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Endocr Connect. 2019 Oct 1. pii: EC-19-0407.R1. doi: 10.1530/EC-19-0407. [Epub ahead of print]

Midnight salivary cortisol associated with high systolic blood pressure in type 1 diabetes.

Author information

1
E Melin, BMC, Diabetes Laboratory, Lunds University Faculty of Medicine, Lund, 22362, Sweden.
2
M Hillman, Clinical Sciences, Diabetes Laboratory, Lunds University Faculty of Medicine, Lund, Sweden.
3
M Landin-Olsson, Clinical Sciences, Diabetes Laboratory, Lunds University Faculty of Medicine, Lund, Sweden.

Abstract

OBJECTIVE:

To explore associations between high midnight salivary cortisol (MSC) secretion and high blood pressure (BP) in type 1 diabetes (T1D).

METHODS:

Cross sectional study of 196 adult patients with T1D (54% men). Associations between high MSC (≥9.3 nmol/l) and high systolic BP (>130 mm Hg), and high diastolic BP (>80 mm Hg) were explored for all patients, users and non-users of antihypertensive drugs (AHD). Adjustments were performed for age, sex, diabetes related variables, p-creatinine, smoking, physical inactivity, depression and medication.

RESULTS:

The prevalence of high MSC differed between patients with high and low systolic BP in all 196 patients: 39% versus 13 % (p = 0.001); in 60 users of AHD: 37% versus 12% (p = 0.039), and in 136 non-users of AHD: 43% versus 13% (p = 0.012). Significant associations with high systolic BP were for all patients: physical inactivity (adjusted odds ratio (AOR) 6.5), high MSC (AOR 3.9), abdominal obesity (AOR 3.7), AHD (AOR 2.9), age (per year) (AOR 1.07), and p-creatinine (per µmol/l) (AOR 1.03); for 60 users of AHD: high MSC (AOR 4.1) and age (per year) (AOR 1.11); for 136 non-users of AHD: abdominal obesity (AOR 27.4), physical inactivity (AOR 14.7), male sex (AOR 9.0), smoking (AOR 7.9), and age (per year) (AOR 1.08). High MSC was not associated with high DBP.

CONCLUSIONS:

In adult patients with T1D, high systolic BP was associated with physical inactivity, high MSC secretion, abdominal obesity, p-creatinine, age, and AHD, the latter indicating treatment failure.

PMID:
31671407
DOI:
10.1530/EC-19-0407
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