Effects of Teriparatide Treatment and Discontinuation in Postmenopausal Women and Eugonadal Men with Osteoporosis

被引:101
作者
Leder, Benjamin Z. [1 ]
Neer, Robert M. [1 ]
Wyland, Jason J. [1 ]
Lee, Hang W. [2 ]
Burnett-Bowie, Sherri-Ann M. [1 ]
Finkelstein, Joel S. [1 ]
机构
[1] Massachusetts Gen Hosp, Endocrine Unit, Dept Med, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Ctr Biostat, Boston, MA 02114 USA
关键词
GROWTH-FACTOR-I; FRACTURE RISK REDUCTION; BONE-MINERAL DENSITY; LONG-TERM EXTENSION; PARATHYROID-HORMONE; SKELETAL SENSITIVITY; LONGITUDINAL CHANGES; RANDOMIZED-TRIAL; ALENDRONATE; RESPONSIVENESS;
D O I
10.1210/jc.2008-2630
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Context: In postmenopausal women, bone mineral density (BMD) declines after teriparatide therapy is stopped. The pattern of BMD loss after teriparatide therapy is stopped in men is less clear. Objective: The aim of the study was to determine whether the pattern of teriparatide-induced bone accrual and post-teriparatide bone loss differs between postmenopausal women and eugonadal men. Design: We conducted a prospective cohort substudy. Patients: The study included 14 postmenopausal women and 17 eugonadal men, ages 46-85 yr, with lumbar spine or femoral neck BMD T-scores below -2. Intervention: Teriparatide (37 mu g sc daily) was administered for 24 months, followed by 12 months off therapy. Main Outcome Measures: We measured BMD at various anatomic sites by dual-energy x-ray absorptiometry, trabecular spine BMD by quantitative computed tomography, and bone turnover markers during the treatment and observation periods. The response to teriparatide administration and discontinuation was compared between females and males. Results: BMD of the spine, femoral neck, total hip, and trabecular spine increased similarly during the treatment period in men and women, whereas BMD at the radius was stable in men but decreased by 8.1 +/- 3.3% in women (P < 0.0001). After teriparatide was stopped, BMD at the posterior-anterior spine decreased by 7.1 +/- 3.8% in women and by 4.1 +/- 3.5% in men (P = 0.036). BMD at the total hip and femoral neck decreased by 3.8 +/- 3.9 and 3.1 +/- 4.3%, respectively, in women but remained stable in men (P < 0.05 for both sites). BMD at the distal radius remained stable in men but increased in women by 1.6 +/- 3.1% (P = 0.069). Conclusions: Teriparatide appears to increase BMD similarly in postmenopausal women and eugonadal men with osteoporosis. After teriparatide is stopped, the decline in BMD is greater in women than in men. If confirmed in larger cohorts, these findings would suggest that the indication for immediate antiresorptive therapy after teriparatide may not be as urgent in men as in women. (J Clin Endocrinol Metab 94: 2915-2921, 2009)
引用
收藏
页码:2915 / 2921
页数:7
相关论文
共 30 条
[1]
Effect of raloxifene after recombinant teriparatide [hPTH(1-34)] treatment in postmenopausal women with osteoporosis [J].
Adami, S. ;
Martin, J. San ;
Munoz-Torres, M. ;
Econs, M. J. ;
Xie, L. ;
Dalsky, G. P. ;
McClung, M. ;
Felsenberg, D. ;
Brown, J. P. ;
Brandi, M. L. ;
Sipos, A. .
OSTEOPOROSIS INTERNATIONAL, 2008, 19 (01) :87-94
[2]
[Anonymous], 2004, Bone Health and Osteoporosis: A report of the Surgeon General
[3]
Insulin-like growth factor I is required for the anabolic actions of parathyroid hormone on mouse bone [J].
Bikle, DD ;
Sakata, T ;
Leary, C ;
Elalieh, H ;
Ginzinger, D ;
Rosen, CJ ;
Beamer, W ;
Majumdar, S ;
Halloran, BP .
JOURNAL OF BONE AND MINERAL RESEARCH, 2002, 17 (09) :1570-1578
[4]
Effects of continuing or stopping alendronate after 5 years of treatment - The Fracture Intervention Trial long-term extension (FLEX): A randomized trial [J].
Black, Dennis M. ;
Schwartz, Ann V. ;
Ensrud, Kristine E. ;
Cauley, Jane A. ;
Levis, Silvina ;
Quandt, Sara A. ;
Satterfield, Suzanne ;
Wallace, Robert B. ;
Bauer, Douglas C. ;
Palermo, Lisa ;
Wehren, Lois E. ;
Lombardi, Antonio ;
Santora, Arthur C. ;
Cummings, Steven R. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 296 (24) :2927-2938
[5]
One year of alendronate after one year of parathyroid hormone (1-84) for osteoporosis [J].
Black, DM ;
Bilezikian, JP ;
Ensrud, KE ;
Greenspan, SL ;
Palermo, L ;
Hue, T ;
Lang, TF ;
McGowan, JA ;
Rosen, CJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (06) :555-565
[6]
Normal levels of serum IGF-I: determinants and validity of current reference ranges [J].
Brabant, G. ;
Wallaschofski, H. .
PITUITARY, 2007, 10 (02) :129-133
[7]
INSULIN-LIKE GROWTH FACTOR-I MEDIATES SELECTIVE ANABOLIC EFFECTS OF PARATHYROID-HORMONE IN BONE CULTURES [J].
CANALIS, E ;
CENTRELLA, M ;
BURCH, W ;
MCCARTHY, TL .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (01) :60-65
[8]
ESTROGEN PROTECTION AGAINST BONE RESORBING EFFECTS OF PARATHYROID-HORMONE INFUSION - ASSESSMENT BY USE OF BIOCHEMICAL MARKERS [J].
COSMAN, F ;
SHEN, V ;
XIE, F ;
SEIBEL, M ;
RATCLIFFE, A ;
LINDSAY, R .
ANNALS OF INTERNAL MEDICINE, 1993, 118 (05) :337-343
[9]
Parathyroid hormone treatment for osteoporosis [J].
Cosman, Felicia .
CURRENT OPINION IN ENDOCRINOLOGY DIABETES AND OBESITY, 2008, 15 (06) :495-501
[10]
Randomized trial of effect of alendronate continuation versus discontinuation in women with low BMD: Results from the Fracture Intervention Trial long-term extension [J].
Ensrud, KE ;
Barrett-Connor, EL ;
Schwartz, A ;
Santora, AC ;
Bauer, DC ;
Suryawanshi, S ;
Feldstein, A ;
Haskell, WL ;
Hochberg, MC ;
Torner, JC ;
Lombardi, A ;
Black, DM .
JOURNAL OF BONE AND MINERAL RESEARCH, 2004, 19 (08) :1259-1269