Evidence map›Paper›PMID 36831140›Full record

ArticleBiomedicines2023

High-Dose Intravenous Steroid Treatment Seems to Have No Long-Term Negative Effect on Bone Mineral Density of Young and Newly Diagnosed Multiple Sclerosis Patients: A Pilot Study.

George Simeakis, Maria Anagnostouli, Nikolaos Fakas, John Koutsikos, Athanasios Papatheodorou, Konstantinos Chanopoulos, Kwnstantinos Athanasiou, George Papatheodorou, Evangelia Zapanti, Maria Alevizaki and 2 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. 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
1.0field-weighted citation impact, top 24% 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, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

12 authors at 3 institutions in 1 country.

George SimeakisEndocrine Department, 401 General Military Hospital of Athens, 115 25 Athens, Greece.ORCID 0000-0002-3348-7340
Maria AnagnostouliMultiple Sclerosis and Demyelinating Diseases Unit, 1st Neurology Department, School of Medicine, Aeginition University Hospital, National and Kapodistrian University of Athens, 115 28 Athens, Greece.ORCID 0000-0001-8934-670X
Nikolaos FakasNeurology Department, 401 General Military Hospital of Athens, 115 25 Athens, Greece.
John KoutsikosDepartment of Nuclear Medicine, 401 Military Hospital of Athens, 115 25 Athens, Greece.
Athanasios PapatheodorouDepartment for Biomedical Research, 251 Air Force General Hospital, 115 25 Athens, Greece.
Konstantinos ChanopoulosCenter for Molecular Biology-Research Unit, 401 Military Hospital of Athens, 115 25 Athens, Greece.
Kwnstantinos AthanasiouDepartment of Nuclear Medicine, 401 Military Hospital of Athens, 115 25 Athens, Greece.
George PapatheodorouCenter for Molecular Biology-Research Unit, 401 Military Hospital of Athens, 115 25 Athens, Greece.
Evangelia ZapantiDepartment of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, 115 28 Athens, Greece.
Maria AlevizakiDepartment of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, 115 28 Athens, Greece.
Gregory KaltsasEndocrine Oncology Unit, First Department of Propaedeutic and Internal Medicine, Laiko Hospital, National and Kapodistrian University of Athens, 115 27 Athens, Greece.
Evangelos TerposDepartment of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, 115 28 Athens, Greece.ORCID 0000-0001-5133-1422
National and Kapodistrian University of Athens · GR401 General Military Hospital of Athens · GRHellenic Air Force · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-dose intravenous steroid treatment (HDIST) represents the first choice of treatment for multiple sclerosis (MS) relapses. Chronic oral glucocorticoid (GC) administration correlates with bone loss whereas data regarding HDIST in MS are still conflicting. Twenty-five newly diagnosed MS patients (NDMSP) (median age: 37 years) were prospectively studied for the effects of HDIST on bone mineral density (BMD) and bone metabolism. Patients received 1000 mg methylprednisolone intravenously every day for 5 days followed by oral prednisolone tapering over 21 days. Bone metabolism indices were determined prior to GC, on days 2, 4, 6, and 90, and at months 6, 12, 18, and 24 post GC therapy. Femoral, lumbar-spine BMD, and whole-body measurement of adipose/lean tissue were assessed prior to GC-administration and then every six months. Ten patients completed the study. N-terminal-propeptide-procollagen-type-1 and bone-specific alkaline phosphatase showed a significant increase at day-90 (

Indexed as

25-hydroxyvitamin DBMDbone-turnovercytokinesglucocorticoidsmultiple sclerosisosteoporosisperiostin

Identifiers

PMID36831140
PMCPMC9952957
OpenAlexW4321378199

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.