Evidence map›Paper›PMID 26808523›Full record

ArticlePloS one2016

Postprandial Hypertriglyceridemia Predicts Development of Insulin Resistance Glucose Intolerance and Type 2 Diabetes.

Mohammad Aslam, Sarla Aggarwal, Krishna Kumar Sharma, Vikas Galav, Sri Venkata Madhu

Open access · goldFull text read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 53 citations in OpenAlex.

  1. Vitamin DEuropean journal of clinical nutrition · 2018
    Trial
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  5. Review
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  10. Observational
  11. Frontiers in endocrinology · 2022
    Article
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  15. Review
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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

5 authors at 3 institutions in 1 country.

Mohammad AslamCenter for Diabetes Endocrinology & Metabolism, Department of Medicine, University College of Medical Sciences (University of Delhi) & GTB Hospital, Delhi, India.
Sarla AggarwalDepartment of Pathology, University College of Medical Sciences (University of Delhi) & GTB Hospital, Delhi, India.
Krishna Kumar SharmaDepartment of Pharmacology, University College of Medical Sciences (University of Delhi) & GTB Hospital, Delhi, India.
Vikas GalavDepartment of Pharmacology, University College of Medical Sciences (University of Delhi) & GTB Hospital, Delhi, India.
Sri Venkata MadhuCenter for Diabetes Endocrinology & Metabolism, Department of Medicine, University College of Medical Sciences (University of Delhi) & GTB Hospital, Delhi, India.
University College of Medical Sciences · INUniversity of Delhi · INGuru Teg Bahadur Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insulin resistance (IR) and type 2 diabetes mellitus (T2DM) have been found to be associated with postprandial hypertriglyceridemia (PPHTg). However, whether PPHTg can cause IR and diabetes is not clear. We therefore investigated the role of PPHTg in development of T2DM in rat model of T2DM. 96 male Wistar rats were randomized into four groups (24 rats each). Control Group A, high sucrose diet (HSD) Group B, HSD+Pioglitazone (10 mg/kg/day) Group C and HSD+Atorvastatin (20 mg/kg/day) Group D. Fat and glucose tolerance tests were done at regular intervals in all groups besides insulin and body weight measurement. At 26 weeks, low dose streptozotocin (15 mg/kg, i.p.) was given to half of the rats. All rats were followed up till 48 weeks. PPHTg developed as early as week 2 in Group B and stabilized by week 14. Group B displayed highest PPHTg compared to other groups. Atorvastatin treatment (Group D) abolished PPHTg which became comparable to controls, pioglitazone treatment partially blunted PPHTg resulting in intermediate PPHTg. Group B with highest PPHTg showed highest subsequent IR, glucose intolerance (GI) and highest incidence of prediabetes at week 26 and diabetes at week 34 and 46 compared to other groups. Group D rats displayed lower IR, GI, low incidence of prediabetes and diabetes at these time points compared to Groups B and C. ROC analysis showed that triglyceride area under the curve of each time point significantly predicts the risk of diabetes. Present study provides the evidence that PPHTg predicts the development of IR, GI and T2DM in rat model of diet induced T2DM.

Indexed as

Insulin ResistancePostprandial PeriodAnimalsAtorvastatinBlood GlucoseBody WeightCausalityDiabetes Mellitus, Type 2Dietary FatsDietary SucroseDisease ProgressionGlucose IntoleranceGlucose Tolerance TestHydroxymethylglutaryl-CoA Reductase InhibitorsHypertriglyceridemiaHypoglycemic AgentsAtorvastatinBlood GlucoseDietary FatsDietary SucroseHydroxymethylglutaryl-CoA Reductase InhibitorsHypoglycemic AgentsLipidsPioglitazoneThiazolidinediones

Identifiers

PMID26808523
PMCPMC4725668
OpenAlexW2410717969

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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.