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. Author manuscript; available in PMC: 2016 May 20.
Published in final edited form as: Osteoporos Int. 2014 Sep 26;26(1):419–420. doi: 10.1007/s00198-014-2883-2

International management of bone health in glucocorticoid-exposed individuals in the observational GLOW study

Stuart Silverman 1, Jeffrey Curtis 2, Kenneth Saag 2, Julie Flahive 3, Jonathan Adachi 4, Frederick Anderson 3, Roland Chapurlat 5, Cyrus Cooper 6, Adolfo Diez-Perez 7, Susan Greenspan 8, Frederick Hooven 3, Andrea Le Croix 9, Lyn March 10, J Coen Netelenbos 11, Jeri Nieves 12, Johannes Pfeilschifter 13, Maurizio Rossini 14, Christian Roux 15, Ethel Siris 16, Nelson Watts 17, Juliet Compston 18
PMCID: PMC4873770  NIHMSID: NIHMS786598  PMID: 25257932

We used the GLOW database to study the bone health management postmenopausal women with glucocorticoid exposure. GLOW is a five year observational study of 60,000 postmenopausal women enrolled in 17 sites in 10 countries in Europe, North America, and Australia. We studied the use of BMD testing within the past 3 years of the study, and medical management in glucocorticoid-exposed individuals during the third year of survey in GLOW.

Of the 40,058 women with complete data over the five years, 893 (2%) reported continuous use of glucocorticoids over the past 2 or more years at the 3-year survey and 29,080 (73%) were non-users. Our study demonstrated considerable differences in BMD management in glucocorticoid users by site and region.. (see Table 1). Glucocorticoid-exposed individuals had greater use of BMD testing and medical management than non-users, although the number of individuals remained low (≤51%) worldwide in current continuous users. The proportion of individuals with current continuous use who were on calcium and vitamin D varied worldwide (35% to 80% and 32% to 89%, respectively) as did AOM use (41% to 51%). Among women who underwent BMD testing within the past 3 years, AOM and calcium/vitamin D use in glucocorticoid-exposed individuals was 1.8 times higher than that of non-users (33% versus 18%). 50% of CC users were aware of an osteoporosis diagnosis while 29% of nonusers were aware of an osteoporosis diagnosis.

Table 1.

Characteristics of GLOW women with 3 years of follow-up who were current continuous (CC) users versus non-users.

Region Calcium use Vitamin D use AOM use BMD testing

CC
n=880
Non-user
n=28,992
CC
n=881
Non-user
n=28,985
CC
n=806
Non-user
n=24,241
CC
n=857
Non-user
n=27,959
Northern Europe* (n=7976) 58 (47, 64) 14 (10, 21) 31 (22, 50) 13 (6, 19) 43 (39, 53) 11 (8, 16) 46 (34, 65) 23 (16, 29)
Southern Europe (n=5610) 35 (22, 55) 22 (7, 31) 32 (22, 41) 22 (12, 32) 38 (26, 55) 23 (19, 27) 57 (27, 66) 47 (43, 50)
USA and Canada **(n=14,649) 80 (71, 95) 70 (63, 78) 89 (77, 100) 79 (72, 86) 42 (20, 67) 22 (8, 28) 71 (59, 86) 62 (35, 81)
Total 67 45 68 49 42 19 65 48

Data given as per cent (minimum, maximum of sites within region). CC = current continuous user

*

Belgium, Germany, Netherlands, UK (4 sites)

France, Italy, Spain (4 sites)

**

7 US sites and 1 Canadian site

Including Australia

Limitations include our inability to determine glucocorticoid dose or confirm duration of therapy. Limitations include the use of self-reported data that were not confirmed by chart review. Our sites may not be fully representative of a country or region.

We conclude that management of bone health for glucocorticoid exposed individuals is not optimal worldwide.

Acknowledgments

The researchers were not specifically funded to do this research. The GLOW study was financed through a grant from Warner Chilcott and Sanofi to the Center for Outcomes Research, University of Massachusetts, Worcester, MA.

Footnotes

Stuart Silverman, Jeffrey Curtis, Kenneth Saag, Julie Flahive, Frederick Anderson, Roland Chapurlat, Christian Roux, JC Netelenbos, Johannes Pfeilschiffer, Nelson Watts, Juliet Compston declare no conflict of interest.

Jonathan Adachi declares that he is a consultant to Actavis, Amgen, Lilly, Merck and Novartis and is doing clinical trials with Amgen, Lilly, Merck and Novartis.

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