Evidence map›Paper›PMID 23918528›Full record

ArticleIrish journal of medical science2014

Osteogenesis imperfecta in adults: phenotypic characteristics and response to treatment in an Irish cohort.

E S O'Sullivan, S van der Kamp, M Kilbane, M McKenna

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Article in Irish journal of medical science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

3 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Developments in rare bone diseases and mineral disorders.Therapeutic advances in chronic disease · 2018
    Review
  3. 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

4 authors at 2 institutions in 1 country.

E S O'SullivanDepartment of Endocrinology, St Vincent's University Hospital, Dublin, Ireland, esther.osullivan2@hse.ie.
S van der Kamp
M Kilbane
M McKenna
St. Vincent's University Hospital · IEUniversity Hospital Galway · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteogenesis imperfecta (OI) is a heritable disorder of variable phenotype that is characterised by bone fragility and frequent fractures, with deformities and short stature in more severe cases.

aimsWe sought to review the response to treatment in a cohort of adult patients with OI.

methodsCharts of 16 patients with OI attending a metabolic bone disease clinic were reviewed, particularly with respect to the response to treatment using bisphosphonates and recombinant human parathyroid hormone (rhPTH). The response to treatment was assessed by monitoring bone mineral density (BMD) and bone turnover markers (BTMs).

resultsIn response to bisphosphonate therapy, median (range) BMD increased at the spine by 15.1(6.9-43.7) %. In response to rhPTH in 2 cases, spinal BMD increased by 40.3 and 27.2 %.

conclusionOI is debilitating disorder, but the course of the disease may be altered by treatment that increases BMD such as bisphosphonates and rhPTH. Both serial BMD and BTM aid in assessing response to intervention. Further study is needed with regard to fracture prevention.

Indexed as

AdolescentAdultBone DensityBone Density Conservation AgentsDiphosphonatesFemaleFractures, BoneHumansIrelandMaleMiddle AgedOsteogenesis ImperfectaParathyroid HormonePelvic BonesPhenotypeRecombinant ProteinsBone Density Conservation AgentsDiphosphonatesParathyroid HormonePTH protein, humanRecombinant Proteins

Identifiers

PMID23918528
OpenAlexW2041527538

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.