Journal Article FZJ-2021-01045

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Early identification of postpartum depression using demographic, clinical, and digital phenotyping

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2021
Nature Publishing Group London

Translational Psychiatry 11(1), 121 () [10.1038/s41398-021-01245-6]

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Abstract: Postpartum depression (PPD) and adjustment disorder (AD) affect up to 25% of women after childbirth. However, there are no accurate screening tools for either disorder to identify at-risk mothers and enable them to benefit from early intervention. Combinations of anamnestic, clinical, and remote assessments were evaluated for an early and accurate identification of PPD and AD. Two cohorts of mothers giving birth were included in the study (N = 308 and N = 193). At baseline, participants underwent a detailed sociodemographic-anamnestic and clinical interview. Remote assessments were collected over 12 weeks comprising mood and stress levels as well as depression and attachment scores. At 12 weeks postpartum, an experienced clinician assigned the participants to three distinct groups: women with PPD, women with AD, and healthy controls (HC). Combinations of these assessments were assessed for an early an accurate detection of PPD and AD in the first cohort and, after pre-registration, validated in a prospective second cohort. Combinations of postnatal depression, attachment (for AD) and mood scores at week 3 achieved balanced accuracies of 93 and 79% for differentiation of PPD and AD from HC in the validation cohort and balanced accuracies of 87 and 91% in the first cohort. Differentiation between AD and PPD, with a balanced accuracy of 73% was possible at week 6 based on mood levels only with a balanced accuracy of 73% in the validation cohort and a balanced accuracy of 76% in the first cohort. Combinations of in clinic and remote self-assessments allow for early and accurate detection of PPD and AD as early as three weeks postpartum, enabling early intervention to the benefit of both mothers and children.

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Note: 410314797/Deutsche Forschungsgemeinschaft (German Research Foundation) 410314797/Deutsche Forschungsgemeinschaft (German Research Foundation) 410314797/Deutsche Forschungsgemeinschaft (German Research Foundation) 410314797/Deutsche Forschungsgemeinschaft (German Research Foundation) 785907/EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) The study was supported by the DFG (Grant number: 410314797). NC wassupported by the Clinical Scientist Program (rotation program) of the medicalfaculty RWTH, Aachen (2015–2017). S.B.E. was supported by the EuropeanUnion’s Horizon 2020 Research and Innovation Programme under GrantAgreement No. 785907 (HBP SGA2). Open Access funding enabled andorganized by Projekt DEAL.

Contributing Institute(s):
  1. Gehirn & Verhalten (INM-7)
Research Program(s):
  1. 525 - Decoding Brain Organization and Dysfunction (POF4-525) (POF4-525)
  2. HBP SGA2 - Human Brain Project Specific Grant Agreement 2 (785907) (785907)

Appears in the scientific report 2021
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Medline ; Creative Commons Attribution CC BY 4.0 ; DOAJ ; OpenAccess ; Article Processing Charges ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; DOAJ Seal ; Essential Science Indicators ; Fees ; IF >= 5 ; JCR ; PubMed Central ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2021-02-15, last modified 2022-09-30


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