TY - JOUR
T1 - Factors associated with depressive state in patients with myasthenia gravis
T2 - A multicentre cross-sectional study
AU - Suzuki, Yasushi
AU - Utsugisawa, Kimiaki
AU - Suzuki, Shigeaki
AU - Nagane, Yuriko
AU - Masuda, Masayuki
AU - Kabasawa, Chiaki
AU - Shimizu, Yuko
AU - Utsumi, Hiroya
AU - Uchiyama, Shinichiro
AU - Fujihara, Kazuo
AU - Suzuki, Norihiro
PY - 2011
Y1 - 2011
N2 - Objectives: The objective of this study was to examine clinical factors associated with depressive state in patients with myasthenia gravis (MG). Design: Cross-sectional study. Setting and participants: We evaluated 287 consecutive cases of MG seen at six neurological centres located in Eastern Japan. Outcome measures: All MG patients completed the Japanese version of the Beck Depression InventoryeSecond Edition (BDI-II). Disease severity was determined according to the MG Foundation of America (MGFA) quantitative MG score, MG activities of daily living scale and MG composite scale (MG composite). Clinical state following treatment was categorised according to MGFA postintervention status. Associations between detailed clinical parameters of MG and BDI-II score were then examined statistically. Results: Mean BDI-II score for patients with MG (11.0±8.1) did not differ substantially from and overlapped with that reported as the Japanese standard (8.7±6.4). The mean +2 SDs for the Japanese standard is 21.5, approximately equal to the cut-off level indicative of moderate or worse depression (> 20 points) in the original English version. We thus defined BDI-II >21.5 as depressive state, with a frequency of 13.6% in patients with MG. Multivariate logistic regression analysis revealed current dose of oral prednisolone (OR 1.09, 95% CI 1.02 to 1.17; p=0.01), unchanged MGFA postintervention status (OR 3.55, 95% CI 1.18 to 10.71; p=0.02), time since onset (OR 0.93, 95% CI 0.87 to 0.99; p=0.03) and MG composite (OR 1.16, 95% CI 1.00 to 1.34; p=0.046) as factors independently associated with depressive state in MG. Conclusions: Dose of oral corticosteroids appears to represent the major factor associated with depressive state in MG. Unchanged status despite treatment and early disease stage are also significant background factors for depressive state, along with disease severity.
AB - Objectives: The objective of this study was to examine clinical factors associated with depressive state in patients with myasthenia gravis (MG). Design: Cross-sectional study. Setting and participants: We evaluated 287 consecutive cases of MG seen at six neurological centres located in Eastern Japan. Outcome measures: All MG patients completed the Japanese version of the Beck Depression InventoryeSecond Edition (BDI-II). Disease severity was determined according to the MG Foundation of America (MGFA) quantitative MG score, MG activities of daily living scale and MG composite scale (MG composite). Clinical state following treatment was categorised according to MGFA postintervention status. Associations between detailed clinical parameters of MG and BDI-II score were then examined statistically. Results: Mean BDI-II score for patients with MG (11.0±8.1) did not differ substantially from and overlapped with that reported as the Japanese standard (8.7±6.4). The mean +2 SDs for the Japanese standard is 21.5, approximately equal to the cut-off level indicative of moderate or worse depression (> 20 points) in the original English version. We thus defined BDI-II >21.5 as depressive state, with a frequency of 13.6% in patients with MG. Multivariate logistic regression analysis revealed current dose of oral prednisolone (OR 1.09, 95% CI 1.02 to 1.17; p=0.01), unchanged MGFA postintervention status (OR 3.55, 95% CI 1.18 to 10.71; p=0.02), time since onset (OR 0.93, 95% CI 0.87 to 0.99; p=0.03) and MG composite (OR 1.16, 95% CI 1.00 to 1.34; p=0.046) as factors independently associated with depressive state in MG. Conclusions: Dose of oral corticosteroids appears to represent the major factor associated with depressive state in MG. Unchanged status despite treatment and early disease stage are also significant background factors for depressive state, along with disease severity.
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U2 - 10.1136/bmjopen-2011-000313
DO - 10.1136/bmjopen-2011-000313
M3 - Article
C2 - 22184587
AN - SCOPUS:84855512395
SN - 2044-6055
VL - 1
JO - BMJ open
JF - BMJ open
IS - 2
M1 - e000313
ER -