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2 odium excretion was directly associated with systolic (4.58 mm Hg; 95% confidence interval [CI], 2.64
3 sessed using the following parameters: early systolic (_ES); slope of -volume relationship during sys
4 e primary outcome was placebo-corrected 24-h systolic ambulatory blood pressure reduction after 4 wee
5 tihypertensive medications while maintaining systolic and diastolic blood pressure <140 mm Hg and 90
6 ndations for the definition of hypertension, systolic and diastolic blood pressure (BP) thresholds fo
7 rs (SD 11) and mean baseline office and 24-h systolic and diastolic blood pressure levels were 154 (1
8 (GERA) cohort individuals provided 1,342,814 systolic and diastolic blood pressure measurements for a
9 ge range, the average rate of change in both systolic and diastolic blood pressure was greater among
11 s and others in biological (body-mass index, systolic and diastolic blood pressure, and handgrip stre
12 ) cholesterol, triglycerides, fat mass (FM), systolic and diastolic blood pressure, fasting insulin a
13 ts across eight cardiometabolic traits (BMI, systolic and diastolic blood pressure, LDL cholesterol,
14 ositively associated with self-reported IHD, systolic and diastolic blood pressure, low-density lipop
15 and identified several cis-eGenes (ALDH2 for systolic and diastolic blood pressure, MCM6 and DARS for
16 difference in the average rate of change in systolic and diastolic blood pressure, respectively, whe
18 ratio of TC to HDL cholesterol (TC:HDL), and systolic and diastolic blood pressures (SBP and DBP, res
19 (n = 11,767), we found significantly higher systolic and diastolic blood pressures among those who e
20 strongly associated with BP (P<10(-320)) for systolic and diastolic BP and CVD events regardless of t
21 e coprimary outcomes were the differences in systolic and diastolic BP changes from baseline to the e
22 lysis of the cross-sectional associations of systolic and diastolic BP with blood-derived genome-wide
26 ss hypertrophy, smaller left atria, and less systolic and diastolic dysfunction than FG+ probands wit
28 h LV concentric remodeling and impairment of systolic and diastolic function parameters, whereas an i
30 stitial collagen deposition and a decline in systolic and diastolic function were present only in WT
33 BK application in CHF rats increased cardiac systolic and diastolic volumes and further increased the
36 e adults with resistant hypertension (office systolic blood pressure >/=160 mm Hg despite taking at l
37 response syndrome criteria) and hypotension (systolic blood pressure </=90 mm Hg or mean arterial pre
39 gnificant between-group mean differences for systolic blood pressure (-1.26 mm Hg [95% CI, -1.77 to -
40 icantly lower adjusted time-weighted average systolic blood pressure (-17 mm Hg; 95% CI, -25 to -8; p
41 sium excretion was inversely associated with systolic blood pressure (-3.72 mm Hg; 95% CI, -6.01 to -
43 sion (OR = 1.6, 95% CI = 1.2-2.3), increased systolic blood pressure (1.2 per 20mmHg, 95% CI = 1.1-1.
44 ed in a factorial design to target levels of systolic blood pressure (130-149mmHg vs <130mmHg; open l
45 genes were associated with a 23 mm Hg higher systolic blood pressure (95% CI, 12-34; P=5.6*10(-5)) an
46 sly, an inverse association was observed for systolic blood pressure (hazard ratio=0.79 [95% CI: 0.68
47 R: 2.18; 95% CI: 1.58, 3.02), new-onset high systolic blood pressure (OR: 1.34; 95% CI: 1.05, 1.70),
48 compared with the HabDiet, resulted in lower systolic blood pressure (P-diet x time interaction = 0.0
50 6.9% = 1.33, OR7-7.9% = 1.86, OR8%+ = 3.22), systolic blood pressure (SBP) (ORper 10mmHg+ = 1.19), an
51 e aimed to test the hypothesis that elevated systolic blood pressure (SBP) across its usual spectrum
52 were associated under an additive model with systolic blood pressure (SBP) and age at diagnosis of hy
53 ement of Aortic Transcatheter Valve) who had systolic blood pressure (SBP) and an echocardiogram obta
54 cemic index (GI) and glycemic load (GL) with systolic blood pressure (SBP) and diastolic blood pressu
55 rom baseline to the end of the trial in both systolic blood pressure (SBP) and diastolic blood pressu
56 mference (WC), waist-to-height ratio (WHtR), systolic blood pressure (SBP) and diastolic blood pressu
58 anol users and control subjects (P = 0.040); systolic blood pressure (SBP) did not differ (P = 0.86).
60 servational studies have shown that elevated systolic blood pressure (SBP) is associated with future
64 vascular disease (ASCVD) risk to personalize systolic blood pressure (SBP) treatment goals is a topic
65 zed management strategy aimed at achieving a systolic blood pressure (SBP) within 10% of the referenc
67 ion of FR167653, p38 MAPK inhibitor, reduced systolic blood pressure (SBP), urinary albumin excretion
68 h interleukin-6 (Spearman r=0.33, P<0.0001), systolic blood pressure (Spearman r=0.28, P<0.0001), bod
69 1.4]; 22 trials, 2721 participants), diurnal systolic blood pressure (WMD, -2.4 points [95% CI, -3.9
70 re (hazard ratio=0.79 [95% CI: 0.68-0.92] at systolic blood pressure 160 vs 110 mm Hg) but not for di
71 % CI, -8.6 to -4.2; 6 studies; I2 = 51%) for systolic blood pressure and -4.0 mm Hg (95% CI, -5.6 to
72 ockers was associated with better control of systolic blood pressure and attenuation of decline in bo
73 ract surgery, PEX was associated with higher systolic blood pressure and more frequent ECG abnormalit
74 alysis to understand the indirect effects of systolic blood pressure and serum aldosterone on the rel
75 sity lipoprotein-cholesterol, triglycerides, systolic blood pressure and the incidence of the metabol
76 pressure, a slowdown in the increase of both systolic blood pressure and waist circumference, and a r
77 omparison with MESA, HealthLNK overestimated systolic blood pressure by 6.5 mm Hg (95% confidence int
80 nsin-aldosterone system genes associate with systolic blood pressure individually in both sexes, indi
83 nd 19.5% (95% CI, 18.5-20.5) met the SPRINT (Systolic Blood Pressure Intervention Trial) eligibility
84 he primary end point considering the SPRINT (Systolic Blood Pressure Intervention Trial) target reach
85 no diabetes mellitus from the SPRINT trial (Systolic Blood Pressure Intervention Trial): 4086 random
86 this population, we defined hypertension as systolic blood pressure of at least 140 mm Hg, or diasto
87 er among those who were assigned to a target systolic blood pressure of less than 120 mm Hg (intensiv
88 ceived intensive treatment, which targeted a systolic blood pressure of less than 120 mm Hg, were sim
89 dividualized assessment, to achieve a target systolic blood pressure of less than 140 mm Hg to reduce
90 ransient ischemic attack to achieve a target systolic blood pressure of less than 140 mm Hg to reduce
91 ly at or above 150 mm Hg to achieve a target systolic blood pressure of less than 150 mm Hg to reduce
92 atment in adults aged 60 years or older with systolic blood pressure persistently at or above 150 mm
94 poor neighborhoods was associated with lower systolic blood pressure than was consistent residence in
95 e analyses adjusting for age and sex, higher systolic blood pressure values were noted for the PEX gr
96 itional antihypertensive medication, and the systolic blood pressure was 14.8 mm Hg (95% confidence i
98 TR1) were individually associated with lower systolic blood pressure with significant (P<0.00076) eff
100 ng, rectal examination findings, heart rate, systolic blood pressure, and haemoglobin concentration s
101 rmediate outcomes of hemoglobin A1c, weight, systolic blood pressure, and heart rate; all-cause morta
102 seline in glycated hemoglobin level, weight, systolic blood pressure, and mean daily bolus dose of in
103 , injury severity score, Glascow Coma Scale, systolic blood pressure, base excess, platelet count, he
104 adjustment for age, sex, diabetes diagnosis, systolic blood pressure, BMI, smoking status, estimated
105 risk, management targeting an individualized systolic blood pressure, compared with standard manageme
107 or cognitive ability in youth), BMI, height, systolic blood pressure, coronary artery disease, and ty
108 educational attainment predicted lower BMI, systolic blood pressure, coronary artery disease, type 2
109 eristics following stratification, including systolic blood pressure, history of diabetes mellitus or
110 adjusting for age, race, body surface area, systolic blood pressure, history of hypertension, curren
111 SGLT2 inhibition caused marked decreases in systolic blood pressure, kidney weight/body weight ratio
112 ment for age, sex, heart rate, hypertension, systolic blood pressure, left ventricular ejection fract
113 lder, had longer hemodialysis vintage, lower systolic blood pressure, lower ultrafiltration rates, hi
114 14) with more than 1 million measurements of systolic blood pressure, total cholesterol, and high-den
120 ardiovascular disease who received intensive systolic blood-pressure control (target, <120 mm Hg) had
122 ned 9361 participants with hypertension to a systolic blood-pressure target of less than 120 mm Hg or
123 etes mellitus, intensive BP lowering (target systolic BP <120 mm Hg) compared with standard BP loweri
124 hypertensive patients, intensive BP control (systolic BP <140 mm Hg) decreased MACE, including cardio
125 ) compared with standard BP lowering (target systolic BP <140 mm Hg) resulted in lower rates of devel
126 women, black race, and 3 levels of baseline systolic BP (</=132 versus >132 to <145 versus >/=145 mm
127 an increase in the low frequency spectra of systolic BP (13.9 +/- 4.3% total power; P < 0.001), indi
129 ociated with a 1.04-mm Hg decrement in adult systolic BP (95% confidence interval (CI): -2.14, 0.06)
131 regression models, each 1-mm Hg increment in systolic BP (SBP) was associated with 0.8% (95% confiden
135 to percentiles from the 81.6th to 99.9th for systolic BP and from the 92.9th to 98.9th for diastolic
136 ice with Tmem27(Y/-) kidneys had the highest systolic BP and were the only group to exhibit glomerula
137 tervention period, but in the intensive arm, systolic BP decreased from 160 mmHg at baseline to 143 m
138 the standard arm, the 2-week moving average systolic BP did not change significantly during the inte
139 yle score) had 3.6, 3.5, and 3.6 mm Hg lower systolic BP in low, middle, and high genetic risk groups
140 e is a modest but significant improvement in systolic BP in randomized controlled trials of self-meas
143 versus -6.8/-3.5 mm Hg, respectively, Delta systolic BP P=3x10(-4), Delta diastolic BP P=5x10(-5)).
145 e and the increased low frequency spectra of systolic BP response were fully maintained despite RVLM
146 stolic BP target <140 mm Hg) with intensive (systolic BP target <120 mm Hg) BP treatment and data fro
149 trends were not consistent, for both sexes, systolic BP z-score was stable from 1999, decreased slig
152 ng treatment interactions with age, baseline systolic BP, and diastolic BP, and the SAE model had 8 v
153 served no significant difference in achieved systolic BP, AngII-treated APA-KO mice developed a signi
154 risk of CKD per 1-SD decrease in mean asleep systolic BP, independent of changes in mean clinic BP or
155 isk exposure between ages 6 and 24 years) of systolic BP, total-cholesterol, and smoking associated i
158 ydrochlorothiazide versus noncarriers (Delta systolic BP/Delta diastolic BP: -12.3/-8.2 versus -6.8/-
159 ism by which changes of the amplitude of the systolic Ca transient control diastolic [Ca(2+) ]i .
160 panied by a decrease of the amplitude of the systolic Ca transient, such that there was no change of
161 show that the ability to dynamically change systolic Ca(2+) , through changes in expression of key C
164 the aortic banding model, the sensitivity of systolic Ca(2+) to LCC density and diastolic Ca(2+) to S
169 olic peak (peak ); and diastolic uncoupling (systolic -diastolic at same volume) during early diastol
170 changes on electrocardiography; decreased LV systolic, diastolic diameter, or septal E' velocity; hig
172 plained 2.9%, 2.5%, and 3.1% of variation in systolic, diastolic, and pulse pressure, respectively, i
174 eport genetic association of blood pressure (systolic, diastolic, pulse pressure) among UK Biobank pa
175 icipants, 40 to 79 years of age, with clinic systolic/diastolic BP <140/90 mm Hg, who completed ambul
176 mg/L reduction in sodium in drinking water, systolic/diastolic BP was lower on average by 0.95/0.57
178 ed whether an internally scaled index of end-systolic dimension is incremental to well-validated prog
179 failure, and increased left ventricular end-systolic dimension zscore at diagnosis were independentl
181 hat all LV parameters (LV end-diastolic and -systolic dimensions, ejection fraction, and fractional s
183 trial fibrillation (AF) and left ventricular systolic dysfunction (LVSD) frequently co-exist despite
185 ical Rate Control in Atrial Fibrillation and Systolic Dysfunction [CAMERA-MRI]; ACTRN12613000880741).
186 pendently associated with the development of systolic dysfunction among moderate-severe traumatic bra
187 trial and ventricular remodeling, along with systolic dysfunction and comparable intra-cardiac fibros
189 Patients with concomitant moderate AS and LV systolic dysfunction are at high risk for clinical event
190 cal data of patients with moderate AS and LV systolic dysfunction between 2010 and 2015 from 4 large
192 valve area between 1.0 and 1.5 cm(2) and LV systolic dysfunction defined as LV ejection fraction <50
193 dinal course, and admission risk factors for systolic dysfunction in patients with moderate-severe tr
196 of future arrhythmic events in patients with systolic dysfunction using the gold standard of cardiova
197 ssessed by transthoracic echocardiogram, and systolic dysfunction was defined as fractional shortenin
199 t ventricular ejection fraction, isolated RV systolic dysfunction was found in 7 (4.4%) patients, 2 o
200 osis was present in 55 patients (72%) and LV systolic dysfunction was identified in 13 patients (24%)
201 on was used to verify the relationship of RV systolic dysfunction with age, sex, functional class, us
202 0%) mild traumatic brain injury patients had systolic dysfunction within the first day after injury (
203 re commonly associated with left ventricular systolic dysfunction, although isolated and early RV dys
205 (-/-) mice developed cardiac hypertrophy and systolic dysfunction, evidenced by a 5-fold greater hear
211 years) complicated by left ventricular (LV) systolic dysfunction; (2) an age- and sex- matched hyper
213 g-axis function-lateral mitral annular plane systolic excursion (MAPSE)-in a large multicenter popula
215 ranscranial Doppler (vTCD) of straight sinus systolic flow velocity (FVsv), and methods derived from
218 mary outcome measures: left ventricular (LV) systolic function (left ventricular ejection fraction),
219 AAS users demonstrated relatively reduced LV systolic function (mean+/-SD left ventricular ejection f
220 nylephrine was inversely related to baseline systolic function (P < 0.05) and associated with markers
221 ndices to characterize left ventricular (LV) systolic function and its relationship to activation of
224 erload stress induces a deeper impairment of systolic function in patients with more advanced degrees
225 is the unexplained loss of maternal cardiac systolic function in the period surrounding parturition.
228 infarct size and preserving left ventricular systolic function is primary percutaneous coronary inter
230 s, 86+/-41 [46-195] g/m(2)) was progressive, systolic function mainly preserved (cardiac index 2.8+/-
231 lysis included 21 cohorts for structural and systolic function traits (n = 32,212) and 17 cohorts for
234 dimension, and RV and left ventricular (LV) systolic function were determined by RV fractional area
237 ng at night ("sleep apnea") in patients with systolic heart failure (HF) have failed to improve progn
238 valuated and is used in select patients with systolic heart failure and chronic stable angina without
240 efibrillators] in Patients With Non-Ischemic Systolic Heart Failure on Mortality) did not demonstrate
241 prevention ICD in patients with nonischemic systolic heart failure warrants further investigation.
245 eeks in patients with recently decompensated systolic HF treated with anakinra, whereas an improvemen
249 ation (N=58) showed significantly reduced LV systolic (left ventricular ejection fraction = 49+/-10%
253 therapy), blood pressure control (<140 mm Hg systolic, <90 mm Hg diastolic), angiotensin-converting e
255 ts analysis was used to identify patterns of systolic motion that were most strongly predictive of su
256 MWS was associated with lower, whereas early systolic MWS was associated with greater LA function, in
257 independent correlates of LA function, late systolic MWS was associated with lower, whereas early sy
261 essure (dp/dtmax ), and the slope of the end-systolic P-V relationship (ESPVR), suggesting that acute
262 me relationship during systole (Sslope); end-systolic peak (peak ); and diastolic uncoupling (systoli
264 ongitudinal motion (decreased mitral annular systolic peak velocities: control median, 0.11 m/s [inte
265 ular diameters compared with sizing based on systolic-phase multidetector computerized tomographic (M
266 Participants were exposed to intensive (goal systolic pressure < 120 mm Hg) versus standard (<140 mm
267 increased heart rate (HR), left ventricular systolic pressure (LVSP), the maximum first derivative o
268 able echocardiogram-derived pulmonary artery systolic pressure (PASP) from the Jackson Heart Study (N
269 n fraction) with PH (HF-PH; pulmonary artery systolic pressure [PASP] >/=40 mm Hg) were compared to n
271 ity score of 3 or greater) and a prehospital systolic pressure between 40 and 119 mm Hg were included
274 horacic Surgeons score and right ventricular systolic pressure were 2+/-3 and 15+/-16 mm Hg, respecti
275 ces in age, country, hospital location, era, systolic pressure, mean arterial pressure, lactate, bund
276 A TR signals, echocardiographic measures of systolic pulmonary arterial pressure correlated reasonab
277 trial than left atrial enlargement and lower systolic pulmonary artery pressure compared with left-si
280 inal systolic strain and strain rate (SR) at systolic (SRs), early diastolic (SRe), and late diastoli
281 demonstrated higher peak atrial longitudinal systolic strain (39.34+/-7.99% versus 37.95+/-7.96%; P<0
284 ent more pronounced peak atrial longitudinal systolic strain functional decay than those of men (P va
285 d the relationship between the ADC value and systolic strain in hypertensive patients with left ventr
286 tricular pressure difference (EIVPD) and the systolic strain rate were higher in patients with cirrho
288 nds assembled as a functional syncytium; (2) systolic twitch forces at a similar level as observed in
290 d-diastolic volume (-18 mL; P=0.009) and end-systolic volume (-14 mL; P=0.005) occurred at end infusi
292 s of death (P < 0.01): right ventricular end-systolic volume index adjusted for age and sex, and the
293 anatomy, and left ventricular function, end-systolic volume index and B-type natriuretic peptide wer
294 f left ventricular ejection fraction and end-systolic volume, but not with the severity of brain or b
296 t reduction of left ventricular volumes (end-systolic volume: -4.3 [11.3] versus 7.4 [11.8], P=0.02;
297 indexed RV end-diastolic volumes and RV end-systolic volumes (RVESVi) (indexed RV end-diastolic volu
298 ry were associated primarily with changes in systolic volumes, longitudinal and circumferential strai
300 ess (hypertrophy) and function (diastolic or systolic), which lack mechanistic specificity, paradigms
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