Evidence map›Paper›PMID 26788515›Full record

ArticleJournal of diabetes research2016

Insulin Secretory Defect and Insulin Resistance in Isolated Impaired Fasting Glucose and Isolated Impaired Glucose Tolerance.

Sae Aoyama-Sasabe, Mitsuo Fukushima, Xin Xin, Ataru Taniguchi, Yoshikatsu Nakai, Rie Mitsui, Yoshitaka Takahashi, Hideaki Tsuji, Daisuke Yabe, Koichiro Yasuda and 3 more

Open access · goldAbstract readComparative StudyMulticenter Study
In one paragraph

Article in Journal of diabetes research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 27 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

13 authors at 8 institutions in 1 country.

Sae Aoyama-SasabeDivision of Clinical Nutrition and Internal Medicine, Okayama Prefectural University, Okayama 719-1197, Japan.
Mitsuo FukushimaDivision of Clinical Nutrition and Internal Medicine, Okayama Prefectural University, Okayama 719-1197, Japan; Preemptive Medicine and Lifestyle-Related Disease Research Center, Kyoto University Hospital, Kyoto 606-8507, Japan.
Xin XinFaculty of Computer Science and Systems Engineering, Okayama Prefectural University, Okayama 719-1197, Japan.
Ataru TaniguchiDivision of Diabetes and Endocrinology, Kyoto Preventive Medical Center, Kyoto 604-8491, Japan.
Yoshikatsu NakaiKyoto Institute of Health Science, Kyoto 604-0845, Japan.
Rie MitsuiCenter for Preventive Medicine, St. Luke's International Hospital, Tokyo 104-6591, Japan.
Yoshitaka TakahashiFaculty of Health and Welfare Science, Okayama Prefectural University, Okayama 719-1197, Japan.
Hideaki TsujiFaculty of Health and Welfare Science, Okayama Prefectural University, Okayama 719-1197, Japan.
Daisuke YabeCenter for Diabetes, Endocrinology and Metabolism, Kansai Electric Power Hospital, Osaka 553-0003, Japan; Yutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe 650-0047, Japan.
Koichiro YasudaDepartment of Diabetes and Endocrinology, Saiseikai Noe Hospital, Osaka 536-0001, Japan.
Takeshi KuroseCenter for Diabetes, Endocrinology and Metabolism, Kansai Electric Power Hospital, Osaka 553-0003, Japan; Yutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe 650-0047, Japan.
Nobuya InagakiDepartment of Diabetes and Clinical Nutrition, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Yutaka SeinoCenter for Diabetes, Endocrinology and Metabolism, Kansai Electric Power Hospital, Osaka 553-0003, Japan; Yutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe 650-0047, Japan.
Okayama Prefectural University · JPKansai Electric Power (Japan) · JPKansai Electric Power Hospital · JPKyoto Medical Center · JPKyoto University · JPKyoto University Hospital · JPSaiseikai Ibaraki Hospital · JPSt. Luke's International Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the characteristics of isolated impaired glucose tolerance (IGT) and isolated impaired fasting glucose (IFG), we analyzed the factors responsible for elevation of 2-hour postchallenge plasma glucose (2 h PG) and fasting plasma glucose (FPG) levels.

methodsWe investigated the relationship between 2 h PG and FPG levels who underwent 75 g OGTT in 5620 Japanese subjects at initial examination for medical check-up. We compared clinical characteristics between isolated IGT and isolated IFG and analyzed the relationships of 2 h PG and FPG with clinical characteristics, the indices of insulin secretory capacity, and insulin sensitivity.

resultsIn a comparison between isolated IGT and isolated IFG, insulinogenic index was lower in isolated IGT than that of isolated IFG (0.43 ± 0.34 versus 0.50 ± 0.47, resp.; p < 0.01). ISI composite was lower in isolated IFG than that of isolated IGT (6.87 ± 3.38 versus 7.98 ± 4.03, resp.; p < 0.0001). In isolated IGT group, insulinogenic index showed a significant correlation with 2 h PG (r = -0.245, p < 0.0001) and had the strongest correlation with 2 h PG (β = -0.290). In isolated IFG group, ISI composite showed a significant correlation with FPG (r = -0.162, p < 0.0001) and had the strongest correlation with FPG (β = -0.214).

conclusionsWe have elucidated that decreased early-phase insulin secretion is the most important factor responsible for elevation of 2 h PG levels in isolated IGT subjects, and decreased insulin sensitivity is the most important factor responsible for elevation of FPG levels in isolated IFG subjects.

Indexed as

Insulin ResistanceAdultAgedBiomarkersBlood GlucoseCross-Sectional StudiesFastingFemaleGlucose IntoleranceGlucose Tolerance TestHumansInsulinInsulin-Secreting CellsInsulin SecretionJapanMaleBiomarkersBlood GlucoseInsulin

Identifiers

PMID26788515
PMCPMC4693016
OpenAlexW1930811513

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.