Evidence map›Paper›PMID 28502917›Full record

ArticleJournal of atherosclerosis and thrombosis2017

The Role of Heparin Cofactor Ⅱ in the Regulation of Insulin Sensitivity and Maintenance of Glucose Homeostasis in Humans and Mice.

Kiyoe Kurahashi, Seika Inoue, Sumiko Yoshida, Yasumasa Ikeda, Kana Morimoto, Ryoko Uemoto, Kazue Ishikawa, Takeshi Kondo, Tomoyuki Yuasa, Itsuro Endo and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of atherosclerosis and thrombosis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

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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

16 authors at 1 institution in 1 country.

Kiyoe KurahashiDepartment of Hematology, Endocrinology and Metabolism, Tokushima University Graduate School of Biomedical Sciences.
Seika InoueDepartment of Nutrition and Metabolism, Tokushima University Graduate School of Biomedical Sciences.
Sumiko YoshidaDepartment of Hematology, Endocrinology and Metabolism, Tokushima University Graduate School of Biomedical Sciences.
Yasumasa IkedaDepartment of Pharmacology, Tokushima University Graduate School of Biomedical Sciences.
Kana MorimotoDepartment of Community Medicine for Diabetes and Metabolic Disorders, Tokushima University Graduate School of Biomedical Sciences.
Ryoko UemotoDepartment of Community Medicine for Diabetes and Metabolic Disorders, Tokushima University Graduate School of Biomedical Sciences.
Kazue IshikawaDepartment of Hematology, Endocrinology and Metabolism, Tokushima University Graduate School of Biomedical Sciences.
Takeshi KondoDepartment of Hematology, Endocrinology and Metabolism, Tokushima University Graduate School of Biomedical Sciences.
Tomoyuki YuasaDepartment of Community Medicine for Diabetes and Metabolic Disorders, Tokushima University Graduate School of Biomedical Sciences.
Itsuro EndoDepartment of Hematology, Endocrinology and Metabolism, Tokushima University Graduate School of Biomedical Sciences.
Masato MiyakeDivision of Molecular Biology, Institute for Genome Research, Institute of Advanced Medical Sciences, Tokushima University.
Seiichi OyadomariDivision of Molecular Biology, Institute for Genome Research, Institute of Advanced Medical Sciences, Tokushima University.
Toshio MatsumotoFujii Memorial Institute of Medical Sciences, Tokushima University.
Masahiro AbeDepartment of Hematology, Endocrinology and Metabolism, Tokushima University Graduate School of Biomedical Sciences.
Hiroshi SakaueDepartment of Nutrition and Metabolism, Tokushima University Graduate School of Biomedical Sciences.
Ken-Ichi AiharaDepartment of Community Medicine for Diabetes and Metabolic Disorders, Tokushima University Graduate School of Biomedical Sciences.
Tokushima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimAccelerated thrombin action is associated with insulin resistance. It is known that upon activation by binding to dermatan sulfate proteoglycans, heparin cofactor Ⅱ(HCⅡ) inactivates thrombin in tissues. Because HCⅡ may be involved in glucose metabolism, we investigated the relationship between plasma HCⅡ activity and insulin resistance. METHODS AND

resultsIn a clinical study, statistical analysis was performed to examine the relationships between plasma HCⅡ activity, glycosylated hemoglobin (HbA1c), fasting plasma glucose (FPG), and homeostasis model assessment-insulin resistance (HOMA-IR) in elderly Japanese individuals with lifestyle-related diseases. Multiple regression analysis showed significant inverse relationships between plasma HCⅡ activity and HbA1c (p=0.014), FPG (p=0.007), and HOMA-IR (p= 0.041) in elderly Japanese subjects. In an animal study, HCⅡ

conclusionsThe present studies provide evidence to support the idea that HCⅡ plays an important role in the maintenance of glucose homeostasis by regulating insulin sensitivity in both humans and mice. Stimulators of HCⅡ production may serve as novel therapeutic tools for the treatment of type 2 diabetes.

Indexed as

HomeostasisInsulin ResistanceAnimalsBiomarkersBlood GlucoseDiet, High-FatFemaleHeparin Cofactor IIHumansHyperglycemiaHyperinsulinismInsulinMaleMiceMice, Inbred C57BLMiddle AgedBiomarkersBlood GlucoseHeparin Cofactor IIInsulinGlucose homeostasisHeparin cofactor ⅡHigh-fat dietHumansMice

Identifiers

PMID28502917
PMCPMC5742367
OpenAlexW2612033774

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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Registered trials

None linked

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.