ArticleHealth science reports2025
The Association of Serum Level of TGF-β
Article in Health science reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
7 authors.
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Abstract
Background and Aims: Sickle cell anemia (SCA) is an inherited red blood cell disorder resulting from the polymerization of Hemoglobin S. Acute vaso-occlusive crisis and multiple organ damage are the most common complications of SCA. Because of its multifunctional role in inflammation, endothelial dysfunction, and fibrosis, TGF-β Methods: The level of TGF-β Results: The laboratory parameters including hemoglobin, red blood cell (RBC), hematocrit (HCT), mean corpuscular volume (MCV), and mean corpuscular hemoglobin (MCH) were lower in SCA patients compared to the control group, and white blood count (WBC), red cell distribution width-coefficient of variation (RDW-CV), platelet count, mean platelet volume (MPV), and lactate dehydrogenase (LDH) were higher in these patients. No significant correlation was observed between laboratory parameters and Transforming Growth Factor Beta 1 (TGF-β Conclusion: We observed a higher prevalence of certain complications in SCA patients in the Arab population of Khuzestan Province. There was no significant correlation between the clinical manifestation of SCA and TGF-β
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