IGF-1 as an early marker for low bone mass or osteoporosis in premenopausal and postmenopausal women

• Published in: Journal of bone and mineral metabolism 2008-03, Vol.26 (2), p.159-164
• Main Authors: Liu, Jian-min, Zhao, Hong-yan, Ning, Guang, Chen, Ying, Zhang, Lian-zhen, Sun, Li-hao, Zhao, Yong-ju, Xu, Man-yin, Chen, Jia-lun
• Format: Article
• Language: English
• Subjects: Adult; Age Distribution; Aged; Aging; Area Under Curve; Biological and medical sciences; Biomarkers - blood; Bone and Bones - physiopathology; Bone Density; Bones; Cytokines - blood; Diagnosis, Differential; Diseases of the osteoarticular system; Female; Femur Neck - physiopathology; Humans; Insulin-Like Growth Factor I - metabolism; Insulin-like growth factors; Leptin - blood; Medical sciences; Medicine; Medicine & Public Health; Metabolic Diseases; Middle Aged; Organ Size; Original Article; Orthopedics; Osteoporosis; Osteoporosis - blood; Osteoporosis - diagnosis; Osteoporosis - physiopathology; Osteoporosis. Osteomalacia. Paget disease; Osteoprotegerin - blood; Postmenopause - physiology; Premenopause - physiology; ROC Curve; Women
• ISSN: 0914-8779; 1435-5604
• DOI: 10.1007/s00774-007-0799-z

To find out which of the following parameters—serum levels of insulin-like growth factor 1 (IGF-1), osteoprotegerin (OPG), leptin, osteocalcin (OC), and urinary excretion of N-terminal telopeptide of type I collagen (NTx), can be used as an early marker for osteopenia/osteoporosis in women diagnosed by dual-energy X-ray absorptiometry (DXA), 282 premenopausal and 222 postmenopausal women aged 20–75 years were investigated by the measurement of bone mineral densities (BMDs) at lumbar spine (LS) and femoral neck (FN) by DXA, together with serum concentrations of IGF-1, OPG, leptin, OC, and urinary NTx. The characteristics of the earliest marker(s) were tested with the receiver operating characteristic (ROC) analysis. The area under the curve (AUC), sensitivity, and specificity parameters were determined. It was revealed that serum levels of IGF-1 and leptin changed the earliest, with both markers significantly decreasing ( P < 0.0001) or increasing ( P = 0.020), respectively, at age 30. However, in ROC analysis, IGF-1 was the only early parameter that had the capacity to differentiate the low bone mass/osteoporosis women from the normal ones ( P < 0.0001). If the serum level of IGF-1 at 1.5 SD below its peak was adopted as a cutoff point, it could identify women with low bone mass/osteoporosis with a sensitivity of 73% and specificity of 67%. In the premenopausal women subgroup analysis, the low bone mass women (30/282, 10.6%) were older (38.2 ± 1.7 vs. 34.5 ± 0.5 years; P = 0.026), with lower serum levels of IGF-1 (215.1 ± 22.4 vs. 278.8 ± 9.4 ng/ml; P = 0.02) and less lean mass (33.1 ± 0.6 vs. 34.8 ± 0.2 kg; P = 0.010) than the normal ones. After controlling for age, the serum level of IGF-1 had a weak, but still significant, positive correlation with lean mass ( r = 0.17, P < 0.001). In conclusion, measurement of serum IGF-1 in young women may help in the early identification of those at risk for developing low bone mass and osteoporosis.