Evidence map›Paper›PMID 26204844›Full record

Trial reportJournal of bone and mineral metabolism2016

Effects of strontium ranelate on bone mass and bone turnover in women with thalassemia major-related osteoporosis.

Nunziata Morabito, Antonino Catalano, Agostino Gaudio, Elisabetta Morini, Lucia Maria Bruno, Giorgio Basile, Eleni Tsiantouli, Federica Bellone, Rita Maria Agostino, Basilia Piraino and 3 more

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Journal of bone and mineral metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
1.7field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 30 citations in OpenAlex.

  1. Treatment for osteoporosis in people with beta-thalassaemia.The Cochrane database of systematic reviews · 2023
    Pooled it
  2. Thalassemia-associated osteoporosis: a systematic review on treatment and brief overview of the disease.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2016
    Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Observational
  11. Sclerostin and Vascular Pathophysiology.International journal of molecular sciences · 2020
    Review
  12. Hematological Diseases and Osteoporosis.International journal of molecular sciences · 2020
    Review
  13. Article
  14. Review
  15. Rheumatic Manifestations of Haemoglobinopathies.Current rheumatology reports · 2018
    Review
  16. Review
  17. Review
  18. Article
  19. 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

13 authors at 2 institutions in 1 country.

Nunziata MorabitoDepartment of Clinical and Experimental Medicine, University Hospital of Messina, A.O.U. Policlinico "G. Martino", Via C. Valeria, 98125, Messina, Italy.
Antonino CatalanoDepartment of Clinical and Experimental Medicine, University Hospital of Messina, A.O.U. Policlinico "G. Martino", Via C. Valeria, 98125, Messina, Italy. catalanoa@unime.it.
Agostino GaudioDepartment of Medical and Pediatric Sciences, University of Catania, Catania, Italy.
Elisabetta MoriniDepartment of Clinical and Experimental Medicine, University Hospital of Messina, A.O.U. Policlinico "G. Martino", Via C. Valeria, 98125, Messina, Italy.
Lucia Maria BrunoDepartment of Clinical and Experimental Medicine, University Hospital of Messina, A.O.U. Policlinico "G. Martino", Via C. Valeria, 98125, Messina, Italy.
Giorgio BasileDepartment of Clinical and Experimental Medicine, University Hospital of Messina, A.O.U. Policlinico "G. Martino", Via C. Valeria, 98125, Messina, Italy.
Eleni TsiantouliDepartment of Clinical and Experimental Medicine, University Hospital of Messina, A.O.U. Policlinico "G. Martino", Via C. Valeria, 98125, Messina, Italy.
Federica BelloneDepartment of Clinical and Experimental Medicine, University Hospital of Messina, A.O.U. Policlinico "G. Martino", Via C. Valeria, 98125, Messina, Italy.
Rita Maria AgostinoDepartment of Human Pathology, University of Messina, Messina, Italy.
Basilia PirainoDepartment of Pediatric Sciences, University Hospital of Messina, Messina, Italy.
Maria Angela La RosaDepartment of Pediatric Sciences, University Hospital of Messina, Messina, Italy.
Carmelo SalpietroDepartment of Pediatric Sciences, University Hospital of Messina, Messina, Italy.
Antonino LascoDepartment of Clinical and Experimental Medicine, University Hospital of Messina, A.O.U. Policlinico "G. Martino", Via C. Valeria, 98125, Messina, Italy.
University of Messina · ITUniversity of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Subjects affected by thalassemia major (TM) often have reduced bone mass and increased fracture risk. Strontium ranelate (SrR) is an effective treatment for postmenopausal and male osteoporosis. To date, no data exist on the use of SrR in the treatment of TM-related osteoporosis. Our aim was to evaluate the effects of SrR on bone mineral density (BMD), bone turnover markers and inhibitors of Wnt signaling (sclerostin and DKK-1). Twenty-four TM osteoporotic women were randomized to receive daily SrR 2 g or placebo in addition to calcium carbonate (1,000 mg) and vitamin D (800 IU). BMD at the lumbar spine and femoral neck, bone turnover markers (C-terminal telopeptide of procollagen type I [CTX], bone-specific alkaline phosphatase [BSAP]) and insulin-like growth factor-1 (IGF-1), sclerostin and DKK-1 were assessed at baseline and after 24 months. Back pain was measured by visual analog scale (VAS) every 6 months. After 24 months, TM women treated with SrR had increased their spine BMD values in comparison to baseline (p < 0.05). Moreover, they also exhibited a reduction of CTX and sclerostin levels (but not DKK-1) and exhibited an increase of BSAP and IGF-1 (p < 0.05); however, no significant changes were observed in the placebo group. In the SrR group, a reduction of back pain was observed after 18 months in comparison to baseline (p < 0.05) and after 24 months in comparison to placebo (p < 0.05). Our study reports for the first time the effects of SrR in the treatment of TM-related osteoporosis. SrR treatment improved BMD and normalized bone turnover markers, as well as lowering sclerostin serum levels.

Indexed as

Adaptor Proteins, Signal TransducingAdultbeta-ThalassemiaBone DensityBone Density Conservation AgentsBone Morphogenetic ProteinsBone RemodelingFemaleGenetic MarkersHumansInsulin-Like Growth Factor IIntercellular Signaling Peptides and ProteinsOsteoporosisThiophenesAdaptor Proteins, Signal TransducingBone Density Conservation AgentsBone Morphogenetic ProteinsDKK1 protein, humanGenetic MarkersInsulin-Like Growth Factor IIntercellular Signaling Peptides and ProteinsSOST protein, humanstrontium ranelateThiophenesDKK-1OsteoporosisSclerostinStrontium ranelateThalassemia

Identifiers

PMID26204844
OpenAlexW1958541311

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.