Evidence map›Paper›PMID 26358172›Full record

Trial reportThe Journal of clinical endocrinology and metabolism2015

Bone Density After Teriparatide Discontinuation in Premenopausal Idiopathic Osteoporosis.

Adi Cohen, Mafo Kamanda-Kosseh, Robert R Recker, Joan M Lappe, David W Dempster, Hua Zhou, Serge Cremers, Mariana Bucovsky, Julie Stubby, Elizabeth Shane

Registry-linked trialOpen access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in The Journal of clinical endocrinology and metabolism, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03396315 (Bisphosphonates for Prevention of Post-Denosumab Bone Loss in Premenopausal Women With Idiopathic Osteoporosis), which is not on this map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03396315 phase2completednot on this mapstarted 2018, after this paper: background citation

Bisphosphonates for Prevention of Post-Denosumab Bone Loss in Premenopausal Women With Idiopathic Osteoporosis

TypeinterventionalSponsorColumbia UniversityRan2018 to 2023Enrolled24ConditionsIOP, OsteoporosisArmsAlendronate, Zoledronic Acid
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Denosumab After Teriparatide in Premenopausal Women With Idiopathic Osteoporosis.The Journal of clinical endocrinology and metabolism · 2022
    Trial
  4. Four-Year Teriparatide Followed by DenosumabFrontiers in endocrinology · 2021
    Trial
  5. Trial
  6. Trial
  7. Article
  8. Article
  9. Review
  10. Distinct Responses of Modeling- and Remodeling-Based Bone Formation to the Discontinuation of Intermittent Parathyroid Hormone Treatment in Ovariectomized Rats.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  11. Short Cyclic Regimen With Parathyroid Hormone (PTH) Results in Prolonged Anabolic Effect Relative to Continuous Treatment Followed by Discontinuation in Ovariectomized Rats.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Updates in CKD-Associated Osteoporosis.Current osteoporosis reports · 2018
    Review
  18. Article
  19. Premenopausal Osteoporosis.Endocrinology and metabolism clinics of North America · 2017
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Adi CohenColumbia University (A.C., M.K.-K., S.C., M.B., E.S.), New York, New York 10032; Creighton University (R.R.R., J.M.L., J.S.), Omaha, Nebraska 68178; and Helen Hayes Hospital (D.W.D., H.Z.), West Haverstraw, New York 10993.
Mafo Kamanda-KossehColumbia University (A.C., M.K.-K., S.C., M.B., E.S.), New York, New York 10032; Creighton University (R.R.R., J.M.L., J.S.), Omaha, Nebraska 68178; and Helen Hayes Hospital (D.W.D., H.Z.), West Haverstraw, New York 10993.
Robert R ReckerColumbia University (A.C., M.K.-K., S.C., M.B., E.S.), New York, New York 10032; Creighton University (R.R.R., J.M.L., J.S.), Omaha, Nebraska 68178; and Helen Hayes Hospital (D.W.D., H.Z.), West Haverstraw, New York 10993.
Joan M LappeColumbia University (A.C., M.K.-K., S.C., M.B., E.S.), New York, New York 10032; Creighton University (R.R.R., J.M.L., J.S.), Omaha, Nebraska 68178; and Helen Hayes Hospital (D.W.D., H.Z.), West Haverstraw, New York 10993.
David W DempsterColumbia University (A.C., M.K.-K., S.C., M.B., E.S.), New York, New York 10032; Creighton University (R.R.R., J.M.L., J.S.), Omaha, Nebraska 68178; and Helen Hayes Hospital (D.W.D., H.Z.), West Haverstraw, New York 10993.
Hua ZhouColumbia University (A.C., M.K.-K., S.C., M.B., E.S.), New York, New York 10032; Creighton University (R.R.R., J.M.L., J.S.), Omaha, Nebraska 68178; and Helen Hayes Hospital (D.W.D., H.Z.), West Haverstraw, New York 10993.
Serge CremersColumbia University (A.C., M.K.-K., S.C., M.B., E.S.), New York, New York 10032; Creighton University (R.R.R., J.M.L., J.S.), Omaha, Nebraska 68178; and Helen Hayes Hospital (D.W.D., H.Z.), West Haverstraw, New York 10993.
Mariana BucovskyColumbia University (A.C., M.K.-K., S.C., M.B., E.S.), New York, New York 10032; Creighton University (R.R.R., J.M.L., J.S.), Omaha, Nebraska 68178; and Helen Hayes Hospital (D.W.D., H.Z.), West Haverstraw, New York 10993.
Julie StubbyColumbia University (A.C., M.K.-K., S.C., M.B., E.S.), New York, New York 10032; Creighton University (R.R.R., J.M.L., J.S.), Omaha, Nebraska 68178; and Helen Hayes Hospital (D.W.D., H.Z.), West Haverstraw, New York 10993.
Elizabeth ShaneColumbia University (A.C., M.K.-K., S.C., M.B., E.S.), New York, New York 10032; Creighton University (R.R.R., J.M.L., J.S.), Omaha, Nebraska 68178; and Helen Hayes Hospital (D.W.D., H.Z.), West Haverstraw, New York 10993.
Columbia University · USHelen Hayes Hospital · USCreighton University · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR024156 · NCRR · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GINSBERG, HENRY N · 2006 to 2011
$53.0M
IDIOPATHIC OSTEOPOROSIS IN PREMENOPAUSAL WOMENR01AR049896 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SHANE, ELIZABETH J · 2005 to 2009
$2.8M
Idiopathic Osteoporosis in Premenopausal WomenK24AR052665 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SHANE, ELIZABETH J · 2005 to 2014
$1.8M
Bone Quality in Premenopausal Women with Idiopathic Fragility FracturesK23AR054127 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI COHEN, ADI · 2007 to 2011
$642k
NCRR NIH HHS UL1 RR024156NCRR NIH HHS UL1RR024156NIAMS NIH HHS 1K23 AR054127NIAMS NIH HHS 2K24 AR052665NIAMS NIH HHS K23 AR054127NIAMS NIH HHS K24 AR052665NIAMS NIH HHS R01 AR049896NIAMS NIH HHS R01 AR49896
6 · The paper itself

Abstract

contextWithout antiresorptive therapy, postmenopausal women lose bone mass after teriparatide (TPTD) discontinuation; estrogen treatment prevents bone loss in this setting. It is not known whether premenopausal women with regular menses lose bone mass after teriparatide discontinuation.

objectiveThis study aimed to test the hypothesis that normally menstruating premenopausal women with idiopathic osteoporosis (IOP) will maintain teriparatide-associated bone mineral density (BMD) gains after medication cessation.

designTwenty-one premenopausal IOP women previously enrolled in an open-label pilot study of teriparatide (20 mcg for 18-24 mo), had substantial BMD increases at the lumbar spine (LS; 10.8 ± 8.3%), total hip (TH; 6.2 ± 5.6%), and femoral neck (7.6 ± 3.4%). For this study, BMD was remeasured 2.0 ± 0.6 years after teriparatide cessation.

participantsFifteen women, who had gained 11.1 ± 7.2% at LS and 6.1 ± 6.5% at TH and were premenopausal at teriparatide completion, were followed without antiresorptive treatment.

resultsTwo years after completing teriparatide, BMD declined by 4.8 ± 4.3% (P = .0007) at the LS. In contrast, BMD remained stable at the femoral neck (-1.5 ± 4.2%) and TH (-1.1 ± 3.7%). Those who sustained LS bone loss >3% (-7.3 ± 2.9%; n = 10), did not differ from those with stable LS BMD (0.1 ± 1.1%; n=5) with regard to baseline body mass index, BMD at any site, or duration of followup, but were significantly older at re-evaluation (46 ± 3 vs 38 ± 7; P = .046), had larger increases in LS BMD during teriparatide treatment and higher cancellous bone remodeling on transiliac biopsy at baseline and completion of teriparatide treatment. Serum bone turnover markers did not differ at baseline or teriparatide completion, but tended to be higher at the re-evaluation timepoint in those with post-teriparatide bone loss.

conclusionsThese findings lead us to conclude that premenopausal women with IOP, particularly those over 40, may require antiresorptive treatment to prevent bone loss after teriparatide.

Indexed as

AdultAgedBiomarkersBone DensityBone Density Conservation AgentsBone DevelopmentFemaleHumansMiddle AgedMineralsOsteoporosis, PostmenopausalPilot ProjectsPremenopauseSpineTeriparatideTreatment OutcomeBiomarkersBone Density Conservation AgentsMineralsTeriparatide

Identifiers

PMID26358172
PMCPMC4702457
OpenAlexW2141615036

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.