Comprehensive metabolic modulations of sphingolipids are promising severity indicators in COVID‐19

The COVID‐19 pandemic, caused by SARS‐CoV‐2, has had a significant worldwide impact, affecting millions of people. COVID‐19 is characterized by a heterogenous clinical phenotype, potentially involving hyperinflammation and prolonged tissue damage, although the exact underlying mechanisms are yet to...

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Published inThe FASEB journal Vol. 38; no. 14; pp. e23827 - n/a
Main Authors Uranbileg, Baasanjav, Isago, Hideaki, Nakayama, Hitoshi, Jubishi, Daisuke, Okamoto, Koh, Sakai, Eri, Kubota, Masayuki, Tsutsumi, Takeya, Moriya, Kyoji, Kurano, Makoto
Format Journal Article
LanguageEnglish
Published United States 31.07.2024
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Abstract The COVID‐19 pandemic, caused by SARS‐CoV‐2, has had a significant worldwide impact, affecting millions of people. COVID‐19 is characterized by a heterogenous clinical phenotype, potentially involving hyperinflammation and prolonged tissue damage, although the exact underlying mechanisms are yet to be fully understood. Sphingolipid metabolites, which govern cell survival and proliferation, have emerged as key players in inflammatory signaling and cytokine responses. Given the complex metabolic pathway of sphingolipids, this study aimed to understand their potential role in the pathogenesis of COVID‐19. We conducted a comprehensive examination of sphingolipid modulations across groups classified based on disease severity, incorporating a time‐course in serum and urine samples. Several sphingolipids, including sphingosine, lactosylceramide, and hexosylceramide, emerged as promising indicators of COVID‐19 severity, as validated by correlation analyses conducted on both serum and urine samples. Other sphingolipids, such as sphingosine 1‐phosphate, ceramides, and deoxy‐dihydroceramides, decreased in both COVID‐19 patients and individuals with non‐COVID infectious diseases. This suggests that these sphingolipids are not specifically associated with COVID‐19 but rather with pathological conditions caused by infectious diseases. Our analysis of urine samples revealed elevated levels of various sphingolipids, with changes dependent on disease severity, potentially highlighting the acute kidney injury associated with COVID‐19. This study illuminates the intricate relationship between disturbed sphingolipid metabolism, COVID‐19 severity, and clinical factors. These findings provide valuable insights into the broader landscape of inflammatory diseases. Several sphingolipids, including sphingosine, lactosylceramide, and hexosylceramide, emerged as promising indicators of COVID‐19 severity, while others, such as sphingosine 1‐phosphate and ceramides, decreased in both COVID‐19 and non‐COVID infectious diseases, indicating a broader association with infectious diseases. Urine analysis revealed elevated sphingolipid levels dependent on disease severity, potentially highlighting acute kidney injury linked to COVID‐19.
AbstractList The COVID-19 pandemic, caused by SARS-CoV-2, has had a significant worldwide impact, affecting millions of people. COVID-19 is characterized by a heterogenous clinical phenotype, potentially involving hyperinflammation and prolonged tissue damage, although the exact underlying mechanisms are yet to be fully understood. Sphingolipid metabolites, which govern cell survival and proliferation, have emerged as key players in inflammatory signaling and cytokine responses. Given the complex metabolic pathway of sphingolipids, this study aimed to understand their potential role in the pathogenesis of COVID-19. We conducted a comprehensive examination of sphingolipid modulations across groups classified based on disease severity, incorporating a time-course in serum and urine samples. Several sphingolipids, including sphingosine, lactosylceramide, and hexosylceramide, emerged as promising indicators of COVID-19 severity, as validated by correlation analyses conducted on both serum and urine samples. Other sphingolipids, such as sphingosine 1-phosphate, ceramides, and deoxy-dihydroceramides, decreased in both COVID-19 patients and individuals with non-COVID infectious diseases. This suggests that these sphingolipids are not specifically associated with COVID-19 but rather with pathological conditions caused by infectious diseases. Our analysis of urine samples revealed elevated levels of various sphingolipids, with changes dependent on disease severity, potentially highlighting the acute kidney injury associated with COVID-19. This study illuminates the intricate relationship between disturbed sphingolipid metabolism, COVID-19 severity, and clinical factors. These findings provide valuable insights into the broader landscape of inflammatory diseases.
The COVID‐19 pandemic, caused by SARS‐CoV‐2, has had a significant worldwide impact, affecting millions of people. COVID‐19 is characterized by a heterogenous clinical phenotype, potentially involving hyperinflammation and prolonged tissue damage, although the exact underlying mechanisms are yet to be fully understood. Sphingolipid metabolites, which govern cell survival and proliferation, have emerged as key players in inflammatory signaling and cytokine responses. Given the complex metabolic pathway of sphingolipids, this study aimed to understand their potential role in the pathogenesis of COVID‐19. We conducted a comprehensive examination of sphingolipid modulations across groups classified based on disease severity, incorporating a time‐course in serum and urine samples. Several sphingolipids, including sphingosine, lactosylceramide, and hexosylceramide, emerged as promising indicators of COVID‐19 severity, as validated by correlation analyses conducted on both serum and urine samples. Other sphingolipids, such as sphingosine 1‐phosphate, ceramides, and deoxy‐dihydroceramides, decreased in both COVID‐19 patients and individuals with non‐COVID infectious diseases. This suggests that these sphingolipids are not specifically associated with COVID‐19 but rather with pathological conditions caused by infectious diseases. Our analysis of urine samples revealed elevated levels of various sphingolipids, with changes dependent on disease severity, potentially highlighting the acute kidney injury associated with COVID‐19. This study illuminates the intricate relationship between disturbed sphingolipid metabolism, COVID‐19 severity, and clinical factors. These findings provide valuable insights into the broader landscape of inflammatory diseases. Several sphingolipids, including sphingosine, lactosylceramide, and hexosylceramide, emerged as promising indicators of COVID‐19 severity, while others, such as sphingosine 1‐phosphate and ceramides, decreased in both COVID‐19 and non‐COVID infectious diseases, indicating a broader association with infectious diseases. Urine analysis revealed elevated sphingolipid levels dependent on disease severity, potentially highlighting acute kidney injury linked to COVID‐19.
Author Tsutsumi, Takeya
Jubishi, Daisuke
Kurano, Makoto
Sakai, Eri
Okamoto, Koh
Isago, Hideaki
Kubota, Masayuki
Uranbileg, Baasanjav
Nakayama, Hitoshi
Moriya, Kyoji
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Issue 14
Keywords COVID‐19
hexosylceramide (HexCer)
sphingolipid
lactosylceramide (LacCer)
sphingosine (Sph)
Language English
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Snippet The COVID‐19 pandemic, caused by SARS‐CoV‐2, has had a significant worldwide impact, affecting millions of people. COVID‐19 is characterized by a heterogenous...
The COVID-19 pandemic, caused by SARS-CoV-2, has had a significant worldwide impact, affecting millions of people. COVID-19 is characterized by a heterogenous...
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wiley
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StartPage e23827
SubjectTerms Adult
Aged
Biomarkers - blood
Biomarkers - metabolism
COVID-19 - blood
COVID-19 - metabolism
COVID-19 - virology
COVID‐19
Female
hexosylceramide (HexCer)
Humans
lactosylceramide (LacCer)
Male
Middle Aged
SARS-CoV-2
Severity of Illness Index
sphingolipid
Sphingolipids - blood
Sphingolipids - metabolism
sphingosine (Sph)
Sphingosine - analogs & derivatives
Sphingosine - metabolism
Title Comprehensive metabolic modulations of sphingolipids are promising severity indicators in COVID‐19
URI https://onlinelibrary.wiley.com/doi/abs/10.1096%2Ffj.202401099R
https://www.ncbi.nlm.nih.gov/pubmed/39012295
Volume 38
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