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DOI: 10.1055/a-1712-4009
Osteoporose-Management während der COVID-19 Pandemie
Management of Osteoporosis During the COVID-19 Pandemic![](https://www.thieme-connect.de/media/10.1055-s-00034914/202201/lookinside/thumbnails/0013-10-2021_10-1055-a-1712-4009-1.jpg)
Abstract
Aim The COVID-19 pandemic has influenced the management of many chronic conditions including osteoporosis as resources are re-allocated to urgent care.
Methods This mini-review summarizes the effects of COVID-19 on diagnosis and management of osteoporosis. Evidence regarding possible effects of osteoporosis medications on COVID-19 outcomes and the relationship of COVID-19 vaccination to osteoporosis care is reviewed. Finally, initiation and maintenance of osteoporosis treatment during the pandemic are highlighted.
Results The use of standard procedures for the diagnosis of osteoporosis and assessment of fracture risk significantly decreased during the COVID-19 pandemic, while the incidence of fragility fractures was mostly unaltered. Both COVID-19 per se and its treatments are associated with a negative impact on bone health. Osteoporosis medications do not aggravate the clinical course of COVID-19, while preclinical data suggests possible beneficial effects of some therapies. While vitamin D deficiency is clearly associated with a worse clinical course of COVID-19, evidence of outcome improvement through vitamin D supplementation is lacking. Osteoporosis treatment should not be generally discontinued, and recommendations for substituting therapies are available. Osteoporosis therapies do not interfere with the efficacy or side-effect profiles of COVID-19 vaccines and should not be stopped or indefinitely delayed because of vaccination.
Conclusion The diagnosis and management of osteoporosis are challenging during the COVID-19 pandemic. Osteoporosis medications are safe and effective and should be continued. Further studies will elucidate the impact of the COVID-19 pandemic on long-term bone health.
Zusammenfassung
Ziel Die COVID-19-Pandemie hat die Behandlung vieler chronischer Erkrankungen, einschließlich Osteoporose, beeinflusst, da Ressourcen für die Notfallversorgung umgewidmet wurden.
Methoden Dieser Übersichtsartikel fasst zusammen die Auswirkungen von COVID-19 auf das Management der Osteoporose. Mögliche Effekte von Osteoporose-Medikamenten auf die COVID-19-Verläufe sowie die Beziehung zwischen COVID-19-Impfung und Osteoporose-Behandlung werden evaluiert. Schließlich wird die Einleitung und Fortsetzung der Osteoporose-Behandlung während der Pandemie diskutiert.
Ergebnisse Die Osteoporose-Diagnostik ging in den frühen Phasen der COVID-19-Pandemie deutlich zurück, während die Inzidenz von Fragilitätsfrakturen weitgehend unverändert blieb. Sowohl COVID-19 an sich als auch seine Behandlung sind mit potentiellen negativen Auswirkungen auf die Knochengesundheit verbunden. Osteoporose-Medikamente aggravieren nicht den klinischen Verlauf von COVID-19, während präklinische Daten auf mögliche positive Auswirkungen einiger Substanzen hinweisen. Obwohl ein Vitamin-D-Mangel eindeutig mit schweren klinischen Verläufen von COVID-19 einhergeht, gibt es keine Evidenz für eine Verbesserung der Erkrankung durch eine Vitamin-D-Supplementation. Die Osteoporose-Behandlung sollte generell nicht abgebrochen werden. Osteoporose-Medikamente beeinträchtigen weder die Wirksamkeit noch das Nebenwirkungsprofil der COVID-19-Impfstoffe und sollten wegen der Impfung nicht unterbrochen werden.
Schlussfolgerung Die Diagnose und Behandlung der Osteoporose während der COVID-19-Pandemie stellt eine Herausforderung dar. Osteoporose-Medikamente sind sicher und wirksam und sollten nach Möglichkeit weiter eingenommen werden. Weitere Studien werden mehr Aufschluss über die Auswirkungen der COVID-19-Pandemie auf die langfristige Knochengesundheit geben.
Publication History
Received: 27 October 2021
Accepted: 01 December 2021
Article published online:
21 February 2022
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Literatur
- 1 Dong E, Du H, Gardner L. An interactive web-based dashboard to track COVID-19 in real time. Lancet Infect Dis 2020; 20: 533-534
- 2 Peeters JJM, van den Berg P, van den Bergh JP. et al. Osteoporosis care during the COVID-19 pandemic in the Netherlands: A national survey. Arch Osteoporos 2021; 16: 11
- 3 Fuggle NR, Singer A, Gill C. et al. How has COVID-19 affected the treatment of osteoporosis? An IOF-NOF-ESCEO global survey. Osteoporos Int 2021; 32: 611-617
- 4 Barton DW, Behrend CJ, Carmouche JJ. Rates of osteoporosis screening and treatment following vertebral fracture. Spine J 2019; 19: 411-417
- 5 Nuñez JH, Sallent A, Lakhani K. et al. Impact of the COVID-19 pandemic on an emergency traumatology service: experience at a tertiary trauma centre in Spain. Injury 2020; 51: 1414-1418
- 6 Miranda I, Sangüesa-Nebot MJ, González A. et al. Impact of strict population confinement on fracture incidence during the COVID-19 pandemic. Experience from a public health care department in Spain. J Orthop Sci 2021;
- 7 Arafa M, Nesar S, Abu-Jabeh H. et al. COVID-19 pandemic and hip fractures: impact and lessons learned. Bone Jt Open 2020; 1: 530-540
- 8 di Filippo L, Formenti AM, Doga M. et al. Radiological thoracic vertebral fractures are highly prevalent in COVID-19 and predict disease outcomes. J Clin Endocrinol Metab 2021; 106: e602-e614
- 9 Tahtabasi M, Kilicaslan N, Akin Y. et al. The prognostic value of vertebral bone density on chest CT in hospitalized COVID-19 patients. J Clin Densitom 2021;
- 10 Krege JH, Kendler D, Krohn K. et al. Relationship between vertebral fracture burden, height loss, and pulmonary function in postmenopausal women with osteoporosis. J Clin Densitom 2015; 18: 506-511
- 11 di Filippo L, Formenti AM, Rovere-Querini P. et al. Hypocalcemia is highly prevalent and predicts hospitalization in patients with COVID-19. Endocrine 2020; 68: 475-478
- 12 Xue X, Ma J, Zhao A. et al. Correlation between hypophosphatemia and the severity of Corona Virus Disease 2019 patients. medRxiv 2020;
- 13 Akchurin O, Meza K, Biswas S. et al. COVID-19 in Patients with CKD in New York City. Kidney360 2021; 2: 63-70
- 14 Sarvazad H, Cahngaripour SH, Eskandari Roozbahani N. et al. Evaluation of electrolyte status of sodium, potassium and magnesium, and fasting blood sugar at the initial admission of individuals with COVID-19 without underlying disease in Golestan Hospital, Kermanshah. New Microbes New Infect 2020; 38: 100807
- 15 Stevens JS, Moses AA, Nickolas TL. et al. Increased mortality associated with hypermagnesemia in severe COVID-19 illness. Kidney360 2021; 2: 1087-1094
- 16 Watkins RR, Lemonovich TL, Salata RA. An update on the association of vitamin D deficiency with common infectious diseases. Can J Physiol Pharmacol 2015; 93: 363-3688
- 17 Bergman P, Lindh AU, Björkhem-Bergman L. et al. Vitamin D and respiratory tract infections: a systematic review and meta-analysis of randomized controlled trials. PLoS One 2013; 8: e65835
- 18 Pham H, Waterhouse M, Baxter C. et al. The effect of vitamin D supplementation on acute respiratory tract infection in older Australian adults: an analysis of data from the D-Health Trial. Lancet Diabetes Endocrinol 2021; 9: 69-81
- 19 Mok CK, Ng YL, Ahidjo BA. et al. Calcitriol, the active form of vitamin D, is a promising candidate for COVID-19 prophylaxis. Microbiology 2020;
- 20 Carpagnano GE, Di Lecce V, Quaranta VN. et al. Vitamin D deficiency as a predictor of poor prognosis in patients with acute respiratory failure due to COVID-19. J Endocrinol Invest 2021; 44: 765-771
- 21 Radujkovic A, Hippchen T, Tiwari-Heckler S. et al. Vitamin D deficiency and outcome of COVID-19 patients. Nutrients 2020; 12: 2757
- 22 Alcala-Diaz JF, Limia-Perez L, Gomez-Huelgas R. et al. Calcifediol treatment and hospital mortality due to COVID-19: a cohort study. Nutrients 2021; 13: 1760
- 23 Ling SF, Broad E, Murphy R. et al. High-dose cholecalciferol booster therapy is associated with a reduced risk of mortality in patients with COVID-19: a cross-sectional multi-centre observational study. Nutrients 2020; 12: 3799
- 24 Entrenas Castillo M, Entrenas Costa LM, Vaquerto Barrios JM. et al. Effect of calcifediol treatment and best available therapy versus best available therapy on intensive care unit admission and mortality among patients hospitalized for COVID-19: A pilot randomized clinical study. J Steroid Biochem Mol Biol 2020; 203: 105751
- 25 Sabico S, Enani MA, Sheshah E. et al. Effects of a 2-week 5000 IU versus 1000 IU vitamin D3 supplementation on recovery of symptoms in patients with mild to moderate Covid-19: a randomized clinical trial. Nutrients 2021; 13: 2170
- 26 Lakkireddy M, Gadiga SG, Malathi RD. et al. Impact of daily high dose oral vitamin D therapy on the inflammatory markers in patients with COVID 19 disease. Sci Rep 2021; 11: 10641
- 27 Murai IH, Fernandes AL, Sales LP. et al. Effect of a single high dose of vitamin D3 on hospital length of stay in patients with moderate to severe COVID-19: a randomized clinical trial. JAMA 2021; 325: 1053-1060
- 28 Grant WB, Lahore H, McDonnell SL. et al. Evidence that vitamin D supplementation could reduce risk of influenza and COVID-19 infections and deaths. Nutrients 2020; 12: 988
- 29 Horby P, Lim WS, Emberson JR. et al. Dexamethasone in hospitalized patients with Covid-19. N Engl J Med 2021; 384: 693-704
- 30 Zhao R, Wang H, Wang X. et al. Steroid therapy and the risk of osteonecrosis in SARS patients: a dose-response meta-analysis. Osteoporos Int 2017; 28: 1027-1034
- 31 Murakami K, Kobayashi Y, Uehara S. et al. A Jak1/2 inhibitor, baricitinib, inhibits osteoclastogenesis by suppressing RANKL expression in osteoblasts in vitro. PLoS One 2017; 12: e0181126
- 32 Kortebein P, Ferrando A, Lombeida J. et al. Effect of 10 days of bed rest on skeletal muscle in healthy older adults. JAMA 2007; 297: 1769-1774
- 33 Yu EW, Tsourdi E, Clarke BL. et al. Osteoporosis management in the era of COVID-19. J Bone Miner Res 2020; 35: 1009-1013
- 34 Napoli N, Elderkin AL, Kiel DP. et al. Managing fragility fractures during the COVID-19 pandemic. Nat Rev Endocrinol 2020; 16: 467-468
- 35 Gittoes NJ, Criseno S, Appelman-Dijkstra NM. et al. ENDOCRINOLOGY IN THE TIME OF COVID-19: Management of calcium metabolic disorders and osteoporosis. Eur J Endocrinol 2020; 183: G57-G65
- 36 Reid IR, Horne AM, Mihov B. et al. Fracture prevention with zoledronate in older women with osteopenia. N Engl J Med 2018; 379: 2407-2416
- 37 Grey A, Horne A, Gamble G. et al. Ten years of very infrequent zoledronate therapy in older women: an open-label extension of a randomized trial. J Clin Endocrinol Metab 2020; 105: dgaa062
- 38 Tsourdi E, Zillikens MC, Meier C. et al. Fracture risk and management of discontinuation of denosumab therapy: a systematic review and position statement by ECTS. J Clin Endocrinol Metab 2021; 106: 264-281
- 39 Leder BZ, Neer R, Wyland JJ. et al. Effects of teriparatide treatment and discontinuation in postmenopausal women and eugonadal men with osteoporosis. J Clin Endocrinol Metab 2009; 94: 2915-2921
- 40 Blanch- Rubió J, Soldevila-Domenech N, Tío L. et al. Influence of anti-osteoporosis treatments on the incidence of COVID-19 in patients with non-inflammatory rheumatic conditions. Aging (Albany NY) 2020; 12: 19923-19937
- 41 Watts NB, Roux C, Modlin JF. et al. Infections in postmenopausal women with osteoporosis treated with denosumab or placebo: coincidence or causal association?. Osteoporos Int 2012; 23: 327-337
- 42 Cummings SR, San Martin J, McClung MR. et al. Denosumab for prevention of fractures in postmenopausal women with osteoporosis. N Engl J Med 2009; 361: 756-765
- 43 Anastasilakis AD, Toulis KA, Goulis DG. et al. Efficacy and safety of denosumab in postmenopausal women with osteopenia or osteoporosis: a systematic review and a meta-analysis. Horm Metab Res 2009; 41: 721-729
- 44 Guerrini MM, Takayanagi H. The immune system, bone and RANKL. Arch Biochem Biophys 2014; 561: 118-123
- 45 Diker-Cohen T, Rosenberg D, Avni T. et al. Risk for infections during treatment with denosumab for osteoporosis: a systematic review and meta-analysis. J Clin Endocrinol Metab 2020; 105: dgz322
- 46 Formenti AM, Pedone E, di Filippo L. et al. Are women with osteoporosis treated with denosumab at risk of severe COVID-19?. Endocrine 2020; 70: 203-205
- 47 Sing C-W, Kiel DP, Hubbard RB. et al. Nitrogen-containing bisphosphonates are associated with reduced risk of pneumonia in patients with hip fracture. J Bone Miner Res 2020; 35: 1676-1684
- 48 Reid IR, Horne AM, Mihov B. et al. Effect of zoledronate on lower respiratory infections in older women: secondary analysis of a randomized controlled trial. Calcif Tissue Int 2021; 109: 12-16
- 49 Smetana K, Rosel D, BrÁbek J. Raloxifene and bazedoxifene could be promising candidates for preventing the COVID-19 related cytokine storm, ARDS and mortality. In Vivo 2020; 34: 3027-3028
- 50 Pirhadi R, Sinai Talaulikar V, Onwude J. et al. Could estrogen protect women From COVID-19?. J Clin Med Res 2020; 12: 634-639
- 51 Calderone A, Menichetti F, Santini F. et al. Selective estrogen receptor modulators in COVID-19: A possible therapeutic option?. Front Pharmacol 2020; 11: 1085
- 52 La Vignera S, Cannarela R, Condorelli RA. et al. Sex-specific SARS-CoV-2 mortality: among hormone-modulated ACE2 expression, risk of venous thromboembolism and hypovitaminosis D. Int J Mol Sci 2020; 21: 2948
- 53 Engelmann F, Rivera A, Park B. et al. Impact of estrogen therapy on lymphocyte homeostasis and the response to seasonal influenza vaccine in post-menopausal women. PLoS One 2016; 11: e0149045
- 54 Peretz J, Pekosz A, Lane AP. et al. Estrogenic compounds reduce influenza A virus replication in primary human nasal epithelial cells derived from female, but not male, donors. Am J Physiol Lung Cell Mol Physiol 2016; 310: L415-L425
- 55 Artero A, Tarín JJ, Cano A. The adverse effects of estrogen and selective estrogen receptor modulators on hemostasis and thrombosis. Semin Thromb Hemost 2012; 38: 797-807
- 56 Tsourdi E, Yu EW, Jan de Beur SM. et al. Vaccination for coronavirus disease 2019 (COVID-19) and relationship to osteoporosis care: current evidence and suggested approaches. J Bone Miner Res 2021; 36: 1042-1047
- 57 Annweiler C, Hanotte B, Grandin de l’Eprevier C. et al. Vitamin D and survival in COVID-19 patients: A quasi-experimental study. J Steroid Biochem Mol Biol 2020; 204: 105771
- 58 Wang R, DeGruttola V, Lei Q. et al. The vitamin D for COVID-19 (VIVID) trial: A pragmatic cluster-randomized design. Contemp Clin Trials 2021; 100: 106176