Publications by authors named "S Jalkanen"

Purpose: The complex pathogenesis of hypertension, potentially involving inflammatory pathways, remains elusive. This study aimed to evaluate the relationship between 24-hour urinary sodium excretion and inflammatory cytokines alongside C-reactive protein (CRP) in a nationwide Finnish sample.

Materials And Methods: 265 participants from the FINRISK 2002 study were included in the analyses.

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We investigated the effects of 35 inflammatory cytokines on respiratory outcomes, including COVID-19, asthma (atopic and non-atopic), chronic obstructive pulmonary disease (COPD), and pulmonary function indices, using Mendelian randomization and colocalization analyses. The emerging associations were further explored using observational analyses in the UK Biobank. We found an inverse association between genetically predicted macrophage colony stimulating factor (MCSF), soluble intercellular adhesion molecule-1 (sICAM), and soluble vascular cell adhesion molecule-1 with risk of COVID-19 outcomes.

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Article Synopsis
  • * It involved 452 patients who underwent coronary angiography, measuring 48 cytokines to determine their association with CAD severity assessed by the SYNTAX Score.
  • * Findings revealed that higher levels of certain cytokines like IL-9, IL-17, and TNF-α were linked to CAD, indicating that specific cytokines play crucial roles in the disease's progression.
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  • * A study with 308 patients found that ACS has lower interleukin-4 levels and higher levels of IL-8, hepatocyte growth factor (HGF), and macrophage colony-stimulating factor (M-CSF) compared to stable CAD.
  • * The findings suggest that cytokine levels vary between ACS and stable CAD, and these differences can change within three months after an ACS event, indicating that a targeted approach to treating inflammation in CAD might need to be personalized rather than generalized.
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Peptide folding is a dynamic process driven by non-covalent cross-linking leading to functional nanostructures for essential biochemical activities. However, replicating this process in synthetic systems is challenging due to the difficulty in mimicking nature's real-time regulation of non-covalent crosslinking for single-chain polymer folding. Here, we address this by employing anionic dithiol building blocks to create macrocyclic disulfides as non-covalent crosslinkers that adapted to the folding process.

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