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Τρίτη 3 Οκτωβρίου 2017

Decrease of salivary cortisol levels after glucocorticoid dose reduction in patients with adrenal insufficiency: a prospective proof-of-concept study

Abstract

Background and aim

Patients with adrenal insufficiency (AI) require life-long glucocorticoid (GC) replacement therapy. Cortisol measurement in saliva is increasingly being used: we assessed salivary cortisol rhythm in outpatients with AI, in order to provide new insights regarding the management of GC treatment.

Materials and methods

19 AI outpatients collected six saliva samples from awakening (Fa, before taking the morning GC therapy), during the day (F1.5h, F6h before the afternoon GC dose, F8.5h, F12h)until bedtime (Fb).We measured daily cortisol exposure by calculating the area under the curve (AUCFa[RIGHTWARDS ARROW]Fb).Saliva samples were collected at baseline and one year after GG dose reduction (by at least 5 mg of hydrocortisone)

Results

Hydrocortisone equivalents decreased from median 25 mg/day (baseline, interquartile range IQR 20-27.5) to 15 mg/day (IQR 15-20, p<0.01). As expected, we observed a reduction of both daily cortisol exposure (AUCFa[RIGHTWARDS ARROW]Fb 23982 nmol·h/L, IQR 12635-45369, to 14689 nmol·h/L, IQR 7168-25378, p<0.001) and salivary cortisol levels at F6h (24.8 nmol/l, IQR 20.1-35.7, to 21 nmol/l, IQR 8.7-29.2, p<0.05) and Fb (8.7 nmol/l, IQR 3.4-20.2, to 3.7 nmol/l, IQR 3.0-5.8, p<0.05). None of the patients developed signs or symptoms consistent with AI after GC reduction. Median diastolic blood pressure (DPB) values fell from baseline to the end of follow-up (87.5 mmHg, IQR 80-90, to 80 mmHg, IQR 80-85, p<0.05). The AUCFa[RIGHTWARDS ARROW]Fb of patients at baseline was above the reference value (90th percentile of controls) in 12 patients (60%); after the dosage reduction, 30% of patients normalized their daily cortisol exposure (AUCFa[RIGHTWARDS ARROW]Fb).

Conclusions

The reduction of GC treatment in patients with AI resulted in better control of daily cortisol rhythm, measured with salivary cortisol, and in an improvement of DPB. Further studies are needed to ascertain if salivary cortisol could be used as a biomarker to manage GC replacement therapy.

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