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Investigation of the relationship between serum creatine kinase and genetic polymorphisms in military recruits
Genetic polymorphisms may explain why certain individuals will develop exertional rhabdomyolysis (ER) or markedly elevated serum creatine kinase (CK) levels following exertion, while others in the same environment, performing the same exertion, do not. Prospectively, 499 recruits were evaluated duri...
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Published in: | Military medicine 2012-11, Vol.177 (11), p.1359-1365 |
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container_title | Military medicine |
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creator | Landau, Mark E Kenney, Kimbra Deuster, Patricia Gonzalez, Rodney S Contreras-Sesvold, Carmen Sambuughin, Nyamkhishig O'Connor, Francis G Campbell, William W |
description | Genetic polymorphisms may explain why certain individuals will develop exertional rhabdomyolysis (ER) or markedly elevated serum creatine kinase (CK) levels following exertion, while others in the same environment, performing the same exertion, do not. Prospectively, 499 recruits were evaluated during the initial fortnight of Army basic training. Serum CK levels were determined before and during that time. Eleven candidate genetic polymorphisms were studied and compared to CK levels. No subjects developed ER. Baseline CK was significantly greater in interleukin-6 G174C GG and myosin light chain kinase 2 (MLCK 2) AA subjects. Intertraining levels were significantly greater in angiotensin I-converting enzyme D/D and interleukin-6 GG subjects. Among African-Americans, those with MLCK2 AA had greater baseline CK (1,352 +/- 1,102.8 IU/L) than AC and CC genotypes (536.9 +/- 500.6). African-American men have the highest baseline levels and are more likely to have MLCK AA genotype. Whether this finding is associated with an increased incidence of ER requires further study. |
doi_str_mv | 10.7205/MILMED-D-12-00086 |
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Prospectively, 499 recruits were evaluated during the initial fortnight of Army basic training. Serum CK levels were determined before and during that time. Eleven candidate genetic polymorphisms were studied and compared to CK levels. No subjects developed ER. Baseline CK was significantly greater in interleukin-6 G174C GG and myosin light chain kinase 2 (MLCK 2) AA subjects. Intertraining levels were significantly greater in angiotensin I-converting enzyme D/D and interleukin-6 GG subjects. Among African-Americans, those with MLCK2 AA had greater baseline CK (1,352 +/- 1,102.8 IU/L) than AC and CC genotypes (536.9 +/- 500.6). African-American men have the highest baseline levels and are more likely to have MLCK AA genotype. Whether this finding is associated with an increased incidence of ER requires further study.</description><identifier>ISSN: 0026-4075</identifier><identifier>EISSN: 1930-613X</identifier><identifier>DOI: 10.7205/MILMED-D-12-00086</identifier><identifier>PMID: 23198514</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Adolescent ; Adult ; Chemokines ; Creatine Kinase - blood ; Cytokines ; Deoxyribonucleic acid ; DNA ; DNA - analysis ; Enzymes ; Female ; Genes ; Genetic testing ; Genetic Testing - methods ; Genotype & phenotype ; Humans ; Hyperthermia ; Illnesses ; Interleukin-6 - genetics ; Kinases ; Male ; Middle Aged ; Military Personnel ; Mutation ; Physical Exertion - physiology ; Polymorphism ; Polymorphism, Genetic ; Prospective Studies ; Reference Values ; Rhabdomyolysis ; Rhabdomyolysis - enzymology ; Rhabdomyolysis - etiology ; Rhabdomyolysis - genetics ; Young Adult</subject><ispartof>Military medicine, 2012-11, Vol.177 (11), p.1359-1365</ispartof><rights>Copyright Association of Military Surgeons of the United States Nov 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-f8a6eed85820783593ea1b5850c5ceb4630577de6fcd1c5d438ded0db9cbebb43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23198514$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Landau, Mark E</creatorcontrib><creatorcontrib>Kenney, Kimbra</creatorcontrib><creatorcontrib>Deuster, Patricia</creatorcontrib><creatorcontrib>Gonzalez, Rodney S</creatorcontrib><creatorcontrib>Contreras-Sesvold, Carmen</creatorcontrib><creatorcontrib>Sambuughin, Nyamkhishig</creatorcontrib><creatorcontrib>O'Connor, Francis G</creatorcontrib><creatorcontrib>Campbell, William W</creatorcontrib><title>Investigation of the relationship between serum creatine kinase and genetic polymorphisms in military recruits</title><title>Military medicine</title><addtitle>Mil Med</addtitle><description>Genetic polymorphisms may explain why certain individuals will develop exertional rhabdomyolysis (ER) or markedly elevated serum creatine kinase (CK) levels following exertion, while others in the same environment, performing the same exertion, do not. Prospectively, 499 recruits were evaluated during the initial fortnight of Army basic training. Serum CK levels were determined before and during that time. Eleven candidate genetic polymorphisms were studied and compared to CK levels. No subjects developed ER. Baseline CK was significantly greater in interleukin-6 G174C GG and myosin light chain kinase 2 (MLCK 2) AA subjects. Intertraining levels were significantly greater in angiotensin I-converting enzyme D/D and interleukin-6 GG subjects. Among African-Americans, those with MLCK2 AA had greater baseline CK (1,352 +/- 1,102.8 IU/L) than AC and CC genotypes (536.9 +/- 500.6). African-American men have the highest baseline levels and are more likely to have MLCK AA genotype. Whether this finding is associated with an increased incidence of ER requires further study.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Chemokines</subject><subject>Creatine Kinase - blood</subject><subject>Cytokines</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA - analysis</subject><subject>Enzymes</subject><subject>Female</subject><subject>Genes</subject><subject>Genetic testing</subject><subject>Genetic Testing - methods</subject><subject>Genotype & phenotype</subject><subject>Humans</subject><subject>Hyperthermia</subject><subject>Illnesses</subject><subject>Interleukin-6 - genetics</subject><subject>Kinases</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Military Personnel</subject><subject>Mutation</subject><subject>Physical Exertion - physiology</subject><subject>Polymorphism</subject><subject>Polymorphism, Genetic</subject><subject>Prospective Studies</subject><subject>Reference Values</subject><subject>Rhabdomyolysis</subject><subject>Rhabdomyolysis - 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blood</topic><topic>Cytokines</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA - analysis</topic><topic>Enzymes</topic><topic>Female</topic><topic>Genes</topic><topic>Genetic testing</topic><topic>Genetic Testing - methods</topic><topic>Genotype & phenotype</topic><topic>Humans</topic><topic>Hyperthermia</topic><topic>Illnesses</topic><topic>Interleukin-6 - genetics</topic><topic>Kinases</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Military Personnel</topic><topic>Mutation</topic><topic>Physical Exertion - physiology</topic><topic>Polymorphism</topic><topic>Polymorphism, Genetic</topic><topic>Prospective Studies</topic><topic>Reference Values</topic><topic>Rhabdomyolysis</topic><topic>Rhabdomyolysis - enzymology</topic><topic>Rhabdomyolysis - etiology</topic><topic>Rhabdomyolysis - genetics</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Landau, Mark E</creatorcontrib><creatorcontrib>Kenney, Kimbra</creatorcontrib><creatorcontrib>Deuster, Patricia</creatorcontrib><creatorcontrib>Gonzalez, Rodney S</creatorcontrib><creatorcontrib>Contreras-Sesvold, Carmen</creatorcontrib><creatorcontrib>Sambuughin, Nyamkhishig</creatorcontrib><creatorcontrib>O'Connor, Francis G</creatorcontrib><creatorcontrib>Campbell, William W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>ProQuest Nursing & Allied Health Database</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Military Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Military Collection</collection><collection>Psychology Database (ProQuest)</collection><collection>ProQuest Science Journals</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Military medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Landau, Mark E</au><au>Kenney, Kimbra</au><au>Deuster, Patricia</au><au>Gonzalez, Rodney S</au><au>Contreras-Sesvold, Carmen</au><au>Sambuughin, Nyamkhishig</au><au>O'Connor, Francis G</au><au>Campbell, William W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation of the relationship between serum creatine kinase and genetic polymorphisms in military recruits</atitle><jtitle>Military medicine</jtitle><addtitle>Mil Med</addtitle><date>2012-11</date><risdate>2012</risdate><volume>177</volume><issue>11</issue><spage>1359</spage><epage>1365</epage><pages>1359-1365</pages><issn>0026-4075</issn><eissn>1930-613X</eissn><abstract>Genetic polymorphisms may explain why certain individuals will develop exertional rhabdomyolysis (ER) or markedly elevated serum creatine kinase (CK) levels following exertion, while others in the same environment, performing the same exertion, do not. Prospectively, 499 recruits were evaluated during the initial fortnight of Army basic training. Serum CK levels were determined before and during that time. Eleven candidate genetic polymorphisms were studied and compared to CK levels. No subjects developed ER. Baseline CK was significantly greater in interleukin-6 G174C GG and myosin light chain kinase 2 (MLCK 2) AA subjects. Intertraining levels were significantly greater in angiotensin I-converting enzyme D/D and interleukin-6 GG subjects. Among African-Americans, those with MLCK2 AA had greater baseline CK (1,352 +/- 1,102.8 IU/L) than AC and CC genotypes (536.9 +/- 500.6). African-American men have the highest baseline levels and are more likely to have MLCK AA genotype. Whether this finding is associated with an increased incidence of ER requires further study.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>23198514</pmid><doi>10.7205/MILMED-D-12-00086</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Chemokines Creatine Kinase - blood Cytokines Deoxyribonucleic acid DNA DNA - analysis Enzymes Female Genes Genetic testing Genetic Testing - methods Genotype & phenotype Humans Hyperthermia Illnesses Interleukin-6 - genetics Kinases Male Middle Aged Military Personnel Mutation Physical Exertion - physiology Polymorphism Polymorphism, Genetic Prospective Studies Reference Values Rhabdomyolysis Rhabdomyolysis - enzymology Rhabdomyolysis - etiology Rhabdomyolysis - genetics Young Adult |
title | Investigation of the relationship between serum creatine kinase and genetic polymorphisms in military recruits |
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