Evidence map›Paper›PMID 29893365›Full record

ArticleChinese medical journal2018

Muscle Magnetic Resonance Imaging in Patients with Various Clinical Subtypes of

Hui-Ting Lin, Xiao Liu, Wei Zhang, Jing Liu, Yue-Huan Zuo, Jiang-Xi Xiao, Ying Zhu, Yun Yuan, Zhao-Xia Wang

Open access · goldAbstract read
In one paragraph

Article in Chinese medical journal, 2018. 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
0.6field-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

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. [Magnetic resonance imaging for the diagnosis of muscular dystrophy].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2022
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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 2 institutions in 1 country.

Hui-Ting LinDepartment of Neurology, Peking University First Hospital, Beijing 100034, China.
Xiao LiuDepartment of Neurology, Peking University First Hospital, Beijing 100034, China.
Wei ZhangDepartment of Neurology, Peking University First Hospital, Beijing 100034, China.
Jing LiuDepartment of Neurology, Peking University First Hospital, Beijing 100034, China.
Yue-Huan ZuoDepartment of Neurology, Peking University First Hospital, Beijing 100034, China.
Jiang-Xi XiaoDepartment of Radiology, Peking University First Hospital, Beijing 100034, China.
Ying ZhuDepartment of Radiology, Peking University First Hospital, Beijing 100034, China.
Yun YuanDepartment of Neurology, Peking University First Hospital, Beijing 100034, China.
Zhao-Xia WangDepartment of Neurology, Peking University First Hospital, Beijing 100034, China.
Peking University · CNPeking University First Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLMNA-related muscular dystrophy can manifest in a wide variety of disorders, including Emery-Dreifuss muscular dystrophy (EDMD), limb-girdle muscular dystrophy (LGMD), and LMNA-associated congenital muscular dystrophy (L-CMD). Muscle magnetic resonance imaging (MRI) has become a useful tool in the diagnostic workup of patients with muscle dystrophies. This study aimed to investigate whether there is a consistent pattern of MRI changes in patients with LMNA mutations in various muscle subtypes.

methodsTwenty-two patients with LMNA-related muscular dystrophies were enrolled in this study. MRI of the thigh and/or calf muscles was performed in them. The muscle MRI features of the three subtypes were compared by the Mann-Whitney U-test. The relationship between the clinical and MRI findings was also investigated by Spearman's rank analyses.

resultsThe present study included five EDMD, nine LGMD, and eight L-CMD patients. The thigh muscle MRI revealed that the fatty infiltration of the adductor magnus, semimembranosus, long and short heads of the biceps femoris, and vasti muscles, with relative sparing of the rectus femoris, was the predominant change observed in the EDMD, LGMD, and advanced-stage L-CMD phenotypes, although the involvement of the vasti muscles was not prominent in the early stage of L-CMD. At the level of the calf, six patients (one EDMD, four LGMD, and one L-CMD) also showed a similar pattern, in which the soleus and the medial and lateral gastrocnemius muscles were most frequently observed to have fatty infiltration. The fatty infiltration severity demonstrated higher scores associated with disease progression, with a corresponding rate of 1.483 + 0.075 × disease duration (X) (r = 0.444, P = 0.026). It was noteworthy that in six L-CMD patients with massive inflammatory cell infiltration in muscle pathology, no remarkable edema-like signals were observed in muscle MRI.

conclusionsEDMD, LGMD and advanced-staged L-CMD subtypes showed similar pattern of muscle MRI changes, while early-staged L-CMD showed somewhat different changes. Muscle MRI of L-CMD with a muscular dystrophy pattern in MRI provided important clues for differentiating it from childhood inflammatory myopathy. The fatty infiltration score could be used as a reliable biomarker for outcome measure of disease progression.

Indexed as

AdolescentAdultChildChild, PreschoolFemaleHumansMagnetic Resonance ImagingMaleMuscular DystrophiesMuscular Dystrophies, Limb-GirdleMuscular Dystrophy, Emery-DreifussYoung AdultCongenital Muscular DystrophyEmery-Dreifuss Muscular DystrophyLimb-Girdle Muscular DystrophyLMNAMuscle Magnetic Resonance Imaging

Identifiers

PMID29893365
PMCPMC6006825
OpenAlexW2806820174

What OpenQuestion holds

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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.