Evidence-based approach for managing hypertension in type 2 diabetes
Integrated Blood Pressure Control
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Evidence-based approach for managing
hypertension in type 2 diabetes
This article was published in the following Dove Press journal:
Integrated Blood Pressure Control
24 May 2010
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Gerti Tashko 1
Robert A Gabbay 2
Division of Endocrinology, Diabetes,
and Metabolism, Penn State College of
Medicine, Hershey, PA, USA; 2Penn State
Institute for Diabetes and Obesity,
Penn State College of Medicine, Penn
State Milton S Hershey Medical Center,
Hershey, PA, USA
1
Introduction
Correspondence: Robert A Gabbay, MD, PhD
Diabetes Program, Penn State Milton S
Hershey Medical Center, 500 University
Drive, H044, Room C6630, Hershey, PA
17033, USA
Tel +1 (717) 531-3592
Fax +1 (717) 531-5726
Email
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Abstract: Blood pressure (BP) control is a critical part of managing patients with type 2 diabetes.
Perhaps it is the single most important aspect of diabetes care, which unlike hyperglycemia and
dyslipidemia can reduce both micro- and macrovascular complications. Hypertension is more
prevalent in individuals with diabetes than general population, and in most cases its treatment
requires two or more pharmacological agents (about 30% of individuals with diabetes need 3 or
more medications to control BP). In this article we describe the key evidence that has contributed
to our understanding that reduced BP translates into positive micro- and macrovascular outcomes. We review the data supporting current recommendation for BP target , 130/80 mmHg.
Two studies suggest that a lower BP goal could be even more beneficial. We also present the
comparative benefits of various antihypertensive drugs in reducing diabetes-related micro- and
macrovascular complications. Finally we propose an evidence-based algorithm of how to initiate and titrate antihypertensive pharmacotherapy in affected individuals. Overall, achieving
BP , 130/80 mmHg is more important than searching for the “best” antihypertensive agent
in patients with diabetes.
Keywords: blood pressure control, treatment protocol, fixed dose combination, clinical inertia,
adherence
Diabetes is very prevalent and places high financial burden to our society. In the United
States during 2009 to 2034 the number of persons with diabetes is anticipated to increase
from 23.7 million to 44.1 million. The relative annual cost is also expected to rise from
$113 billion to $336 billion during the same period.1 Worldwide, 366 million individuals are projected to have diabetes by year 2030.2 Type 2 diabetes, the predominant
form, comprises 90% to 95% of all cases.
Macrovascular disorders are common in affected individuals. Specifically, cardiovascular disease (CVD) is 2 to 5 times more prevalent in persons with diabetes than general
population.3–5 Importantly it is the most serious complication by contributing 70% to
all-cause mortality in affected patients.6 In the United States, diabetes is also the leading
cause of microvascular disorders of end stage renal disease (ESRD)7,8 and retinopathy.9
Hypertension is 1.5 to 2.0 times more common in patients with diabetes than without
diabetes,10 and more so in females than males.11 For example, about 40% of individuals
between ages 25 to 65 already have high blood pressure (BP) at the time of diagnosis
of diabetes.11 This figure increases further with age.4,11 Coexistence of hypertension
with diabetes is likely due to the confounding effect of metabolic syndrome that often
predates both conditions.
Integrated Blood Pressure Control 2010:3 31–43
31
© 2010 Tashko and Gabbay, publisher and licensee Dove Medical Press Ltd. This is an Open Access
article which permits unrestricted noncommercial use, provided the original work is properly cited.
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Tashko and Gabbay
Hypertension is not only common but also a major cause
of cardiovascular (CV) pathology11–14 and thus mortality
in individuals with diabetes. It is also a direct contributor
to microvascular complications of nephropathy 7,15,16 and
retinopathy.16–18 As described in the main text, many randomized clinical trials have documented that good BP control
reduces both micro- and macrovascular complications. This
could make hypertension the single most important determinant of diabetes-related morbidity and mortality compared
to hyperglycemia that mainly causes microvascular disease
and dyslipidemia that mostly contributes to macrovascular
complications.
For this review article, we searched the literature for
clinical studies related to treatment of hypertension in type 2
diabetes. We utilized PubMed to find trials published in 2005
to 2010. We then used citations from identified articles to
select landmark studies printed before 2005. For this paper
we chose mainly randomized clinical trials with large sample
size and long duration of follow up. We narrowed further
our selection to original works that emphasized renal and CV
outcomes of various antihypertensive therapies in subjects
with type 2 diabetes.
The purpose of this article is 5-fold. First, to provide
evidence that reducing BP is beneficial in patients with
diabetes; second, to demonstrate that optimal BP target
is ,130/80 mmHg; third, to show that hypertension is poorly
controlled in clinical practice worldwide; fourth, to explain
the rationale of choosing the right antihypertensive medications; and fifth, to provide a descriptive algorithm of how to
initiate and titrate pharmacotherapy.
Reducing BP is beneficial
Critical evidence from 2 major trials, UKPDS18,19 and
SHEP,20 shows that reduced BP prevents complications in
patients with type 2 diabetes.
UKPDS 3818 was a landmark study that examined if
decreased BP in persons with new type 2 diabetes lowered
micro- and macrovascular complications. At study entry,
1148 subjects with less than 3 years of diabetes and mean
BP 164/94 mmHg were randomized into “tight” BP and
“less-tight” BP control groups. Patients in the tight BP control group received either angiotensin converting enzyme
inhibitor (ACEi) captopril or β-blocker atenolol to bring
BP to ,150/85 mmHg. The less-tight BP control group
could use medications other than ACEi or β-blocker to attain
BP ,180/105 mmHg.
After 8.4 years of follow up, the tight BP control group
achieved a lower BP than the less-tight BP control arm
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(∆10/∆5 mmHg), resulting in greater relative reductions
(P , 0.05) for both micro and macrovascular complications:
24% in any diabetes related end-points (...truncated)