Abstract

The chronic autoimmune disease myasthenia gravis (MG) is characterized by fluctuating muscle weakness, which can lead to a large amount of stress in the patient. The current investigation plans to assess the risk of depressive disorders in MG patients. A retrospective cohort study of patients ageing 20 years and older and also newly diagnosed with MG between January 1, 2000, and December 31, 2008, was conducted from the National Health Insurance Research Database (NHIRD) in Taiwan. Observations of all 349 MG patients and 1,396 control individuals were made until a diagnosis of a depressive disorder by a psychiatrist, until death, or until December 31, 2013. A range of comorbidities were found, such as coronary artery disease, hypertension, diabetes mellitus, and dyslipidemia, with cerebrovascular disease being reported more frequently in MG patients in comparison with control subjects. After adjustment of patients’ sex, age, urbanization, comorbidities, and monthly income, results indicated that MG individuals are 1.94 times more at risk (95% confidence interval [CI], 1.15–3.27, P = 0.014) of developing depressive disorders than are controls. This showed an increased risk in the development of depressive disorders in people with MG. Thus, depressive symptoms in MG patients should be regularly assessed.

Highlights

  • Myasthenia gravis (MG), one of the chronic immune diseases, is described with symptoms of unpredictable fluctuating weakness and fatigue in neck muscles, eye muscles, limb muscles, swallowing, chewing, breathing, and talking throughout the day by having an impact on the skeletal neuromuscular junction

  • We analyzed the risk of depressive disorder in myasthenia gravis (MG) patients by conducting a nationwide study

  • Results revealed that in MG patients, in comparison with control individuals, the hazard ratio (HR) for developing depressive disorders during the follow-up period increased to 1.94 times, after adjustment for age, sex, comorbidities, urbanization, and monthly income

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Summary

Introduction

Myasthenia gravis (MG), one of the chronic immune diseases, is described with symptoms of unpredictable fluctuating weakness and fatigue in neck muscles, eye muscles, limb muscles, swallowing, chewing, breathing, and talking throughout the day by having an impact on the skeletal neuromuscular junction. In a previous study using the National Health Insurance Research Database (NHIRD) to investigate the epidemiology of myasthenia gravis in Taiwan, the average annual incidence was 2.1/100,000. The prevalence increased steadily during the study period from 8.4/100,000 in 2000 to 14.0/100,000 in 2007 [4]. MG is a life-long and remitting/relapsing disease with an unpredictable course [3]. On the other hand, continued treatment and chronic symptoms may lead to significant restraint and diminution of health-related quality of life [7,8,9,10]

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