Objective: Nonadherence with scheduled saliva sampling, as encountered in ambulatory settings, can bias the estimation of salivary cortisol concentrations. This study is the first to estimate if such nonadherence is also associated with biased salivary testosterone concentration estimates. Methods: Using a standard ambulatory saliva-sampling protocol, we instructed pregnant women to collect saliva samples on two consecutive days at awakening, 1100 h, 1500h, 2000h, and 2200 h. We estimated testosterone concentrations in the saliva samples and participants' actual sampling times with an electronic medication event-monitoring system. We classified a saliva sample as adherent if it was sampled within a specific time window relative to its scheduled sampling time. We used a mixed-model analysis to distinguish between trait (number of adherent saliva samples per participant) and state (adherence status of a specific sample) adherence. Results: We included 60 pregnant women in this study. Seventy-five percent (448 of 600) of the scheduled samples indicated adherence with the sampling schedule. Participants' trait adherence was associated with their diurnal profiles of salivary testosterone estimates; that is, adherent participants had higher salivary testosterone estimates compared with nonadherent participants, F(1,58) = 5.41, p = 0.023, Cohen's d = 0.67. The state adherence of a sample was associated with the salivary testosterone estimate of the related sample, F(1,469) = 4.48, p = 0.035, Cohen's d = 0.20, with delayed sampling associated with lower salivary testosterone estimates. Conclusions: The results suggest that common ambulatory nonadherence with scheduled saliva sampling is associated with biased salivary testosterone estimates. They will inform further studies estimating salivary testosterone with ambulatory saliva-sampling designs and highlight the relevance of strategies to improve or confirm adherence, beyond routinely used instructions. (C) 2014 Elsevier Ltd. All rights reserved.
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North West Univ, Fac Hlth Sci, Hypertens Africa Res Team, ZA-2520 Potchefstroom, South AfricaNorth West Univ, Fac Hlth Sci, Hypertens Africa Res Team, ZA-2520 Potchefstroom, South Africa
Malan, N. T.
Stalder, T.
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Tech Univ Dresden, Dept Psychol, D-01062 Dresden, GermanyNorth West Univ, Fac Hlth Sci, Hypertens Africa Res Team, ZA-2520 Potchefstroom, South Africa
Stalder, T.
Schlaich, M. P.
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Monash Univ, Human Neurotransmitters & Neurovasc Hypertens Lab, Melbourne, Vic 3004, Australia
Monash Univ, Baker IDI Heart & Diabet Inst, Kidney Dis Labs, Melbourne, Vic 3004, Australia
Monash Univ, Fac Med Nursing & Hlth Sci, Melbourne, Vic 3004, AustraliaNorth West Univ, Fac Hlth Sci, Hypertens Africa Res Team, ZA-2520 Potchefstroom, South Africa
Schlaich, M. P.
Lambert, G. W.
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Monash Univ, Human Neurotransmitters & Neurovasc Hypertens Lab, Melbourne, Vic 3004, Australia
Monash Univ, Baker IDI Heart & Diabet Inst, Kidney Dis Labs, Melbourne, Vic 3004, Australia
Monash Univ, Fac Med Nursing & Hlth Sci, Melbourne, Vic 3004, AustraliaNorth West Univ, Fac Hlth Sci, Hypertens Africa Res Team, ZA-2520 Potchefstroom, South Africa
Lambert, G. W.
Hamer, M.
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North West Univ, Fac Hlth Sci, Hypertens Africa Res Team, ZA-2520 Potchefstroom, South Africa
UCL, Dept Epidemiol & Publ Hlth, London, EnglandNorth West Univ, Fac Hlth Sci, Hypertens Africa Res Team, ZA-2520 Potchefstroom, South Africa
Hamer, M.
Schutte, A. E.
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North West Univ, Fac Hlth Sci, Hypertens Africa Res Team, ZA-2520 Potchefstroom, South AfricaNorth West Univ, Fac Hlth Sci, Hypertens Africa Res Team, ZA-2520 Potchefstroom, South Africa