Exploring blood microbial communities and their influence on human cardiovascular disease
Background Cardiovascular disease (CVD) is the single biggest contributor to global mortality. CVD encompasses multiple disorders, including atherosclerosis, hypertension, platelet hyperactivity, stroke, hyperlipidemia, and heart failure. In addition to traditional risk factors, the circulating micr...
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Published in | Journal of clinical laboratory analysis Vol. 36; no. 4; pp. e24354 - n/a |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
John Wiley & Sons, Inc
01.04.2022
John Wiley and Sons Inc |
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Abstract | Background
Cardiovascular disease (CVD) is the single biggest contributor to global mortality. CVD encompasses multiple disorders, including atherosclerosis, hypertension, platelet hyperactivity, stroke, hyperlipidemia, and heart failure. In addition to traditional risk factors, the circulating microbiome or the blood microbiome has been analyzed recently in chronic inflammatory diseases, including CVD in humans.
Methods
For this review, all relevant original research studies were assessed by searching in electronic databases, including PubMed, Google Scholar, and Web of Science, by using relevant keywords.
Results
This review demonstrated that elevated markers of systemic bacterial exposure are associated with noncommunicable diseases, including CVD. Studies have shown that the bacterial DNA sequence found in healthy blood belongs mainly to the Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria phyla. In cardiac events, such as stroke, coronary heart disease, and myocardial infarction, the increased proportion of Proteobacteria and Actinobacteria phyla was found. Lipopolysaccharides are a major component of Proteobacteria, which play a key role in the onset of CVD. Moreover, recently, a study reported the lower cholesterol‐degrading bacteria, including Caulobacterales order and Caulobacteraceae family were both considerably reduced in myocardial infarction.
Conclusion
Proteobacteria and Actinobacteria were shown to be independent markers of the risk of CVD. This finding is evidence for the new concept of the role played by blood microbiota dysbiosis in CVD. However, the association between blood microbiota and CVD is still inconsistent. Thus, more deep investigations are required in future to fully understand the role of the bacteria community in causing and preventing CVD.
In this study, we highlight the origin of the blood microbiota, alteration in the blood microbial makeup, and their association with the etiology and progression of cardiovascular disease. |
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AbstractList | Cardiovascular disease (CVD) is the single biggest contributor to global mortality. CVD encompasses multiple disorders, including atherosclerosis, hypertension, platelet hyperactivity, stroke, hyperlipidemia, and heart failure. In addition to traditional risk factors, the circulating microbiome or the blood microbiome has been analyzed recently in chronic inflammatory diseases, including CVD in humans.BACKGROUNDCardiovascular disease (CVD) is the single biggest contributor to global mortality. CVD encompasses multiple disorders, including atherosclerosis, hypertension, platelet hyperactivity, stroke, hyperlipidemia, and heart failure. In addition to traditional risk factors, the circulating microbiome or the blood microbiome has been analyzed recently in chronic inflammatory diseases, including CVD in humans.For this review, all relevant original research studies were assessed by searching in electronic databases, including PubMed, Google Scholar, and Web of Science, by using relevant keywords.METHODSFor this review, all relevant original research studies were assessed by searching in electronic databases, including PubMed, Google Scholar, and Web of Science, by using relevant keywords.This review demonstrated that elevated markers of systemic bacterial exposure are associated with noncommunicable diseases, including CVD. Studies have shown that the bacterial DNA sequence found in healthy blood belongs mainly to the Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria phyla. In cardiac events, such as stroke, coronary heart disease, and myocardial infarction, the increased proportion of Proteobacteria and Actinobacteria phyla was found. Lipopolysaccharides are a major component of Proteobacteria, which play a key role in the onset of CVD. Moreover, recently, a study reported the lower cholesterol-degrading bacteria, including Caulobacterales order and Caulobacteraceae family were both considerably reduced in myocardial infarction.RESULTSThis review demonstrated that elevated markers of systemic bacterial exposure are associated with noncommunicable diseases, including CVD. Studies have shown that the bacterial DNA sequence found in healthy blood belongs mainly to the Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria phyla. In cardiac events, such as stroke, coronary heart disease, and myocardial infarction, the increased proportion of Proteobacteria and Actinobacteria phyla was found. Lipopolysaccharides are a major component of Proteobacteria, which play a key role in the onset of CVD. Moreover, recently, a study reported the lower cholesterol-degrading bacteria, including Caulobacterales order and Caulobacteraceae family were both considerably reduced in myocardial infarction.Proteobacteria and Actinobacteria were shown to be independent markers of the risk of CVD. This finding is evidence for the new concept of the role played by blood microbiota dysbiosis in CVD. However, the association between blood microbiota and CVD is still inconsistent. Thus, more deep investigations are required in future to fully understand the role of the bacteria community in causing and preventing CVD.CONCLUSIONProteobacteria and Actinobacteria were shown to be independent markers of the risk of CVD. This finding is evidence for the new concept of the role played by blood microbiota dysbiosis in CVD. However, the association between blood microbiota and CVD is still inconsistent. Thus, more deep investigations are required in future to fully understand the role of the bacteria community in causing and preventing CVD. In this study, we highlight the origin of the blood microbiota, alteration in the blood microbial makeup, and their association with the etiology and progression of cardiovascular disease. Background Cardiovascular disease (CVD) is the single biggest contributor to global mortality. CVD encompasses multiple disorders, including atherosclerosis, hypertension, platelet hyperactivity, stroke, hyperlipidemia, and heart failure. In addition to traditional risk factors, the circulating microbiome or the blood microbiome has been analyzed recently in chronic inflammatory diseases, including CVD in humans. Methods For this review, all relevant original research studies were assessed by searching in electronic databases, including PubMed, Google Scholar, and Web of Science, by using relevant keywords. Results This review demonstrated that elevated markers of systemic bacterial exposure are associated with noncommunicable diseases, including CVD. Studies have shown that the bacterial DNA sequence found in healthy blood belongs mainly to the Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria phyla. In cardiac events, such as stroke, coronary heart disease, and myocardial infarction, the increased proportion of Proteobacteria and Actinobacteria phyla was found. Lipopolysaccharides are a major component of Proteobacteria, which play a key role in the onset of CVD. Moreover, recently, a study reported the lower cholesterol‐degrading bacteria, including Caulobacterales order and Caulobacteraceae family were both considerably reduced in myocardial infarction. Conclusion Proteobacteria and Actinobacteria were shown to be independent markers of the risk of CVD. This finding is evidence for the new concept of the role played by blood microbiota dysbiosis in CVD. However, the association between blood microbiota and CVD is still inconsistent. Thus, more deep investigations are required in future to fully understand the role of the bacteria community in causing and preventing CVD. In this study, we highlight the origin of the blood microbiota, alteration in the blood microbial makeup, and their association with the etiology and progression of cardiovascular disease. Cardiovascular disease (CVD) is the single biggest contributor to global mortality. CVD encompasses multiple disorders, including atherosclerosis, hypertension, platelet hyperactivity, stroke, hyperlipidemia, and heart failure. In addition to traditional risk factors, the circulating microbiome or the blood microbiome has been analyzed recently in chronic inflammatory diseases, including CVD in humans. For this review, all relevant original research studies were assessed by searching in electronic databases, including PubMed, Google Scholar, and Web of Science, by using relevant keywords. This review demonstrated that elevated markers of systemic bacterial exposure are associated with noncommunicable diseases, including CVD. Studies have shown that the bacterial DNA sequence found in healthy blood belongs mainly to the Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria phyla. In cardiac events, such as stroke, coronary heart disease, and myocardial infarction, the increased proportion of Proteobacteria and Actinobacteria phyla was found. Lipopolysaccharides are a major component of Proteobacteria, which play a key role in the onset of CVD. Moreover, recently, a study reported the lower cholesterol-degrading bacteria, including Caulobacterales order and Caulobacteraceae family were both considerably reduced in myocardial infarction. Proteobacteria and Actinobacteria were shown to be independent markers of the risk of CVD. This finding is evidence for the new concept of the role played by blood microbiota dysbiosis in CVD. However, the association between blood microbiota and CVD is still inconsistent. Thus, more deep investigations are required in future to fully understand the role of the bacteria community in causing and preventing CVD. BackgroundCardiovascular disease (CVD) is the single biggest contributor to global mortality. CVD encompasses multiple disorders, including atherosclerosis, hypertension, platelet hyperactivity, stroke, hyperlipidemia, and heart failure. In addition to traditional risk factors, the circulating microbiome or the blood microbiome has been analyzed recently in chronic inflammatory diseases, including CVD in humans.MethodsFor this review, all relevant original research studies were assessed by searching in electronic databases, including PubMed, Google Scholar, and Web of Science, by using relevant keywords.ResultsThis review demonstrated that elevated markers of systemic bacterial exposure are associated with noncommunicable diseases, including CVD. Studies have shown that the bacterial DNA sequence found in healthy blood belongs mainly to the Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria phyla. In cardiac events, such as stroke, coronary heart disease, and myocardial infarction, the increased proportion of Proteobacteria and Actinobacteria phyla was found. Lipopolysaccharides are a major component of Proteobacteria, which play a key role in the onset of CVD. Moreover, recently, a study reported the lower cholesterol‐degrading bacteria, including Caulobacterales order and Caulobacteraceae family were both considerably reduced in myocardial infarction.ConclusionProteobacteria and Actinobacteria were shown to be independent markers of the risk of CVD. This finding is evidence for the new concept of the role played by blood microbiota dysbiosis in CVD. However, the association between blood microbiota and CVD is still inconsistent. Thus, more deep investigations are required in future to fully understand the role of the bacteria community in causing and preventing CVD. |
Author | Kakakhel, Mian Adnan Xiaohua, Zhang Zhiqiang, Li Khan, Ikram Khan, Imran Jianye, Zhou Hilal, Mian Gul Mehmood, Arshad Khan, Murad Lizhe, An |
AuthorAffiliation | 5 71213 Department of Neurology The Second Hospital of Hebei Medical University Shijiazhuang China 3 66293 Key Laboratory of Oral Diseases of Gansu Province School of Stomatology Northwest Minzu University Lanzhou China 4 12553 Department of Genetics Hebei Key Laboratory Animal Hebei Medical University Shijiazhuang China 2 Department of Microbiology Khyber Medical University Peshawar Peshawar Pakistan 1 12426 School of Life Sciences Lanzhou University Lanzhou China |
AuthorAffiliation_xml | – name: 1 12426 School of Life Sciences Lanzhou University Lanzhou China – name: 5 71213 Department of Neurology The Second Hospital of Hebei Medical University Shijiazhuang China – name: 3 66293 Key Laboratory of Oral Diseases of Gansu Province School of Stomatology Northwest Minzu University Lanzhou China – name: 2 Department of Microbiology Khyber Medical University Peshawar Peshawar Pakistan – name: 4 12553 Department of Genetics Hebei Key Laboratory Animal Hebei Medical University Shijiazhuang China |
Author_xml | – sequence: 1 givenname: Ikram surname: Khan fullname: Khan, Ikram organization: Lanzhou University – sequence: 2 givenname: Imran surname: Khan fullname: Khan, Imran organization: Khyber Medical University Peshawar – sequence: 3 givenname: Zhou surname: Jianye fullname: Jianye, Zhou organization: Northwest Minzu University – sequence: 4 givenname: Zhang surname: Xiaohua fullname: Xiaohua, Zhang organization: Northwest Minzu University – sequence: 5 givenname: Murad surname: Khan fullname: Khan, Murad organization: Hebei Medical University – sequence: 6 givenname: Mian Gul surname: Hilal fullname: Hilal, Mian Gul organization: Lanzhou University – sequence: 7 givenname: Mian Adnan surname: Kakakhel fullname: Kakakhel, Mian Adnan organization: Lanzhou University – sequence: 8 givenname: Arshad orcidid: 0000-0002-7547-4767 surname: Mehmood fullname: Mehmood, Arshad organization: The Second Hospital of Hebei Medical University – sequence: 9 givenname: An surname: Lizhe fullname: Lizhe, An email: yxlzq@xbmu.edu.cn organization: Lanzhou University – sequence: 10 givenname: Li surname: Zhiqiang fullname: Zhiqiang, Li email: lizhiqiang6767@163.com organization: Northwest Minzu University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35293034$$D View this record in MEDLINE/PubMed |
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Cardiovascular disease (CVD) is the single biggest contributor to global mortality. CVD encompasses multiple disorders, including atherosclerosis,... Cardiovascular disease (CVD) is the single biggest contributor to global mortality. CVD encompasses multiple disorders, including atherosclerosis,... BackgroundCardiovascular disease (CVD) is the single biggest contributor to global mortality. CVD encompasses multiple disorders, including atherosclerosis,... In this study, we highlight the origin of the blood microbiota, alteration in the blood microbial makeup, and their association with the etiology and... |
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SubjectTerms | Actinobacteria Alzheimer's disease Anthrax Arteriosclerosis Bacteria bacterial translocation Blood blood circulation Cardiovascular disease Cardiovascular diseases Cardiovascular Diseases - epidemiology Cattle Cerebral infarction Cholesterol Congestive heart failure Coronary artery disease Diabetes Dysbacteriosis Dysbiosis - microbiology Heart Humans Hyperactivity Hyperlipidemia Infectious diseases Inflammatory diseases Investigations Lipopolysaccharides Metabolism Metabolites Microbiomes Microbiota Microorganisms Myocardial Infarction noncommunicable diseases Nucleotide sequence Proteobacteria Review Risk factors Stroke Vein & artery diseases |
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Title | Exploring blood microbial communities and their influence on human cardiovascular disease |
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