4.4 Article

Bone Density After Teriparatide Discontinuation With or Without Antiresorptive Therapy in Pregnancy- and Lactation-Associated Osteoporosis

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CALCIFIED TISSUE INTERNATIONAL
卷 109, 期 5, 页码 544-553

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SPRINGER
DOI: 10.1007/s00223-021-00869-6

关键词

Osteoporosis; Anabolics; Antiresorptives; DXA

资金

  1. 'SENTINEL (Severance ENdocrinology daTa scIeNcE pLatform)' program of the Endocrinology Division, Department of Internal medicine, Yonsei University College of Medicine, Seoul, Korea [4-2018-1215, DUCD000002]

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This retrospective cohort study found that treatment with teriparatide (TPTD) in premenopausal women with pregnancy- and lactation-associated osteoporosis (PLO) can effectively maintain bone mineral density (BMD) without the need for sequential antiresorptive therapy (ART).
Pregnancy- and lactation-associated osteoporosis (PLO) is a rare and severe disorder that causes low-trauma or spontaneous fractures, most commonly multiple vertebral fractures, in the late pregnancy or lactation period [1]. In severe PLO, teriparatide (TPTD) might aid in bone mineral density (BMD) recovery and subsequent fracture risk reduction. However, it is unclear whether TPTD can be discontinued without sequential antiresorptive therapy (ART) in premenopausal women with PLO. In this retrospective cohort study, we investigated the changes in BMD in premenopausal women with PLO treated with TPTD 20 mcg daily with or without sequential ART. Data for 67 patients diagnosed with PLO from 2007 through 2017 were reviewed. Among 43 women with annual follow-up dual-energy X-ray absorptiometry data for 3 years, 33 were treated with TPTD (median 12 months) with (TPTD-ART, n = 13; median, 18 months) or without (TPTD-no ART, n = 20) sequential ART. The two groups showed no differences in the mean age (31 vs. 31 years), body mass index (BMI, 20.5 vs. 21.0 kg/m(2)), and baseline lumbar spine (LS) BMD (0.666 vs. 0.707 g/cm(2); p > 0.05 for all). LSBMD increased at 1, 2, and 3 years from baseline in both the TPTD-ART (14.1%, 21.8%, and 24.0%, respectively) and TPTD-no ART (17.3%, 24.1%, and 23.4%, respectively) groups, without significant between-group differences. Similar results were observed for the total hip BMD. LSBMD gain at 3 years did not differ by ART use (adjusted beta, 0.40; p = 0.874) in univariable and multivariable models adjusted for age, BMI, and baseline LSBMD. In summary, BMD gain by TPTD administration in premenopausal women with PLO can be well maintained without sequential ART treatment.

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