Evidence map›Paper›PMID 29033896›Full record

ArticleFrontiers in endocrinology2017

The Influence of a KDT501, a Novel Isohumulone, on Adipocyte Function in Humans.

Brian S Finlin, Beibei Zhu, Bernard P Kok, Cristina Godio, Philip M Westgate, Neile Grayson, Robert Sims, Jeffrey S Bland, Enrique Saez, Philip A Kern

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02444910 (Effects of KDT501 on Metabolic Features in Insulin Resistant Subjects), which is not on this map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 30% 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.

NCT02444910 phase2completednot on this map

Effects of KDT501 on Metabolic Features in Insulin Resistant Subjects

TypeinterventionalSponsorKinDex Pharmaceuticals, Inc.Ran2015 to 2015Enrolled9ConditionsDiabetes Mellitus, Type 2ArmsKDT501
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. The Promising Ability ofMolecules (Basel, Switzerland) · 2021
    Pooled it
  2. Trial
  3. Enantioselectivity of Isomerization ofMolecules (Basel, Switzerland) · 2026
    Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
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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

10 authors at 2 institutions in 1 country.

Brian S FinlinThe Department of Internal Medicine, Division of Endocrinology, The Barnstable Brown Diabetes and Obesity Center, University of Kentucky, Lexington, KY, United States.
Beibei ZhuThe Department of Internal Medicine, Division of Endocrinology, The Barnstable Brown Diabetes and Obesity Center, University of Kentucky, Lexington, KY, United States.
Bernard P KokDepartment of Molecular Medicine, Scripps Research Institute, La Jolla, CA, United States.
Cristina GodioDepartment of Molecular Medicine, Scripps Research Institute, La Jolla, CA, United States.
Philip M WestgateCollege of Public Health, University of Kentucky, Lexington, KY, United States.
Neile GraysonKindex Pharmaceuticals, Seattle, WA, United States.
Robert SimsKindex Pharmaceuticals, Seattle, WA, United States.
Jeffrey S BlandKindex Pharmaceuticals, Seattle, WA, United States.
Enrique SaezDepartment of Molecular Medicine, Scripps Research Institute, La Jolla, CA, United States.
Philip A KernThe Department of Internal Medicine, Division of Endocrinology, The Barnstable Brown Diabetes and Obesity Center, University of Kentucky, Lexington, KY, United States.
University of Kentucky · USScripps Research Institute · US

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
The role of IKKß in linking obesity to adipose tissue inflammation and adipogeneP20GM103527 · NIGMS · UNIVERSITY OF KENTUCKY · PI CASSIS, LISA A · 2012 to 2017
$13.7M
Cold Induced Changed in Human Subcutaneous White AdiposeR01DK107646 · NIDDK · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2015 to 2017
$1.5M
Seahorse XF96 Extracellular Flux AnalyzerS10OD016357 · OD · SCRIPPS RESEARCH INSTITUTE, THE · PI SAEZ, ENRIQUE · 2013 to 2013
$175k
NCATS NIH HHS UL1 TR001998NIDDK NIH HHS R01 DK107646NIGMS NIH HHS P20 GM103527NIH HHS S10 OD016357
6 · The paper itself

Abstract

objectiveIn a phase II clinical trial in nine obese, insulin-resistant humans, we observed that treatment with KDT501, a novel isohumulone drug, increased total and high-molecular weight (HMW) adiponectin in plasma. The objective was to determine whether KDT501 increased adiponectin secretion from subcutaneous white adipose tissue (SC WAT) and the underlying mechanism(s).

methodsNine obese participants with either prediabetes or with normal glucose tolerance plus three features of metabolic syndrome were part of the study. SC WAT biopsies were performed before and after 28 days of KDT501 treatment in a clinical research setting. In addition, a cold stimulus was used to induce thermogenic gene expression. Adiponectin secretion was measured, and gene expression of 130 genes involved in adipose tissue function was determined. The effect of KDT501 on adipocyte mitochondrial function was analyzed

resultsSC WAT explants secreted more total and HMW adiponectin after KDT501 treatment (

conclusionKDT501 induced adiponectin secretion posttranscriptionally and increased gene expression of thermogenic and lipolytic genes in response to cold stimulation. These beneficial effects on SC WAT may be explained by the ability of KDT501 to potentiate β-adrenergic signaling and enhance mitochondrial function in adipocytes. CLINICAL

trial registrationhttps://www.ClinicalTrials.gov, ID number: NCT02444910.

Indexed as

adipocyte secretionadiponectinadipose tissue biologygene expression profilingmetabolic syndromemitochondria

Identifiers

PMID29033896
PMCPMC5626816
OpenAlexW2759682790

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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.