Evidence map›Paper›PMID 27579211›Full record

ArticleJournal of osteoporosis2016

Effect of Denosumab on Bone Mineral Density and Markers of Bone Turnover among Postmenopausal Women with Osteoporosis.

A Sánchez, L R Brun, H Salerni, P R Costanzo, D González, A Bagur, B Oliveri, M B Zanchetta, V Farías, L Maffei and 9 more

Open access · goldAbstract read
In one paragraph

Article in Journal of osteoporosis, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 20% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Denosumab-efficacy, safety, persistence and sequential strategies-a systematic review.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. A Review on the Role of Denosumab in Fracture Prevention.Drug design, development and therapy · 2020
    Review
  9. Effects of osteoporosis drug treatments on cortical and trabecular bone in the femur using DXA-based 3D modeling.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2018
    Article
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

19 authors at 9 institutions in 1 country.

A SánchezCentro de Endocrinología, Rosario, Argentina.ORCID 0000-0002-0761-4385
L R BrunLaboratorio de Biología Ósea, Facultad de Ciencias Médicas, Universidad Nacional de Rosario, Rosario, Argentina.ORCID 0000-0001-6281-2096
H SalerniConsultorios de Investigación Clínica Endocrinológica y del Metabolismo Óseo (CICEMO), Buenos Aires, Argentina.
P R CostanzoConsultorios de Investigación Clínica Endocrinológica y del Metabolismo Óseo (CICEMO), Buenos Aires, Argentina.ORCID 0000-0002-6130-2155
D GonzálezMautalen Salud e Investigación, Buenos Aires, Argentina.
A BagurMautalen Salud e Investigación, Buenos Aires, Argentina.
B OliveriMautalen Salud e Investigación, Buenos Aires, Argentina; Laboratorio Osteoporosis y Enfermedades Metabólicas Óseas, INIGEM, UBA-CONICET, Hospital de Clínicas, Buenos Aires, Argentina.
M B ZanchettaInstituto de Diagnóstico e Investigaciones Metabólicas (IDIM), Cátedra de Osteología y Metabolismo Mineral, Universidad del Salvador, Buenos Aires, Argentina.ORCID 0000-0002-9397-1847
V FaríasInstituto de Diagnóstico e Investigaciones Metabólicas (IDIM), Cátedra de Osteología y Metabolismo Mineral, Universidad del Salvador, Buenos Aires, Argentina.
L MaffeiConsultorios Asociados de Endocrinología Dra. Laura Maffei, Buenos Aires, Argentina.
V PremrouConsultorios Asociados de Endocrinología Dra. Laura Maffei, Buenos Aires, Argentina.ORCID 0000-0002-5351-5222
J L MansurCentro de Endocrinología y Osteoporosis, La Plata, Argentina.
M S LarroudéHospital Milstein, Buenos Aires, Argentina.
M A SarliInstituto de Diagnóstico e Investigaciones Metabólicas (IDIM), Cátedra de Osteología y Metabolismo Mineral, Universidad del Salvador, Buenos Aires, Argentina.ORCID 0000-0003-4615-6820
P ReyInstituto de Diagnóstico e Investigaciones Metabólicas (IDIM), Cátedra de Osteología y Metabolismo Mineral, Universidad del Salvador, Buenos Aires, Argentina.ORCID 0000-0003-4041-8594
M R UllaCentro de Endocrinología y Osteopatías Médicas, Córdoba, Argentina.ORCID 0000-0003-3729-878X
M M PavloveHospital Durand, Buenos Aires, Argentina.
S KarlsbrumHospital Durand, Buenos Aires, Argentina.
M L BranceCentro de Reumatología, Rosario, Argentina.ORCID 0000-0002-6749-9921
Universidad del Salvador · AREl Hospital General de Agudos Carlos G. Durand · ARHelios Salud · ARInstituto de Neurología Cognitiva · ARCentro Científico Tecnólogico - Rosario · ARConsejo Nacional de Investigaciones Científicas y Técnicas · ARHospital César Milstein · ARHospital Provincial de Rosario · ARNational University of Rosario · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to evaluate the effect of denosumab (Dmab) on bone mineral density (BMD) and bone turnover markers after 1 year of treatment. Additionally, the effect of Dmab in bisphosphonate-naïve patients (BP-naïve) compared to patients previously treated with bisphosphonates (BP-prior) was analyzed. This retrospective study included 425 postmenopausal women treated with Dmab for 1 year in clinical practice conditions in specialized centers from Argentina. Participants were also divided according to previous bisphosphonate treatment into BP-naïve and BP-prior. A control group of patients treated with BP not switched to Dmab matched by sex, age, and body mass index was used. Data are expressed as mean ± SEM. After 1 year of treatment with Dmab the bone formation markers total alkaline phosphatase and osteocalcin were significantly decreased (23.36% and 43.97%, resp.), as was the bone resorption marker s-CTX (69.61%). Significant increases in BMD were observed at the lumbar spine, femoral neck, and total hip without differences between BP-naïve and BP-prior. A better BMD response was found in BP-prior group compared with BP treated patients not switched to Dmab. Conclusion. Dmab treatment increased BMD and decreased bone turnover markers in the whole group, with similar response in BP-naïve and BP-prior patients. A better BMD response in BP-prior patients versus BP treated patients not switched to Dmab was observed.

Identifiers

PMID27579211
PMCPMC4992763
OpenAlexW2480607838

What OpenQuestion holds

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Registered trials

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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.