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Low acylation stimulating protein levels are associated with cardiometabolic disorders-secondary to autoimmune activation?

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  • معلومة اضافية
    • المصدر:
      Publisher: KARE publishing Country of Publication: Turkey NLM ID: 101652981 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2149-2271 (Electronic) Linking ISSN: 21492263 NLM ISO Abbreviation: Anatol J Cardiol Subsets: MEDLINE
    • بيانات النشر:
      Publication: 2023- : İstanbul, Turkey : KARE publishing
      Original Publication: İstanbul, Turkey : Aves, [2015]-
    • الموضوع:
    • نبذة مختصرة :
      Objective: We investigated the possible association of serum acylation stimulating protein (ASP) with cardiometabolic disorders and the evidence of autoimmune activation.
      Methods: Population-based randomly selected 1024 participants were cross-sectionally and prospectively analyzed. ASP concentrations were measured with a validated ELISA kit. Correlations were sought separately in subjects with no cardiometabolic disorders (n=427) designated as "healthy."
      Results: ASP was positively correlated with total testosterone and inversely correlated with platelet activating factor (PAF), PAF-acetylhydrolase (AH), in each gender, and positively correlated in "healthy" men with lipoprotein [Lp](a) and apolipoprotein B. Correlations of ASP with PAF values ≥22 nmol/L were abolished, contrasted to a strongly inverse one in subjects with PAF <22 nmol/L. In linear regression analyses in the whole sample, ASP was inversely associated independently with PAF and PAF-AH and, in men, positively with Lp(a) and sex hormone-binding globulin. Prevalent and (at 2.0 years' follow-up) incident metabolic syndrome (MetS, n=393), diabetes (n=154), and coronary heart disease (CHD, n=171) were analyzed by sex-, age-, and Lp(a)-adjusted logistic regression, using tertiles of ASP and PAF. The lower two (<42 nmol/L) ASP tertiles were a risk factor in combined sexes for MetS and diabetes. In women, incident CHD was predicted by either reduced or elevated ASP tertiles.
      Conclusion: Findings can be explained by the notion of operation of immune responses against both ASP and oxidized PAF-like lipids of Lp(a) to yield for "reduced" values and increased likelihood of cardiometabolic disorders.
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    • الرقم المعرف:
      0 (complement C3a, des-Arg-(77)-)
      80295-42-7 (Complement C3a)
      EC 3.1.1.47 (1-Alkyl-2-acetylglycerophosphocholine Esterase)
      EC 3.1.1.47 (PLA2G7 protein, human)
    • الموضوع:
      Date Created: 20160908 Date Completed: 20190408 Latest Revision: 20190408
    • الموضوع:
      20231215
    • الرقم المعرف:
      PMC5336773
    • الرقم المعرف:
      10.14744/AnatolJCardiol.2016.7024
    • الرقم المعرف:
      27599666