Evidence map›Paper›PMID 27009489›Full record

ReviewInternational dental journal2016

Non-antibacterial tetracycline formulations: host-modulators in the treatment of periodontitis and relevant systemic diseases.

Lorne M Golub, Muna S Elburki, Clay Walker, Maria Ryan, Timo Sorsa, Howard Tenenbaum, Michael Goldberg, Mark Wolff, Ying Gu

Open access · bronzeAbstract readReview
In one paragraph

Review in International dental journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 83 citations in OpenAlex.

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  13. Role of bestatin as a treatment for periodontitis.Frontiers in dental medicine · 2025
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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

9 authors at 7 institutions in 6 countries.

Lorne M GolubDepartment of Oral Biology and Pathology, School of Dental Medicine, Stony Brook University, Stony Brook, NY, USA.
Muna S ElburkiDepartment of Oral Biology and Pathology, School of Dental Medicine, Stony Brook University, Stony Brook, NY, USA.
Clay WalkerDepartment of Oral Biology, College of Dentistry, University of Florida, Gainesville, FL, USA.
Maria RyanDepartment of Oral Biology and Pathology, School of Dental Medicine, Stony Brook University, Stony Brook, NY, USA.
Timo SorsaDepartment of Oral and Maxillofacial Diseases, Helsinki University Central Hospital, Institute of Dentistry, University of Helsinki, Helsinki, Finland.
Howard TenenbaumDepartment of Periodontics, Faculty of Dentistry, University of Toronto, Toronto, Ontario, Canada.
Michael GoldbergDepartment of Periodontics, Faculty of Dentistry, University of Toronto, Toronto, Ontario, Canada.
Mark WolffDepartment of Cariology and Comprehensive Care, College of Dentistry, New York University, New York City, NY, USA.
Ying GuDepartment of General Dentistry, School of Dental Medicine, Stony Brook University, Stony Brook, NY, USA.
Stony Brook School · USNew York University · USTel Aviv University · ILUniversity of Benghazi · LYUniversity of Florida · USUniversity of Helsinki · FIUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traditionally, the dental profession has primarily treated periodontitis using a mechanical/surgical, rather than a pharmaceutical, approach. However, based on experiments several decades ago which demonstrated that tetracyclines, unexpectedly, inhibit collagen- and bone-destructive mammalian-derived enzymes (e.g. the collagenases), and through non-antibiotic mechanisms, the concept of host-modulation therapy (HMT) was developed. Accordingly, two drug-development strategies evolved: (i) the development of non-antimicrobial formulations of doxycycline; and (ii) the chemical modification of tetracyclines to eliminate their antibiotic activity but retain (or even enhance) their anti-collagenase properties. Regarding the latter, these chemically modified tetracyclines (CMTs) showed efficacy in vitro, in animal models of periodontal (and relevant systemic) disease, and in preliminary clinical trials on patients with Kaposi's sarcoma (however, at the high doses used, photosensitivity was a significant side-effect). In the first strategy, subantimicrobial-dose doxycycline (SDD) demonstrated safety and efficacy in human clinical trials and was approved by the U S Food and Drug Administration (U S FDA) and in other countries for the treatment of periodontitis (20 mg, twice daily, i.e. once every 12 hours) adjunctive to scaling and root planing, and for chronic inflammatory skin diseases (40-mg sustained-release 'beads'). SDD also showed efficacy in patients with systemic diseases relevant to periodontitis, including diabetes mellitus and arthritis, and in postmenopausal women with local and systemic bone loss. Importantly, long-term administration of SDD, of up to 2 years, in clinical trials did not produce antibiotic side-effects. SDD (and in the future, new HMTs, such as low-dose CMT-3, resolvins and chemically modified curcumins) may shift the paradigm of periodontal therapy from a predominantly surgical approach to the greater use of medicinal/pharmacologic strategies, ultimately to benefit larger numbers of patients.

Indexed as

AnimalsDoxycyclineHumansMatrix Metalloproteinase InhibitorsPeriodontitisTetracyclinesDoxycyclineMatrix Metalloproteinase InhibitorsTetracyclineshost-modulation therapynon-antibacterial tetracyclinesPeriodontitissystemic disease

Identifiers

PMID27009489
PMCPMC9376645
OpenAlexW2307480902

What OpenQuestion holds

Textmetadata
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.