Prevention of hypertension in patients with prehypertension in the rural areas of China: a community-based quasi-experiment
Haijian Guo MPH, Xuanxuan Wang PhD, Jinshui Xu
MPH, Tao Mao MPH 及 Jiaying Chen Prof
Lancet, The, 2018-10-01, 卷 392, 頁面 S82-S82, Copyright
© 2018 Elsevier Ltd
People with prehypertension are highly likely to develop
hypertension and other cardiovascular diseases. Lifestyle modifications
may prevent hypertension in patients with prehypertension, but evidence
remains scarce in developing countries. This study aimed to investigate
whether a community-based intervention could prevent hypertension
through lifestyle modifications in people with prehypertension in the
rural areas of China.
A community-based quasi-experiment design was applied. Eighteen
villages from six townships in Sheyang county, a rural area in eastern
China, were randomly sampled. Of these local residents, patients with
prehypertension—a systolic blood pressure (SBP) of 120–139 mm Hg or a
diastolic blood pressure (DBP) of 80–89 mm Hg—and who were 30–60 years
old were screened. Participants from three of the townships (n=206)
were randomly assigned to the intervention group, and those from the
other three townships (n=250) were assigned to the control group. At
the outset, intervention group participants received individual
consultations from a community health management team to assess their
self-management ability, determine their lifestyle, set goals for a
healthier lifestyle, and design individualised action plans. A
guideline booklet was provided to intervention group participants,
which contained detailed explanations of hypertension, prehypertension,
healthy lifestyles and their impacts, and methods to lose weight, cease
smoking, and deal with mental pressure. Intervention group participants
also received quarterly follow-ups to assess the implementation of
action plans, identify difficulties in changing unhealthy lifestyles,
and find feasible solutions. In both intervention and control groups,
usual care was provided to participants according to national
guidelines, and the available resources were the same across the
townships. Evaluations were conducted at baseline, and at the end of
months 6, 12, 18, and 30. Between-group analyses were performed using
repeated measures ANOVA. Written informed consent was obtained from the
participants.
At 30 months, 18 participants in the intervention group (n=188) showed progression to hypertension, whereas 47 in the control group (n=234) developed hypertension. This difference between intervention and control groups was statistically significant (9.6 vs 20.1%, p=0.007). Significant changes in DBP (–2.7 vs 0.7 mmHg, p<0·0001), weight (–0.79 vs −0.66 kg, p=0.029), and daily walking steps (11 500 vs 8000 steps, p<0.0001) were observed between intervention and control groups. No differential effects were found for SBP, drinking, and smoking, with both groups showing substantial improvements.
Long-term mortality after blood pressure-lowering and lipid-lowering treatment in patients with hypertension in the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT) Legacy study: 16-year follow-up results of a randomised factorial trial
Ajay Gupta MRCP, Judith Mackay MRCP, Andrew
Whitehouse MBBS, Thomas Godec MSc, Tim Collier MSc, Stuart Pocock Prof,
Neil Poulter Prof 及 Peter Sever Prof
Lancet, The, 2018-09-29, 卷 392, 期 10153, 頁面 1127-1137,
Copyright © 2018 Elsevier Ltd
In patients with hypertension, the long-term cardiovascular and
all-cause mortality effects of different blood pressure-lowering
regimens and lipid-lowering treatment are not well documented,
particularly in clinical trial settings. The Anglo-Scandinavian Cardiac
Outcomes Trial (ASCOT) Legacy Study reports mortality outcomes after 16
years of follow-up of the UK participants in the original ASCOT trial.
ASCOT was a multicentre randomised trial with a 2 × 2 factorial
design. UK-based patients with hypertension were followed up for
all-cause and cardiovascular mortality for a median of 15.7 years (IQR
9.7–16.4 years). At baseline, all patients enrolled into the blood
pressure-lowering arm (BPLA) of ASCOT were randomly assigned to receive
either amlodipine-based or atenolol-based blood pressure-lowering
treatment. Of these patients, those who had total cholesterol of 6.5
mmol/L or lower and no previous lipid-lowering treatment underwent
further randomisation to receive either atorvastatin or placebo as part
of the lipid-lowering arm (LLA) of ASCOT. The remaining patients formed
the non-LLA group. A team of two physicians independently adjudicated
all causes of death.
Of 8580 UK-based patients in ASCOT, 3282 (38.3%) died, including 1640 (38.4%) of 4275 assigned to atenolol-based treatment and 1642 (38.1%) of 4305 assigned to amlodipine-based treatment. 1768 of the 4605 patients in the LLA died, including 903 (39.5%) of 2288 assigned placebo and 865 (37.3%) of 2317 assigned atorvastatin. Of all deaths, 1210 (36.9%) were from cardiovascular-related causes. Among patients in the BPLA, there was no overall difference in cardiovascular mortality between treatments (adjusted hazard ratio [HR] 0.90, 95% CI 0.81–1.01, p=0.0776]), although significantly fewer deaths from stroke (adjusted HR 0.71, 0.53–0.97, p=0.0305) occurred in the amlodipine-based treatment group than in the atenolol-based treatment group. There was no interaction between treatment allocation in the BPLA and in the LLA. However, in the 3975 patients in the non-LLA group, there were fewer cardiovascular deaths (adjusted HR 0.79, 0.67–0.93, p=0.0046) among those assigned to amlodipine-based treatment compared with atenolol-based treatment (p=0.022 for the test for interaction between the two blood pressure treatments and allocation to LLA or not). In the LLA, significantly fewer cardiovascular deaths (HR 0.85, 0.72–0.99, p=0.0395) occurred among patients assigned to statin than among those assigned placebo.
Angiotensin-Converting Enzyme Inhibitors vs.
Angiotensin Receptor Blockers for the Treatment of Hypertension in
Adults With Type 2 Diabetes: Why We Favour Angiotensin Receptor
Blockers
Thomas A. Mavrakanas MD 及 Mark L. Lipman MD
Canadian Journal of Diabetes, 2018-04-01, 卷 42, 期 2,
頁面 118-123, Copyright © 2017 Diabetes Canada
Prevention and Control of Hypertension
Robert M. Carey MD, Paul Muntner PhD, Hayden B.
Bosworth PhD 及 Paul K. Whelton MB, MD, MSc
JACC (Journal of the American College of Cardiology),
2018-09-11, 卷 72, 期 11, 頁面 1278-1293, Copyright © 2018 American College
of Cardiology Foundation
Blood Pressure Control and Cardiovascular Outcomes in Patients With Atrial Fibrillation (From the ORBIT-AF Registry)
Sreekanth Vemulapalli MD, Taku Inohara MD,
Sunghee Kim PhD, Laine Thomas PhD, Jonathan P. Piccini MD, MHS, Manesh
R. Patel MD, Paul Chang MD, Gregg C. Fonarow MD, Michael D. Ezekowitz
MB, ChB, Elaine Hylek MD, Alan S. Go MD, Peter R. Kowey MD, Kenneth W.
Mahaffey MD, Bernard J. Gersh MB, ChB, DPhil 及 Eric D. Peterson MD, MPH
American Journal of Cardiology, The, 2019-05-15, 卷
123, 期 10, 頁面 1628-1636, Copyright © 2019 Elsevier Inc.
Arterial hypertension in cancer: The elephant in the room
Giacomo Tini, Matteo Sarocchi, Giuliano Tocci,
Eleonora Arboscello, Giorgio Ghigliotti, Giuseppina Novo, Claudio
Brunelli, Daniel Lenihan, Massimo Volpe 及 Paolo Spallarossa
International Journal of Cardiology, 2019-04-15, 卷
281, 頁面 133-139, Copyright © 2019 Elsevier B.V.
The great therapeutical success achieved by
oncology is counterbalanced by growing evidences of cardiovascular (CV)
toxicity due to many antineoplastic treatments. Cardiac adverse events
may cause premature discontinuation of effective oncologic treatments
or occur as late events undermining the oncologic success. Arterial
hypertension is both the most common comorbidity in cancer patients and
a frequent adverse effect of anticancer therapies.
A pre-existing hypertension is known to increase the risk of other
cardiac adverse events due to oncologic treatments, in particular heart
failure. Moreover, as a strict association between cancer and CV
diseases has emerged over the recent years, various analyses have shown
a direct relationship between hypertension and cancer incidence and
mortality. Finally, many antineoplastic treatments may cause a rise in
blood pressure (BP) values, particularly the novel anti VEGF agents,
this possibly compromising efficacy of chemotherapy.
Aim of this review is to revise the topic and the many aspects linking
arterial hypertension and cancer, and to provide a comprehensive and
practical guide of the current treatment approaches.
Endovascular ultrasound renal denervation to treat hypertension (RADIANCE-HTN SOLO): a multicentre, international, single-blind, randomised, sham-controlled trial
Michel Azizi Prof, Roland E Schmieder Prof, Felix
Mahfoud Prof, Michael A Weber Prof, Joost Daemen MD, Justin Davies
MBBS, Jan Basile MD, Ajay J Kirtane MD, Yale Wang MD, Melvin D Lobo
PhD, Manish Saxena MBBS, Lida Feyz MD, Florian Rader MD, Philipp Lurz
MD, Jeremy Sayer MD, Marc Sapoval Prof, Terry Levy MBChB, Kintur
Sanghvi MD, Josephine Abraham MD, Andrew S P Sharp MD, Naomi D L Fisher
MD, Michael J Bloch MD, Helen Reeve-Stoffer PhD, Leslie Coleman DVM,
Christopher Mullin MS 及 Laura Mauri Prof
Lancet, The, 2018-06-09, 卷 391, 期 10137, 頁面 2335-2345,
Copyright © 2018 Elsevier Ltd
Impact of antihypertensive agents on arterial stiffness in hypertensive patients
Liwen Ye, Xixi Yang, Jie Hu, Qingwei Chen, Jian
Wang 及 Xingsheng Li
International Journal of Cardiology, 2018-12-15, 卷
273, 頁面 207-212, Copyright © 2018
Flavonoids in hypertension: a brief review of the underlying mechanisms
Dina Maaliki, Abdullah A Shaito, Gianfranco
Pintus, Ahmed El-Yazbi 及 Ali H Eid
Current Opinion in Pharmacology, 2019-04-01, 卷 45, 頁面
57-65, Copyright © 2019 Elsevier Ltd
• Increased flavonoid consumption imparts antihypertensive
benefits.
• Luteolin, Quercetin, Kaempferol, Epicatechin, and Daidzein increase
eNOS activity.
• Many flavonoids reduce oxidative stress and improve endothelial
function.
• Many flavonoids induce vasodilation by modulating K + and
Ca 2+ ion
channels.
Flavonoids are a diverse group of bioactive polyphenolic
compounds abundant in dietary plants and herbs. Regular consumption of
flavonoids exerts cardio-vasculoprotective effects and may reduce the
onset or progression of many cardiovascular diseases, particularly
hypertension. Observational studies suggest inverse associations among
either of these three combinations: a) anthocyanin intake and risk of
myocardial infarction (MI), b) flavanone intake and risk of ischemic
stroke and c) flavonol intake and risk of type 2 diabetes mellitus.
Human randomized controlled trials (RCTs) show that catechins and
quercetin impart significant blood pressure lowering effects.
Mechanistically, flavonoids mediate their antihypertensive effects
through increasing nitric oxide (NO) bioavailability, reducing
endothelial cell oxidative stress or modulating vascular ion channel
activity. In this review, we focus on the six main subgroups of
flavonoids, namely flavones, flavonols, flavanols, flavanones,
anthocyanins, and isoflavones. We further discuss their
antihypertensive effects, and their possible mechanisms of regulating
blood pressure. We conclude by addressing the safety of these compounds
as well as their potential use in hypertension management and treatment.
Effects of exercise training on endothelial function in individuals with hypertension: a systematic review with meta-analysis
Marinei L. Pedralli MSc, Bruna Eibel PhD, Gustavo
Waclawovsky MSc, Maximiliano I. Schaun PhD, Walter Nisa-Castro-Neto
PhD, Daniel Umpierre PhD, Linda S. Pescatello PhD, Hirofumi Tanaka PhD
及 Alexandre Machado Lehnen PhD
Journal of the American Society of Hypertension,
2018-12-01, 卷 12, 期 12, 頁面 e65-e75, Copyright © 2018 American Heart
Association