Intra-individual variability in the urine concentrations of inhaled salmeterol in male subjects with reference to doping analysis – impact of urine specific gravity correction

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Intra-individual variability in the urine concentrations of inhaled salmeterol in male subjects with reference to doping analysis – impact of urine specific gravity correction. / Hostrup, Morten; Kalsen, Anders; Hemmersbach, Peter; Backer, Vibeke.

In: Journal of Sports Medicine & Doping Studies, Vol. 2, No. 6, 2012.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hostrup, M, Kalsen, A, Hemmersbach, P & Backer, V 2012, 'Intra-individual variability in the urine concentrations of inhaled salmeterol in male subjects with reference to doping analysis – impact of urine specific gravity correction', Journal of Sports Medicine & Doping Studies, vol. 2, no. 6. https://doi.org/10.4172/2161-0673.1000118

APA

Hostrup, M., Kalsen, A., Hemmersbach, P., & Backer, V. (2012). Intra-individual variability in the urine concentrations of inhaled salmeterol in male subjects with reference to doping analysis – impact of urine specific gravity correction. Journal of Sports Medicine & Doping Studies, 2(6). https://doi.org/10.4172/2161-0673.1000118

Vancouver

Hostrup M, Kalsen A, Hemmersbach P, Backer V. Intra-individual variability in the urine concentrations of inhaled salmeterol in male subjects with reference to doping analysis – impact of urine specific gravity correction. Journal of Sports Medicine & Doping Studies. 2012;2(6). https://doi.org/10.4172/2161-0673.1000118

Author

Hostrup, Morten ; Kalsen, Anders ; Hemmersbach, Peter ; Backer, Vibeke. / Intra-individual variability in the urine concentrations of inhaled salmeterol in male subjects with reference to doping analysis – impact of urine specific gravity correction. In: Journal of Sports Medicine & Doping Studies. 2012 ; Vol. 2, No. 6.

Bibtex

@article{027e9e252ba94d66acdb8f2443cc1748,
title = "Intra-individual variability in the urine concentrations of inhaled salmeterol in male subjects with reference to doping analysis – impact of urine specific gravity correction",
abstract = "Since 2010, the World Anti-Doping Agency (WADA) has introduced urinary thresholds for some beta2-agonists. In doping analysis urine samples of beta2-agonists are not corrected for the Urine Specific Gravity (USG) by theWADA laboratories. Several studies have observed high differences in the urine concentrations of beta2-agonists when correction for USG is compared with no correction, as well as high inter-individual variability between subjects. However, no studies have measured the intra-individual variability after inhalation of the long-acting beta2-agonist salmeterol. As such, the purpose of this study was to measure the intra-individual variability in the urine concentrations of salmeterol and its metabolite a-hydroxysalmeterol. Furthermore, to highlight the variability between corrected and uncorrected urine samples for USG. Urine samples from 20 subjects were analyzed for USG, urine excretion and urine concentrations of salmeterol and a-hydroxysalmeterol. Seven of the subjects underwent a second visit with the same procedures. At each visit 100 µg salmeterol was administered by inhalation. Urine samples were collected before administration of the drug (T0) and 4 (T4), 8 (T8) and 12 (T12) hours after administration. The mean relativedifferences in the urine concentrations of salmeterol and a-hydroxysalmeterol between USG corrected and uncorrected samples were 43 ± 44, 27 ± 42 and 56 ± 87% at T4, T8 and T12, respectively. The intra-individual variability in theurine excretion of salmeterol and a-hydroxysalmeterol during visits one and two were 12.6 and 21.8%, respectively. The intra-individual variability of salmeterol and a-hydroxysalmeterol in the urine concentrations were significantly higher when uncorrected for USG with 43.0 and 43.7% versus 20.4% (p<0.01) and 28.0% (p<0.05), respectively. Correction for USG reduces inter-individual and intra-individual variability in urine concentrations of salmeterol anda-hydroxysalmeterol.",
author = "Morten Hostrup and Anders Kalsen and Peter Hemmersbach and Vibeke Backer",
note = "CURIS 2012 5200 079",
year = "2012",
doi = "10.4172/2161-0673.1000118",
language = "English",
volume = "2",
journal = "Journal of Sports Medicine & Doping Studies",
issn = "2161-0673",
publisher = "OMICS Publishing Group, Los Angeles, CA",
number = "6",

}

RIS

TY - JOUR

T1 - Intra-individual variability in the urine concentrations of inhaled salmeterol in male subjects with reference to doping analysis – impact of urine specific gravity correction

AU - Hostrup, Morten

AU - Kalsen, Anders

AU - Hemmersbach, Peter

AU - Backer, Vibeke

N1 - CURIS 2012 5200 079

PY - 2012

Y1 - 2012

N2 - Since 2010, the World Anti-Doping Agency (WADA) has introduced urinary thresholds for some beta2-agonists. In doping analysis urine samples of beta2-agonists are not corrected for the Urine Specific Gravity (USG) by theWADA laboratories. Several studies have observed high differences in the urine concentrations of beta2-agonists when correction for USG is compared with no correction, as well as high inter-individual variability between subjects. However, no studies have measured the intra-individual variability after inhalation of the long-acting beta2-agonist salmeterol. As such, the purpose of this study was to measure the intra-individual variability in the urine concentrations of salmeterol and its metabolite a-hydroxysalmeterol. Furthermore, to highlight the variability between corrected and uncorrected urine samples for USG. Urine samples from 20 subjects were analyzed for USG, urine excretion and urine concentrations of salmeterol and a-hydroxysalmeterol. Seven of the subjects underwent a second visit with the same procedures. At each visit 100 µg salmeterol was administered by inhalation. Urine samples were collected before administration of the drug (T0) and 4 (T4), 8 (T8) and 12 (T12) hours after administration. The mean relativedifferences in the urine concentrations of salmeterol and a-hydroxysalmeterol between USG corrected and uncorrected samples were 43 ± 44, 27 ± 42 and 56 ± 87% at T4, T8 and T12, respectively. The intra-individual variability in theurine excretion of salmeterol and a-hydroxysalmeterol during visits one and two were 12.6 and 21.8%, respectively. The intra-individual variability of salmeterol and a-hydroxysalmeterol in the urine concentrations were significantly higher when uncorrected for USG with 43.0 and 43.7% versus 20.4% (p<0.01) and 28.0% (p<0.05), respectively. Correction for USG reduces inter-individual and intra-individual variability in urine concentrations of salmeterol anda-hydroxysalmeterol.

AB - Since 2010, the World Anti-Doping Agency (WADA) has introduced urinary thresholds for some beta2-agonists. In doping analysis urine samples of beta2-agonists are not corrected for the Urine Specific Gravity (USG) by theWADA laboratories. Several studies have observed high differences in the urine concentrations of beta2-agonists when correction for USG is compared with no correction, as well as high inter-individual variability between subjects. However, no studies have measured the intra-individual variability after inhalation of the long-acting beta2-agonist salmeterol. As such, the purpose of this study was to measure the intra-individual variability in the urine concentrations of salmeterol and its metabolite a-hydroxysalmeterol. Furthermore, to highlight the variability between corrected and uncorrected urine samples for USG. Urine samples from 20 subjects were analyzed for USG, urine excretion and urine concentrations of salmeterol and a-hydroxysalmeterol. Seven of the subjects underwent a second visit with the same procedures. At each visit 100 µg salmeterol was administered by inhalation. Urine samples were collected before administration of the drug (T0) and 4 (T4), 8 (T8) and 12 (T12) hours after administration. The mean relativedifferences in the urine concentrations of salmeterol and a-hydroxysalmeterol between USG corrected and uncorrected samples were 43 ± 44, 27 ± 42 and 56 ± 87% at T4, T8 and T12, respectively. The intra-individual variability in theurine excretion of salmeterol and a-hydroxysalmeterol during visits one and two were 12.6 and 21.8%, respectively. The intra-individual variability of salmeterol and a-hydroxysalmeterol in the urine concentrations were significantly higher when uncorrected for USG with 43.0 and 43.7% versus 20.4% (p<0.01) and 28.0% (p<0.05), respectively. Correction for USG reduces inter-individual and intra-individual variability in urine concentrations of salmeterol anda-hydroxysalmeterol.

U2 - 10.4172/2161-0673.1000118

DO - 10.4172/2161-0673.1000118

M3 - Journal article

VL - 2

JO - Journal of Sports Medicine & Doping Studies

JF - Journal of Sports Medicine & Doping Studies

SN - 2161-0673

IS - 6

ER -

ID: 42015437