Characterizing the phenotype of multiple sclerosis-associated depression in comparison with idiopathic major depression
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Characterizing the phenotype of multiple sclerosis-associated depression in comparison with idiopathic major depression. / Hasselmann, Helge; Bellmann-Strobl, Judith; Ricken, Roland; Oberwahrenbrock, Timm; Rose, Matthias; Otte, Christian; Adli, Mazda; Paul, Friedemann; Brandt, Alexander U; Finke, Carsten; Gold, Stefan M.
In: MULT SCLER J, Vol. 22, No. 11, 10.2016, p. 1476-1484.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Characterizing the phenotype of multiple sclerosis-associated depression in comparison with idiopathic major depression
AU - Hasselmann, Helge
AU - Bellmann-Strobl, Judith
AU - Ricken, Roland
AU - Oberwahrenbrock, Timm
AU - Rose, Matthias
AU - Otte, Christian
AU - Adli, Mazda
AU - Paul, Friedemann
AU - Brandt, Alexander U
AU - Finke, Carsten
AU - Gold, Stefan M
N1 - © The Author(s), 2016.
PY - 2016/10
Y1 - 2016/10
N2 - BACKGROUND: Depression is a common co-morbidity in patients with multiple sclerosis (MS). While somatic symptoms of MS correlate with depression levels, it is unclear whether the clinical presentation of MS-associated depression differs from patients with "idiopathic" major depressive disorder (MDD).OBJECTIVE: To compare the clinical phenotype of depression among MS and idiopathic MDD patients.METHODS: Mean relative contribution of individual Beck Depression Inventory-II (BDI-II) items was evaluated among n = 139 patients with relapsing-remitting MS and n = 85 MDD patients without somatic illness. Next, comparisons were repeated in n = 38 MS with clinically relevant depressive symptoms (BDI-II > 19) and n = 38 MDD patients matched for sex, age, and depression severity. Finally, the underlying construct of depression was compared across groups using confirmatory factor analysis (CFA).RESULTS: Comparisons on a whole-group level produced the expected differences along somatic/non-somatic symptoms. However, when appropriately controlling for depression severity, age, and sex, only four items contributed differentially to BDI-II total scores in MS versus MDD. CFA suggested that the underlying depression construct is essentially identical in both groups.CONCLUSION: The clinical phenotype of "idiopathic" MDD and MS-associated depression appears similar when adequately examined. The relevance of these findings for psychotherapeutic approaches for MS-associated depression should be explored in future studies.
AB - BACKGROUND: Depression is a common co-morbidity in patients with multiple sclerosis (MS). While somatic symptoms of MS correlate with depression levels, it is unclear whether the clinical presentation of MS-associated depression differs from patients with "idiopathic" major depressive disorder (MDD).OBJECTIVE: To compare the clinical phenotype of depression among MS and idiopathic MDD patients.METHODS: Mean relative contribution of individual Beck Depression Inventory-II (BDI-II) items was evaluated among n = 139 patients with relapsing-remitting MS and n = 85 MDD patients without somatic illness. Next, comparisons were repeated in n = 38 MS with clinically relevant depressive symptoms (BDI-II > 19) and n = 38 MDD patients matched for sex, age, and depression severity. Finally, the underlying construct of depression was compared across groups using confirmatory factor analysis (CFA).RESULTS: Comparisons on a whole-group level produced the expected differences along somatic/non-somatic symptoms. However, when appropriately controlling for depression severity, age, and sex, only four items contributed differentially to BDI-II total scores in MS versus MDD. CFA suggested that the underlying depression construct is essentially identical in both groups.CONCLUSION: The clinical phenotype of "idiopathic" MDD and MS-associated depression appears similar when adequately examined. The relevance of these findings for psychotherapeutic approaches for MS-associated depression should be explored in future studies.
U2 - 10.1177/1352458515622826
DO - 10.1177/1352458515622826
M3 - SCORING: Journal article
C2 - 26746809
VL - 22
SP - 1476
EP - 1484
JO - MULT SCLER J
JF - MULT SCLER J
SN - 1352-4585
IS - 11
ER -