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. 2021 May 31;16(1):351.
doi: 10.1186/s13018-021-02497-0.

Potential of biomarkers during pharmacological therapy setting for postmenopausal osteoporosis: a systematic review

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Potential of biomarkers during pharmacological therapy setting for postmenopausal osteoporosis: a systematic review

Filippo Migliorini et al. J Orthop Surg Res. .

Abstract

Background: Biochemical markers of bone turnover (BTMs), such as the bone alkaline phosphatase (bALP), procollagen type I N propeptide (PINP), serum cross-linked C-telopeptides of type I collagen (bCTx), and urinary cross-linked N-telopeptides of type I collagen (NTx), are used to manage therapy monitoring in osteoporotic patients. This systematic review analyzed the potential of these BMTs in predicting the clinical outcomes in terms of BMD, t-score, rate of fractures, and adverse events during the therapy setting in postmenopausal osteoporosis.

Methods: All randomized clinical trials (RCTs) reporting data on biomarkers for postmenopausal osteoporosis were accessed. Only articles reporting quantitative data on the level of biomarkers at baseline and on the outcomes of interest at the last follow-up were eligible.

Results: A total of 36,706 patients were retrieved. Greater values of bALP were associated with a greater rate of vertebral (P = 0.001) and non-vertebral fractures (P = 0.0001). Greater values of NTx at baseline were associated with a greater rate of adverse events at the last follow-up (P = 0.02). Greater values of CTx at baseline were associated with a greater rate of adverse events leading to discontinuation (P = 0.04), gastrointestinal adverse events (P = 0.0001), musculoskeletal adverse events (P = 0.04), and mortality (P = 0.04). Greater values of PINP at baseline were associated with greater rates of gastrointestinal adverse events (P = 0.02) at the last follow-up.

Conclusion: The present analysis supports the adoption of BMTs during pharmacological therapy setting of patients suffering from osteoporosis.

Level of evidence: I, systematic review of RCTs.

Keywords: Biomarkers; NTx; Osteoporosis; PINP; bALP; bCTx.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

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Fig. 1
Flow chart of the literature search
Fig. 2
Fig. 2
Methodological quality assessment

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References

    1. Borgstrom F, Sobocki P, Strom O, et al. The societal burden of osteoporosis in Sweden. Bone. 2007;40(6):1602–1609. doi: 10.1016/j.bone.2007.02.027. - DOI - PubMed
    1. Burge R, Dawson-Hughes B, Solomon DH, Wong JB, King A, Tosteson A. Incidence and economic burden of osteoporosis-related fractures in the United States, 2005-2025. J Bone Miner Res. 2007;22(3):465–475. doi: 10.1359/jbmr.061113. - DOI - PubMed
    1. Ray NF, Chan JK, Thamer M, Melton LJ., III Medical expenditures for the treatment of osteoporotic fractures in the United States in 1995: report from the National Osteoporosis Foundation. J Bone Miner Res. 1997;12(1):24–35. doi: 10.1359/jbmr.1997.12.1.24. - DOI - PubMed
    1. Bennett JE, Li G, Foreman K, Best N, Kontis V, Pearson C, Hambly P, Ezzati M. The future of life expectancy and life expectancy inequalities in England and Wales: Bayesian spatiotemporal forecasting. Lancet. 2015;386(9989):163–170. doi: 10.1016/S0140-6736(15)60296-3. - DOI - PMC - PubMed
    1. Kontis V, Bennett JE, Mathers CD, Li G, Foreman K, Ezzati M. Future life expectancy in 35 industrialised countries: projections with a Bayesian model ensemble. Lancet. 2017;389(10076):1323–1335. doi: 10.1016/S0140-6736(16)32381-9. - DOI - PMC - PubMed

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