Evidence map›Paper›PMID 36971206›Full record

ArticleCNS neuroscience & therapeutics2023

Brain metabolic signatures in patients with genetic and nongenetic amyotrophic lateral sclerosis.

Pan Liu, Yongxiang Tang, Wanzhen Li, Zhen Liu, Ming Zhou, Jian Li, Yanchun Yuan, Liangjuan Fang, Jifeng Guo, Lu Shen and 4 more

Open access · goldAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 11 citations in OpenAlex.

  1. Cerebral metabolic patterns onEuropean journal of nuclear medicine and molecular imaging · 2026
    Article
  2. Systemic brain-body metabolic coupling patterns in amyotrophic lateral sclerosis: a whole-body [European journal of nuclear medicine and molecular imaging · 2026
    Article
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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

14 authors at 2 institutions in 2 countries.

Pan LiuDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Yongxiang TangDepartment of Neurology, The Central Hospital of Shaoyang, Shaoyang, China.
Wanzhen LiDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Zhen LiuDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Ming ZhouDepartment of Nuclear Medicine, Xiangya Hospital, Central South University, Changsha, China.
Jian LiDepartment of Nuclear Medicine, Xiangya Hospital, Central South University, Changsha, China.
Yanchun YuanDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Liangjuan FangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Jifeng GuoDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0002-3658-3928
Lu ShenDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0002-3393-8578
Hong JiangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0002-7646-5950
Beisha TangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Shuo HuDepartment of Nuclear Medicine, Xiangya Hospital, Central South University, Changsha, China.
Junling WangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0001-5117-5204
Central South University · CNThe Central Hospital of Shaoyang · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsTo study the brain metabolic signature in Chinese amyotrophic lateral sclerosis (ALS) patients and compare the difference in brain metabolic patterns between ALS with and without genetic variants.

methodsWe included 146 patients with ALS and 128 healthy controls (HCs). All patients with ALS underwent genetic testing to screen for ALS related genetic variants and were then divided into genetic (n = 22) and nongenetic ALS (n = 93) subgroups. All participants underwent brain

resultsWe identified a large of hypometabolic clusters in ALS patients as compared with HCs, especially in the bilateral basal ganglia, midbrain, and cerebellum. Moreover, hypometabolism in the bilateral temporal lobe, precentral gyrus and hypermetabolism in the left anterior cingulate, occipital lobe, and bilateral frontal lobe were also found in ALS patients as compared with HCs. Compared with nongenetic ALS patients, genetic ALS patients showed hypometabolism in the right postcentral gyrus, precuneus, and middle occipital gyrus. The incidence of sensory disturbance in patients with genetic ALS was higher than that in patients with nongenetic ALS (5 of 22 [22.72%] vs. 7 of 93 [7.52%], p = 0.036).

conclusionsOur investigation provided unprecedented evidence of relative hypometabolism in the midbrain and cerebellum in ALS patients. Genetic ALS patients showed a specific signature of brain metabolism and a higher incidence of sensory disturbance, indicating that genetic factors may be an underlying cause affecting the brain metabolism and increasing the risk of sensory disturbance in ALS.

Indexed as

Amyotrophic Lateral SclerosisBrainCerebellumFluorodeoxyglucose F18HumansMesencephalonFluorodeoxyglucose F1818F-FDG-PETamyotrophic lateral sclerosisbrain metabolismgeneticwhole exome sequencing

Identifiers

PMID36971206
PMCPMC10401109
OpenAlexW4361005903

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.