiesTomography, X-Ray ComputedComputed tomographyDialysisFirst lumbar vertebra levelPrognosisSkeletal muscle quality

Identifiers

PMID37722854
PMCPMC10751407
OpenAlexW4386820083

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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.