Evidence map›Paper›PMID 30774454›Full record

ArticleJournal of experimental pharmacology2019

Enhanced efficacy of chemically modified curcumin in experimental periodontitis: systemic implications.

Howard H Wang, Hsi-Ming Lee, Veena Raja, Wei Hou, Vincent J Iacono, Joseph Scaduto, Francis Johnson, Lorne M Golub, Ying Gu

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of experimental pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 20 citations in OpenAlex.

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  7. Effect ofFrontiers in microbiology · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Howard H WangDepartment of Periodontology and Endodontology, School of Dental Medicine, State University of New York at Buffalo, Buffalo, NY, USA.
Hsi-Ming LeeDepartment of Oral Biology and Pathology, School of Dental Medicine, Stony Brook University, Stony Brook, NY, USA.
Veena RajaDepartment of Oral Biology and Pathology, School of Dental Medicine, Stony Brook University, Stony Brook, NY, USA.
Wei HouDepartment of Preventive Medicine, School of Medicine, Stony Brook University, Stony Brook, NY, USA.
Vincent J IaconoDepartment of Periodontology, School of Dental Medicine, Stony Brook University, Stony Brook, NY, USA.
Joseph ScadutoTraverse Biosciences Inc., Stony Brook, NY, USA.
Francis JohnsonDepartment of Chemistry, Stony Brook University, Stony Brook, NY, USA.
Lorne M GolubDepartment of Oral Biology and Pathology, School of Dental Medicine, Stony Brook University, Stony Brook, NY, USA.
Ying GuDepartment of General Dentistry, School of Dental Medicine, Stony Brook University, Stony Brook, NY, USA, ying.gu@stonybrook.edu.
Stony Brook School · USStony Brook University · USTraverse Biosciences (United States) · USUniversity at Buffalo, State University of New York · US

Funding

Evaluation of TRB-N0224, a Proprietary Chemically Modified Curcumin, for the Treatment of Periodontal Disease in a LPS-Induced Rat ModelR41DE024946 · NIDCR · TRAVERSE BIOSCIENCES, INC. · PI GOLUB, LORNE M, GU, YING · 2015 to 2015
$206k
NIDCR NIH HHS R41 DE024946
6 · The paper itself

Abstract

introductionDental microbial biofilm initiates gingival inflammation, and its suppression is the current dominant strategy for treating periodontitis. However, the host response to the biofilm is largely responsible for the connective tissue breakdown including alveolar bone loss, which is mediated by proinflammatory cytokines and matrix metalloproteinases (MMPs).

methodsThe current study compared the efficacy of a novel host-modulation compound, a chemically modified curcumin (CMC 2.24), to that of its parent compound (natural curcumin), in both lipopolysaccharide (LPS) (a bacterial endotoxin)-induced cell culture and in vivo models of periodontitis.

resultsIn cell culture, both CMC 2.24 and curcumin appeared similarly effective in suppressing LPS-induced cytokine (IL-1β and TNF-α) secretion by mononuclear inflammatory cells; however, CMC 2.24 significantly reduced MMP-9 secretion by 78% (

conclusionThese data, plus that from previous studies, support the therapeutic potential of CMC 2.24 in the management of inflammatory periodontal disease and its ability to reduce the risk of associated systemic diseases. The current study also indicates that the MMP-9 inhibitor efficacy is associated with the ability of CMC 2.24 (but not curcumin) to inhibit alveolar bone loss in this rat model of periodontitis.

Indexed as

chemically modified curcumincytokinesmatrix metalloproteinasesMMPsperiodontitisrats

Identifiers

PMID30774454
PMCPMC6350653
OpenAlexW2911953538

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.