Evidence map›Paper›PMID 32912928›Full record

ArticleBMJ open diabetes research & care2020

Diabetes mellitus is associated with elevated urinary pyrrole markers of γ-diketones known to cause axonal neuropathy.

Xiao Chen, Wei Liu, Lu Wang, Dafeng Lin, Lulin Nie, Kaiwu He, Zhiwei Guo, Feiqi Zhu, Wenting Feng, Weimin Liu and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMJ open diabetes research & care, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
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 6 institutions in 2 countries.

Xiao ChenKey Laboratory of Modern Toxicology of Shenzhen, Shenzhen Medical Key Subject of Health Toxicology, (2020-2024), Shenzhen Center for Disease Control and Prevention, Shenzhen, Guangdong, China.
Wei LiuKey Laboratory of Modern Toxicology of Shenzhen, Shenzhen Medical Key Subject of Health Toxicology, (2020-2024), Shenzhen Center for Disease Control and Prevention, Shenzhen, Guangdong, China.
Lu WangKey Laboratory of Modern Toxicology of Shenzhen, Shenzhen Medical Key Subject of Health Toxicology, (2020-2024), Shenzhen Center for Disease Control and Prevention, Shenzhen, Guangdong, China.
Dafeng LinPoison Detection Center, Shenzhen Prevention and Treatment Center for Occupational Diseases, Shenzhen, Guangdong, China.
Lulin NieKey Laboratory of Modern Toxicology of Shenzhen, Shenzhen Medical Key Subject of Health Toxicology, (2020-2024), Shenzhen Center for Disease Control and Prevention, Shenzhen, Guangdong, China.
Kaiwu HeKey Laboratory of Modern Toxicology of Shenzhen, Shenzhen Medical Key Subject of Health Toxicology, (2020-2024), Shenzhen Center for Disease Control and Prevention, Shenzhen, Guangdong, China.
Zhiwei GuoShenzhen Luohu Hospital for Traditional Chinese Medicine, Shenzhen, Guangdong, China.
Feiqi ZhuCognitive Impairment ward of Neurology, The 3rd Affiliated Hospital of Shenzhen University, Shenzhen, Guangdong, China.
Wenting FengPoison Detection Center, Shenzhen Prevention and Treatment Center for Occupational Diseases, Shenzhen, Guangdong, China.
Weimin LiuShenzhen Luohu Center for Disease Control and Prevention, Shenzhen, Guangdong, China.
Jing YuanDepartment of Occupational and Environmental Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Xifei YangKey Laboratory of Modern Toxicology of Shenzhen, Shenzhen Medical Key Subject of Health Toxicology, (2020-2024), Shenzhen Center for Disease Control and Prevention, Shenzhen, Guangdong, China.
Peter SpencerNeurology, School of Medicine, and Oregon Institute of Occupational Health Sciences, Oregon Health & Science University, Portland, Oregon, USA spencer@ohsu.edu junii8@126.com.ORCID 0000-0003-3994-2639
Jianjun LiuKey Laboratory of Modern Toxicology of Shenzhen, Shenzhen Medical Key Subject of Health Toxicology, (2020-2024), Shenzhen Center for Disease Control and Prevention, Shenzhen, Guangdong, China spencer@ohsu.edu junii8@126.com.
Shenzhen Center for Disease Control and Prevention · CNShenzhen Occupational Disease Prevention Hospital · CNMinistry of Ecology and Environment · CNOregon Health & Science University · USShenzhen Luohu People's Hospital · CNShenzhen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionProgressive distal symmetrical axonal neuropathy, a complication of diabetes mellitus (DM), has an unknown cause. Normal physiological metabolism and diabetic dysmetabolism are associated with the generation of γ-diketones. γ-Diketones form pyrroles with protein amines, notably with axonal proteins required for the maintenance of nerve fiber integrity, especially elongate, large-diameter peripheral nerve fibers innervating the extremities. We tested the hypothesis that neuropathy-associated γ-diketone pyrroles are elevated in DM. RESEARCH DESIGN AND

methodsWe measured the urinary concentration of γ-diketone pyrroles in age-matched and gender-matched elderly (60-84 years) persons with (n=267) or without (n=267) indicators of DM based in a community population (9411 community older adults aged ≥60 years) in Shenzhen city, Guangdong, China. We used statistical methods, including a generalized linear model, multivariate logistic regression analysis and restricted cubic splines, to assess linear and nonlinear relationships between urinary γ-diketone pyrroles and indicators of DM.

resultsCompared with healthy controls, those with DM had significantly higher levels of fasting blood glucose, glycated hemoglobin A1c, urinary ketone bodies and urinary γ-diketone pyrroles. The median concentration of urinary γ-diketone pyrrole adducts was significantly higher (p<0.0001) in individuals with DM (7.5 (5.4) μM) compared with healthy controls (5.9 (4.3) μM). Both linear and non-linear relations were found between urinary γ-diketone pyrroles and indicators of DM.

conclusionsDiabetic dysmetabolism includes increased generation and excretion of neuropathy-associated γ-diketone pyrroles. These findings form the foundation for studies to test whether γ-diketone pyrrole concentration correlates with quantitative sensory (vibration and temperature) and electrodiagnostic testing.

Indexed as

Diabetes MellitusPeripheral Nervous System DiseasesAgedAged, 80 and overAxonsChinaHumansMiddle AgedPyrrolesPyrrolesdiabetic ketoacidosisdiabetic neuropathiesmetabolism

Identifiers

PMID32912928
PMCPMC7484872
OpenAlexW3084212325

What OpenQuestion holds

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LicenceCC BY-NC
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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.