Position Statement
What Is the Role of Serial Bone Mineral Density Measurements in Patient Management?

https://doi.org/10.1385/JCD:5:3S:S29Get rights and content

Abstract

The ability of dual X-ray absorptiometry (DXA) to monitor bone mineral density (BMD) has been well documented in epidemiologic and pharmaceutical trials. However, its application to monitoring of patients in clinical practice has been subject to recent controversies. Despite these controversies, most clinical centers rely on DXA for monitoring of patients, and therefore guidance is needed. In this article, we report the positions developed by an expert panel of the International Society for Clinical Densitometry on the use of densitometry for the serial measurement of bone mass for monitoring change in BMD. The panel found DXA to be a precise method of measuring change in BMD if used with an appropriate level of least significant change (LSC), at anatomic sites with good precision and response to therapy, and at 1- to 2-yr time intervals. Monitoring is acceptable for determining when therapy is indicated, and if an agent is not therapeutically effective (i.e., when bone loss occurs despite treatment). Each densitometry center should perform an in vivo precision study on individuals similar to the patient population at the center and determine LSC at a 95% confidence level. If such a precision study cannot be performed, benchmark precision might be used, although there was no agreement on what values should be used. The PA spine is the preferred anatomic site for monitoring. The total hip can be used when the spine study is technically invalid. We conclude with recommendations for further research.

References (62)

  • SL Silverman et al.

    Effect of bone density information on decisions about hormone replacement therapy: a randomized trial

    Obstet Gynecol

    (1997)
  • L Lenchik et al.

    Regression to the mean: what does it mean? Using bone density results to monitor treatment of osteoporosis

    J Clin Densitom

    (2001)
  • HK Genant et al.

    Noninvasive assessment of bone mineral and structure: state of the art

    J Bone Miner Res

    (1996)
  • ME Arlot et al.

    Apparent pre- and postmenopausal bone loss evaluated by DXA at different, skeletal sites in women: the OFELY cohort

    J Bone Miner Res

    (1997)
  • ES Orwoll et al.

    The rate of bone mineral loss in normal men and the effects of calcium and cholecalciferol supplementation

    Ann Intern Med

    (1990)
  • JM Pouilles et al.

    The effects of menopause on longitudinal bone loss from the spine

    Calcif Tissue Int

    (1993)
  • KG Saag et al.

    Alendronate for the prevention and treatment of glucocorticoid-induced osteoporosis

    N Engl J Med

    (1998)
  • SJ Silverberg et al.

    Longitudinal measurements of bone density and biochemical indices in untreated primary hyperparathyroidism

    J Clin Endocrinol Metab

    (1995)
  • H Stempfle et al.

    Prevention of osteoporosis after cardiac transplantation

    Transplantation

    (1999)
  • B Dawson-Hughes et al.

    Effect of calcium and vitamin D supplementation on bone density in men and women 65 years of age or older

    N Engl J Med

    (1997)
  • PD Delmas et al.

    Effects of raloxifene on bone mineral density, serum cholesterol concentrations, and uterine endometrium in postmenopausal women

    N Engl J Med

    (1997)
  • DT Felson et al.

    The effect of postmenopausal estrogen therapy on bone density in elderly women

    N Engl J Med

    (1993)
  • RM Francis

    The effects of testosterone on osteoporosis in men

    Clin Endocrinol

    (1999)
  • EG Lufkin et al.

    Treatment of postmenopausal osteoporosis with transdermal estrogen

    Ann Intern Med

    (1992)
  • MR McClung et al.

    Effect of risedronate on the risk of hip fracture in elderly women. Hip Intervention Program Study Group

    N Engl J Med

    (2001)
  • CY Pak et al.

    Treatment of postmenopausal osteoporosis with slow-release sodium fluoride

    Ann Intern Med

    (1995)
  • NB Watts et al.

    Intermittent cyclical etidronate treatment of postmenopausal osteoporosis

    N Engl J Med

    (1990)
  • CE Cann et al.

    Precise measurement of vertebral mineral content using computed tomography

    J Comput Assist Tomogr

    (1980)
  • JW Davis et al.

    Long-term precision of bone loss rate measurements among postmenopausal women

    Calcif Tissue Int

    (1991)
  • MJ Haddaway et al.

    Bone mineral density in healthy normal women and reproducibility of measurements in spine and hip using dual-energy X-ray absorptiometry

    Br J Radiol

    (1992)
  • R Mazess et al.

    Enhanced precision with dual-energy X-ray absorptiometry

    Calcif Tissue Int

    (1992)
  • Cited by (149)

    • Comparison of the Lunar Prodigy and Stratos DR Dual-Energy X-Ray Absorptiometers to Assess Regional Bone Mineral Density

      2022, Journal of Clinical Densitometry
      Citation Excerpt :

      Consequently, regression equations for translating scans between the Stratos DR and Prodigy are valid only for the conditions presented in this study. Evaluation of lumbar spine aBMD is essential for diagnosing osteoporosis because this bone site is preferentially affected by demineralisation after menopause(21) and also because the effect of osteoporotic drugs is particularly marked at this bone site (24). Experimental study has demonstrated that projectional DXA measurements in human cadaveric spine phantom are significantly affected by the positioning of the lumbar spine, but more severely by kyphotic than lordotic curvature (13).

    • Utility of DXA for monitoring, technical aspects of DXA BMD measurement and precision testing

      2017, Bone
      Citation Excerpt :

      A common problem for DXA reporters and clinicians is when to perform the next DXA scan. A repeat DXA scan in 1–2 years makes sense following most interventions [7,22,24,28–32,90], particularly after commencing osteoporosis therapy. The majority of patients would be expected to meet or exceed the LSC at the lumbar spine within 1–2 years in a quality DXA facility, but not perhaps the hip (Fig. 3).

    View all citing articles on Scopus
    View full text