AI Article Synopsis

  • The study aimed to evaluate the effectiveness of a 2-year treatment with doxycycline on alveolar bone in post-menopausal women with osteopenia undergoing periodontal care.
  • One hundred and twenty-eight participants were randomly assigned to receive either doxycycline or a placebo, with various measures taken to assess bone density and height over the study period.
  • While overall results showed no significant differences between the treatment and placebo groups, some subgroup analyses indicated potential benefits for specific populations, suggesting a need for further research in those areas.

Article Abstract

Aim: Determine the efficacy of 2-year continuous subantimicrobial dose doxycycline (SDD; 20 mg bid) on alveolar bone in post-menopausal osteopenic, oestrogen-deficient women undergoing periodontal maintenance in a 2-year double-blind, placebo-controlled, randomized clinical trial.

Material And Methods: One-hundred and twenty-eight subjects randomized to SDD or placebo (n=64 each). Posterior vertical bite wings taken at baseline, 1 and 2 years for alveolar bone density (ABD), using radiographic absorptiometry (RA) and computer-assisted densitometric image analysis (CADIA), and alveolar bone height (ABH). Statistical analyses utilized generalized estimating equations; primary analyses were intent to treat (ITT). Results are presented as SDD versus placebo.

Results: Under ITT, there was no statistically significant effect of SDD on ABD loss (RA: p=0.8; CADIA: p=0.2) or ABH loss (p=0.2). Most sites (81-95%) were inactive. For subgroup analyses, mean CADIA was higher with SDD for non-smokers (p=0.05) and baseline probing depths > or =5 mm (p=0.003). SDD was associated with 29% lower odds of more progressive ABH loss in women >5 years post-menopausal (p=0.05) and 36% lower among protocol-adherent subjects (p=0.03).

Conclusions: In post-menopausal osteopenic women with periodontitis, SDD did not differ overall from placebo. Based on exploratory subgroup analyses, additional research is needed to determine the usefulness of SDD in non-smokers, subjects >5 years post-menopausal and in deeper pockets. Protocol registered at (ClinicalTrials.gov). Identifier: NCT00066027.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174266PMC
http://dx.doi.org/10.1111/j.1600-051X.2007.01115.xDOI Listing

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