(Biochemistry) |
Investigation | : | β-CTX | ||||||||||
Specimen type | : | Plasma | ||||||||||
Spec container | : | EDTA | ||||||||||
Volume required | : | 4 ml | ||||||||||
Reference range | : | See Below μg/l | ||||||||||
Turnaround | : | <72 hours | ||||||||||
Patient preparation: Fasting morning sample (09:00-12:00) preferred. A baseline pre-treatment measurement is required if assessing response to antiresorption therapy.
Sample requirements for external users: EDTA plasma. Store frozen at -20° prior to dispatch and send frozen. Mininum sample requirement - 0.5 ml of EDTA plasma. Haemolysed samples are unsuitable for analysis.
Interpretation:
Osteoporosis Treatment
β-CTX reposnse to potent bisphosphonate (3/12 post commencing treatment):
"The least significant change (LSC) was determined to be 36%, meaning that an individual should display a ≥ 36% decrease of plasma βCTx concentrations when receiving antiresorptive therapy to have a < 5 % chance (p < 0.05) of the decrease being the result of random variation in marker concentration."
No baseline B-CTx (3/12 post commencing treatment):
B-CTx should be <0.30 ug/L
Pre-menopausal Geometric Mean: 0.306 ug/L
Post-menopausal Geometric Mean: 0.424 ug/L
If poor response to therapy check compliance
Additional information on CTXand its clinical use can be found here: CTX.