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Bone Specific Drugs and Osteonecrosis of Sites Other than the Jaw: A Nationwide Cohort Study
Umeå universitet, Medicinska fakulteten, Institutionen för samhällsmedicin och rehabilitering, Geriatrik.ORCID-id: 0000-0003-2924-508X
Umeå universitet, Medicinska fakulteten, Institutionen för samhällsmedicin och rehabilitering, Geriatrik.
Umeå universitet, Medicinska fakulteten, Institutionen för samhällsmedicin och rehabilitering, Geriatrik. Umeå universitet, Medicinska fakulteten, Institutionen för folkhälsa och klinisk medicin, Avdelningen för hållbar hälsa.
Umeå universitet, Medicinska fakulteten, Institutionen för folkhälsa och klinisk medicin, Avdelningen för hållbar hälsa.ORCID-id: 0000-0002-8107-2860
Visa övriga samt affilieringar
2020 (Engelska)Ingår i: Journal of Bone and Mineral Research, ISSN 0884-0431, E-ISSN 1523-4681, Vol. 35, nr 9, s. 1703-1710Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Bone specific drugs (BSDs) increase the risk of osteonecrosis of the jaw, but whether they increase the risk of osteonecrosis at other sites is not known. Two studies, a cohort study and a case-control study, were conducted using registry data on everyone who was residing in Sweden on December 31, 2005, and who was 50 years of age or older at the time (N = 3,523,912). In the cohort study, individuals prescribed a BSD during 2006-2017 (n = 217 387) were 1:1 matched with nonusers on birth year, sex, hip fracture status and Swedish or foreign origin. In the case-control study, individuals diagnosed with osteonecrosis during 2006-2017 (n = 12 614) were 1:1 matched with individuals without a diagnosis of osteonecrosis on birth year, sex, and Swedish or foreign background. In the cohort study, osteonecrosis was diagnosed in 983 BSD users and 214 nonusers (adjusted hazard ratio [aHR], 4.02; 95% CI, 3.32-4.87), during a mean treatment time of 2.8 years. A similar association was observed in a subcohort where all indivuals diagnosed with cancer (HR, 4.82, 95% CI, 2.52-9.22). The greatest difference in incidence between BSD users and nonusers was observed in patients with a femoral neck fracture that was not treated with total hip arthroplasty or hemiarthroplasty (Incidence rate difference, 77.8 cases per 10,000 person-years, p < 0.05). The risk of osteonecrosis was higher in users of denosumab (HR, 1.93; 95% CI, 1.33-2.79) and users of zoledronic acid (HR, 1.95; 95% CI, 1.31-2.91) than in users of other BSDs. The increased risk of osteonecrosis decreased after the end of therapy (p < 0.001 for time trend). The results were confirmed in the case-control study. In summary, use of BSDs, especially more potent BSDs, is associated with increased risk of osteonecrosis of sites other than the jaw. This increased risk decreases after the final dose of BSD.

Ort, förlag, år, upplaga, sidor
John Wiley & Sons, 2020. Vol. 35, nr 9, s. 1703-1710
Nyckelord [en]
Bisphosphonates, Hip fracture, Osteonecrosis
Nationell ämneskategori
Ortopedi
Identifikatorer
URN: urn:nbn:se:umu:diva-170775DOI: 10.1002/jbmr.4040ISI: 000533442700001PubMedID: 32379370Scopus ID: 2-s2.0-85084788234OAI: oai:DiVA.org:umu-170775DiVA, id: diva2:1430445
Tillgänglig från: 2020-05-15 Skapad: 2020-05-15 Senast uppdaterad: 2023-03-24Bibliografiskt granskad
Ingår i avhandling
1. Benefits and harms of Bisphosphonates: an observational study
Öppna denna publikation i ny flik eller fönster >>Benefits and harms of Bisphosphonates: an observational study
2022 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Alternativ titel[sv]
Positiva och negativa effekter av bisfosfonater : en observationsstudie
Abstract [en]

Background: Bisphosphonates are first-line treatment for osteoporosis, but osteoporosis is considered an undertreated disease. The general aim of this dissertation was to further study the benefits and harms of bisphosphonates. There were four specific research questions: (1) Do bisphosphonates reduce the risk of new fractures in older adults who have a history of fracture? (2) Do bisphosphonates reduce the risk of fracture in people taking glucocorticoids? (3) Does confounding explain why bisphosphonates are associated with lower mortality in observational studies? (4) Do bisphosphonates increase the risk of non-jaw osteonecrosis?

Methods: To answer these questions, we used Swedish register data on deaths, diagnoses, and prescription medications to conduct four matched cohort studies of bisphosphonate users and nonusers. The cohorts were selected from patients registered in the Hip Fracture Register and from all residents of Sweden who were aged 50 years or older on December 31, 2005.

Results: (1) Bisphosphonate users had an initially increased risk of sustaining new fractures, which appeared to be due to an underlying high risk of fracture. This increased risk diminished over time, which is consistent with a gradual treatment effect, but it is also consistent with a bias known as depletion of susceptibles. (2) Bisphosphonate users had a lower risk of fracture during glucocorticoid therapy. (3) Bisphosphonate users had a lower mortality rate from day 2 of treatment. Although such an early treatment effect cannot be ruled out, this finding is consistent with confounding. (4) Bisphosphonate users had an increased risk of developing non-jaw osteonecrosis. 

Conclusion: Most of the results were difficult to interpret as true benefits or harms of bisphosphonates because alternative explanations, arising from bias or confounding, were likely. The exception was the results of Study 2, where alternative explanations are more difficult to find. Therefore, Study 2 suggests that bisphosphonates reduce the risk of fractures in glucocorticoid-treated patients. Further research is needed to clarify the potential effects of bisphosphonates on mortality, non-jaw osteonecrosis, and new fractures after a previous fracture.

Ort, förlag, år, upplaga, sidor
Umeå: Umeå universitet, 2022. s. 89
Serie
Umeå University medical dissertations, ISSN 0346-6612 ; 2184
Nyckelord
osteoporosis, fracture, alendronate, risedronate, zoledronic acid, glucocorticoid, mortality, osteonecrosis, register, registry, real-world evidence, epidemiology
Nationell ämneskategori
Geriatrik Folkhälsovetenskap, global hälsa och socialmedicin
Forskningsämne
geriatrik; epidemiologi
Identifikatorer
urn:nbn:se:umu:diva-194452 (URN)978-91-7855-807-0 (ISBN)978-91-7855-808-7 (ISBN)
Disputation
2022-06-03, Hörsal F, Humanisthuset, Universitetsområdet, Umeå, 13:00 (Svenska)
Opponent
Handledare
Tillgänglig från: 2022-05-13 Skapad: 2022-05-05 Senast uppdaterad: 2025-02-20Bibliografiskt granskad

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Nordström, PeterBergman, JonathanBallin, MarcelBjörk, SabineNordström, Anna

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