4.2 Article

Associations between depressive symptom profiles and immunometabolic characteristics in individuals with depression and their siblings

期刊

WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY
卷 22, 期 2, 页码 128-138

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/15622975.2020.1761562

关键词

Atypical depression; siblings; inflammation; BMI; familial resemblance

资金

  1. Netherlands Organisation for Health Research and Development (ZonMw) [10-000-1002]
  2. VU University Medical Centre
  3. GGZ inGeest
  4. Leiden University Medical Centre
  5. Leiden University
  6. GGZ Rivierduinen
  7. University Medical Centre Groningen
  8. University of Groningen
  9. Lentis
  10. GGZ Friesland
  11. GGZ Drenthe
  12. Rob Giel Onderzoekscentrum

向作者/读者索取更多资源

The study found that in individuals with lifetime diagnoses of depression and/or anxiety disorders and their siblings, BMI and waist circumference were associated with somatic and atypical-like symptom profiles, while other immunometabolic characteristics were significantly related to depressive symptom profiles. However, there was no apparent familial link between depressive symptom profiles and immunometabolic characteristics.
Objectives: The present study examined associations between immunometabolic characteristics (IMCs) and depressive symptom profiles (DSPs) in probands with lifetime diagnoses of depression and/or anxiety disorders and their siblings. Methods: Data were from the Netherlands Study of Depression and Anxiety, comprising 256 probands with lifetime diagnoses of depression and/or anxiety and their 380 siblings. Measured IMCs included blood pressure, waist circumference, and levels of glucose, triglycerides, HDL cholesterol, CRP, TNF-alpha and IL-6. DSPs included mood, cognitive, somatic and atypical-like profiles. We cross-sectionally examined whether DSPs were associated with IMCs within probands and within siblings, and whether DSPs were associated with IMCs between probands and siblings. Results: Within probands and within siblings, higher BMI and waist circumference were associated with higher somatic and atypical-like profiles. Other IMCs (IL-6, glucose and HDL cholesterol) were significantly related to DSPs either within probands or within siblings. DSPs and IMCs were not associated between probands and siblings. Conclusions: The results suggest that there is a familial component for each trait, but no common familial factors for the association between DSPs and IMCs. Alternative mechanisms, such as direct causal effects or non-shared environmental risk factors, may better fit these results.

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