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1 kers have vascular protective effects beyond blood pressure lowering.
2 lt of CHF, even in the setting of aggressive blood pressure lowering.
3 at with losartan monotherapy, independent of blood pressure lowering.
4 e vast amount of evidence on the benefits of blood pressure lowering accumulated to date, elevated bl
5 ral bioavailability in rats and demonstrated blood pressure lowering activity in the double-transgeni
6 l dogs to assess its biological actions as a blood pressure-lowering agent and as a natriuretic facto
7 mised trials from around the world comparing blood pressure-lowering agents in adults with diabetic k
8 s a factorial randomized controlled trial of blood pressure lowering and blood glucose control in pat
9 r likelihood of new-onset AF, independent of blood pressure lowering and treatment modality in essent
10 f CV morbidity and mortality, independent of blood pressure lowering and treatment modality in person
11 linical end points, additional to effects of blood pressure lowering and treatment modality.
12  that a novel conjugated oral hBNP possesses blood pressure-lowering and natriuretic actions over a 6
13 erapy (polypill) that combines antiplatelet, blood pressure-lowering, and cholesterol-lowering medica
14 eview focuses on the role of lipid-lowering, blood pressure-lowering, antithrombotic drugs and diet a
15 he Anglo-Scandinavian Cardiac Outcomes Trial Blood Pressure Lowering Arm (ASCOT-BPLA) compared amlodi
16 he Anglo-Scandinavian Cardiac Outcomes Trial-Blood Pressure Lowering Arm (ASCOT-BPLA) show significan
17 e Anglo-Scandinavian Cardiac Outcomes Trial--Blood Pressure Lowering Arm (ASCOT-BPLA) whose BP remain
18 n (Anglo-Scandinavian Cardiac Outcomes Trial Blood Pressure Lowering Arm [ASCOT-BPLA]).
19 A (Anglo-Scandinavian Cardiac Outcomes Trial-Blood Pressure Lowering Arm).
20 iting picomolar binding affinity and in vivo blood pressure lowering at pharmaceutically relevant dos
21 ve important mechanisms of action apart from blood pressure lowering but also that effective treatmen
22 t-trial follow-up for a median of 5.9 years (blood-pressure-lowering comparison) or 5.4 years (glucos
23 rtension from households able to afford four blood pressure-lowering drug classes were more likely to
24 tment with antiplatelet, lipid-lowering, and blood pressure lowering drugs (all p<0.0001).
25 -controlled trials of 4 different classes of blood pressure-lowering drugs (thiazides, beta-blockers,
26  were 17,641 participants who were allocated blood pressure-lowering drugs and 6603 who were allocate
27  a quadpill-a single capsule containing four blood pressure-lowering drugs each at quarter-dose (irbe
28 ct from the practical benefits of the use of blood pressure-lowering drugs in preventing headaches an
29 med to investigate the benefits and harms of blood pressure-lowering drugs in this population of pati
30                        Our results show that blood pressure-lowering drugs prevent a significant prop
31              Uncertainty exists over whether blood pressure-lowering drugs prevent headache.
32   The availability of two or more classes of blood pressure-lowering drugs was lower in low-income an
33  pressure >/=140/90 mm Hg or those receiving blood pressure-lowering drugs) had a lifetime risk of ov
34 tihypertensive action of diuretics and other blood pressure-lowering drugs.
35 kidney disease comparing orally administered blood pressure-lowering drugs.
36          To prevent stroke most effectively, blood-pressure-lowering drugs should reduce mean blood p
37 y disease) who were receiving at least three blood-pressure-lowering drugs, including a diuretic, at
38 hypothalamic NPYergic mechanisms mediate the blood pressure lowering effect of caloric restriction in
39 ypertension in mice and exerts a significant blood pressure lowering effect on preexisting hypertensi
40 r the renal protection, independent from its blood pressure lowering effect, have not yet been fully
41                 Finally, fish oil has a mild blood pressure-lowering effect in both normal and mildly
42 hose affecting BNP did not, highlighting the blood pressure-lowering effect of ANP in the general pop
43                                            A blood pressure-lowering effect of calcium supplementatio
44 e effect of kallistatin yet it abolished the blood pressure-lowering effect of kinin and kallikrein.
45                                          The blood pressure-lowering effect of SKA-31 suggests KCa3.1
46 iologic effects of angiotensin-(1-7) favor a blood pressure-lowering effect.
47 nction, and fibrosis, despite the absence of blood pressure-lowering effect.
48 sensitive model was inversely related to its blood pressure-lowering effect.
49 ebo-controlled trials probably result from a blood-pressure-lowering effect.
50 new class of direct renin inhibitors exerted blood pressure lowering effects in a hypertensive double
51 ber indicate that the strongest evidence for blood pressure lowering effects is in hypertensive as op
52                        The selective central blood pressure-lowering effects of nitrite have therapeu
53                       It is assumed that the blood pressure-lowering effects of reducing sodium intak
54 e of 80-89 mm Hg to test the feasibility and blood pressure-lowering effects of seven nonpharmacologi
55                                 Although the blood pressure-lowering effects of sodium-glucose cotran
56 m vegetables and fruit may contribute to the blood pressure-lowering effects of the Dietary Approache
57                        However, evidence for blood pressure-lowering effects of vitamin C in clinical
58 n contrast, in monkeys, EGF had dose-related blood pressure-lowering effects only; significant hypote
59                 The pooled placebo-corrected blood pressure-lowering effects were 5/2 mm Hg and 7/5 m
60                          We investigated the blood-pressure-lowering effects of the new vasodilatory,
61  Denervation for Hypertension) confirmed the blood pressure-lowering efficacy of renal denervation ad
62 rovide biological proof of principle for the blood-pressure-lowering efficacy of renal denervation.
63                                 In contrast, blood pressure lowering, estimated glomerular filtration
64  an event rate of 1.2% per year in intensive blood pressure-lowering group participants, compared wit
65 istent across patient groups, and additional blood pressure lowering had a clear benefit even in pati
66 vity profile and demonstrated robust in vivo blood pressure lowering in a spontaneously hypertensive
67 icyclic thiazepinone, demonstrated excellent blood pressure lowering in a variety of animal models ch
68 ubstituted azepinone, demonstrated excellent blood pressure lowering in animal models.
69              Thus, the long-term benefits of blood pressure lowering in early adulthood are promising
70       The net absolute benefits of intensive blood pressure lowering in high-risk individuals are lar
71 geted hemorrhagic shock, icatibant prevented blood pressure lowering in the angiotensin-converting en
72 based renal denervation produced significant blood pressure lowering in treatment-resistant patients
73  are additional benefits from more intensive blood pressure lowering, including for those with systol
74                            Finally, although blood pressure lowering is undoubtedly beneficial, the c
75 se risk in middle-aged people mainly through blood pressure-lowering mechanisms.
76 )albuminuria, the use of lipid-modifying and blood pressure-lowering medication, and prior cardiovasc
77       To examine whether treatment with oral blood-pressure-lowering medication or statins influences
78 d-lowering (19.2% versus 4.8%; P<0.001), and blood pressure-lowering medications (23.3% versus 12.1%;
79 s, treatment was based on the regular use of blood pressure-lowering medications, and control was def
80 ated patients were taking 2 or more types of blood pressure-lowering medications.
81 ailable were more likely to use at least one blood pressure-lowering medicine (adjusted odds ratio [O
82 classes were more likely to use at least one blood pressure-lowering medicine (adjusted OR 1.42, 95%
83 ountries do not have access to more than one blood pressure-lowering medicine and, when available, th
84                Ensuring access to affordable blood pressure-lowering medicines is essential for contr
85 roportion of households unable to afford two blood pressure-lowering medicines was 31% in low-income
86 0.0001) than were those in communities where blood pressure-lowering medicines were not available.
87 he availability, costs, and affordability of blood pressure-lowering medicines with data recorded fro
88 assess the availability and affordability of blood pressure-lowering medicines, and the association w
89 vascular disease (a statin, aspirin, and two blood-pressure-lowering medicines) in 23 such countries.
90 e prevention beyond the expected benefits of blood pressure lowering per se.
91 ne system inhibiting, cardiac unloading, and blood pressure lowering properties when compared with na
92 s of BTPs points toward antiinflammatory and blood pressure-lowering properties and improvement in pl
93                                          Its blood pressure-lowering properties were particularly fav
94 ions of the natriuretic peptides, which have blood pressure-lowering properties.
95                                    Intensive blood pressure lowering provided greater vascular protec
96  control (placebo or less intensive regimen) blood pressure-lowering regimen.
97                                              Blood pressure lowering significantly reduces vascular r
98 nts uncertainty about whether more intensive blood pressure-lowering strategies are associated with g
99    These findings emphasise the need for new blood pressure-lowering strategies, and will help to inf
100  assess the efficacy and safety of intensive blood pressure-lowering strategies.
101                                           No blood pressure-lowering strategy prolonged survival in a
102 sive low-density lipoprotein cholesterol and blood pressure lowering therapy slowed disease progressi
103 efficacy and safety of quarter-standard-dose blood pressure-lowering therapy against placebo.
104                                              Blood pressure-lowering therapy is likely to prevent str
105 hat the main driver of clinical benefit from blood pressure-lowering therapy is the magnitude of bloo
106 served among patients originally assigned to blood-pressure-lowering therapy were attenuated but stil
107     In PAD patients with diabetes, intensive blood pressure lowering to a mean of 128/75 mm Hg result
108                              The benefits of blood pressure lowering treatment for prevention of card
109  pressures less than 130 mm Hg and providing blood pressure lowering treatment to individuals with a
110          All randomised controlled trials of blood pressure lowering treatment were eligible for incl
111                                    Intensive blood pressure-lowering treatment achieved RR reductions
112 he benefit or risk associated with intensive blood pressure-lowering treatment can be established onl
113 andomisation, patients in the more intensive blood pressure-lowering treatment group had mean blood p
114 w of evidence that the risks and benefits of blood pressure-lowering treatment in acute stroke might
115 s that caution should be taken in the use of blood pressure-lowering treatment in patients with coron
116 n or placebo therapy was not modified by the blood pressure-lowering treatment strategy in the factor
117        Spironolactone was the most effective blood pressure-lowering treatment, throughout the distri
118 ants to more intensive versus less intensive blood pressure-lowering treatment, with different blood
119  been observed in the group receiving active blood-pressure-lowering treatment during the trial were
120 alizations for heart failure, independent of blood pressure lowering, treatment method, and other ris
121 iovascular disease, a fifth of whom received blood pressure-lowering treatments.
122 the beneficial effects of lipid-reducing and blood pressure-lowering treatments.
123 nalysis, we searched MEDLINE for large-scale blood pressure lowering trials, published between Jan 1,
124                                          For blood pressure-lowering trials (n=13), 3 were not congru
125       Serious adverse events associated with blood pressure lowering were only reported by six trials

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