Effects of periodontal and bisphosphonate treatment on the gingival crevicular levels of sclerostin and dickkopf‐1 in postmenopausal osteoporosis with and without periodontitis
Objective and Background Both periodontitis and osteoporosis are associated with osteoclast‐related bone resorption. Bone metabolism is regulated by wingless‐type MMTV integration site family (WNT), and WNT/β‐catenin signals are controlled by physiological antagonists including dickkopf‐1 (DKK‐1) an...
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Veröffentlicht in: | Journal of periodontal research 2022-08, Vol.57 (4), p.849-858 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Objective and Background
Both periodontitis and osteoporosis are associated with osteoclast‐related bone resorption. Bone metabolism is regulated by wingless‐type MMTV integration site family (WNT), and WNT/β‐catenin signals are controlled by physiological antagonists including dickkopf‐1 (DKK‐1) and sclerostin (SOST). This study examined the effects of periodontal and bisphosphonate (BP) treatment on the gingival crevicular fluid (GCF) sclerostin (SOST) and dickkopf‐related protein‐1 (DKK‐1) levels in osteoporotic and systemically healthy postmenopausal women with and without periodontitis.
Materials and Methods
A total of 48 postmenopausal women were divided into 4 groups (n = 12) according to periodontal health and osteoporosis status, as follows: Group OP/P: subjects with both osteoporosis and periodontitis; Group P: systemically healthy subjects with periodontitis; Group OP: periodontally healthy subjects with osteoporosis; Group H: systemically and periodontally healthy controls. Clinical data and GCF SOST and DKK‐1 levels of the participants were collected at baseline and at 6 and 12 months following the initiation of periodontal and/or BP treatment in the experimental groups. GCF SOST and DKK‐1 data were obtained by ELISA.
Results
Clinical improvements were observed in all experimental groups. GCF SOST and DKK1 baseline levels varied significantly between groups due to periodontal disease (p |
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ISSN: | 0022-3484 1600-0765 |
DOI: | 10.1111/jre.13023 |