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For hours, walk-ins and appointments.Synonyms
- Bone GLA Protein
Expected Turnaround Time
2 - 4 days
Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.
Related Documents
Specimen Requirements
Specimen
Serum, frozen
Volume
0.8 mL
Minimum Volume
0.4 mL (Note: This volume does not allow for repeat testing.)
Container
Red-top tube or gel-barrier tube
Collection
Transfer the serum into a LabCorp PP transpak frozen purple tube with screw cap (LabCorp No 49482). Freeze immediately and maintain frozen until tested. To avoid delays in turnaround time when requesting multiple tests on frozen samples, please submit separate frozen specimens for each test requested.
Storage Instructions
Freeze.
Stability Requirements
Temperature | Period |
|---|---|
Room temperature | unstable |
Refrigerated | unstable |
Frozen | -20 = 30 days; -70 = 90 days |
Test Details
Use
Evaluate bone disease. Increased levels of osteocalcin are found in bone diseases characterized by increased bone turnover. Osteocalcin has been found to be elevated in Paget disease of the bone, cancer accompanied by bone metastases, primary hyperparathyroidism and renal osteodystrophy. Osteocalcin levels may serve as useful index in evaluating the therapeutic management of the patient.
Methodology
Enzyme-linked immunosorbent assay (ELISA)
Reference Interval
• Male: 3.2−39.6 ng/mL
• Female:
− Premenopausal: 4.9−30.9 ng/mL
− Postmenopausal: 9.4−47.4 ng/mL
Additional Information
Osteocalcin, or bone Gla protein (BGP), is the major noncollagenous protein of bone matrix. It has a molecular weight of approximately 5.8 kilodaltons and consists of 49 amino acids, including three residues of γ-carboxyglutamic acid. Osteocalcin is synthesized in bone by osteoblasts. After production, it is partly incorporated into the bone matrix and partly delivered to the circulatory system. The precise physiological function of osteocalcin is still unclear. A large number of studies have shown that the circulating level of osteocalcin reflects the rate of bone formation.
Determination of serum osteocalcin has proven to be valuable as an aid in identifying women at risk of developing osteoporosis, for monitoring bone metabolism during perimenopause and postmenopause, and during antiresorptive therapy.
References
Bjarnason NH, Bjarnason K, Haarbo J, Rosenquist C, Christiansen C. Tibolone: prevention of bone loss in late postmenopausal women. J Clin Endocrinol Metab. 1996 Jul; 81(7):2419-2422. 8675554
Christian C, Tanko LB, Warming L, et al. Dose dependent effects on bone resorption and formation of intermittently administered intravenous ibandronate. Osteoporos Int. 2003; 14(7):609-613. 12830369
Junqueira PA, da Fonseca AM, Bagnoli VR, et al. Comparison of bone remodeling indicators in climacteric women. Int J Fertil Womens Med. 2002; 47(4):174-181. 12199414
Marcus R, Holloway L, Wells B, et al. The relationship of biochemical markers of bone turnover to bone density changes on postmenopausal women: Results from the postmenopausal estrogen/progestin interventions (PEPI) trial. J Bone Miner Res. 1999; 14(9):1583-1595. 10469288
McClung M, Clemmesen B, Daifotis A. Alendronate prevents postmenopausal bone loss in women without osteoporosis. A double-blind, randomized, controlled trial. Alendronate Osteoporosis Prevention Study Group. Ann Intern Med. 1998 Feb 15; 128(4):253-261. 9471927
Meunier PJ, Confaveux E, Tupinon I. Prevention of early postmenopausal bone loss with cyclical etidronate therapy (A double-blind, placebo-controlled study and 1-year follow-up). J Clin Endocrinol Metab. 1997; 82(9):2784-2791; erratum: J Clin Endocrinol Metab. 1997; 82(11):3740. 9284696
Ohishi T, Takahashi M, Kushida K, et al. Changes of biochemical markers during fracture healing. Arch Orthop Trama Surg. 1998; 118(3):126-130. 9932185
Ravn P, Clemmesen B, Christiansen C. Biochemical markers can predict the response in bone mass during alendronate treatment in early postmenopausal women. Alendronate Osteoporosis Prevention Study Group. Bone. 1999; 24(3):237-244. 10071916
Ravn P, Clemmesen B, Riis BJ, et al. The effects on bone mass and bone markers of different doses of ibandronate: A new bisphosphate for prevention and treatment of postmenopausal osteoporosis: A 1-year, randomized, double-blind, placebo-controlled, dose-finding study. Bone. 1996; 19(5):527-533. 8922653
Ravn P, Christensen JO, Baumann M. Changes in biochemical markers and bone mass after withdrawal of ibandronate treatment: Prediction of bone mass changes during treatment. Bone. 1998; 22(5):559-564. 9600792
Ravn P, Rix M, Andreassen H. High bone turnover is associated with low bone mass and spinal fracture in postmenopausal women. Calcif Tissue Int. 1997; 6(30):255-260. 9069162
Rosenquist C, Qvist P, Bjarnason NH, et al. Measurement of a more stable region of osteocalcin in serum by ELISA with two monoclonal antibodies. Clin Chem. 1995; 41(10):1439-1445. 7586514
Takahashi M, Kushida K, Nagano A, et al. Comparison of the analytical and clinical performance characteristics of an N-MID versus an intact osteocalcin immunoradiometric assay. Clin Chim Acta. 2000; 294(1-2):67-76. 10727674
Tanko LB, Mouritzen U, Lehmann HJ, et al. Oral ibandronate: Changes in markers of bone turnover during adequately dosed continuous and weekly therapy and during different suboptimally dosed treatment regimens. Bone. 2003; 32(6):687-693.12810176
LOINC® Map
| Order Code | Order Code Name | Order Loinc | Result Code | Result Code Name | UofM | Result LOINC |
|---|---|---|---|---|---|---|
| 010249 | Osteocalcin, Serum | 2697-1 | 010250 | Osteocalcin, Serum | ng/mL | 2697-1 |
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