Tumor Necrosis Factor Alpha Influences the Inflammatory Response After Coronary Surgery
A systemic inflammatory response is not uncommonly observed after coronary revascularization. Tumor necrosis factor alpha is one of a number of modulators of this response. A functional polymorphism within the TNFα gene at position G-308A has been associated with increased TNFα levels. The relations...
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Veröffentlicht in: | The Annals of thoracic surgery 2006, Vol.81 (1), p.132-137 |
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container_title | The Annals of thoracic surgery |
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description | A systemic inflammatory response is not uncommonly observed after coronary revascularization. Tumor necrosis factor alpha is one of a number of modulators of this response. A functional polymorphism within the TNFα gene at position G-308A has been associated with increased TNFα levels. The relationship between predicted TNFα genotype and circulating TNFα levels in patients undergoing coronary revascularization surgery has yet to be defined. We examined the relationship between TNFα G-308A polymorphism, TNFα postoperative levels, and clinical outcome after coronary revascularization surgery.
We obtained DNA from 96 consecutive patients who underwent elective coronary revascularization. Patients were genotyped for TNFα G-308A polymorphism using sequence specific primer–polymerase chain reaction (SSP-PCR). Tumor necrosis factor alpha levels were measured on serum samples taken 3 hours postoperatively using enzyme-linked immunosorbent assay (ELISA).
The prevalence of AA, AG, and GG TNFα-308 genotype was 12%, 40%, and 48%, respectively. Patients homozygous for A had higher circulating levels of TNFα (
p = 0.009). Higher levels of TNFα were significantly associated with prolonged intensive care unit stay (
p = 0.008), increase usage of an inotropic agent (
p = 0.024), increased mortality risk (
p = 0.018), and diabetes (
p = 0.019). These remained statistically significant after risk stratification.
Patients of the AA-308 TNFα genotype showed significantly higher TNFα plasma levels. Higher plasma levels of TNFα were associated with less favorable outcome after coronary revascularization surgery. It may prove useful to utilize TNFα serum levels as a marker for identifying high-risk patients in the future. |
doi_str_mv | 10.1016/j.athoracsur.2005.07.037 |
format | Article |
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We obtained DNA from 96 consecutive patients who underwent elective coronary revascularization. Patients were genotyped for TNFα G-308A polymorphism using sequence specific primer–polymerase chain reaction (SSP-PCR). Tumor necrosis factor alpha levels were measured on serum samples taken 3 hours postoperatively using enzyme-linked immunosorbent assay (ELISA).
The prevalence of AA, AG, and GG TNFα-308 genotype was 12%, 40%, and 48%, respectively. Patients homozygous for A had higher circulating levels of TNFα (
p = 0.009). Higher levels of TNFα were significantly associated with prolonged intensive care unit stay (
p = 0.008), increase usage of an inotropic agent (
p = 0.024), increased mortality risk (
p = 0.018), and diabetes (
p = 0.019). These remained statistically significant after risk stratification.
Patients of the AA-308 TNFα genotype showed significantly higher TNFα plasma levels. Higher plasma levels of TNFα were associated with less favorable outcome after coronary revascularization surgery. It may prove useful to utilize TNFα serum levels as a marker for identifying high-risk patients in the future.</description><identifier>ISSN: 0003-4975</identifier><identifier>EISSN: 1552-6259</identifier><identifier>DOI: 10.1016/j.athoracsur.2005.07.037</identifier><identifier>PMID: 16368349</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Aged ; Cardiopulmonary Bypass - adverse effects ; DNA Mutational Analysis ; Elective Surgical Procedures ; Female ; Genetic Predisposition to Disease ; Genotype ; Humans ; Male ; Middle Aged ; Myocardial Revascularization ; Polymerase Chain Reaction ; Polymorphism, Single Nucleotide ; Postoperative Complications - etiology ; Postoperative Complications - physiopathology ; Risk Factors ; Systemic Inflammatory Response Syndrome - etiology ; Systemic Inflammatory Response Syndrome - genetics ; Systemic Inflammatory Response Syndrome - physiopathology ; Treatment Outcome ; Tumor Necrosis Factor-alpha - analysis ; Tumor Necrosis Factor-alpha - genetics ; Tumor Necrosis Factor-alpha - physiology</subject><ispartof>The Annals of thoracic surgery, 2006, Vol.81 (1), p.132-137</ispartof><rights>2006 The Society of Thoracic Surgeons</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c457t-45ebeeb0b0f3aa73c240fc39576221ef71639b91bd450ba3ece9576b2a3fbeec3</citedby><cites>FETCH-LOGICAL-c457t-45ebeeb0b0f3aa73c240fc39576221ef71639b91bd450ba3ece9576b2a3fbeec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16368349$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bittar, Mohamad N.</creatorcontrib><creatorcontrib>Carey, John A.</creatorcontrib><creatorcontrib>Barnard, James B.</creatorcontrib><creatorcontrib>Pravica, Vera</creatorcontrib><creatorcontrib>Deiraniya, Abdul K.</creatorcontrib><creatorcontrib>Yonan, Nizar</creatorcontrib><creatorcontrib>Hutchinson, Ian V.</creatorcontrib><title>Tumor Necrosis Factor Alpha Influences the Inflammatory Response After Coronary Surgery</title><title>The Annals of thoracic surgery</title><addtitle>Ann Thorac Surg</addtitle><description>A systemic inflammatory response is not uncommonly observed after coronary revascularization. Tumor necrosis factor alpha is one of a number of modulators of this response. A functional polymorphism within the TNFα gene at position G-308A has been associated with increased TNFα levels. The relationship between predicted TNFα genotype and circulating TNFα levels in patients undergoing coronary revascularization surgery has yet to be defined. We examined the relationship between TNFα G-308A polymorphism, TNFα postoperative levels, and clinical outcome after coronary revascularization surgery.
We obtained DNA from 96 consecutive patients who underwent elective coronary revascularization. Patients were genotyped for TNFα G-308A polymorphism using sequence specific primer–polymerase chain reaction (SSP-PCR). Tumor necrosis factor alpha levels were measured on serum samples taken 3 hours postoperatively using enzyme-linked immunosorbent assay (ELISA).
The prevalence of AA, AG, and GG TNFα-308 genotype was 12%, 40%, and 48%, respectively. Patients homozygous for A had higher circulating levels of TNFα (
p = 0.009). Higher levels of TNFα were significantly associated with prolonged intensive care unit stay (
p = 0.008), increase usage of an inotropic agent (
p = 0.024), increased mortality risk (
p = 0.018), and diabetes (
p = 0.019). These remained statistically significant after risk stratification.
Patients of the AA-308 TNFα genotype showed significantly higher TNFα plasma levels. Higher plasma levels of TNFα were associated with less favorable outcome after coronary revascularization surgery. It may prove useful to utilize TNFα serum levels as a marker for identifying high-risk patients in the future.</description><subject>Aged</subject><subject>Cardiopulmonary Bypass - adverse effects</subject><subject>DNA Mutational Analysis</subject><subject>Elective Surgical Procedures</subject><subject>Female</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotype</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Myocardial Revascularization</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Postoperative Complications - etiology</subject><subject>Postoperative Complications - physiopathology</subject><subject>Risk Factors</subject><subject>Systemic Inflammatory Response Syndrome - etiology</subject><subject>Systemic Inflammatory Response Syndrome - genetics</subject><subject>Systemic Inflammatory Response Syndrome - physiopathology</subject><subject>Treatment Outcome</subject><subject>Tumor Necrosis Factor-alpha - analysis</subject><subject>Tumor Necrosis Factor-alpha - genetics</subject><subject>Tumor Necrosis Factor-alpha - physiology</subject><issn>0003-4975</issn><issn>1552-6259</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkF9LwzAUxYMobk6_gvTJt9akaZr1cQ6ng6GgEx9Dkt64jraZSSvs25u6wR59Cif3nPvnh1BEcEIwye-3iew21knte5ekGLME8wRTfobGhLE0zlNWnKMxxpjGWcHZCF15vw0yDeVLNCI5zac0K8boc9031kUvoJ31lY8WUndBz-rdRkbL1tQ9tBp81G3gT8qmkcGwj97A72zrIZqZDlw0t862Mvy_9-4L3P4aXRhZe7g5vhP0sXhcz5_j1evTcj5bxTpjvIszBgpAYYUNlZJTnWbYaFownqcpAcPDpoUqiCozhpWkoGGoqVRSE4KaTtDdoe_O2e8efCeaymuoa9mC7b3IOZsGPkUwTg_G4VDvwIidq5qwsSBYDFDFVpygigGqwFwEqCF6e5zRqwbKU_BIMRgeDgYIl_5U4ITX1cCtrBzoTpS2-n_KL1oMj7U</recordid><startdate>2006</startdate><enddate>2006</enddate><creator>Bittar, Mohamad N.</creator><creator>Carey, John A.</creator><creator>Barnard, James B.</creator><creator>Pravica, Vera</creator><creator>Deiraniya, Abdul K.</creator><creator>Yonan, Nizar</creator><creator>Hutchinson, Ian V.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>2006</creationdate><title>Tumor Necrosis Factor Alpha Influences the Inflammatory Response After Coronary Surgery</title><author>Bittar, Mohamad N. ; Carey, John A. ; Barnard, James B. ; Pravica, Vera ; Deiraniya, Abdul K. ; Yonan, Nizar ; Hutchinson, Ian V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c457t-45ebeeb0b0f3aa73c240fc39576221ef71639b91bd450ba3ece9576b2a3fbeec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Aged</topic><topic>Cardiopulmonary Bypass - adverse effects</topic><topic>DNA Mutational Analysis</topic><topic>Elective Surgical Procedures</topic><topic>Female</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Myocardial Revascularization</topic><topic>Polymerase Chain Reaction</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Postoperative Complications - etiology</topic><topic>Postoperative Complications - physiopathology</topic><topic>Risk Factors</topic><topic>Systemic Inflammatory Response Syndrome - etiology</topic><topic>Systemic Inflammatory Response Syndrome - genetics</topic><topic>Systemic Inflammatory Response Syndrome - physiopathology</topic><topic>Treatment Outcome</topic><topic>Tumor Necrosis Factor-alpha - analysis</topic><topic>Tumor Necrosis Factor-alpha - genetics</topic><topic>Tumor Necrosis Factor-alpha - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bittar, Mohamad N.</creatorcontrib><creatorcontrib>Carey, John A.</creatorcontrib><creatorcontrib>Barnard, James B.</creatorcontrib><creatorcontrib>Pravica, Vera</creatorcontrib><creatorcontrib>Deiraniya, Abdul K.</creatorcontrib><creatorcontrib>Yonan, Nizar</creatorcontrib><creatorcontrib>Hutchinson, Ian V.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Annals of thoracic surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bittar, Mohamad N.</au><au>Carey, John A.</au><au>Barnard, James B.</au><au>Pravica, Vera</au><au>Deiraniya, Abdul K.</au><au>Yonan, Nizar</au><au>Hutchinson, Ian V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tumor Necrosis Factor Alpha Influences the Inflammatory Response After Coronary Surgery</atitle><jtitle>The Annals of thoracic surgery</jtitle><addtitle>Ann Thorac Surg</addtitle><date>2006</date><risdate>2006</risdate><volume>81</volume><issue>1</issue><spage>132</spage><epage>137</epage><pages>132-137</pages><issn>0003-4975</issn><eissn>1552-6259</eissn><abstract>A systemic inflammatory response is not uncommonly observed after coronary revascularization. Tumor necrosis factor alpha is one of a number of modulators of this response. A functional polymorphism within the TNFα gene at position G-308A has been associated with increased TNFα levels. The relationship between predicted TNFα genotype and circulating TNFα levels in patients undergoing coronary revascularization surgery has yet to be defined. We examined the relationship between TNFα G-308A polymorphism, TNFα postoperative levels, and clinical outcome after coronary revascularization surgery.
We obtained DNA from 96 consecutive patients who underwent elective coronary revascularization. Patients were genotyped for TNFα G-308A polymorphism using sequence specific primer–polymerase chain reaction (SSP-PCR). Tumor necrosis factor alpha levels were measured on serum samples taken 3 hours postoperatively using enzyme-linked immunosorbent assay (ELISA).
The prevalence of AA, AG, and GG TNFα-308 genotype was 12%, 40%, and 48%, respectively. Patients homozygous for A had higher circulating levels of TNFα (
p = 0.009). Higher levels of TNFα were significantly associated with prolonged intensive care unit stay (
p = 0.008), increase usage of an inotropic agent (
p = 0.024), increased mortality risk (
p = 0.018), and diabetes (
p = 0.019). These remained statistically significant after risk stratification.
Patients of the AA-308 TNFα genotype showed significantly higher TNFα plasma levels. Higher plasma levels of TNFα were associated with less favorable outcome after coronary revascularization surgery. It may prove useful to utilize TNFα serum levels as a marker for identifying high-risk patients in the future.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>16368349</pmid><doi>10.1016/j.athoracsur.2005.07.037</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Cardiopulmonary Bypass - adverse effects DNA Mutational Analysis Elective Surgical Procedures Female Genetic Predisposition to Disease Genotype Humans Male Middle Aged Myocardial Revascularization Polymerase Chain Reaction Polymorphism, Single Nucleotide Postoperative Complications - etiology Postoperative Complications - physiopathology Risk Factors Systemic Inflammatory Response Syndrome - etiology Systemic Inflammatory Response Syndrome - genetics Systemic Inflammatory Response Syndrome - physiopathology Treatment Outcome Tumor Necrosis Factor-alpha - analysis Tumor Necrosis Factor-alpha - genetics Tumor Necrosis Factor-alpha - physiology |
title | Tumor Necrosis Factor Alpha Influences the Inflammatory Response After Coronary Surgery |
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