Altered Lipid Metabolism in Recovered SARS Patients Twelve Years after Infection
Severe acute respiratory syndrome-coronavirus (SARS-CoV) and SARS-like coronavirus are a potential threat to global health. However, reviews of the long-term effects of clinical treatments in SARS patients are lacking. Here a total of 25 recovered SARS patients were recruited 12 years after infectio...
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Published in | Scientific reports Vol. 7; no. 1; pp. 9110 - 12 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
22.08.2017
Nature Publishing Group Nature Portfolio |
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Abstract | Severe acute respiratory syndrome-coronavirus (SARS-CoV) and SARS-like coronavirus are a potential threat to global health. However, reviews of the long-term effects of clinical treatments in SARS patients are lacking. Here a total of 25 recovered SARS patients were recruited 12 years after infection. Clinical questionnaire responses and examination findings indicated that the patients had experienced various diseases, including lung susceptibility to infections, tumors, cardiovascular disorders, and abnormal glucose metabolism. As compared to healthy controls, metabolomic analyses identified significant differences in the serum metabolomes of SARS survivors. The most significant metabolic disruptions were the comprehensive increase of phosphatidylinositol and lysophospha tidylinositol levels in recovered SARS patients, which coincided with the effect of methylprednisolone administration investigated further in the steroid treated non-SARS patients with severe pneumonia. These results suggested that high-dose pulses of methylprednisolone might cause long-term systemic damage associated with serum metabolic alterations. The present study provided information for an improved understanding of coronavirus-associated pathologies, which might permit further optimization of clinical treatments. |
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AbstractList | Severe acute respiratory syndrome-coronavirus (SARS-CoV) and SARS-like coronavirus are a potential threat to global health. However, reviews of the long-term effects of clinical treatments in SARS patients are lacking. Here a total of 25 recovered SARS patients were recruited 12 years after infection. Clinical questionnaire responses and examination findings indicated that the patients had experienced various diseases, including lung susceptibility to infections, tumors, cardiovascular disorders, and abnormal glucose metabolism. As compared to healthy controls, metabolomic analyses identified significant differences in the serum metabolomes of SARS survivors. The most significant metabolic disruptions were the comprehensive increase of phosphatidylinositol and lysophospha tidylinositol levels in recovered SARS patients, which coincided with the effect of methylprednisolone administration investigated further in the steroid treated non-SARS patients with severe pneumonia. These results suggested that high-dose pulses of methylprednisolone might cause long-term systemic damage associated with serum metabolic alterations. The present study provided information for an improved understanding of coronavirus-associated pathologies, which might permit further optimization of clinical treatments. Severe acute respiratory syndrome-coronavirus (SARS-CoV) and SARS-like coronavirus are a potential threat to global health. However, reviews of the long-term effects of clinical treatments in SARS patients are lacking. Here a total of 25 recovered SARS patients were recruited 12 years after infection. Clinical questionnaire responses and examination findings indicated that the patients had experienced various diseases, including lung susceptibility to infections, tumors, cardiovascular disorders, and abnormal glucose metabolism. As compared to healthy controls, metabolomic analyses identified significant differences in the serum metabolomes of SARS survivors. The most significant metabolic disruptions were the comprehensive increase of phosphatidylinositol and lysophospha tidylinositol levels in recovered SARS patients, which coincided with the effect of methylprednisolone administration investigated further in the steroid treated non-SARS patients with severe pneumonia. These results suggested that high-dose pulses of methylprednisolone might cause long-term systemic damage associated with serum metabolic alterations. The present study provided information for an improved understanding of coronavirus-associated pathologies, which might permit further optimization of clinical treatments.Severe acute respiratory syndrome-coronavirus (SARS-CoV) and SARS-like coronavirus are a potential threat to global health. However, reviews of the long-term effects of clinical treatments in SARS patients are lacking. Here a total of 25 recovered SARS patients were recruited 12 years after infection. Clinical questionnaire responses and examination findings indicated that the patients had experienced various diseases, including lung susceptibility to infections, tumors, cardiovascular disorders, and abnormal glucose metabolism. As compared to healthy controls, metabolomic analyses identified significant differences in the serum metabolomes of SARS survivors. The most significant metabolic disruptions were the comprehensive increase of phosphatidylinositol and lysophospha tidylinositol levels in recovered SARS patients, which coincided with the effect of methylprednisolone administration investigated further in the steroid treated non-SARS patients with severe pneumonia. These results suggested that high-dose pulses of methylprednisolone might cause long-term systemic damage associated with serum metabolic alterations. The present study provided information for an improved understanding of coronavirus-associated pathologies, which might permit further optimization of clinical treatments. Abstract Severe acute respiratory syndrome-coronavirus (SARS-CoV) and SARS-like coronavirus are a potential threat to global health. However, reviews of the long-term effects of clinical treatments in SARS patients are lacking. Here a total of 25 recovered SARS patients were recruited 12 years after infection. Clinical questionnaire responses and examination findings indicated that the patients had experienced various diseases, including lung susceptibility to infections, tumors, cardiovascular disorders, and abnormal glucose metabolism. As compared to healthy controls, metabolomic analyses identified significant differences in the serum metabolomes of SARS survivors. The most significant metabolic disruptions were the comprehensive increase of phosphatidylinositol and lysophospha tidylinositol levels in recovered SARS patients, which coincided with the effect of methylprednisolone administration investigated further in the steroid treated non-SARS patients with severe pneumonia. These results suggested that high-dose pulses of methylprednisolone might cause long-term systemic damage associated with serum metabolic alterations. The present study provided information for an improved understanding of coronavirus-associated pathologies, which might permit further optimization of clinical treatments. |
ArticleNumber | 9110 |
Author | Li, Yu Liu, Huiling Chen, Huaiyong Yan, Zhongfang Wu, Junping Li, Kuan Hu, Chunxiu Zhao, Jieyu Zhou, Lina Wu, Qi Xu, Long Zhang, Qiuyang Li, Xue Sun, Xin Wang, Xiaolin Yin, Peiyuan Li, Yanli Xu, Guowang |
Author_xml | – sequence: 1 givenname: Qi surname: Wu fullname: Wu, Qi organization: Key Research Laboratory for Infectious Disease Prevention for State Administration of Traditional Chinese Medicine, Tianjin Institute of Respiratory Diseases, Haihe Clinical College of Tianjin Medical University – sequence: 2 givenname: Lina surname: Zhou fullname: Zhou, Lina organization: CAS Key Laboratory of Separation Sciences for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences – sequence: 3 givenname: Xin surname: Sun fullname: Sun, Xin organization: Department of Respiratory Medicine, Tianjin Haihe Hospital – sequence: 4 givenname: Zhongfang surname: Yan fullname: Yan, Zhongfang organization: Department of Nutrition, Tianjin Haihe Hospital – sequence: 5 givenname: Chunxiu surname: Hu fullname: Hu, Chunxiu organization: CAS Key Laboratory of Separation Sciences for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences – sequence: 6 givenname: Junping surname: Wu fullname: Wu, Junping organization: Department of Respiratory Medicine, Tianjin Haihe Hospital – sequence: 7 givenname: Long surname: Xu fullname: Xu, Long organization: Department of Respiratory Medicine, Tianjin Haihe Hospital – sequence: 8 givenname: Xue surname: Li fullname: Li, Xue organization: Department of Basic Medicine, Tianjin Haihe Hospital – sequence: 9 givenname: Huiling surname: Liu fullname: Liu, Huiling organization: Department of Gastroenterology, Tianjin Haihe Hospital – sequence: 10 givenname: Peiyuan surname: Yin fullname: Yin, Peiyuan organization: CAS Key Laboratory of Separation Sciences for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences – sequence: 11 givenname: Kuan surname: Li fullname: Li, Kuan organization: Department of Basic Medicine, Tianjin Haihe Hospital – sequence: 12 givenname: Jieyu surname: Zhao fullname: Zhao, Jieyu organization: CAS Key Laboratory of Separation Sciences for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences – sequence: 13 givenname: Yanli surname: Li fullname: Li, Yanli organization: CAS Key Laboratory of Separation Sciences for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences – sequence: 14 givenname: Xiaolin surname: Wang fullname: Wang, Xiaolin organization: CAS Key Laboratory of Separation Sciences for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences – sequence: 15 givenname: Yu surname: Li fullname: Li, Yu organization: Department of Basic Medicine, Tianjin Haihe Hospital – sequence: 16 givenname: Qiuyang surname: Zhang fullname: Zhang, Qiuyang organization: Department of Basic Medicine, Tianjin Haihe Hospital – sequence: 17 givenname: Guowang orcidid: 0000-0003-4298-3554 surname: Xu fullname: Xu, Guowang email: xugw@dicp.ac.cn organization: CAS Key Laboratory of Separation Sciences for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences – sequence: 18 givenname: Huaiyong surname: Chen fullname: Chen, Huaiyong email: huaiyong.chen@foxmail.com organization: Key Research Laboratory for Infectious Disease Prevention for State Administration of Traditional Chinese Medicine, Tianjin Institute of Respiratory Diseases, Haihe Clinical College of Tianjin Medical University, Department of Basic Medicine, Tianjin Haihe Hospital |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28831119$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
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Snippet | Severe acute respiratory syndrome-coronavirus (SARS-CoV) and SARS-like coronavirus are a potential threat to global health. However, reviews of the long-term... Abstract Severe acute respiratory syndrome-coronavirus (SARS-CoV) and SARS-like coronavirus are a potential threat to global health. However, reviews of the... |
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SubjectTerms | 692/699/1785/3193 692/699/255/2514 Coronaviridae Coronaviruses COVID-19 Global health Glucose metabolism Humanities and Social Sciences Lipid metabolism Long-term effects Lung diseases Metabolism Metabolomics Methylprednisolone multidisciplinary Phosphatidylinositol Science Science (multidisciplinary) Severe acute respiratory syndrome Tumors |
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Title | Altered Lipid Metabolism in Recovered SARS Patients Twelve Years after Infection |
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