Evidence map›Paper›PMID 26909149›Full record

ArticleBoneKEy reports2016

Sclerostin serum levels in patients with systemic autoimmune diseases.

Concepción Fernández-Roldán, Fernanda Genre, Raquel López-Mejías, Begoña Ubilla, Verónica Mijares, Daniel Sánchez Cano, Concepción López Robles, José Luis Callejas-Rubio, Raquel Ríos Fernández, Manuela Expósito Ruiz and 2 more

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In one paragraph

Article in BoneKEy reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

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  5. 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

12 authors at 3 institutions in 1 country.

Concepción Fernández-RoldánUnidad de Enfermedades Autoinmunes y Sistémicas, Servicio de Medicina Interna, Hospital Universitario San Cecilio , Granada, España.
Fernanda GenreLaboratorio de Epidemiología Genética y Arteriosclerosis en Enfermedades Inflamatorias Sistémicas, IDIVAL , Santander, España.
Raquel López-MejíasLaboratorio de Epidemiología Genética y Arteriosclerosis en Enfermedades Inflamatorias Sistémicas, IDIVAL , Santander, España.
Begoña UbillaLaboratorio de Epidemiología Genética y Arteriosclerosis en Enfermedades Inflamatorias Sistémicas, IDIVAL , Santander, España.
Verónica MijaresLaboratorio de Epidemiología Genética y Arteriosclerosis en Enfermedades Inflamatorias Sistémicas, IDIVAL , Santander, España.
Daniel Sánchez CanoUnidad de Enfermedades Autoinmunes y Sistémicas, Servicio de Medicina Interna, Hospital Universitario San Cecilio , Granada, España.
Concepción López RoblesUnidad de Enfermedades Autoinmunes y Sistémicas, Servicio de Medicina Interna, Hospital Universitario San Cecilio , Granada, España.
José Luis Callejas-RubioUnidad de Enfermedades Autoinmunes y Sistémicas, Servicio de Medicina Interna, Hospital Universitario San Cecilio , Granada, España.
Raquel Ríos FernándezUnidad de Enfermedades Autoinmunes y Sistémicas, Servicio de Medicina Interna, Hospital Universitario San Cecilio , Granada, España.
Manuela Expósito RuizFIBAO (Fundación Pública Andaluza para la Investigación Biosanitaria de Andalucía Oriental - Alejandro Otero) , Granada, España.
Miguel Á González-GayLaboratorio de Epidemiología Genética y Arteriosclerosis en Enfermedades Inflamatorias Sistémicas, IDIVAL , Santander, España.
Norberto Ortego CentenoUnidad de Enfermedades Autoinmunes y Sistémicas, Servicio de Medicina Interna, Hospital Universitario San Cecilio , Granada, España.
Instituto de Investigación Biosanitaria de Granada · ESCentro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESFundación Pública Andaluza para la Gestión de la Investigación en Salud de Sevilla · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic autoimmune diseases (SADs) are associated with lower bone mass and an increased risk of fractures. Sclerostin has a pivotal role in bone metabolism. Available data on circulating sclerostin levels in healthy subjects are limited, whereas those in SAD patients are absent. Our objective was to determine circulating sclerostin concentrations in systemic lupus erythematosus (SLE), systemic sclerosis (SSc) and Crohn's disease (CD) patients, and to analyze the factors associated with sclerostin concentrations. In this cross-sectional case-control study, serum sclerostin levels were measured in 38 SLE patients, 20 CD patients, 8 SSc patients and 20 healthy controls using a sclerostin ELISA. The mean values of the sclerostin (95% confidence interval) were 35.36 pmol l(-1) (12-101) in patients and 33.92 pmol l(-1) (2.31-100) in control subjects. The mean sclerostin value was 36.4 pmol l(-1) (22.1-48.5) in SLE patients, 26.7 pmol l(-1) (17.3-36.3) in CD patients and 51.8 pmol l(-1) (26.5-77.1) in SSc patients (P=0.001). Serum sclerostin levels were positively correlated with age (P<0.001), body mass index (BMI) (P=0.01) and lumbar spine Z-score (P=0.001) and negatively with creatinine clearance (P=0.001). Glucocorticoid treatment did not affect sclerostin levels. Sclerostin levels seem to have a heterogeneous pattern in different autoimmune diseases. SLE and SSc patients did not differ from healthy controls regarding sclerostin levels. The CD group had significantly lower values compared with SSc patients. Factors associated with sclerostin levels in autoimmune diseases seem to be the same than in the general population.

Identifiers

PMID26909149
PMCPMC4747078
OpenAlexW2267268572

What OpenQuestion holds

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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.