TY - JOUR
T1 - Effects of teriparatide in postmenopausal women with osteoporosis on prior alendronate or raloxifene
T2 - Differences between stopping and continuing the antiresorptive agent
AU - Cosman, Felicia
AU - Wermers, Robert A.
AU - Recknor, Christopher
AU - Mauck, Karen F.
AU - Xie, Li
AU - Glass, Emmett V.
AU - Krege, John H.
N1 - Funding Information:
Disclosure Summary: F.C. has received lecture fees, consulting fees and/or grant support from Eli Lilly and Company, Novartis, Merck, Zosano, Procter and Gamble, Amgen, and Pfizer. C.R. has received consulting fees from and is an advisor for Eli Lilly and Company, Roche, and Procter and Gamble and has received honoraria from Eli Lilly and Company, Roche, Procter and Gamble, GlaxoSmithKline, Merck, and Aventis. L.X., E.V.G., and J.H.K. are employees of Eli Lilly and Company. R.A.W. and K.F.M. have nothing to declare.
PY - 2009
Y1 - 2009
N2 - Objective: The aim of the study was to assess adding vs. switching to teriparatide 20μg/d in patients on alendronate or raloxifene. Design: We conducted a randomized, open-label trial. Patients and Interventions: Postmenopausal women with osteoporosis on alendronate or raloxifene for at least 18 months added teriparatide (Add groups) or switched to teriparatide (Switch groups) for 18 months. Main Outcome Measures:Wemeasured bone turnover markers (BTM) and bone mineral density (BMD). Results: In the alendronate stratum, increases in BTM were smaller in the Add vs. Switch group [6-month PINP (64 vs. 401%); bone ALP (15 vs. 71%); βCTX (27 vs. 250%); all P < 0.001]. However, at 6 months, total hip BMD increased more in the Add vs. Switch group (1.4 vs. -0.8%; P = 0.002). In the Add vs. Switch group, 18-month BMD increments were higher in lumbar spine (8.4 vs. 4.8%; P = 0.003) and total hip (3.2 vs. 0.9%; P = 0.02), but not in femoral neck (2.7 vs. 2.3%; P = 0.75). In the raloxifene stratum, increases in BTM were also smaller in the Add vs. Switch group [6-month PINP (131 vs. 259%; P<0.001), bone ALP (31 vs. 44%; P=0.035), and βCTX (67 vs. 144%; P=0.001)]. At 6 months, total hip BMD increase was greater in the Add vs. Switch group (1.8 vs. 0.5%; P = 0.028). At 18 months, increases in lumbar spine (9.2 vs. 8.1%), total hip (2.8 vs. 1.8%), and femoral neck (3.8 vs. 2.2%) were not significantly different between groups. Conclusions: In women with osteoporosis treated with antiresorptives, greater bone turnover increases were achieved by switching to teriparatide, whereas greater BMD increases were achieved by adding teriparatide.
AB - Objective: The aim of the study was to assess adding vs. switching to teriparatide 20μg/d in patients on alendronate or raloxifene. Design: We conducted a randomized, open-label trial. Patients and Interventions: Postmenopausal women with osteoporosis on alendronate or raloxifene for at least 18 months added teriparatide (Add groups) or switched to teriparatide (Switch groups) for 18 months. Main Outcome Measures:Wemeasured bone turnover markers (BTM) and bone mineral density (BMD). Results: In the alendronate stratum, increases in BTM were smaller in the Add vs. Switch group [6-month PINP (64 vs. 401%); bone ALP (15 vs. 71%); βCTX (27 vs. 250%); all P < 0.001]. However, at 6 months, total hip BMD increased more in the Add vs. Switch group (1.4 vs. -0.8%; P = 0.002). In the Add vs. Switch group, 18-month BMD increments were higher in lumbar spine (8.4 vs. 4.8%; P = 0.003) and total hip (3.2 vs. 0.9%; P = 0.02), but not in femoral neck (2.7 vs. 2.3%; P = 0.75). In the raloxifene stratum, increases in BTM were also smaller in the Add vs. Switch group [6-month PINP (131 vs. 259%; P<0.001), bone ALP (31 vs. 44%; P=0.035), and βCTX (67 vs. 144%; P=0.001)]. At 6 months, total hip BMD increase was greater in the Add vs. Switch group (1.8 vs. 0.5%; P = 0.028). At 18 months, increases in lumbar spine (9.2 vs. 8.1%), total hip (2.8 vs. 1.8%), and femoral neck (3.8 vs. 2.2%) were not significantly different between groups. Conclusions: In women with osteoporosis treated with antiresorptives, greater bone turnover increases were achieved by switching to teriparatide, whereas greater BMD increases were achieved by adding teriparatide.
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U2 - 10.1210/jc.2008-2719
DO - 10.1210/jc.2008-2719
M3 - Article
C2 - 19584192
AN - SCOPUS:70349897684
SN - 0021-972X
VL - 94
SP - 3772
EP - 3780
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 10
ER -