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Module 8. Diabetes Complications and Comorbidities
Background
Diabetes is a growing global health concern that affects all age groups and genders. Analysts predict a
worldwide prevalence of 552 million people with diabetes by 2030.1 According to the 2017 National Diabetes
Statistics Report, in 2015, there are an estimated 30.3 million individuals with diabetes in the United States (U.S.), which
approximates 9.4% of the population. Of these people, 8.1 million (27.8%) are undiagnosed.2 This increased
diabetes prevalence is attributed to an aging population with increased obesity.3
The damaging effects of hyperglycemia on the vasculature contribute to diabetes complications and
comorbidities and between 30% and 50% of all diabetic patients have some organ damage, which can
potentially progress to long-term complications.4 Studies show that 2 or more complications are diagnosed in
almost one-fifth of people with diabetes.4 Life expectancy is also shorter for the diabetes community. For
example, in the United Kingdom Prospective Diabetes Study (UKPDS) Outcomes Model, men with diabetes
aged 55 years were predicted to live 3.6 to 11.5 years less than their age-matched peers.5
In addition to the societal and humanistic effects, the management of diabetes and its complications has
substantial economic impact. The estimated total direct and indirect cost of diabetes in 2012 in the U.S. is $245 billion.2 If diabetes is undetected or its
complications are poorly managed, patients can experience a poor health-related quality of life (QoL) with
significant morbidity and mortality, so optimal prevention and treatment strategies are necessary. Therefore, the purpose of this activity is to provide an overview of the complications and comorbidities affecting those with
diabetes and describe some of the proposed treatment options.
Complications of Diabetes: Microvascular Versus Macrovascular
Patients with either type 1 diabetes mellitus (T1DM) or type 2 diabetes mellitus (T2DM) are at potential risk for
long-term microvascular and/or macrovascular complications. Those at greatest risk are patients whose diabetes is uncontrolled.6 Microvascular diseases occur in small blood
vessel tissues, such as the kidney, the retina of the eyes, and the nerves, where exposure to glucose correlates
closely with plasma glucose levels. The resulting complications include nephropathy, retinopathy, and
neuropathy.6
Diabetic retinopathy (DR) is one of the most common microvascular complications and the leading cause of
vision loss among patients with diabetes.6,7 A mechanism postulated for the development of DR is the
conversion of glucose to sorbitol by the enzyme aldose reductase. Hyperglycemia increases the uptake of
glucose molecules via the sorbitol pathway, which accumulate in the cells and result in osmotic stress,
microaneurysm formation, thickening of the basement membrane, and pericyte loss.6 In addition, vascular
endothelial growth factor (VEGF) production increases in response to hypoxia.6 VEGF normally creates new
blood vessels, but it can overexpress and lead to disease and increased oxidative stress. Because oxidative stress
plays a role in cell injury from hyperglycemia, suppression of VEGF has been shown to reduce the progression
of retinopathy.6
DR can be divided into nonproliferative (NPDR) and proliferative diabetic retinopathy (PDR), which is a
progression of NPDR.7 DR risk factors include poor glycemic control and long-standing disease.7,8 NPDR
involves the development of microaneurysms, venous loops, retinal hemorrhages, and hard and soft exudates,
while PDR involves neovascularization or the development of new blood vessels on the retinal surface with or
without vitreous hemorrhage.6,8 According to the Centers for Disease Control and Prevention (CDC), from 2005
to 2008, there were 4.2 million (28.5%) patients with DR aged 40 years and older in the U.S.2 Without therapeutic intervention, blindness can occur, so it is incumbent on the health care provider to stress the importance of good blood glucose control to the patient as a method of helping to delay or prevent diabetes complications.6,8
Another microvascular complication is diabetic neuropathy (DN), which is a group of conditions that involves
nerve damage.8 The pathophysiology of neuropathy is complex and unclear. Dyslipidemia, hyperglycemia,
insulin resistance, and growth factors are associated with nerve glycation. Excess glucose interacts with reactive
oxygen species, proteins, and lipids to form free radical byproducts that contribute to oxidative stress. This
oxidative stress creates inflammation in the nerves. The polyol pathway also assists in the metabolic processes
to promote intracellular variability and deterioration.8-10 DN is classified according to the affected nerves such
as peripheral, proximal, focal, or autonomic.8 Age, height, metabolic control, duration of diabetes, and/or a
presence of nephropathy or retinopathy are potential risk factors that have been correlated with the presence of
DN in clinical studies.9,10 Most patients that present with symptoms of diabetic peripheral neuropathy (DPN) describe burning and tingling of the feet or hands, or numbness with pain worsening at night.6 With no
intervention, people may be subject to amputation after foot ulceration or injury.2 Even though DPN is the most
common form of DN for patients with diabetes, it is important to exclude other diagnostic causes of neuropathy
in this population, such as alcoholism, vitamin B12 deficiency from metformin, hypothyroidism, or uremia.6-10 In 2010, the CDC reported about 73,000 nontraumatic lower limb amputations in patients with diabetes 20 years
of age and older.3 In general, 60% of all nontraumatic lower limb amputations in that age group occur in those
with diabetes.3
Proximal neuropathy is the second most common form of neuropathy, potentially affecting the muscles of the
legs, buttocks, and hips and leading to muscle weakness. This can make it difficult for the individual to stand
from a sitting position.11 Focal neuropathy (FN) results in the sudden weakness of 1 nerve or a group of nerves,
causing muscle weakness or pain. This malady occurs suddenly, but generally resolves in 6 to 8 weeks for
patients with long-standing diabetes. Unlike the other types of neuropathy, the focal kind usually occurs in a single limited area, such as the wrist, and can involve nerve entrapment the likes of carpal tunnel
syndrome.11 Patients with diabetes and FN can develop double vision, aching behind one eye, Bell’s palsy, an
inability to focus the eye; and severe pain in the pelvis, back, thigh, chest, stomach, or shin.11 Diabetic autonomic neuropathy (DAN) can occur in a variety of organ systems and might be manifested by
gastroparesis, hypoglycemic unawareness, constipation, diarrhea, erectile dysfunction, exercise intolerance,
resting tachycardia, silent myocardial ischemia, and even sudden death.11
Diabetic nephropathy is the most common cause of end-stage renal disease (ESRD) in the nation and is a risk
factor for coronary artery disease (CAD) and potentially mortality.12 The CDC cites diabetes as the primary
cause of kidney failure in 44% of all new cases diagnosed in 2011.2 Both the Diabetes Control and
Complications Trial (DCCT) and the UKPDS trial demonstrated that improving hyperglycemia and reducing
elevated glycated hemoglobin (A1C) decrease the risk of microvascular complications for those with T1DM
and T2DM, respectively.7,13
Unlike microvascular complications, macrovascular complications affect large blood vessels of the heart, brain,
and arteries, thereby contributing to atherosclerosis, CAD, peripheral vascular disease (PVD) and
cerebrovascular disease.6 The risk of patients with diabetes dying from cardiovascular (CV) complications is
twice that of people without diabetes.14 Cardiovascular disease (CVD) accounts for 70% of overall mortality in
patients with diabetes and is the most common cause of death.14
The benefit of blood glucose (BG) lowering in mitigating macrovascular disorders is unclear.6,7 The lack of clarity was fueled by more recent trials, such as the ACCORD (Action to Control Cardiovascular Risk in
Diabetes) trial, the ADVANCE (Action in Diabetes and Vascular Disease: Preterax and Diamicron Modified
Release Controlled Evaluation) trial, and the VADT (Veterans Affairs Diabetes Trial), which all sought to determine the effect of lowering BG to near-normal levels on CV risk in those with T2DM.15-17 Results of the
ACCORD and ADVANCE trials concluded that that near-normal glycemic control for a median of 3.5 to 5
years does not reduce CV events and substantially increased the risks of death from all causes as well as CV
disease.15,16 The VADT concluded that intensive BG control in patients with poorly controlled T2DM had no
substantial effect on the rates of major CV events, death, or microvascular complications, except for the
progression of proteinuria.17 In addition, the complications of CVD, PVD, and stroke also occur in patients
without diabetes, but with risk factors of hypertension (HTN), dyslipidemia, and insulin resistance, which
indicate that hyperglycemia may not necessarily be involved.18 Because the risk of macrovascular disease is
increased in individuals with diabetes and obesity, the management of dyslipidemia, HTN, obesity, and/or
tobacco cessation is quite urgent.2
Common Comorbidities in Diabetic Patients
Most people with diabetes have at least 1 comorbidity, but approximately 40% have at least 3 of them.19 Patients with diabetes are at increased risk for comorbidities at higher rates than individuals the same age but
without diabetes.19 Comorbidities with worse outcomes are highly prevalent for those with diabetes and are
listed in Table 1.19,20 Comorbid disorders can be classified into clinically dominant conditions—concordant
versus discordant chronic conditions, and symptomatic versus asymptomatic chronic conditions.19 Clinically dominant comorbid conditions, such as severe depression, stage IV cancer, or newly diagnosed
breast cancer, are serious conditions and clinicians may potentially focus more on the comorbidity, sometimes at the
expense of diabetes management.19 Concordant comorbid maladies that include diabetes and HTN have a
related pathology and therapeutic management plan, while a discordant comorbidity, such as diabetes or
irritable bowel syndrome, is unrelated both in its pathology and in its treatment strategies.19 Studies show that
having comorbidities increases patients’ exposure to the health care system, thereby allowing for increased
opportunities for foot inspections, eye examinations, and A1C testing, which leads to better glycemic
control.19 Interestingly, symptomatic comorbidities, such as back pain, are not always of greater concern to patients than managing their hyperglycemia, and patients may forgo analgesics to focus on diabetes therapy.19 Asymptomatic conditions, such as HTN or dyslipidemia, might not present symptoms; so, treatment would
highlight the prevention of mortality, improving patient functioning, halting medications’ adverse effects, and
improving health-related QoL.19
Because of the mortality risk seen with intensive BG lowering in the ACCORD and ADVANCE trials and the
VADT to achieve near-normal BG levels, the American Diabetes Association (ADA) recommends selecting
patients with few comorbidities and a long life expectancy to benefit from tight glycemic goals (e.g, an A1C of
less than 6.5%).20
The Impact on Diabetes Treatment Goals According to the DCCT and the UKPDS Trials
Large, randomized, controlled trials such as the DCCT and the UKPDS trial, had significant impact on diabetes
treatment goals and guidelines in those with T1DM and T2DM, respectively.7,13 The DCCT was a major clinical trial conducted involving patients with T1DM in the U.S. and Canada to compare the effects of conventional
versus intensive BG control with A1C as close as possible to the norm on diabetes-related complications.13 The goal A1C was less than 6.05% (within the normal range).13
The study results show that a statistically significant difference in the average A1C value was maintained
between the intensive-therapy and the conventional-therapy groups (P < 0.001). Although 44% of patients in
the study’s intensive-therapy arm achieved an A1C of less than 6.05% at least once during the study, fewer than
5% were able to maintain this value.13 Tight glycemic control reduced microvascular complications of
retinopathy by 76%, microalbuminuria (defined as urinary albumin excretion of 40 mg or more per 24 hours) by
39%, albuminuria (defined as urinary albumin excretion of 300 mg or more per 24 hours) by 54%, and
neuropathy by 60%. In fact, any prolonged BG lowering benefited the patient, even if he or she had a history of
poor control.13 The chief adverse effect, though, was a 2- to 3-fold increase in severe hypoglycemia in the
intensive-treatment group.13
The UKPDS was a large, randomized trial that recruited patients with T2DM in the UK to determine whether
intensive BG therapy reduced CV and microvascular complications and assess the advantage of sulfonylureas,
metformin, or insulin.7,21 Results of the UKPDS study show that as a result of tight glycemic control in the intensively treated group,
participants experienced a decrease in microvascular but not macrovascular complications when compared with
the conventionally treated group.7 There was a decrease, however, in all-cause mortality in overweight T2DM
patients who were on metformin therapy.21 Individuals randomized to metformin in the intensive-treated group
had statistically significant risk reductions of 32% for any diabetes-related endpoint, 42% for diabetes-related
death, and 36% for all-cause mortality compared with sulfonylurea and insulin.21
The UKPDS 38 also evaluated patients with T2DM and HTN, with a mean blood pressure (BP) at study entry
of 160/94 mm Hg. Participantes receiving treatment for tight BP control were compared with participants
receiving BP treatment that was not as tightly controlled.22 The main objective was to determine whether tight
control of BP prevents microvascular and macrovascular complications in patients with T2DM.22 Mean BP
during follow-up was significantly reduced in the group assigned to tight BP control (144/82 mm Hg) compared
with the group assigned to less tight control (154/87 mm Hg) (P < 0.0001).22 In summary, the UKPDS results
demonstrated that reasonably tight treatment goals for BG combinded with tight BP control, ultimately,
achieved reductions in diabetes-related deaths, progression of retinopathy, and deterioration in visual acuity.22
Therefore, several goals, guidelines, and management strategies emerged from these major findings, which
include the following:
- The ADA guidelines, as well as the American Association of Clinical Endocrinologists and the
American College of Endocrinology (AACE/ACE) guidelines, recommend intensive BG control with
a general A1C goal of less than 7% to reduce microvascular complications. These goals should be individualized, however, for patients for whom the benefits would outweigh the risks of severe
hypoglycemia.20,23
- As a result of mortality findings and severe hypoglycemia observed in the ACCORD and ADVANCE
trials and the VADT, the ADA guidelines suggest less stringent goals for patients with long-standing
diabetes, advanced atherosclerosis, a history of severe hypoglycemia, advanced age with significant
comorbidities, and a short life expectancy.20
- Both the UKPDS trial and the DCCT demonstrate that patients with T1DM and those with T2DM
have the same benefits of decreased microvascular events with improved glycemic control.7,13
- Hyperglycemia is toxic whether occurring early in life or later and regardless of its etiology and, in
turn, causes a resulting inflammatory process leading to microvascular complications.24
- Tight BP control, to a mean of 144/82 mm Hg, significantly decreased rates of stroke, diabetes-related
deaths, heart failure, microvascular complications, and vision loss.21,24
- There was no long-term significant reduction in CVD with tight glycemic control, except in the
UKPDS trial, where a risk reduction in both myocardial infarction (MI), of 15%, (P = 0.01) and in
death from any cause, of 13% (P = .007) after 10 years of follow-up, were observed.15-17,24-26
- Metformin significantly decreases the risk of diabetes-related endpoints for patients who are
overweight with diabetes, including those with MI (33%; P = 0.005), and contributes to less weight
gain and fewer hypoglycemic episodes. Therefore, the agent has become the first-line therapy
recommended by leading diabetes experts.22,2325
- Sulfonylureas are as safe as insulin in controlling BG.7
- Long after the trials’ conclusions, there was a sustained benefit in patients with microvascular
complications, indicating that early treatment is beneficial.25
- Sulfonylurea and metformin did not provide sustained BG control over time; studies show that control
worsened. So, as diabetes progresses, clinicians have to intensify therapy to regain glycemic
control.20,24,25
- As a follow-up to the DCCT and the UKPDS trial, the ACCORD and ADVANCE trials and the
VADT, it is prudent to caution against excessively intensive BG goals because aggressive A1C targets
(less than 6.5%) were associated with a 3-fold increased risk of hypoglycemia.15-17
To effectively treat the complications experienced by a patient with diabetes, the clinician should target
diabetes-specific therapeutic goals, as is recommended by leading experts. It is important to implement
prevention and treatment strategies for complications, as well as manage comorbid chronic conditions,
incorporate the patient’s priority goals, and integrate diabetes self-management education and support.
Anything less may result in ineffective diabetes control, increased morbidity and, in the worst-case scenario,
mortality.19,20,23
Prevention and Treatment Options for Common Diabetes Complications
Diabetic Retinopathy (DR)
Both the AACE/ACE guidelines and those of the ADA suggest optimizing glycemic and BP control to reduce
or slow the progression of retinopathy.20,23 Experienced ophthalmologists should screen patients using a dilated
eye examination in adults with T1DM within 5 years of the onset of diabetes and immediately after diagnosis
for patients with T2DM. Yearly eye exams are recommended for patients with diabetes thereafter.20,23
Laser photocoagulation therapy is indicated in individuals with macular edema (ME), severe NPDR, or any
PDR to reduce the risk of vision loss by sealing off leaky blood vessels in the retina close to the macula; but,
this does not necessarily reverse already reduced visual acuity.2 Laser photocoagulation increases the oxygen
tension in the retina, relieves hypoxia, improves retinal circulation, and reduces vision loss.26
Enhancement of the retina’s oxygenation also lessens neovascularization and edema formation by reducing
VEGF production. The antimonoclonal VEGF therapies improve vision, cut down on vessel leakage, and
reduce the necessity for laser photocoagulation in patients with ME.27 The U.S. Food and Drug Administration (FDA) approved antimonoclonal VEGF therapies, such as aflibercept and ranibizumab, for the treatment of ME
and other diabetic retinopathy complications.27-29
Aflibercept (Eyelea) is a recombinant fusion protein that serves as a receptor decoy to prevent the binding and
subsequent activation of the VEGF receptors.28 This agent is indicated for neovascular age-related macular
degeneration, ME following retinal vein occlusion, diabetic macular edema (DME), or DR in patients with
DME.28 It is dosed at 2 mg (0.05 mL) once monthly by intravitreal administration for the first 5 injections,
followed by once every 2 months.28 The most common side effects associated with aflibercept include
conjunctival hemorrhage, eye pain, cataracts, vitreous floaters, increased intraocular pressure (IOP), and
vitreous detachment. Patients should immediately contact their ophthalmologist if they experience vision
changes or develop red, painful eyes that are sensitive to light.28 Serious adverse reactions include
endophthalmitis and retinal detachment. Clinicians should advise patients that they may experience temporary
visual disturbances after the injection, so they should avoid driving or operating machinery until they regain
visual acuity.28
Ranibizumab (Lucentis) is a humanized monoclonal antibody fragment indicated as an intravitreal injection for
the treatment of patients with DR with DME.29 It is dosed at 0.3 mg (0.05 mL) monthly by intravitreal
administration, after which the retina is evaluated for further treatment.29 The main adverse events are similar to
those of aflibercept, which include conjunctival hemorrhage, eye pain, vitreous floaters, and elevated IOP.29 Ranibizumab alone or as an adjunct to laser therapy has been shown to decrease mean retinal thickness, as well
as improve vision and QoL in addition to substantially correcting visual acuity when compared with laser
therapy.27
Diabetic Peripheral Neuropathy (DPN)
There is no cure for this condition, but the standard of treatment includes optimum glycemic
control, foot care, supportive footwear, and pain control.7,13,20,23 Patients must be taught to inspect their feet on a daily basis and look for any signs of dry cracking skin, callus
formations, fissures, cuts, and bruises, as well as infections between the toes and near the toenails.20,30 Individuals with diabetes should be educated about foot injury prevention.31 And because as many as 50% of
DPN cases are asymptomatic, comprehensive annual foot examinations to detect any signs of early DPN are
warranted.20 The ADA recommends that all patients be screened for DPN at the diagnosis of T2DM and, then, 5
years after diagnosis for those with T1DM and yearly thereafter.20
Treatment for DPN is primarily for pain control. There are many agents used for the treatment of DPN, but only
2 medications have U.S. FDA approval—pregabalin and duloxetine.30-32 Other drugs used in DPN therapy include venlafaxine, carbamazepine, topiramate, amitriptyline, imipramine, paroxetine, citalopram, gabapentin,
sodium valproate, dextromethorphan, morphine sulfate, tramadol, oxycodone, transdermal lidocaine, and
capsaicin.30 Although approved for the treatment of DPN in Europe, capsaicin is approved in the U.S. only for
neuropathic pain associated with postherpetic neuralgia, which does not include patients with diabetes.33
A systematic review and network meta-analysis concluded that selective serotonin reuptake inhibitors (SSRIs),
topical capsaicin, tricyclic antidepressants (TCAs), and anticonvulsants were associated with statistically
meaningful reductions in pain.31 Selective norepinephrine reuptake inhibitors (SNRIs) had exhibited a greater
effect on pain control than anticonvulsants and opioids did.31 Amitriptyline, though commonly used for painful
DPN, is limited by such adverse events as sedation, urinary retention, and orthostatic hypotension.34 Both amitriptyline and desipramine showed similar pain relief in 1 study, regardless of whether patients had a
diagnosis of depression or not.34 Therefore, desipramine is an option for DPN because of its safety profile if
patients are unable to tolerate amitriptyline.
Duloxetine is an SNRI that is FDA-approved for painful DPN.32 The drug’s exact mechanism of action is
unknown, but it is thought to potentiate serotonergic and noradrenergic activity in the central nervous system (CNS) to inhibit central pain and anxiety.32 Duloxetine has a black box warning for suicidal thoughts and
behaviors; so, patients have to be monitored.32 The dosage for the treatment of DPN is 60 mg once daily, but in
those with renal impairment, a lower dose is suggested at the outset and then a gradual increase or titration.
Duloxetine is a delayed-release capsule and should not be sprinkled onto food. This agent’s serious adverse
effects include orthostasis, hepatoxicity, suicidal thoughts, abnormal bleeding, and serotonin syndrome (SS). SS
can occur alone or in combination with other serotonergic drugs that encompass triptans, TCAs, fentanyl,
lithium, tramadol, buspirone, St John’s Wort, tryptophan, monoamine oxidase inhibitors (MAOIs), linezolid,
and intravenous (IV) methylene blue.32
A Cochrane review was designed to assess the benefit and harm of duloxetine use for the treatment of painful
DPN or chronic pain.35 The study results show that duloxetine at 60 mg daily was effective for treating
painful DPN in the short-term, with a risk ratio (RR) for 50% or greater pain reduction at 12 weeks. The related
number needed to treat to benefit (NNTB) was 5 (95% confidence interval [CI], 4 to 7). Adverse events were
common in both the treatment and placebo groups, but more common in the former group. Authors concluded
that doses of 60 mg and 120 mg of duloxetine were efficacious for treating painful DPN, but lower doses were
ineffective.35
Pregabalin is an anticonvulsant therapy used for a variety of conditions that include the management of
neuropathic pain associated with DPN, postherpetic neuralgia, fibromyalgia, and partial-onset seizures.36 The mechanism of action is not fully understood, but is thought to bind to the alpha2-delta subunit of calcium
channels in the CNS tissues, thereby resulting in antinociceptive effects.36 Pregabalin is given at a maximum daily dose of 100 mg 3 times daily for the treatment of DN in patients with a
creatinine clearance of 60 mL/minute or more.36 The most common negative side effects are dizziness,
somnolence, dry mouth, edema, blurred vision, weight gain, and abnormal concentration or attention.36 Pregabalin has warnings of angioedema, hypersensitivity reactions, and an increased risk of suicidal thoughts or behavior.36 Results of a meta-analysis show that pregabalin substantially lessened the pain associated with DPN
by more than 50% and boosted patients’ global impression of change.37
A significant challenge with the use of pregabalin and duloxetine is the potential for major drug-drug
interactions (DDIs), especially for older adults. Naproxen and ketorolac reduce pregabalin effectiveness,
eventually resulting in potentially major DDIs.38 Duloxetine is a highly protein-bound agent that undergoes
hepatic metabolism and inhibits the isoenzymes CYP450 (2D6 and 1A2).36,37 Many drugs are contraindicated or
have potentially major DDIs with duloxetine therapy, in turn, causing CNS toxicity, SS, neuroleptic malignant
syndrome (NMS), QT prolongation, and/or an increased risk of bleeding.36,37 A recent retrospective, matched cohort study was conducted using medical and pharmacy claims data to examine the impact of DDIs on newly
initiated treatment with pregabalin or duloxetine for patients with painful DPN.38 A total of 1320 individuals
met the criteria for inclusion in the study, with 570 patients given pregabalin and 750 prescribed duloxetine.
Results show that the percentage of patients with a potential DDI was statistically greater (P < 0.001) in the
duloxetine group (56.7%, n = 253) compared with the pregabalin group (2.9%, n = 13).38 There were 17
potentially major DDIs involving pregabalin, most of them incorporating the use of naproxen. On the other
hand, there were 649 potentially major and moderate DDIs with duloxetine, including 11 contraindicated
interactions.38 Precisely 91 of those interactions involved clopidogrel, while more than 25 interactions occurred
with tramadol, sertraline, trazodone, cyclobenzaprine; meloxicam, citalopram, and/or fluoxetine.38 As a result of
this study, pharmacists should screen patients on multiple therapies for potential DDIs when completing a medication review.
Diabetic Autonomic Neuropathy (DAN)
As diabetes progresses, patients should be assessed for signs and symptoms of diabetic autonomic neuropathy
(DAN), including orthostasis, resting tachycardia, hypoglycemic unawareness, and cardiovascular autonomic
neuropathy (CAN), which is the most important and concerning DAN in terms of mortality.22 In the early stages of CAN, people may be asymptomatic; but, as the disease progresses, there can be changes in heart-rate
variability with deep breathing and abnormal CV reflex. Advanced disease is indicated by resting tachycardia
and orthostasis.22 CAN is best prevented by targeting BG, BP, and lipid control, tobacco cessation, and physical
activity to reduce its progression and development among those with T2DM. Patients who develop CAN should
be referred to a cardiologist.22
Hypoglycemic unawareness is a progressive loss of the autonomic symptoms of sweating, tremors, and
palpitations traceable to reduced counter-regulatory responses to glucagon and epinephrine.39 The patient is
unaware of hypoglycemia and unable to respond appropriately, thus leading to seizures, coma, and even death.
This vicious cycle leads to further decreases in counter-regulatory responses to hypoglycemia.39 Risk factors
include tight glycemic control, low A1C, and a history of T1DM or T2DM in those with long-standing disease.
Patients should be educated to strictly avoid hypoglycemia. Studies show symptom improvement by 3 days and
normalization of hypoglycemic awareness in as 3 weeks. The 2 types of effective patient-education strategies
include a psychological instructional program to improve the person’s ability to detect hypoglycemia and
teaching him or her the proper strategies to help avoid hypoglycemia through dietary education and flexible
insulin dosing strategies in response to exercise and a reduced diet.39
Diabetic Nephropathy
The ADA recommends optimizing both BG and BP control to reduce the risk or slow the progression of chronic
kidney disease (CKD) in the presense of diabetes.22 The ADA now discourages the use of the term
macroalbuminuria becasue albuminuria is a progressive symptom.22 Albuminuria is defined as a urine albumin-to-creatinine ratio (UACR) of 30 mg/g or greater. All patients with T2DM and those who have T1DM for a
duration of 5 or more years should be screened and assessed at least once a year using UACR and estimated
glomerular filtration rate (eGFR).22 The guidelines do not recommend an angiotensin converting enzyme
(ACE) inhibitor or angiotensin receptor blocker (ARB) for the primary prevention of CKD in patients with
diabetes who have normal BP and UACR.22 Either an ACE inhibitor or an ARB is suggested for the treatment of patients who are not pregnant who have a moderately elevated UACR (30 to 299 mg/g); they are also
recommended for the treatment of those with a UACR of more than 300 mg/g.22 When treatment with ACE
inhibitors, ARBs, or diuretics is initiated, clinicians should monitor the patient’s serum creatinine and potassium
levels. They should also be vigilant, especially in patients with an eGFRof less than 60 mL/minute or with
albuminuria, to evaluate, manage, and monitor for the potential complications and progression of CKD. ACE
inhibitors reduce the development of CKD in patients with T1DM and high levels of albuminuria by delaying
the progression of albuminuria and slowing eGFR, as well as reducing the risks of stroke, MI, and death.40 Therefore, such inhibitors are beneficial for the treatment of those at high risk of CVD and CKD.38 ARBs do
not demonstrate the same positive effect on CVD risks, but ARBs reduce the progression of albuminuria in
those with diabetes and ESRD.20,40 The combination of ACE inhibitors and ARBs should be avoided because
combining them therapeutically has no additional benefit on CVD or CKD and leads to higher rates of
hyperkalemia and acute kidney injuries.20 Because the goal for managing CKD involves optimal BP control, the
ADA recommends the use of diuretics, calcium channel blockers, and beta-blockers as additional therapy to
further BP lowering in patients already on maximal dosages of ACE inhibitors or ARBs, or as an alternative for
those intolerant to an ACE inhibitor or an ARB.22
Cardiovascular Disease (CVD)
CVD risk management involves managing HTN, controlling dyslipidemia, using antiplatelet therapy, and
treating obesity where applicable.20 The goal BP is less than 140/90 mm Hg in patients with diabetes and HTN;
for younger patients, though, if it is possible without burden, the goal can be reduced to less than 130/80 mm
Hg.20 For those patients with a BP of more than 120/88 mm Hg, health care practitioners should advise them to
lose weight if they are overweight or obese, using the Dietary Approaches to Stop Hypertension (DASH) diet.
The DASH diet regimen includes reducing sodium and increasing potassium intake, along with moderating
alcohol use and increasing physical activity. Therapies should include an ACE inhibitor or an ARB with multiple-drug therapies that feature a thiazide diuretic combined with an ACE inhibitor or an ARB at maximal
dosages to achieve BP targets.22
The ADA recommends reducing saturated fat, trans-fat, and cholesterol and increasing omega fatty acids,
viscous fiber, and plant stanols and sterols. Add to that, more physical activity and weight loss if indicated to
improve the lipid profile in patienst with diabetes.20 Moderate-dose or high-dose statin therapy is recommended
depending on age and risk factors.20 High-dose statins are indicated in those with diagnosed CVD from ages 40
to 75 years; with a moderate or a high dose suggested for those 75 years of age and older.20 Combining statins
with niacin or fibrate therapies is not recommended because there are no additional benefits.20 Cholesterol
laboratory testing may be helpful in monitoring adherence to therapy, but may not be needed once the patient is
stable on therapy.20
A useful tool for estimating patients’ 10-year atherosclerotic CVD (ASCVD) risk is a risk calculator, which
providers can quickly access at http://cvdrisk.nhlbi.nih.gov/calculator.asp.
Antiplatelet therapy, such as an aspirin dose of 75 to 162 mg per day, should be initiated as a primary
prevention strategy for all patients with diabetes and a 10-year CVD risk of more than 10% and most men with
diabetes older than 50 years of age or women with diabetes older than 60 years of age who have another major
risk factor, such as a family history of CVD, HTN, smoking, dyslipidemia, or albuminuria.20 Aspirin is no
longer suggested as CVD prevention for adults with diabetes who are at a low CVD risk (i.e., less than 5%),
such as women younger than 60 years of age, men younger than 50 years of age with no major CVD risk
factors, or a 10-year CVD risk of less than 5%, because the risk for significant bleeding outweighs the agent’s
benefits.20,23 For patients with a known history of diabetes and CAD, aspirin at a dose of 75 to 162 mg/day
should be initiated. If these individuals are allergic to aspirin, though, clopidogrel at 75 mg a day can be
substituted. If patients had an acute coronary syndrome, dual-antiplatelet therapy can be used for as long as 1
year post-event.20
Obesity is diagnosed according to a body mass index (BMI) of 30 kg/m2 or greater.23 Measurement of waist
circumference may be considered for individuals with a BMI between 25 and 35 kg/m2. Men with a waist
circumference of 40 inches or more or women with a waist circumference of 35 inches or more are at a higher
risk for metabolic disease and should be evaluated for such obesity-related complications as sleep apnea and
osteoarthritis.23 Nonpharmacologic strategies should include lifestyle modifications, such as behavioral change,
reduced-calorie diets, and physical therapy. Weight-loss therapies may be considered if these approaches fail to
achieve the target goals.23
Conclusions
Patients with either T1DM or T2DM are at risk for long-term microvascular and macrovascular complications.
Tight glycemic control remains the main strategy for the prevention of retinopathy, neuropathy, and
nephropathy, while the treatment of HTN and dyslipidemia and the cessation of tobacco use can reduce CV
risk. It is important to manage people with a patient-centered communication and approach to care. They should
be taught about self-care management to prevent complications and that, in turn, may well lead to a good
health-related QoL. Therefore, providers should aggressively focus on the therapeutic goals of both the
prevention and treatment of diabetes and its complications by incorporating both pharmacologic and
nonpharmacologic therapeutic plans of action..
Table 1. Diabetes Comorbidities |
Heart failure (HF)
Chronic kidney disease (CKD)
Obstructive sleep apnea (OSA) and other sleep disorders
Periodontal disease
Low testosterone
Certain cancers
Fractures
Nonalcoholic fatty liver disease
Depression
Anxiety
Arthritis
Cognitive impairment
Dementia
Hearing impairment |
Category |
Counseling Tips |
General Diabetes Education |
- Hyperglycemia can damage small blood vessels such as those in the kidney, the retina of the eyes, and the nerves.6
- It is important to take steps to control your diabetes because complications from uncontrolled diabetes in small blood vessels include, but are not limited to, the following: vision loss, muscle weakness, kidney disease, burning, tingling or numbness of the feet or hands, and limb amputations.6
- In addition, hyperglycemia can damage large blood vessels, such as those in the heart, brain, and arteries.
- The risk of insult to large blood vessels is increased in individuals with diabetes who has 1 of the following risk factors: obesity, high blood pressure, high cholesterol, or those who smoke.6
- Research suggests that keeping your A1C below 7% can decrease the chances for developing the complications of diabetes.13
- To identify foot conditions before they become severe, inspect your feet daily to look for any signs of dry cracking skin, callus formations, fissures, cuts, and bruises, as well as infections between the toes and near the toenails.
|
REFERENCES
- Sangi M, Win KT, Shirvani F, et al. Applying a novel combination of techniques to develop a predictive
model for diabetes complication. PLoS One. 2015;10(4):e0121569.
- Centers for Disease Control and Prevention. National Diabetes Statistics Report 2017. Available
at https://www.cdc.gov/diabetes/pdfs/data/statistics/national-diabetes-statistics-report.pdf. Accessed May 1, 2018.
- Amos AF, McCarty DJ, Zimmet P. The rising global burden of diabetes and its complications: estimates
and projections to the year 2010. Diabet Med. 1997;14 (Suppl 5):S1-S85.
- Girach A, Manner D, Porta M. Diabetes microvascular complications: can patients at risk be identified?
A review. Int J Clin Pract. 2006;60(11):1471-1483.
- Leal J, Gray AM, Clarke PM. Development of life-expectancy tables for people with type 2 diabetes. Eur Heart J. 2009;30(7):834-839.
- Fowler MJ. Microvascular and macrovascular complications of diabetes. Clin Diabetes. 2008;26:77-82.
- UK Prospective Diabetes Study Group. Intensive blood-glucose control with sulphonylureas or insulin
compared with conventional treatment and risk of complications in patients with type 2 diabetes
(UKPDS 33). Lancet. 1998;352(9131):837-853.
- Zimmerman R. Microvascular complications of diabetes. Cleveland Clinic Center for Continuing
Education. Available
from http://www.clevelandclinicmeded.com/medicalpubs/diseasemanagement/endocrinology/microvasc
ular-complications-of-diabetes/ Accessed October 20, 2015.
- Tesfaye S, Stevens LK, Stephenson JM, et al; and the EURODIAB IDDM Study Group. Prevalence of
diabetic peripheral neuropathy and its relation to glycaemic control and potential risk factors: the
EURODIAB IDDM Complications Study. Diabetologia. 1996;39(11):1377-1384.
- Dyck PJ, Davies JL, Wilson DM, et al. Risk factors for severity of diabetic polyneuropathy: intensive
longitudinal assessment of the Rochester Diabetic Neuropathy Study cohort. Diabetes Care.
1999;22(9):1479-1486.
- National Institute of Diabetes and Digestive and Kidney Diseases. Available from
http://www.niddk.nih.gov/health-information/health-topics/Diabetes/diabetic-neuropathies-nerve-damage-diabetes/Pages/diabetic-neuropathies-nerve-damage.aspx. Accessed November 9, 2015.
- Borch-Johnsen K, Kreiner S. Proteinuria: value as predictor of cardiovascular mortality in insulin
dependent diabetes mellitus. Br Med J (Clin Res Ed). 1987;294(6588):1651-1654.
- The Diabetes Control and Complications Trial Research Group. The effect of intensive treatment of
diabetes on the development and progression of long-term complications in insulin-dependent diabetes
mellitus. N Engl J Med. 1993;329(14):977-986.
- Mattila TK, de Boer A. Influence of intensive versus conventional glucose control on microvascular and
macrovascular complications in type 1 and 2 diabetes mellitus. Drugs. 2010;70(17):2229-2245.
- Action to Control Cardiovascular Risk in Diabetes Study Group. Effects of intensive glucose lowering
in type 2 diabetes. N Engl J Med. 2008; 358(24):2545-2559.
- ADVANCE Collaborative Group. Intensive blood glucose control and vascular outcomes in patients
with type 2 diabetes. N Engl J Med. 2008;358(24):2560-2572.
- Duckworth W, Abraira C, Moritz T, et al. Glucose control and vascular complications in veterans with
type 2 diabetes. N Engl J Med. 2009;360(12):129-139.
- Meetoo D. Diabetes: Complications and the economic burden. Br J Healthc Manag. 2014;20(2):60-67.
- Piette JD, Kerr EA. The impact of comorbid chronic conditions on diabetes care. Diabetes Care. 2006;29(3):725-731.
- American Diabetes Association. Standards of Medical Care in Diabetes - 2016. Diabetes Care. 2016;39(Supp 1):S1-S111.
- UK Prospective Diabetes Study (UKPDS) Group. Effect of intensive blood-glucose control with
metformin on complications in overweight patients with type 2 diabetes (UKPDS 34). Lancet. 1998;352(9131):854-865.
- UKPDS 38 UK Prospective Study Group. Tight blood pressure control and risk of macrovascular and
microvascular complications in type 2 diabetes. BMJ. 1998;317(7160):703-713.
- The American Association of Clinical Endocrinologists and American College of Endocrinology
(AACE/ACE). American Association of Clinical Endocrinologists and American College of
Endocrinology Clinical Practice Guidelines for Developing a Diabetes Mellitus Comprehensive Care
Plan. Endocr Pract. 2015;21(Suppl 1):1-87.
- American Diabetes Association. Implications of the United Kingdom prospective diabetes study. Diabetes Care. 2002;25(Suppl 1):S28-S32.
- Murray P, Chune GW, Raghavan VA. Legacy effects from DCCT and UKPDS: what they mean and
implications for future diabetes trials. Curr Atheroscler Rep. 2010;12(16):432-439.
- Bressler NM, Beck RW, Ferris FL 3rd. Panretinal photocoagulation for proliferative diabetic
retinopathy. N Engl J Med. 2011;365(16):1520-1526.
- Gupta N, Mansoor S, Sharma A, et al. Diabetic retinopathy and VEGF. Open Opthalmol J. 2013; 7:4-10.
- Eylea [package insert]. Tarrytown, NY: Regeneron Pharmaceuticals, Inc.;2015.
- Lucentis [package insert]. South San Francisco, CA: Genentech, Inc.;2015.
- Feldman EL, Shefner JM, Dashe DF. Patient information. Diabetic neuropathy beyond the basics. Available from http://www.uptodate.com/contents/diabetic-neuropathy-beyond-the-basics. Accessed
November 13, 2015.
- Griebeler ML, Morey-Vargas OL, Brito JP, et al. Pharmacologic interventions for painful diabetic
neuropathy: an umbrella systematic review and comparative effectiveness network meta-analysis. Ann Intern Med. 2014;161(9):639-649.
- Cymbalta [package insert]. Indianapolis, IN: Lilly USA, LLC;2015.
- Qutenza (capsaicin 8%) patch [package insert]. Ardsley, NY: Acorda Therapeutics, Inc.;2013.
- Max MB, Lynch SA, Muir J, et al. Effects of desipramine, amitriptyline, and fluoxetine on pain in
diabetic neuropathy. N Engl J Med. 1992;326(19):1250-1256.
- Lunn MP, Hughes RA, Wiffen PJ. Duloxetine for treating painful neuropathy, chronic pain or
fibromyalgia. Cochrane Database Syst Rev. 2014, Issue 1. Art. No.: CD007115.
- Lyrica [package insert]. New York, NY: Parke-Davis, Division of Pfizer, Inc;2013.
- Hurley RW, Lesley MR, Adams MC, et al. Pregabalin as a treatment for painful diabetic peripheral
neuropathy: a meta-analysis. Regl Anesth Pain Med. 2008;33(5):389-394.
- Ellis JJ, Sadosky AB, Ten Eyck LL, et al. A retrospective, matched cohort study of potential drug-drug
interaction prevalence and opioid utilization in a diabetic peripheral neuropathy population initiated on
pregabalin or duloxetine. BMC Health Serv Res. 2015;15:159.
- Reno CM, Litvin M, Clark AL, Fisher SJ. Defective counterregulation and hypoglycemia unawareness
in diabetes: mechanisms and emerging treatments. Endocr Metab Clin North Am. 2013;42(1):15-38.
- Lewis EJ, Hunsicker LG, Bain RP, Rohde RD. The Collaborative Study Group. The effect of
angiotensin-converting-enzyme inhibition on diabetic nephropathy. The Collaborative Study Group. N Engl J Med 1993;329(20):1456-1462.
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