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. 2012 Jan;32(1):23-30.
doi: 10.3343/alm.2012.32.1.23. Epub 2011 Dec 20.

Diagnostic utility of osteocalcin, undercarboxylated osteocalcin, and alkaline phosphatase for osteoporosis in premenopausal and postmenopausal women

Affiliations

Diagnostic utility of osteocalcin, undercarboxylated osteocalcin, and alkaline phosphatase for osteoporosis in premenopausal and postmenopausal women

Sacide Atalay et al. Ann Lab Med. 2012 Jan.

Abstract

Background: We aimed to investigate the diagnostic utility of osteocalcin (OC), undercarboxylated osteocalcin (ucOC), and alkaline phosphatase (ALP) in pre- and postmenopausal women for femoral neck, L1-4, and L2-4 bone mineral density (BMD) values by taking into consideration their age, body mass index (BMI), and menopausal status.

Methods: Premenopausal (N=40) and postmenopausal cases (N=42) were classified as 25-34 or 35-45 yr of age and within the first 5 yr or 5 yr or more after the onset of menopause, respectively.

Results: Among the groups, statistical differences were found for age, BMI, OC, ucOC, ALP, femoral neck BMD, L1-4 BMD, and L2-4 BMD. The highest serum OC, ucOC, and ALP levels were observed in cases within the first 5 yr after the onset of menopause, probably due to a more rapid bone turnover rate. The best predictors for the femoral neck osteoporosis were ALP, OC, and calcium (areas under the ROC curve [AUC]=0.882, 0.829, and 0.761, respectively), and those for L1-4 and L2-4 osteoporosis were OC, ALP, and ucOC (AUC=0.949, 0.873, and 0.845; and 0.866, 0.819, and 0.814, respectively). Multiple logistic regression analysis revealed that the most discriminative parameter for osteoporosis was OC.

Conclusions: These results indicate that serum OC levels, with or without ucOC and ALP, may be useful to monitor follow-up changes that currently cannot be assessed with BMD and to diagnose femoral neck, L1-4 spine, and L2-4 spine osteoporosis.

Keywords: Bone mineral density; Menopause; Osteocalcin; Osteoporosis; Undercarboxylated osteocalcin.

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Conflict of interest statement

No potential conflict of interest relevant to this article was reported.

Figures

Fig. 1
Fig. 1
Distribution of serum osteocalcin levels in 4 different groups of menopausal status. *, P=0.001 vs. the 35-45 yr age-group.
Fig. 2
Fig. 2
Distribution of femoral neck, L1-4 spine, and L2-4 spine BMD values in 4 different groups of menopausal status. *, P=0.02 vs. the 25-34 yr age-group and P=0.002 vs. the 35-45 yr age-group; , P=0.03 vs. the 25-34 yr age-group and P=0.006 vs. the 35-45 yr age-group; , P=0.014 vs. the 25-34 yr age-group and P=0.006 vs. the 35-45 yr age-group; §, P<0.001 vs. the 25-34 yr age-group and the 35-45 yr age-group; *†, P<0.001 vs. the 25-34 yr age-group and the 35-45 yr age-group.
Fig. 3
Fig. 3
Distribution of serum osteocalcin levels in normal, osteopenia and osteoporosis groups. *, P=0.017 vs. the normal group; , P=0.029 vs. the normal group; , P=0.001 vs. the normal group and P=0.011 vs. the osteopenia group; §, P<0.001 vs. the normal group and P=0.004 vs. the osteopenia group; *†, P<0.001 vs. the normal group and P=0.029 vs. the osteopenia group.
Fig. 4
Fig. 4
ROC curve analysis of biochemical bone markers for osteoporosis. (A) femoral neck osteoporosis (AUC=0.882, P=0.002 for ALP; AUC=0.829, P=0.008 for OC; AUC=0.761, P=0.034 for calcium), (B) L1-4 spine osteoporosis (AUC=0.949, P=0.003 for OC; AUC=0.873, P=0.012 for ALP; AUC=0.845, P=0.021 for ucOC), and (C) L2-4 spine osteoporosis (AUC=0.866, P=0.003 for OC; AUC=0.819, P=0.010 for ALP; AUC=0.814, P=0.011 for ucOC). Abbreviations: AUC, area under the curve; ALP, alkaline phosphatase; OC, osteocalcin; ucOC, undercarboxylated osteocalcin.

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