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Algorithm for the Use of Biochemical Markers of Bone Turnover in the Diagnosis, Assessment and Follow-Up of Treatment for Osteoporosis

Artikel i vetenskaplig tidskrift
Författare Mattias Lorentzon
J. Branco
M. L. Brandi
O. Bruyere
R. Chapurlat
C. Cooper
B. Cortet
A. Diez-Perez
S. Ferrari
A. Gasparik
M. Herrmann
N. R. Jorgensen
J. Kanis
J. M. Kaufman
A. Laslop
M. Locquet
R. Matijevic
E. McCloskey
S. Minisola
R. Pikner
J. Y. Reginster
R. Rizzoli
P. Szulc
M. Vlaskovska
E. Cavalier
Publicerad i Advances in Therapy
Volym 36
Nummer/häfte 10
Sidor 2811-2824
ISSN 0741-238X
Publiceringsår 2019
Publicerad vid Institutionen för medicin, avdelningen för invärtesmedicin och klinisk nutrition
Sidor 2811-2824
Språk en
Länkar dx.doi.org/10.1007/s12325-019-01063...
Ämnesord Algorithm, Bone, Bone biomarker, CTX, Osteoporosis, P1NP, Rheumatology, postmenopausal women, fracture risk, double-blind, international, osteoporosis, vertebral fractures, metabolism markers, randomized-trial, denosumab, teriparatide, risedronate, Research & Experimental Medicine, Pharmacology & Pharmacy
Ämneskategorier Klinisk medicin


Introduction Increased biochemical bone turnover markers (BTMs) measured in serum are associated with bone loss, increased fracture risk and poor treatment adherence, but their role in clinical practice is presently unclear. The aim of this consensus group report is to provide guidance to clinicians on how to use BTMs in patient evaluation in postmenopausal osteoporosis, in fracture risk prediction and in the monitoring of treatment efficacy and adherence to osteoporosis medication. Methods A working group with clinical scientists and osteoporosis specialists was invited by the Scientific Advisory Board of European Society on Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO). Results Serum bone formation marker PINP and resorption marker beta CTX-I are the preferred markers for evaluating bone turnover in the clinical setting due to their specificity to bone, performance in clinical studies, wide use and relatively low analytical variability. BTMs cannot be used to diagnose osteoporosis because of low sensitivity and specificity, but can be of value in patient evaluation where high values may indicate the need to investigate some causes of secondary osteoporosis. Assessing serum levels of beta CTX-I and PINP can improve fracture prediction slightly, with a gradient of risk of about 1.2 per SD increase in the bone marker in addition to clinical risk factors and bone mineral density. For an individual patient, BTMs are not useful in projecting bone loss or treatment efficacy, but it is recommended that serum PINP and beta CTX-I be used to monitor adherence to oral bisphosphonate treatment. Suppression of the BTMs greater than the least significant change or to levels in the lower half of the reference interval in young and healthy premenopausal women is closely related to treatment adherence. Conclusion In conclusion, the currently available evidence indicates that the principal clinical utility of BTMs is for monitoring oral bisphosphonate therapy.

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