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  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
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We are analyzing https://link.springer.com/article/10.1007/s00406-024-01902-z.

Title:
Longitudinal associations between depressive symptoms and cell deformability: do glucocorticoids play a role? | European Archives of Psychiatry and Clinical Neuroscience
Description:
Cell deformability of all major blood cell types is increased in depressive disorders (DD). Furthermore, impaired glucocorticoid secretion is associated with DD, as well as depressive symptoms in general and known to alter cell mechanical properties. Nevertheless, there are no longitudinal studies examining accumulated glucocorticoid output and depressive symptoms regarding cell deformability. The aim of the present study was to investigate, whether depressive symptoms predict cell deformability one year later and whether accumulated hair glucocorticoids mediate this relationship. In 136 individuals (nfemale = 100; Mage = 46.72, SD = 11.28; age range = 20–65), depressive symptoms (PHQ-9) and hair glucocorticoids (cortisol and cortisone) were measured at time point one (T1), while one year later (T2) both depressive symptoms and hair glucocorticoids were reassessed. Additionally, cell deformability of peripheral blood cells was assessed at T2. Depression severity at T1 predicted higher cell deformability in monocytes and lymphocytes at T2. Accumulated hair cortisol and cortisone concentrations from T1 and T2 were not associated with higher cell deformability and further did not mediate the relationship between depressive symptoms and cell deformability. Elevated depressive symptomatology in a population based sample is longitudinally associated with higher immune cell deformability, while long-term integrated glucocorticoid levels seem not to be implicated in the underlying mechanism.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Health & Fitness
  • Education
  • Telecommunications

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💾}

We can't see how the site brings in money.

Some websites aren't about earning revenue; they're built to connect communities or raise awareness. There are numerous motivations behind creating websites. This might be one of them. Link.springer.com might be making money, but it's not detectable how they're doing it.

Keywords {🔍}

cell, deformability, depressive, pubmed, article, google, scholar, symptoms, immune, cas, hair, study, glucocorticoid, depression, blood, cortisol, increased, cells, levels, central, association, severity, major, participants, disorder, model, sample, dresden, psychiatry, glucocorticoids, analyses, analysis, data, individuals, phq, cortisone, disorders, health, university, secretion, concentrations, mdd, stress, significant, httpsdoiorgs, longitudinal, associations, walther, accumulated, time,

Topics {✒}

column-switching lc-apci-ms/ms assay real-time deformability cytometry computer-assisted dia-x-5 interview entitled mood-related morpho-rheological single-cell morpho-rheological phenotyping cross-sectional case-control study long-term glucocorticoid output long-term glucocorticoid secretion acquisition software shape-in2 long-term hpa-axis article download pdf lc-ms based analysis epstein-barr virus infections cross-lagged panel analysis plasma-based phenotype related american psychiatric publishing hypothalamic-pituitary-adrenal activation classificatory-categorical depression cases lw provided funding small population-based sample lc-ms/ms survive holm-bonferroni correction article eder cross-national meta-analysis steudte-schmiedgen adult psychiatric inpatients explore potential associations university funding sources common mental disorders privacy choices/manage cookies cross-sectional results inter-assay coefficients lam wa case-control analyses jochen guck patient health questionnaire european economic area integrated hormone concentration regression-based approach chronic glucocorticoid secretion low-grade inflammation [15 marlene penz clinical neuroscience aims higher cell deformability accumulated glucocorticoid concentrations accumulated hair cortisol longer-term outcomes continuously elevated levels accumulated glucocorticoid levels hypothalamus-pituitary-adrenal

Questions {❓}

  • Longitudinal associations between depressive symptoms and cell deformability: do glucocorticoids play a role?
  • Longitudinal associations between depressive symptoms and cell deformability: do glucocorticoids play a role?
  • McLachlan G (2018) Treatment resistant depression: what are the options?
  • Moylan S, Berk M, Dean OM et al (2014) Oxidative & nitrosative stress in depression: why so much stress?
  • Munder T, FlĂŒckiger C, Leichsenring F et al (2018) Is psychotherapy effective?
  • Pariante CM (2017) Why are depressed patients inflamed?
  • Psarraki EE, Kokka I, Bacopoulou F et al (2021) Is there a relation between major depression and hair cortisol?
  • Wolkowitz OM, Epel ES, Reus VI, Mellon SH (2010) Depression gets old fast: do stress and depression accelerate cell aging?

Schema {đŸ—ș}

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         headline:Longitudinal associations between depressive symptoms and cell deformability: do glucocorticoids play a role?
         description:Cell deformability of all major blood cell types is increased in depressive disorders (DD). Furthermore, impaired glucocorticoid secretion is associated with DD, as well as depressive symptoms in general and known to alter cell mechanical properties. Nevertheless, there are no longitudinal studies examining accumulated glucocorticoid output and depressive symptoms regarding cell deformability. The aim of the present study was to investigate, whether depressive symptoms predict cell deformability one year later and whether accumulated hair glucocorticoids mediate this relationship. In 136 individuals (nfemale = 100; Mage = 46.72, SD = 11.28; age range = 20–65), depressive symptoms (PHQ-9) and hair glucocorticoids (cortisol and cortisone) were measured at time point one (T1), while one year later (T2) both depressive symptoms and hair glucocorticoids were reassessed. Additionally, cell deformability of peripheral blood cells was assessed at T2. Depression severity at T1 predicted higher cell deformability in monocytes and lymphocytes at T2. Accumulated hair cortisol and cortisone concentrations from T1 and T2 were not associated with higher cell deformability and further did not mediate the relationship between depressive symptoms and cell deformability. Elevated depressive symptomatology in a population based sample is longitudinally associated with higher immune cell deformability, while long-term integrated glucocorticoid levels seem not to be implicated in the underlying mechanism.
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      headline:Longitudinal associations between depressive symptoms and cell deformability: do glucocorticoids play a role?
      description:Cell deformability of all major blood cell types is increased in depressive disorders (DD). Furthermore, impaired glucocorticoid secretion is associated with DD, as well as depressive symptoms in general and known to alter cell mechanical properties. Nevertheless, there are no longitudinal studies examining accumulated glucocorticoid output and depressive symptoms regarding cell deformability. The aim of the present study was to investigate, whether depressive symptoms predict cell deformability one year later and whether accumulated hair glucocorticoids mediate this relationship. In 136 individuals (nfemale = 100; Mage = 46.72, SD = 11.28; age range = 20–65), depressive symptoms (PHQ-9) and hair glucocorticoids (cortisol and cortisone) were measured at time point one (T1), while one year later (T2) both depressive symptoms and hair glucocorticoids were reassessed. Additionally, cell deformability of peripheral blood cells was assessed at T2. Depression severity at T1 predicted higher cell deformability in monocytes and lymphocytes at T2. Accumulated hair cortisol and cortisone concentrations from T1 and T2 were not associated with higher cell deformability and further did not mediate the relationship between depressive symptoms and cell deformability. Elevated depressive symptomatology in a population based sample is longitudinally associated with higher immune cell deformability, while long-term integrated glucocorticoid levels seem not to be implicated in the underlying mechanism.
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                  name:TUD Dresden University of Technology
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            type:Organization
      name:Magdalena Wekenborg
      url:https://orcid.org/0000-0002-4498-107X
      affiliation:
            name:TUD Dresden University of Technology
            address:
               name:Biopsychology, Faculty of Psychology, TUD Dresden University of Technology, Dresden, Germany
               type:PostalAddress
            type:Organization
            name:TUD Dresden University of Technology
            address:
               name:Else Kröner Fresenius Center of Digital Health, Faculty of Medicine and University Hospital Carl Gustav Carus, TUD Dresden University of Technology, Dresden, Germany
               type:PostalAddress
            type:Organization
      name:Marlene Penz
      url:https://orcid.org/0000-0003-0356-1594
      affiliation:
            name:Johannes Kepler UniversitĂ€t Linz
            address:
               name:Institute of Psychology, Johannes Kepler UniversitĂ€t Linz, Linz, Austria
               type:PostalAddress
            type:Organization
      name:Nicole Rothe
      affiliation:
            name:TUD Dresden University of Technology
            address:
               name:Biopsychology, Faculty of Psychology, TUD Dresden University of Technology, Dresden, Germany
               type:PostalAddress
            type:Organization
      name:Jochen Guck
      url:https://orcid.org/0000-0002-1453-6119
      affiliation:
            name:TUD Dresden University of Technology
            address:
               name:Center for Molecular and Cellular Bioengineering, Biotechnology Center, TUD Dresden University of Technology, Dresden, Germany
               type:PostalAddress
            type:Organization
            name:Max Planck Institute for the Science of Light & Max-Planck-Zentrum fĂŒr Physik und Medizin
            address:
               name:Max Planck Institute for the Science of Light & Max-Planck-Zentrum fĂŒr Physik und Medizin, Erlangen, Germany
               type:PostalAddress
            type:Organization
      name:Lucas Daniel Wittwer
      url:https://orcid.org/0000-0002-8892-0025
      affiliation:
            name:Max Planck Institute for the Science of Light & Max-Planck-Zentrum fĂŒr Physik und Medizin
            address:
               name:Max Planck Institute for the Science of Light & Max-Planck-Zentrum fĂŒr Physik und Medizin, Erlangen, Germany
               type:PostalAddress
            type:Organization
            name:Technische UniversitĂ€t Freiberg
            address:
               name:Institut fĂŒr Numerische Mathematik und Optimierung, Technische UniversitĂ€t Freiberg, Freiberg, Germany
               type:PostalAddress
            type:Organization
      name:Andreas Walther
      url:http://orcid.org/0000-0003-4516-1783
      affiliation:
            name:University of Zurich
            address:
               name:Clinical Psychology and Psychotherapy, University of Zurich, Zurich, Switzerland
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Biopsychology, Faculty of Psychology, TUD Dresden University of Technology, Dresden, Germany
      name:Center for Molecular and Cellular Bioengineering, Biotechnology Center, TUD Dresden University of Technology, Dresden, Germany
      name:Max Planck Institute for the Science of Light & Max-Planck-Zentrum fĂŒr Physik und Medizin, Erlangen, Germany
      name:Biopsychology, Faculty of Psychology, TUD Dresden University of Technology, Dresden, Germany
      name:Biopsychology, Faculty of Psychology, TUD Dresden University of Technology, Dresden, Germany
      name:School of Psychology, Nanjing Normal University, Nanjing, China
      name:Biopsychology, Faculty of Psychology, TUD Dresden University of Technology, Dresden, Germany
      name:Else Kröner Fresenius Center of Digital Health, Faculty of Medicine and University Hospital Carl Gustav Carus, TUD Dresden University of Technology, Dresden, Germany
      name:Institute of Psychology, Johannes Kepler UniversitĂ€t Linz, Linz, Austria
      name:Biopsychology, Faculty of Psychology, TUD Dresden University of Technology, Dresden, Germany
      name:Center for Molecular and Cellular Bioengineering, Biotechnology Center, TUD Dresden University of Technology, Dresden, Germany
      name:Max Planck Institute for the Science of Light & Max-Planck-Zentrum fĂŒr Physik und Medizin, Erlangen, Germany
      name:Max Planck Institute for the Science of Light & Max-Planck-Zentrum fĂŒr Physik und Medizin, Erlangen, Germany
      name:Institut fĂŒr Numerische Mathematik und Optimierung, Technische UniversitĂ€t Freiberg, Freiberg, Germany
      name:Clinical Psychology and Psychotherapy, University of Zurich, Zurich, Switzerland

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