Evidence map›Paper›PMID 25105817›Full record

ArticleInternational journal of oral science2014

Oral microbiota and host innate immune response in bisphosphonate-related osteonecrosis of the jaw.

Smruti Pushalkar, Xin Li, Zoya Kurago, Lalitha V Ramanathapuram, Satoko Matsumura, Kenneth E Fleisher, Robert Glickman, Wenbo Yan, Yihong Li, Deepak Saxena

Open access · goldAbstract read
In one paragraph

Article in International journal of oral science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 11% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Actinomyces lesions and acute inflammation predominate in osteonecrosis of the jaw associated with osteoclast-suppressing therapy in contrast to non-medication-related osteonecrosis.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
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  12. Alteration of salivaryFrontiers in pharmacology · 2025
    Article
  13. Review
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  19. Microbial Changes Associated With Oral Cavity Cancer Progression.Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery · 2023
    Article
  20. Article
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.

Smruti PushalkarDepartment of Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, USA.
Xin LiDepartment of Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, USA.
Zoya KuragoDepartment of Oral and Maxillofacial Pathology, Radiology and Medicine, New York University College of Dentistry, New York, USA.
Lalitha V RamanathapuramDepartment of Oral and Maxillofacial Pathology, Radiology and Medicine, New York University College of Dentistry, New York, USA.
Satoko MatsumuraDepartment of Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, USA.
Kenneth E FleisherDepartment of Oral and Maxillofacial Surgery, New York University College of Dentistry, New York, USA.
Robert GlickmanDepartment of Oral and Maxillofacial Surgery, New York University College of Dentistry, New York, USA.
Wenbo YanDepartment of Biology, Nyack College, New York, USA.
Yihong LiDepartment of Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, USA.
Deepak SaxenaDepartment of Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, USA.
New York University · USNyack College · US

Funding

FISH "N" Chips: A Microfluidic Processor for Isolating and Analyzing MicrobesR01DE020891 · NIDCR · SANDIA CORP-SANDIA NATIONAL LABORATORIES · PI SINGH, ANUP K. · 2009 to 2012
$1.8M
(PQA1) Novel epigenetic mechanism mediate metformin inhibition of prostate cancerR01CA180277 · NCI · NEW YORK UNIVERSITY · PI LI, XIN · 2013 to 2016
$1.1M
Metformin as a novel chemopreventive agent for prostate cancerR03CA172894 · NCI · NEW YORK UNIVERSITY · PI LI, XIN · 2013 to 2014
$156k
NCI NIH HHS CA172894NCI NIH HHS CA180277NCI NIH HHS R01 CA180277NCI NIH HHS R03 CA172894NIDCR NIH HHS R01 DE020891
6 · The paper itself

Abstract

Bacterial biofilms have emerged as potential critical triggers in the pathogenesis of bisphosphonate (BP)-related osteonecrosis of the jaw (ONJ) or BRONJ. BRONJ lesions have shown to be heavily colonized by oral bacteria, most of these difficult to cultivate and presents many clinical challenges. The purpose of this study was to characterize the bacterial diversity in BRONJ lesions and to determine host immune response. We examined tissue specimens from three cohorts (n=30); patients with periodontal disease without a history of BP therapy (Control, n=10), patients with periodontal disease having history of BP therapy but without ONJ (BP, n=5) and patients with BRONJ (BRONJ, n=15). Denaturing gradient gel electrophoresis of polymerase chain reaction (PCR)-amplified 16S rRNA gene fragments revealed less bacterial diversity in BRONJ than BP and Control cohorts. Sequence analysis detected six phyla with predominant affiliation to Firmicutes in BRONJ (71.6%), BP (70.3%) and Control (59.1%). Significant differences (P<0.05) in genera were observed, between Control/BP, Control/BRONJ and BP/BRONJ cohorts. Enzyme-linked immunosorbent assay (ELISA) results indicated that the levels of myeloperoxidase were significantly lower, whereas interleukin-6 and tumor necrosis factor-alpha levels were moderately elevated in BRONJ patients as compared to Controls. PCR array showed significant changes in BRONJ patients with downregulation of host genes, such as nucleotide-binding oligomerization domain containing protein 2, and cathepsin G, the key modulators for antibacterial response and upregulation of secretory leukocyte protease inhibitor, proteinase 3 and conserved helix-loop-helix ubiquitous kinase. The results suggest that colonization of unique bacterial communities coupled with deficient innate immune response is likely to impact the pathogenesis of ONJ.

Indexed as

BiofilmsActinobacteriaBacteriaBacteroidetesBisphosphonate-Associated Osteonecrosis of the JawBone Density Conservation AgentsCathepsin GCohort StudiesDown-RegulationFemaleFusobacteriaGram-Negative BacteriaHost-Pathogen InteractionsHumansI-kappa B KinaseImmunity, InnateBone Density Conservation AgentsCathepsin GCHUK protein, humanCTSG protein, humanI-kappa B KinaseIL6 protein, humanInterleukin-6MyeloblastinNOD2 protein, humanNod2 Signaling Adaptor ProteinPeroxidaseTumor Necrosis Factor-alpha

Identifiers

PMID25105817
PMCPMC5153588
OpenAlexW2088776598

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.