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Relationship Between ABCB1 Polymorphisms and Cold Pain Sensitivity Among Healthy Opioid‐naive Malay Males
Background Endogenous and exogenous opioids are substrates of the permeability glycoprotein (P‐gp) efflux transporter, which is encoded by the ABCB1 (MDR1) gene. Genetic polymorphisms of ABCB1 may contribute to interindividual differences in pain modulation and analgesic responses. We investigated t...
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Published in: | Pain practice 2017-09, Vol.17 (7), p.930-940 |
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creator | Zahari, Zalina Lee, Chee Siong Ibrahim, Muslih Abdulkarim Musa, Nurfadhlina Mohd Yasin, Mohd Azhar Lee, Yeong Yeh Tan, Soo Choon Mohamad, Nasir Ismail, Rusli |
description | Background
Endogenous and exogenous opioids are substrates of the permeability glycoprotein (P‐gp) efflux transporter, which is encoded by the ABCB1 (MDR1) gene. Genetic polymorphisms of ABCB1 may contribute to interindividual differences in pain modulation and analgesic responses. We investigated the relationship between ABCB1 polymorphisms and cold pain sensitivity among healthy males.
Methods
Cold pain responses, including pain threshold and pain tolerance, were measured using the cold‐pressor test (CPT). DNA was extracted from whole blood and genotyped for ABCB1 polymorphisms, including c.1236C>T (rs1128503), c.2677G>T/A (rs2032582), and c.3435C>T (rs1045642), using the allelic discrimination real‐time polymerase chain reaction.
Results
A total of 152 participants were recruited in this observational study. Frequencies of mutated allele for c.1236C>T, c.2677G>T/A, and c.3435C>T polymorphisms were 56.6%, 49.7%, and 43.4%, respectively. Our results revealed an association of the CGC/CGC diplotype (c.1236C>T, c.2677G>T/A, and c.3435C>T) with cold pain sensitivity. Participants with the CGC/CGC diplotype had 90% and 72% higher cold pain thresholds (87.62 seconds vs. 46.19 seconds, P = 0.010) and cold pain tolerances (97.24 seconds vs. 56.54 seconds, P = 0.021), respectively, when compared with those without the diplotype.
Conclusion
The CGC/CGC diplotype of ABCB1 polymorphisms was associated with variability in cold pain threshold and pain tolerance in healthy males. |
doi_str_mv | 10.1111/papr.12546 |
format | article |
fullrecord | <record><control><sourceid>wiley_pubme</sourceid><recordid>TN_cdi_pubmed_primary_27996183</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>PAPR12546</sourcerecordid><originalsourceid>FETCH-LOGICAL-p2536-e91f177d27f5504c5f6b0d5a3dd12d3061001ede8990beb392b6e1f920e38bd53</originalsourceid><addsrcrecordid>eNo9kE1OwzAQhS0EoqWw4QDIF0jxT53EyzQCilTUqMA6cvCEGhLHikOr7DgCZ-Qk9AeYxcyT3tNI70PokpIx3c61U64dUyYm4REaUsF5wAQhx3tNgojEYoDOvH8jhEaS81M0YJGUIY35EL0voVKdaaxfGYen0G0ALE6m6ZTirKn6umndyvjaY2U1TptK40wZix_BetOZtel6nNSNfcUzUFW36vHCmcbo788vq8wa8IOqVL_b4M_RSakqDxe_d4Seb2-e0lkwX9zdp8k8cEzwMABJSxpFmkWlEGTyIsqwIFoorjVlmpOQbouAhlhKUkDBJStCoKVkBHhcaMFH6Orw130UNejctaZWbZ__td4G6CGwMRX0_z4l-Y5nvuOZ73nmWZIt94r_ALQfadU</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Relationship Between ABCB1 Polymorphisms and Cold Pain Sensitivity Among Healthy Opioid‐naive Malay Males</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Zahari, Zalina ; Lee, Chee Siong ; Ibrahim, Muslih Abdulkarim ; Musa, Nurfadhlina ; Mohd Yasin, Mohd Azhar ; Lee, Yeong Yeh ; Tan, Soo Choon ; Mohamad, Nasir ; Ismail, Rusli</creator><creatorcontrib>Zahari, Zalina ; Lee, Chee Siong ; Ibrahim, Muslih Abdulkarim ; Musa, Nurfadhlina ; Mohd Yasin, Mohd Azhar ; Lee, Yeong Yeh ; Tan, Soo Choon ; Mohamad, Nasir ; Ismail, Rusli</creatorcontrib><description>Background
Endogenous and exogenous opioids are substrates of the permeability glycoprotein (P‐gp) efflux transporter, which is encoded by the ABCB1 (MDR1) gene. Genetic polymorphisms of ABCB1 may contribute to interindividual differences in pain modulation and analgesic responses. We investigated the relationship between ABCB1 polymorphisms and cold pain sensitivity among healthy males.
Methods
Cold pain responses, including pain threshold and pain tolerance, were measured using the cold‐pressor test (CPT). DNA was extracted from whole blood and genotyped for ABCB1 polymorphisms, including c.1236C>T (rs1128503), c.2677G>T/A (rs2032582), and c.3435C>T (rs1045642), using the allelic discrimination real‐time polymerase chain reaction.
Results
A total of 152 participants were recruited in this observational study. Frequencies of mutated allele for c.1236C>T, c.2677G>T/A, and c.3435C>T polymorphisms were 56.6%, 49.7%, and 43.4%, respectively. Our results revealed an association of the CGC/CGC diplotype (c.1236C>T, c.2677G>T/A, and c.3435C>T) with cold pain sensitivity. Participants with the CGC/CGC diplotype had 90% and 72% higher cold pain thresholds (87.62 seconds vs. 46.19 seconds, P = 0.010) and cold pain tolerances (97.24 seconds vs. 56.54 seconds, P = 0.021), respectively, when compared with those without the diplotype.
Conclusion
The CGC/CGC diplotype of ABCB1 polymorphisms was associated with variability in cold pain threshold and pain tolerance in healthy males.</description><identifier>ISSN: 1530-7085</identifier><identifier>EISSN: 1533-2500</identifier><identifier>DOI: 10.1111/papr.12546</identifier><identifier>PMID: 27996183</identifier><language>eng</language><publisher>United States</publisher><subject>ABCB1 ; Adolescent ; Adult ; Analgesics, Opioid ; ATP Binding Cassette Transporter, Sub-Family B - genetics ; Cold Temperature - adverse effects ; cold‐pressor test ; Cross-Sectional Studies ; Genotype ; Humans ; Malaysia - epidemiology ; Male ; Middle Aged ; Pain - diagnosis ; Pain - epidemiology ; Pain - genetics ; pain threshold ; Pain Threshold - physiology ; pain tolerance ; permeability glycoprotein ; Polymorphism, Single Nucleotide - genetics ; Random Allocation ; Young Adult</subject><ispartof>Pain practice, 2017-09, Vol.17 (7), p.930-940</ispartof><rights>2016 World Institute of Pain</rights><rights>2016 World Institute of Pain.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27996183$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zahari, Zalina</creatorcontrib><creatorcontrib>Lee, Chee Siong</creatorcontrib><creatorcontrib>Ibrahim, Muslih Abdulkarim</creatorcontrib><creatorcontrib>Musa, Nurfadhlina</creatorcontrib><creatorcontrib>Mohd Yasin, Mohd Azhar</creatorcontrib><creatorcontrib>Lee, Yeong Yeh</creatorcontrib><creatorcontrib>Tan, Soo Choon</creatorcontrib><creatorcontrib>Mohamad, Nasir</creatorcontrib><creatorcontrib>Ismail, Rusli</creatorcontrib><title>Relationship Between ABCB1 Polymorphisms and Cold Pain Sensitivity Among Healthy Opioid‐naive Malay Males</title><title>Pain practice</title><addtitle>Pain Pract</addtitle><description>Background
Endogenous and exogenous opioids are substrates of the permeability glycoprotein (P‐gp) efflux transporter, which is encoded by the ABCB1 (MDR1) gene. Genetic polymorphisms of ABCB1 may contribute to interindividual differences in pain modulation and analgesic responses. We investigated the relationship between ABCB1 polymorphisms and cold pain sensitivity among healthy males.
Methods
Cold pain responses, including pain threshold and pain tolerance, were measured using the cold‐pressor test (CPT). DNA was extracted from whole blood and genotyped for ABCB1 polymorphisms, including c.1236C>T (rs1128503), c.2677G>T/A (rs2032582), and c.3435C>T (rs1045642), using the allelic discrimination real‐time polymerase chain reaction.
Results
A total of 152 participants were recruited in this observational study. Frequencies of mutated allele for c.1236C>T, c.2677G>T/A, and c.3435C>T polymorphisms were 56.6%, 49.7%, and 43.4%, respectively. Our results revealed an association of the CGC/CGC diplotype (c.1236C>T, c.2677G>T/A, and c.3435C>T) with cold pain sensitivity. Participants with the CGC/CGC diplotype had 90% and 72% higher cold pain thresholds (87.62 seconds vs. 46.19 seconds, P = 0.010) and cold pain tolerances (97.24 seconds vs. 56.54 seconds, P = 0.021), respectively, when compared with those without the diplotype.
Conclusion
The CGC/CGC diplotype of ABCB1 polymorphisms was associated with variability in cold pain threshold and pain tolerance in healthy males.</description><subject>ABCB1</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Analgesics, Opioid</subject><subject>ATP Binding Cassette Transporter, Sub-Family B - genetics</subject><subject>Cold Temperature - adverse effects</subject><subject>cold‐pressor test</subject><subject>Cross-Sectional Studies</subject><subject>Genotype</subject><subject>Humans</subject><subject>Malaysia - epidemiology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pain - diagnosis</subject><subject>Pain - epidemiology</subject><subject>Pain - genetics</subject><subject>pain threshold</subject><subject>Pain Threshold - physiology</subject><subject>pain tolerance</subject><subject>permeability glycoprotein</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>Random Allocation</subject><subject>Young Adult</subject><issn>1530-7085</issn><issn>1533-2500</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNo9kE1OwzAQhS0EoqWw4QDIF0jxT53EyzQCilTUqMA6cvCEGhLHikOr7DgCZ-Qk9AeYxcyT3tNI70PokpIx3c61U64dUyYm4REaUsF5wAQhx3tNgojEYoDOvH8jhEaS81M0YJGUIY35EL0voVKdaaxfGYen0G0ALE6m6ZTirKn6umndyvjaY2U1TptK40wZix_BetOZtel6nNSNfcUzUFW36vHCmcbo788vq8wa8IOqVL_b4M_RSakqDxe_d4Seb2-e0lkwX9zdp8k8cEzwMABJSxpFmkWlEGTyIsqwIFoorjVlmpOQbouAhlhKUkDBJStCoKVkBHhcaMFH6Orw130UNejctaZWbZ__td4G6CGwMRX0_z4l-Y5nvuOZ73nmWZIt94r_ALQfadU</recordid><startdate>201709</startdate><enddate>201709</enddate><creator>Zahari, Zalina</creator><creator>Lee, Chee Siong</creator><creator>Ibrahim, Muslih Abdulkarim</creator><creator>Musa, Nurfadhlina</creator><creator>Mohd Yasin, Mohd Azhar</creator><creator>Lee, Yeong Yeh</creator><creator>Tan, Soo Choon</creator><creator>Mohamad, Nasir</creator><creator>Ismail, Rusli</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>201709</creationdate><title>Relationship Between ABCB1 Polymorphisms and Cold Pain Sensitivity Among Healthy Opioid‐naive Malay Males</title><author>Zahari, Zalina ; Lee, Chee Siong ; Ibrahim, Muslih Abdulkarim ; Musa, Nurfadhlina ; Mohd Yasin, Mohd Azhar ; Lee, Yeong Yeh ; Tan, Soo Choon ; Mohamad, Nasir ; Ismail, Rusli</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p2536-e91f177d27f5504c5f6b0d5a3dd12d3061001ede8990beb392b6e1f920e38bd53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>ABCB1</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Analgesics, Opioid</topic><topic>ATP Binding Cassette Transporter, Sub-Family B - genetics</topic><topic>Cold Temperature - adverse effects</topic><topic>cold‐pressor test</topic><topic>Cross-Sectional Studies</topic><topic>Genotype</topic><topic>Humans</topic><topic>Malaysia - epidemiology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pain - diagnosis</topic><topic>Pain - epidemiology</topic><topic>Pain - genetics</topic><topic>pain threshold</topic><topic>Pain Threshold - physiology</topic><topic>pain tolerance</topic><topic>permeability glycoprotein</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>Random Allocation</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zahari, Zalina</creatorcontrib><creatorcontrib>Lee, Chee Siong</creatorcontrib><creatorcontrib>Ibrahim, Muslih Abdulkarim</creatorcontrib><creatorcontrib>Musa, Nurfadhlina</creatorcontrib><creatorcontrib>Mohd Yasin, Mohd Azhar</creatorcontrib><creatorcontrib>Lee, Yeong Yeh</creatorcontrib><creatorcontrib>Tan, Soo Choon</creatorcontrib><creatorcontrib>Mohamad, Nasir</creatorcontrib><creatorcontrib>Ismail, Rusli</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Pain practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zahari, Zalina</au><au>Lee, Chee Siong</au><au>Ibrahim, Muslih Abdulkarim</au><au>Musa, Nurfadhlina</au><au>Mohd Yasin, Mohd Azhar</au><au>Lee, Yeong Yeh</au><au>Tan, Soo Choon</au><au>Mohamad, Nasir</au><au>Ismail, Rusli</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relationship Between ABCB1 Polymorphisms and Cold Pain Sensitivity Among Healthy Opioid‐naive Malay Males</atitle><jtitle>Pain practice</jtitle><addtitle>Pain Pract</addtitle><date>2017-09</date><risdate>2017</risdate><volume>17</volume><issue>7</issue><spage>930</spage><epage>940</epage><pages>930-940</pages><issn>1530-7085</issn><eissn>1533-2500</eissn><abstract>Background
Endogenous and exogenous opioids are substrates of the permeability glycoprotein (P‐gp) efflux transporter, which is encoded by the ABCB1 (MDR1) gene. Genetic polymorphisms of ABCB1 may contribute to interindividual differences in pain modulation and analgesic responses. We investigated the relationship between ABCB1 polymorphisms and cold pain sensitivity among healthy males.
Methods
Cold pain responses, including pain threshold and pain tolerance, were measured using the cold‐pressor test (CPT). DNA was extracted from whole blood and genotyped for ABCB1 polymorphisms, including c.1236C>T (rs1128503), c.2677G>T/A (rs2032582), and c.3435C>T (rs1045642), using the allelic discrimination real‐time polymerase chain reaction.
Results
A total of 152 participants were recruited in this observational study. Frequencies of mutated allele for c.1236C>T, c.2677G>T/A, and c.3435C>T polymorphisms were 56.6%, 49.7%, and 43.4%, respectively. Our results revealed an association of the CGC/CGC diplotype (c.1236C>T, c.2677G>T/A, and c.3435C>T) with cold pain sensitivity. Participants with the CGC/CGC diplotype had 90% and 72% higher cold pain thresholds (87.62 seconds vs. 46.19 seconds, P = 0.010) and cold pain tolerances (97.24 seconds vs. 56.54 seconds, P = 0.021), respectively, when compared with those without the diplotype.
Conclusion
The CGC/CGC diplotype of ABCB1 polymorphisms was associated with variability in cold pain threshold and pain tolerance in healthy males.</abstract><cop>United States</cop><pmid>27996183</pmid><doi>10.1111/papr.12546</doi><tpages>11</tpages></addata></record> |
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subjects | ABCB1 Adolescent Adult Analgesics, Opioid ATP Binding Cassette Transporter, Sub-Family B - genetics Cold Temperature - adverse effects cold‐pressor test Cross-Sectional Studies Genotype Humans Malaysia - epidemiology Male Middle Aged Pain - diagnosis Pain - epidemiology Pain - genetics pain threshold Pain Threshold - physiology pain tolerance permeability glycoprotein Polymorphism, Single Nucleotide - genetics Random Allocation Young Adult |
title | Relationship Between ABCB1 Polymorphisms and Cold Pain Sensitivity Among Healthy Opioid‐naive Malay Males |
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