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1 transdermal nor oral ERT had any effects on baroreflex sensitivity.
2 ither baseline cardiovascular parameters nor baroreflex sensitivity.
3 ence between control and occlusion groups in baroreflex sensitivity.
4 ied Oxford technique to assess cardiac vagal baroreflex sensitivity.
5 ivity and negatively correlated with cardiac baroreflex sensitivity.
6 in an increase in HRV and an improvement in baroreflex sensitivity.
7 an increase in parasympathetic activity and baroreflex sensitivity.
8 heart, leading to hypertension and depressed baroreflex sensitivity.
9 vs. sham-operated SHR) and an improvement in baroreflex sensitivity.
10 trual cycle had no influences on cardiovagal baroreflex sensitivity.
11 ssed according to heart rate variability and baroreflex sensitivity.
12 renal sympathetic nerve activity and to test baroreflex sensitivity.
13 ors with a possible reduction in sympathetic baroreflex sensitivity.
14 amic Starling mechanism and arterial-cardiac baroreflex sensitivity.
15 ood pressure and a smaller change in cardiac baroreflex sensitivity.
16 ivity to higher pressures without changes in baroreflex sensitivity.
17 , employing heart rate variability (HRV) and baroreflex sensitivity.
18 ympathetic nerve activity without changes in baroreflex sensitivity.
19 r the Fontan operation, with reduced HRV and baroreflex sensitivity.
20 d more impaired autonomic balance, ie, lower baroreflex sensitivity (1.4 +/- 1.3 versus 5.0 +/- 1.5 m
21 hostatic intolerance had lower cardiac vagal baroreflex sensitivity (12+/-1 versus 25+/-4 ms/mm Hg; P
22 antecedent hypoglycemia leads to 1) reduced baroreflex sensitivity (16.7 +/- 1.8 vs. 13.8 +/- 1.4 ms
23 resulted in greater improvements in resting baroreflex sensitivity (2.3 ms/mm Hg [95% CI, 1.3 to 3.3
24 ntal Young's elastic modulus (-17%; P=0.03), baroreflex sensitivity (+28%; P=0.049), heart rate varia
25 , OR, 10; 95% CI, -1 to 21), lower mean (SD) baroreflex sensitivity (3.77 [0.79] vs 9.76 [2.92] s-3mm
26 One marker of these adaptations is decreased baroreflex sensitivity, a strong predictor of post-MI mo
29 c hypertrophy, pulmonary congestion, loss of baroreflex sensitivity (alpha index: SHAM = 3.64 +/- 1.0
30 eart rate [HR] recovery, HR variability, and baroreflex sensitivity) among 46-year-old adults from th
32 cal responsiveness to ACTH, but had enhanced baroreflex sensitivity and augmented plasma catecholamin
34 rt rate and blood pressure were recorded and baroreflex sensitivity and heart rate variability were d
36 cardiac vagal function, as measured by both baroreflex sensitivity and intrinsic cardiac neural acti
37 ostatic intolerance have lower cardiac vagal baroreflex sensitivity and marginally lower blood volume
40 goal was to test sympathetic and cardiovagal baroreflex sensitivity and the transduction of sympathet
41 ngiotensin II levels, inflammation, impaired baroreflex sensitivity, and autonomic dysfunction, as we
42 oexcitation, autonomic dysfunction, impaired baroreflex sensitivity, and enhanced blood pressure, whe
43 biomarkers included heart rate variability, baroreflex sensitivity, and flow-mediated dilation, alon
45 ormalized indexes of sympathetic outflow and baroreflex sensitivity, and reduced the incidence of apn
46 is an active posture test used in assessing baroreflex sensitivity, and the array of patients a phys
47 c nervous system--heart rate variability and baroreflex sensitivity--are reviewed, and the clinical a
51 aimed to evaluate left ventricular function, baroreflex sensitivity, autonomic modulation, and inflam
52 m, mean and maximum (+/-s.d.) supine control baroreflex sensitivities averaged 5 +/- 3, 18 +/- 6, and
53 fferences in the cardiovagal and sympathetic baroreflex sensitivities between phases under any condit
55 alysis of heart rate variability [HRV]), and baroreflex sensitivity (bolus phenylephrine method and a
56 systolic blood pressure, cardiac parameters, baroreflex sensitivity (BRS) and hyperinsulinemia in the
57 Although heart rate variability (HRV) and baroreflex sensitivity (BRS) are recognized as independe
60 lex function as indicated by the blunting of baroreflex sensitivity (BRS) following the antagonizatio
63 muscle sympathetic nerve activity (MSNA) and baroreflex sensitivity (BRS) in treated patients with hy
65 ter standard tests of autonomic function and baroreflex sensitivity (BRS) measurement, diabetic parti
71 bute to sympathetic overactivity, attenuated baroreflex sensitivity (BRS), and excessive ventilation
72 ventilatory recruitment threshold (VRT-CO2), baroreflex sensitivity (BRS), blood pressure, and blood
75 ailure (CHF) results in blunting of arterial baroreflex sensitivity (BRS), which arises from alterati
79 od pressure or heart rate, or to cardiovagal baroreflex sensitivity, but correlated with muscle sympa
80 /DeltaMAP, which does not involve changes in baroreflex sensitivity, but may involve changes in chemo
82 nism for the decrease in spontaneous cardiac baroreflex sensitivity (cBRS) during exercise in humans.
85 at 0.6 of gestation; however, fetal cardiac baroreflex sensitivity decreased with advancing gestatio
86 ared with baseline euglycemic conditions, 1) baroreflex sensitivity decreases significantly (19.2 +/-
88 d pressure and baroreflex threshold, reduced baroreflex sensitivity, diminished plasma catecholamine
89 d HR increase, systolic function impairment, baroreflex sensitivity drop, as well as pulse interval v
91 athetic neural responses but not sympathetic baroreflex sensitivity during orthostasis, though uprigh
92 x sensitivity with OC differ from changes in baroreflex sensitivity during the normal menstrual cycle
94 sibly 'steady-state' conditions, human vagal baroreflex sensitivity fluctuates in a major way, at ver
95 t during brief periods of observation, human baroreflex sensitivity fluctuates widely and rhythmicall
99 ween arrhythmic events and predictive tests (baroreflex sensitivity, heart rate turbulence, heart rat
101 mpathetic nerve activity and reduced cardiac baroreflex sensitivity heighten cardiovascular risk, alt
104 er, intravenous CV-11974 failed to alter the baroreflex sensitivities in area postrema-lesioned SHRs.
106 es were associated with baseline measures of baroreflex sensitivity in both CLBP and NP participants.
108 y 5959 affects the control of heart rate and baroreflex sensitivity in conscious dogs with pacing-ind
110 hough studies have examined resting arterial baroreflex sensitivity in older subjects, little attenti
111 mpathetic nerve activity and reduced cardiac baroreflex sensitivity in patients with RA compared to m
112 of ANA-12 into the dmNTS greatly diminished baroreflex sensitivity in sham rats, whereas it had less
113 e, and normalized heart rate variability and baroreflex sensitivity in TGA-PE rats compared to contro
115 s measurements of heart rate variability and baroreflex sensitivity in the neuromonitoring setting of
118 upled with impairments in renal function and baroreflex sensitivity, increased neuroinflammatory mark
120 on against sympathetic overdrive and loss of baroreflex sensitivity, independent markers of mortality
121 with laryngopharyngeal symptoms had reduced baroreflex sensitivity, indicating diminished vagal cont
122 eart rate variability, endothelial function, baroreflex sensitivity, inflammation, and platelet funct
126 Not only sympathetic but also cardiovagal baroreflex sensitivity is similar between sexes and mens
127 t, as measured by heart rate variability and baroreflex sensitivity, is significantly associated with
128 ns of physiological abnormalities: depressed baroreflex sensitivity low LF/HF low LF/(HF + LF) low al
131 function, including decreased cardiac vagal baroreflex sensitivity, may contribute directly to morta
132 ing age, left ventricular ejection fraction, baroreflex sensitivity, mean RR interval, standard devia
133 thetic nerve activity (MSNA) and sympathetic baroreflex sensitivity (MSNA-diastolic pressure relation
134 ivity (n=38), heart rate variability (n=34), baroreflex sensitivity (n=20), and ergoreflex activity (
138 No significant differences in cardiovagal baroreflex sensitivity or vascular transduction were obs
139 ent of heart rate variability (P<0.0001) and baroreflex sensitivity (P=0.03), and overactive ergorece
140 , it still decreased heart rate and restored baroreflex sensitivity (PI/SAP slope, 12.7+/-2.8 ms/mm H
141 central chemoreceptor sensitivity, arterial baroreflex sensitivity, plasma norepinephrine, epinephri
142 pathetic activity and increasing sympathetic baroreflex sensitivity plays a key role in promoting the
144 (integrated relaxation pressure) and reduced baroreflex sensitivity (r = -0.33; 95% CI, -0.58 to -0.0
148 emetry), autonomic function, and spontaneous baroreflex sensitivity (SBRS) were not significantly dif
150 fects heart rate, blood pressure regulation, baroreflex sensitivity, tissue oxygenation, and vascular
151 cardiovascular disease biomarkers including baroreflex sensitivity to quantify the influence of the
169 s measurements of heart rate variability and baroreflex sensitivity we aimed to test whether autonomi
171 y-four-hour ambulatory BP, SND, and arterial baroreflex sensitivity were measured before and after 8
172 t subjects, moderate ongoing fluctuations of baroreflex sensitivity were punctuated by brief major pe
176 art rate variability, heart rate turbulence, baroreflex sensitivity) were significant predictors of a
177 stiffness; (2) it is associated with reduced baroreflex sensitivity, which increases blood pressure v
180 amic Starling mechanism and arterial-cardiac baroreflex sensitivity, without changing dynamic arteria