Evidence map›Paper›PMID 27164661›Full record

ArticleNeurology2016

Depression in amyotrophic lateral sclerosis.

Elin Roos, Daniela Mariosa, Caroline Ingre, Cecilia Lundholm, Karin Wirdefeldt, Per M Roos, Fang Fang

Open access · bronzeAbstract read
In one paragraph

Article in Neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 99 citations in OpenAlex.

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  15. Indications and techniques of non-invasive ventilation (NIV) in neuromuscular diseases.Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Elin RoosFrom the Departments of Medical Epidemiology and Biostatistics (E.R., D.M., C.L., K.W., F.F.) and Clinical Neuroscience (C.I., K.W.), and Institute of Environmental Medicine (P.M.R.), Karolinska Institutet, Stockholm, Sweden; and Department of Neurology (P.M.R.), Division of Clinical Neurophysiology, Oslo University Hospital, Oslo, Norway.
Daniela MariosaFrom the Departments of Medical Epidemiology and Biostatistics (E.R., D.M., C.L., K.W., F.F.) and Clinical Neuroscience (C.I., K.W.), and Institute of Environmental Medicine (P.M.R.), Karolinska Institutet, Stockholm, Sweden; and Department of Neurology (P.M.R.), Division of Clinical Neurophysiology, Oslo University Hospital, Oslo, Norway. Daniela.Mariosa@ki.se.
Caroline IngreFrom the Departments of Medical Epidemiology and Biostatistics (E.R., D.M., C.L., K.W., F.F.) and Clinical Neuroscience (C.I., K.W.), and Institute of Environmental Medicine (P.M.R.), Karolinska Institutet, Stockholm, Sweden; and Department of Neurology (P.M.R.), Division of Clinical Neurophysiology, Oslo University Hospital, Oslo, Norway.
Cecilia LundholmFrom the Departments of Medical Epidemiology and Biostatistics (E.R., D.M., C.L., K.W., F.F.) and Clinical Neuroscience (C.I., K.W.), and Institute of Environmental Medicine (P.M.R.), Karolinska Institutet, Stockholm, Sweden; and Department of Neurology (P.M.R.), Division of Clinical Neurophysiology, Oslo University Hospital, Oslo, Norway.
Karin WirdefeldtFrom the Departments of Medical Epidemiology and Biostatistics (E.R., D.M., C.L., K.W., F.F.) and Clinical Neuroscience (C.I., K.W.), and Institute of Environmental Medicine (P.M.R.), Karolinska Institutet, Stockholm, Sweden; and Department of Neurology (P.M.R.), Division of Clinical Neurophysiology, Oslo University Hospital, Oslo, Norway.
Per M RoosFrom the Departments of Medical Epidemiology and Biostatistics (E.R., D.M., C.L., K.W., F.F.) and Clinical Neuroscience (C.I., K.W.), and Institute of Environmental Medicine (P.M.R.), Karolinska Institutet, Stockholm, Sweden; and Department of Neurology (P.M.R.), Division of Clinical Neurophysiology, Oslo University Hospital, Oslo, Norway.
Fang FangFrom the Departments of Medical Epidemiology and Biostatistics (E.R., D.M., C.L., K.W., F.F.) and Clinical Neuroscience (C.I., K.W.), and Institute of Environmental Medicine (P.M.R.), Karolinska Institutet, Stockholm, Sweden; and Department of Neurology (P.M.R.), Division of Clinical Neurophysiology, Oslo University Hospital, Oslo, Norway.
Oslo University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo examine the relative risk of depression among patients with amyotrophic lateral sclerosis (ALS), both in terms of depression diagnosis and use of antidepressant drugs, before and after diagnosis.

methodsWe conducted a nested case-control study including 1,752 patients with ALS diagnosed from July 2005 to December 2010 and 8,760 controls based on the Swedish national health and population registers, to assess the associations of depression diagnosis and use of antidepressant drugs with a subsequent risk of ALS. We further followed the patients with ALS after diagnosis to estimate the association of an ALS diagnosis with the subsequent risk of depression and use of antidepressant drugs.

resultsBefore diagnosis, patients with ALS were at higher risk of receiving a clinical diagnosis of depression compared to controls (odds ratio [OR] 1.7, 95% confidence interval [CI] 1.3-2.3), and the highest risk increase was noted during the year before diagnosis (OR 3.5, 95% CI 2.1-5.6). Patients with ALS also had a highly increased risk of depression within the first year after diagnosis (hazard ratio 7.9, 95% CI 4.4-14.3). Antidepressant use was more common in patients with ALS than in controls, especially during the year before (OR 5.8, 95% CI 4.5-7.5) and the year after (hazard ratio 16.1, 95% CI 11.5-22.6) diagnosis.

conclusionsPatients with ALS are at higher risk of depression diagnosis and use of antidepressant drugs both immediately before and after diagnosis.

Indexed as

AgedAmyotrophic Lateral SclerosisAntidepressive AgentsCase-Control StudiesCohort StudiesDepressive DisorderFemaleHumansMaleMiddle AgedOdds RatioProportional Hazards ModelsPsychiatric Status Rating ScalesRegistriesRiskSensitivity and SpecificityAntidepressive Agents

Identifiers

PMID27164661
PMCPMC4909561
OpenAlexW2340417956

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.