Literature DB >> 27164661

Depression in amyotrophic lateral sclerosis.

Elin Roos1, Daniela Mariosa2, Caroline Ingre1, Cecilia Lundholm1, Karin Wirdefeldt1, Per M Roos1, Fang Fang1.   

Abstract

OBJECTIVE: To 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.
METHODS: We 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.
RESULTS: Before 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.
CONCLUSIONS: Patients with ALS are at higher risk of depression diagnosis and use of antidepressant drugs both immediately before and after diagnosis.
© 2016 American Academy of Neurology.

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Year:  2016        PMID: 27164661      PMCID: PMC4909561          DOI: 10.1212/WNL.0000000000002671

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  29 in total

1.  Depression in amyotrophic lateral sclerosis.

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3.  The Use of Antidepressant Medication before and after the Diagnosis of Amyotrophic Lateral Sclerosis: A Population-Based Cohort Study.

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4.  Prevalence of depressive disorders and change over time in late-stage ALS.

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5.  Increased risk for depression after breast cancer: a nationwide population-based cohort study of associated factors in Denmark, 1998-2011.

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6.  Severity of depressive symptoms and quality of life in patients with amyotrophic lateral sclerosis.

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Review 8.  Risk factors for amyotrophic lateral sclerosis.

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  14 in total

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4.  Neurodegenerative and psychiatric diseases among families with amyotrophic lateral sclerosis.

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Journal:  Neurology       Date:  2017-07-12       Impact factor: 9.910

5.  COMPLEX TREATMENT OF AMYOTROPHIC LATERAL SCLEROSIS PATIENT.

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Review 6.  The Impact of Cognitive and Behavioral Symptoms on ALS Patients and Their Caregivers.

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Review 7.  Palliative care in motor neurone disease: where are we now?

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8.  An observational study on quality of life and preferences to sustain life in locked-in state.

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9.  A Nation-Wide, Multi-Center Study on the Quality of Life of ALS Patients in Germany.

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Review 10.  Beyond Haemostasis and Thrombosis: Platelets in Depression and Its Co-Morbidities.

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