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Clinical and biological subtypes of late-life depression.
Kwak, Seyul; Kim, Hairin; Oh, Dae Jong; Jeon, Yeong-Ju; Oh, Da Young; Park, Su Mi; Lee, Jun-Young.
Afiliação
  • Kwak S; Department of Psychology, Pusan National University, Republic of Korea.
  • Kim H; Department of Psychiatry, Seoul National University College of Medicine & SMG-SNU Boramae Medical Center, Republic of Korea.
  • Oh DJ; Department of Psychiatry, Seoul National University College of Medicine & SMG-SNU Boramae Medical Center, Republic of Korea.
  • Jeon YJ; Department of Psychiatry, Seoul National University College of Medicine & SMG-SNU Boramae Medical Center, Republic of Korea.
  • Oh DY; Department of Psychiatry, Seoul National University College of Medicine & SMG-SNU Boramae Medical Center, Republic of Korea.
  • Park SM; Department of Counseling Psychology, Hannam University, Republic of Korea.
  • Lee JY; Department of Psychiatry, Seoul National University College of Medicine & SMG-SNU Boramae Medical Center, Republic of Korea. Electronic address: benji@snu.ac.kr.
J Affect Disord ; 312: 46-53, 2022 09 01.
Article em En | MEDLINE | ID: mdl-35691418
ABSTRACT

BACKGROUND:

Late-life depression (LDD) results from multiple psychosocial and neurobiological changes occurring in later life. The current study investigated how patterns of clinical symptoms and brain structural features are classified into LDD subtypes.

METHOD:

Self-report scale of depression, behavioral rating of affective symptoms, and brain structural imaging of white matter change and cortical thickness were assessed in 541 older adults with no cognitive impairment or mild cognitive impairment. Latent profile analysis was used to identify distinct subtypes of depression.

RESULTS:

The latent profile analysis identified four classes with mild to severe depressive symptoms and two classes with minimal symptoms. While the classes primarily differed in the overall severity, the combinatory patterns of clinical symptoms and neuropathological signature distinguished the classes with similar severity. The classes were distinguished in terms of whether or not neurodegenerative risk accompanied the corresponding depressive symptoms. The presence of the negative self-scheme and cortical thinning pattern notably characterized the subtypes of LDD.

LIMITATIONS:

The underlying etiologies of the biological subtypes are still speculative, and the current study lacks clinical history that differentiates late- and early-onset depression.

CONCLUSIONS:

Our finding provides insight in identifying heterogeneities of depressive disorder in later life and suggests that self-report and behavioral symptom profile in combination with white matter lesion and cortical thickness effectively characterizes distinct subtypes of LDD.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Disfunção Cognitiva / Substância Branca Tipo de estudo: Prognostic_studies Limite: Aged / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Disfunção Cognitiva / Substância Branca Tipo de estudo: Prognostic_studies Limite: Aged / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article