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Decreased Azithromycin Susceptibility of Neisseria gonorrhoeae Isolates in Patients Recently Treated with Azithromycin. / Wind, Carolien M.; de Vries, Esther; Schim van der Loeff, Maarten F. et al.

In: Clinical infectious diseases, Vol. 65, No. 1, 2017, p. 37-45.

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Wind CM, de Vries E, Schim van der Loeff MF, van Rooijen MS, van Dam AP, Demczuk WHB et al. Decreased Azithromycin Susceptibility of Neisseria gonorrhoeae Isolates in Patients Recently Treated with Azithromycin. Clinical infectious diseases. 2017;65(1):37-45. Epub 2017. doi: 10.1093/cid/cix249

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Wind, Carolien M. ; de Vries, Esther ; Schim van der Loeff, Maarten F. et al. / Decreased Azithromycin Susceptibility of Neisseria gonorrhoeae Isolates in Patients Recently Treated with Azithromycin. In: Clinical infectious diseases. 2017 ; Vol. 65, No. 1. pp. 37-45.

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@article{2917614f8c7745a182ae1aadf8d9c638,
title = "Decreased Azithromycin Susceptibility of Neisseria gonorrhoeae Isolates in Patients Recently Treated with Azithromycin",
abstract = "Background. Increasing azithromycin usage and resistance in Neisseria gonorrhoeae threatens current dual treatment. Because antimicrobial exposure influences resistance, we analyzed the association between azithromycin exposure and decreased susceptibility of N. gonorrhoeae. Methods. We included N. gonorrhoeae isolates of patients who visited the Amsterdam STI Clinic between 1999 and 2013 (t(0)), with another clinic visit in the previous 60 days (t(-1)). Exposure was defined as the prescription of azithromycin at t(-1). Using multivariable linear regression, we assessed the association between exposure and azithromycin minimum inhibitory concentration (MIC). Whole genome sequencing (WGS) was performed to produce a phylogeny and identify multilocus sequence types (MLST), N. gonorrhoeae multiantigen sequence types (NG-MAST), and molecular markers of azithromycin resistance. Results. We included 323 isolates; 212 were unexposed to azithromycin, 14 were exposed <= 30 days, and 97 were exposed between 31 and 60 days before isolation. Mean azithromycin MIC was 0.28 mg/L (range, <0.016-24 mg/L). Linear regression adjusted for age, ethnicity, infection site, and calendar year showed a significant association between azithromycin exposure <= 30 days and MIC (beta, 1.00; 95% confidence interval, 0.44-1.56; P = .002). WGS was performed on 31 isolates: 14 unexposed, 14 exposed to azithromycin <= 30 days before isolation, and 3 t(-1) isolates. Exposure to azithromycin was significantly associated with A39T or G45D mtrR mutations (P = .046) but not with MLST or NG-MAST types. Conclusions. The results suggest that frequent azithromycin use in populations at high risk of contracting N. gonorrhoeae induces an increase in MIC and may result in resistance",
author = "Wind, {Carolien M.} and {de Vries}, Esther and {Schim van der Loeff}, {Maarten F.} and {van Rooijen}, {Martijn S.} and {van Dam}, {Alje P.} and Demczuk, {Walter H. B.} and Irene Martin and {de Vries}, {Henry J. C.}",
year = "2017",
doi = "10.1093/cid/cix249",
language = "English",
volume = "65",
pages = "37--45",
journal = "Clinical infectious diseases",
issn = "1058-4838",
publisher = "Oxford University Press",
number = "1",

}

RIS

TY - JOUR

T1 - Decreased Azithromycin Susceptibility of Neisseria gonorrhoeae Isolates in Patients Recently Treated with Azithromycin

AU - Wind, Carolien M.

AU - de Vries, Esther

AU - Schim van der Loeff, Maarten F.

AU - van Rooijen, Martijn S.

AU - van Dam, Alje P.

AU - Demczuk, Walter H. B.

AU - Martin, Irene

AU - de Vries, Henry J. C.

PY - 2017

Y1 - 2017

N2 - Background. Increasing azithromycin usage and resistance in Neisseria gonorrhoeae threatens current dual treatment. Because antimicrobial exposure influences resistance, we analyzed the association between azithromycin exposure and decreased susceptibility of N. gonorrhoeae. Methods. We included N. gonorrhoeae isolates of patients who visited the Amsterdam STI Clinic between 1999 and 2013 (t(0)), with another clinic visit in the previous 60 days (t(-1)). Exposure was defined as the prescription of azithromycin at t(-1). Using multivariable linear regression, we assessed the association between exposure and azithromycin minimum inhibitory concentration (MIC). Whole genome sequencing (WGS) was performed to produce a phylogeny and identify multilocus sequence types (MLST), N. gonorrhoeae multiantigen sequence types (NG-MAST), and molecular markers of azithromycin resistance. Results. We included 323 isolates; 212 were unexposed to azithromycin, 14 were exposed <= 30 days, and 97 were exposed between 31 and 60 days before isolation. Mean azithromycin MIC was 0.28 mg/L (range, <0.016-24 mg/L). Linear regression adjusted for age, ethnicity, infection site, and calendar year showed a significant association between azithromycin exposure <= 30 days and MIC (beta, 1.00; 95% confidence interval, 0.44-1.56; P = .002). WGS was performed on 31 isolates: 14 unexposed, 14 exposed to azithromycin <= 30 days before isolation, and 3 t(-1) isolates. Exposure to azithromycin was significantly associated with A39T or G45D mtrR mutations (P = .046) but not with MLST or NG-MAST types. Conclusions. The results suggest that frequent azithromycin use in populations at high risk of contracting N. gonorrhoeae induces an increase in MIC and may result in resistance

AB - Background. Increasing azithromycin usage and resistance in Neisseria gonorrhoeae threatens current dual treatment. Because antimicrobial exposure influences resistance, we analyzed the association between azithromycin exposure and decreased susceptibility of N. gonorrhoeae. Methods. We included N. gonorrhoeae isolates of patients who visited the Amsterdam STI Clinic between 1999 and 2013 (t(0)), with another clinic visit in the previous 60 days (t(-1)). Exposure was defined as the prescription of azithromycin at t(-1). Using multivariable linear regression, we assessed the association between exposure and azithromycin minimum inhibitory concentration (MIC). Whole genome sequencing (WGS) was performed to produce a phylogeny and identify multilocus sequence types (MLST), N. gonorrhoeae multiantigen sequence types (NG-MAST), and molecular markers of azithromycin resistance. Results. We included 323 isolates; 212 were unexposed to azithromycin, 14 were exposed <= 30 days, and 97 were exposed between 31 and 60 days before isolation. Mean azithromycin MIC was 0.28 mg/L (range, <0.016-24 mg/L). Linear regression adjusted for age, ethnicity, infection site, and calendar year showed a significant association between azithromycin exposure <= 30 days and MIC (beta, 1.00; 95% confidence interval, 0.44-1.56; P = .002). WGS was performed on 31 isolates: 14 unexposed, 14 exposed to azithromycin <= 30 days before isolation, and 3 t(-1) isolates. Exposure to azithromycin was significantly associated with A39T or G45D mtrR mutations (P = .046) but not with MLST or NG-MAST types. Conclusions. The results suggest that frequent azithromycin use in populations at high risk of contracting N. gonorrhoeae induces an increase in MIC and may result in resistance

U2 - 10.1093/cid/cix249

DO - 10.1093/cid/cix249

M3 - Article

C2 - 28369420

VL - 65

SP - 37

EP - 45

JO - Clinical infectious diseases

JF - Clinical infectious diseases

SN - 1058-4838

IS - 1

ER -

ID: 3527183