Evidence map›Paper›PMID 37904164›Full record

ArticleBMC endocrine disorders2023

Serum anti-PCK1 antibody levels are a prognostic factor for patients with diabetes mellitus.

Toshiki Namiki, Minoru Takemoto, Aiko Hayashi, Hiroki Yamagata, Takahiro Ishikawa, Koutaro Yokote, Shu-Yang Li, Masaaki Kubota, Bo-Shi Zhang, Yoichi Yoshida and 12 more

Abstract read
In one paragraph

Article in BMC endocrine disorders, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
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

22 authors.

Toshiki NamikiDepartment of Diabetes, Metabolism and Endocrinology, School of Medicine, International University of Health and Welfare, Narita Hospital, 852 Hatakeda, Narita City, Chiba, 286-8520, Japan.
Minoru TakemotoDepartment of Diabetes, Metabolism and Endocrinology, School of Medicine, International University of Health and Welfare, Narita Hospital, 852 Hatakeda, Narita City, Chiba, 286-8520, Japan. minoru.takemoto@iuhw.ac.jp.
Aiko HayashiDepartment of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Hiroki YamagataDepartment of Diabetes, Metabolism and Endocrinology, School of Medicine, International University of Health and Welfare, Narita Hospital, 852 Hatakeda, Narita City, Chiba, 286-8520, Japan.
Takahiro IshikawaDepartment of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Koutaro YokoteDepartment of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Shu-Yang LiDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Masaaki KubotaDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Bo-Shi ZhangDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Yoichi YoshidaDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Tomoo MatsutaniDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Seiichiro MineDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Toshio MachidaDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Yoshio KobayashiDepartment of Cardiovascular Medicine, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Jiro TeradaDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Akira NaitoDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Koichiro TatsumiDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Hirotaka TakizawaPort Square Kashiwado Clinic, Kashiwado Memorial Foundation, Chiba, 260-0025, Japan.
Rika NakamuraMedical Project Division, Research Development Center, Fujikura Kasei Co, Saitama, 340-0203, Japan.
Hideyuki KurodaMedical Project Division, Research Development Center, Fujikura Kasei Co, Saitama, 340-0203, Japan.
Yasuo IwadateDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.
Takaki HiwasaDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba, 260-8670, Japan.

Funding

This work was supported, in part, by research grants from the Japan Science and Technology Agency (JST) and JSPS KAKENHI Grant Numbers 20K17953, 19K09451, 17K19810, 19K08596, 20K07810, 16K10520, 20K07810, 21K07395 and 15K10117.
6 · The paper itself

Abstract

backgroundAutoantibodies develop in autoimmune diseases, cancer, diabetes mellitus (DM), and atherosclerosis-related diseases. However, autoantibody biomarkers have not been successfully examined for diagnosis and therapy.

methodsSerological identification of antigens through recombinant cDNA expression cloning (SEREX) was used for primary screening of antigens. The cDNA product was expressed in bacteria and purified. Amplified luminescent proximity homogeneous assay-linked immunosorbent assay (AlphaLISA) was used to evaluate antibody levels in serum samples.

resultsPhosphoenolpyruvate carboxykinase 1 (PCK1) was recognized as an antigen by serum IgG antibodies in the sera of patients with atherosclerosis. AlphaLISA showed significantly higher serum antibody levels against recombinant PCK1 protein in patients with DM and cardiovascular disease than in healthy donors, but not in those with acute ischemic stroke, transient ischemic attack, or obstructive sleep apnea syndrome. The area under the receiver operating characteristic curve for anti-PCK1 antibodies was 0.7024 for DM. The serum anti-PCK1 antibody levels were associated with age, platelet count, and blood pressure. Anti-PCK1-antibody-positive patients showed significantly lower overall survival than the negative patients.

conclusionsSerum anti-PCK1 antibody levels were found to be associated with DM. The anti-PCK1 antibody marker is useful for predicting the overall survival of patients with DM.

Indexed as

AtherosclerosisDiabetes MellitusIschemic StrokeAutoantibodiesDNA, ComplementaryHumansIntracellular Signaling Peptides and ProteinsPhosphoenolpyruvate Carboxykinase (GTP)PrognosisRecombinant ProteinsAutoantibodiesDNA, ComplementaryIntracellular Signaling Peptides and ProteinsPCK1 protein, humanPhosphoenolpyruvate Carboxykinase (GTP)Recombinant ProteinsAntibody biomarkerAtherosclerosisCardiovascular diseaseDiabetes mellitusPhosphoenolpyruvate carboxykinase 1

Identifiers

PMID37904164
PMCPMC10614393

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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.