Literature DB >> 17264390

Salivary isoprostanes indicate increased oxidation injury in periodontitis with additional tobacco abuse.

Roswitha M Wolfram1, Alexandra C Budinsky, Andreas Eder, Christiane Presenhuber, Andrea Nell, Wolfgang Sperr, Helmut Sinzinger.   

Abstract

Isoprostanes (IPs) are indicators of in-vivo oxidative stress, and have been successfully used as markers for chronic inflammatory processes. The presence of chronic periodontal disease and cigarette smoking has been individually linked to the development of atherosclerosis, yet data regarding oxidative stress in this context are not available yet. The aim of this study was to evaluate levels of the salivary prostaglandins (PGs) 8-epi-PGF(2alpha), 6-oxo-PGF(1alpha), thromboxane B(2) (TXB(2)) and PGF(2alpha) in association with periodontal disease status with and without additional cigarette smoking. We analyzed saliva samples from 121 adults, (aged 21-73 years, 90 non-smokers, 31 smokers) for levels of 8-epi-PGF(2alpha), 6-oxo-PGF(1alpha), TXB(2) and PGF(2alpha). On the basis of periodontal disease indices the periodontal status of each subject was assessed and outcomes were then correlated with smoking status and laboratory findings. Salivary 8-epi-PGF(2alpha) levels increased with deteriorating plaque index, and were significantly higher (115.5 +/- 23.5 pg/ml) in smoking individuals, when compared to non-smokers (70.2 +/- 20.4 pg/ml, p<0.0001). In addition, smokers showed higher TXB(2) and PGF(2alphas) and lower 6-oxo-PGF(1alpha) levels p<0.0001). Oxidative stress, as reflected by elevated salivary 8-epi-PGF(2alpha) levels, is associated with the extent of periodontal disease and is significantly aggravated by concomitant tobacco abuse. Chronic inflammation and smoking have been individually associated with the development of atherosclerosis. The results of this study indicate that: 1) salivary IPs can reliably assess the degree of oxidative stress, and: 2) smoking and periodontal disease are two modifiable cardiovascular risk factors, able to potentiate each other.

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Year:  2006        PMID: 17264390     DOI: 10.1002/biof.5520280103

Source DB:  PubMed          Journal:  Biofactors        ISSN: 0951-6433            Impact factor:   6.113


  6 in total

1.  Association of systemic oxidative stress with suppressed serum IgG to commensal oral biofilm and modulation by periodontal infection.

Authors:  R E Singer; K Moss; J D Beck; S Offenbacher
Journal:  Antioxid Redox Signal       Date:  2009-12       Impact factor: 8.401

Review 2.  Oxidative Stress and Antioxidants in the Diagnosis and Therapy of Periodontitis.

Authors:  L'ubomíra Tóthová; Peter Celec
Journal:  Front Physiol       Date:  2017-12-14       Impact factor: 4.566

Review 3.  Oxidative Stress and Antioxidant System in Periodontitis.

Authors:  Yue Wang; Oleh Andrukhov; Xiaohui Rausch-Fan
Journal:  Front Physiol       Date:  2017-11-13       Impact factor: 4.566

4.  Influence of smoking on levels of urinary 8-iso Prostaglandin F2α.

Authors:  Angela van der Plas; Sandrine Pouly; Guillaume de La Bourdonnaye; Gizelle Baker; Frank Lüdicke
Journal:  Toxicol Rep       Date:  2018-11-20

Review 5.  Ethanol- and Cigarette Smoke-Related Alternations in Oral Redox Homeostasis.

Authors:  Sara Zięba; Mateusz Maciejczyk; Anna Zalewska
Journal:  Front Physiol       Date:  2022-01-28       Impact factor: 4.566

6.  Salivary inflammatory mediators as biomarkers for oral mucositis and oral mucosal dryness in cancer patients: A pilot study.

Authors:  Anna Kiyomi; Kensuke Yoshida; Chie Arai; Risa Usuki; Kyosuke Yamazaki; Naoto Hoshino; Akira Kurokawa; Shinobu Imai; Naoto Suzuki; Akira Toyama; Munetoshi Sugiura
Journal:  PLoS One       Date:  2022-04-27       Impact factor: 3.240

  6 in total

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