Hypertension: Pathology review

Hypertension: Pathology review

1H Exam

1H Exam

Bones of the lower limb
Anatomy of the anterior and medial thigh
Vessels and nerves of the gluteal region and posterior thigh
Anatomy of the leg
Anatomy of the hip joint
Fascia, vessels and nerves of the lower limb
Muscles of the gluteal region and posterior thigh
Anatomy of the knee joint
Joints of the ankle and foot
Bones of the upper limb
Anatomy of the brachial plexus
Anatomy of the arm
Vessels and nerves of the forearm
Anatomy of the elbow joint
Anatomy of the sternoclavicular and acromioclavicular joints
Joints of the wrist and hand
Fascia, vessels and nerves of the upper limb
Anatomy of the pectoral and scapular regions
Muscles of the forearm
Anatomy of the glenohumeral joint
Anatomy of the radioulnar joints
Anatomy clinical correlates: Axilla
Anatomy clinical correlates: Clavicle and shoulder
Anatomy clinical correlates: Arm, elbow and forearm
Anatomy clinical correlates: Median, ulnar and radial nerves
Glycolysis
Citric acid cycle
Electron transport chain and oxidative phosphorylation
Gluconeogenesis
Glycogen metabolism
Pentose phosphate pathway
Physiological changes during exercise
Amino acid metabolism
Nitrogen and urea cycle
Fatty acid synthesis
Fatty acid oxidation
Ketone body metabolism
Cholesterol metabolism
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Lactose intolerance
Pyruvate dehydrogenase deficiency
Familial hypercholesterolemia
Hyperlipidemia
Hypertriglyceridemia
Dyslipidemias: Pathology review
Disorders of fatty acid metabolism: Pathology review
Carbohydrates and sugars
Fats and lipids
Proteins
Fat-soluble vitamin deficiency and toxicity: Pathology review
Water-soluble vitamin deficiency and toxicity: B1-B7: Pathology review
Study designs
Cohort study
Clinical trials
Randomized control trial
Case-control study
Cytoskeleton and intracellular motility
Cell membrane
Extracellular matrix
Endocytosis and exocytosis
Resting membrane potential
Nuclear structure
Transcription of DNA
Gene regulation
Amino acids and protein folding
Cell cycle
DNA mutations
DNA replication
DNA damage and repair
Mitosis and meiosis
DNA structure
Translation of mRNA
Human development days 1-4
Human development week 2
Human development days 4-7
Human development week 3
Ectoderm
Endoderm
Mesoderm
Cardiac muscle histology
Artery and vein histology
Pancreas histology
Liver histology
Blood histology
Skin histology
Skeletal muscle histology
Central nervous system histology
Peripheral nervous system histology
Bacterial structure and functions
Ischemia
Necrosis and apoptosis
Hypoxia
Hyperplasia and hypertrophy
Atrophy, aplasia, and hypoplasia
Inflammation
Wound healing
Arterial disease
Hypertension
Deep vein thrombosis
Shock
Shock: Pathology review
Hypertension: Pathology review
Diabetes mellitus
Diabetic retinopathy
Diabetic nephropathy
Diabetes mellitus: Pathology review
Non-alcoholic fatty liver disease
Vitamin B12 deficiency
Microcytic anemia: Pathology review
Intrinsic hemolytic normocytic anemia: Pathology review
Non-hemolytic normocytic anemia: Pathology review
Extrinsic hemolytic normocytic anemia: Pathology review
Heme synthesis disorders: Pathology review
Coagulation disorders: Pathology review
Macrocytic anemia: Pathology review
Myasthenia gravis
Sunburn
Burns
Skin cancer
Skin cancer: Pathology review
Hyponatremia
Introduction to pharmacology
Enzyme function
Pharmacodynamics: Drug-receptor interactions
Pharmacodynamics: Agonist, partial agonist and antagonist
Pharmacodynamics: Desensitization and tolerance
Pharmacokinetics: Drug absorption and distribution
Pharmacokinetics: Drug metabolism
Pharmacokinetics: Drug elimination and clearance
Lipid-lowering medications: Statins
Lipid-lowering medications: Fibrates
Miscellaneous lipid-lowering medications
Anticoagulants: Heparin
Anticoagulants: Warfarin
Anticoagulants: Direct factor inhibitors
Cardiovascular system anatomy and physiology
Cardiac excitation-contraction coupling
Baroreceptors
Chemoreceptors
Renin-angiotensin-aldosterone system
Endocrine system anatomy and physiology
Hunger and satiety
Antidiuretic hormone
Insulin
Glucagon
Somatostatin
Cortisol
Pancreatic secretion
Blood components
Platelet plug formation (primary hemostasis)
Coagulation (secondary hemostasis)
Role of Vitamin K in coagulation
Clot retraction and fibrinolysis
Introduction to the immune system
Cytokines
Innate immune system
Complement system
T-cell development
B-cell development
MHC class I and MHC class II molecules
T-cell activation
B-cell activation, differentiation, and contraction
Cell-mediated immunity of CD4 cells
Cell-mediated immunity of natural killer and CD8 cells
Antibody classes
Somatic hypermutation and affinity maturation
VDJ rearrangement
Contracting the immune response and peripheral tolerance
B- and T-cell memory
Anergy, exhaustion, and clonal deletion
Vaccinations
Type I hypersensitivity
Type II hypersensitivity
Type III hypersensitivity
Type IV hypersensitivity
Skin anatomy and physiology
Muscular system anatomy and physiology
Brachial plexus
Neuromuscular junction and motor unit
Sliding filament model of muscle contraction
Slow twitch and fast twitch muscle fibers
Muscle contraction
Nervous system anatomy and physiology
Neuron action potential
Ascending and descending spinal tracts
Spinal cord reflexes
Motor cortex
Somatosensory pathways
Sympathetic nervous system
Parasympathetic nervous system
Adrenergic receptors
Cholinergic receptors
Pyramidal and extrapyramidal tracts
Body temperature regulation (thermoregulation)
Hydration
Movement of water between body compartments
Osmoregulation
Physiologic pH and buffers
Acid-base map and compensatory mechanisms
Buffering and Henderson-Hasselbalch equation
Respiratory acidosis
Pulmonary changes at high altitude and altitude sickness
Pulmonary changes during exercise
Oxygen binding capacity and oxygen content
Oxygen-hemoglobin dissociation curve
Carbon dioxide transport in blood
Respiratory alkalosis
Metabolic alkalosis
The role of the kidney in acid-base balance
Anorexia nervosa
Eating disorders: Clinical
Muscle weakness: Clinical
Diabetes mellitus: Clinical
Insulins
Hypoglycemics: Insulin secretagogues

Questions

USMLE® Step 1 style questions USMLE

0 of 3 complete

Start
A 55-year-old woman comes to the clinic for a hypertension follow up. She was diagnosed with hypertension 6 months ago and was prescribed a low-sodium diet and exercise. Medical history is significant for diabetes mellitus type 2 that is currently managed with metformin. She has been smoking 1 pack of cigarettes daily for 20 years. Family history is significant for osteoporosis in her mother and diabetes mellitus in her father. Temperature is 37.0 °C (98.6 °F), pulse is 80/min, and blood pressure is 152/95 mmHg. Urinalysis reveals microalbuminuria. DXA scan shows normal bone mineral density. A decision is made to add a pharmacological antihypertensive medication that works by inhibiting the production of angiotensin II. Which of the following types of medications was provided to this patient? 

Transcript

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Anthony is a 40 year old male with a history of type 2 diabetes mellitus presenting to a family medicine clinic for his annual health check-up. His blood pressure measurement is 145 over 95 millimeters of mercury, and his BMI is 32. On further history, he explains that his job as a truck driver has prevented him from exercising regularly. His father had a history of hypertension and passed away from a stroke. A follow-up appointment showed a blood pressure of 150 over 90. Alicia is a 30 year old female who came in because she’s concerned that she might be pregnant. Her pregnancy test is negative, however, her blood pressure is 170 over 90. On her second appointment, her blood pressure remains elevated. She is placed on lisinopril. A couple of days later, she presents with decreased urine output, and an elevated blood urea nitrogen and creatinine. Finally, Vikander is a 62 year old-male with a history of hypertension. He complains of headache, altered mental status, and visual changes. On further history, he mentions he is “sick of all the medications he has to take”. Fundoscopic examination reveals a swollen optic disk, and his blood pressure is 200 over 120.

Okay so all three people present with hypertension. Now normal blood pressure is less than 120 systolic over 80 diastolic. According to the recent 2017 American Heart Association and American College of Cardiology guidelines, hypertension is currently defined as a blood pressure over 130 systolic and 80 diastolic. Now, typically, both systolic and diastolic pressures tend to rise or fall together, but that’s not always the case. Sometimes, you can have systolic or diastolic hypertension. This is referred to as isolated systolic hypertension or isolated diastolic hypertension.

Okay, just because you see an elevated blood pressure on the exam, it does not mean that individual has hypertension. The blood pressure must be persistently elevated in order to define it as hypertension. So on your exam, remember that the diagnosis requires at least 2 separate readings on 2 separate visits. The reason for this is because of the phenomenon of “white coat hypertension”. This is hypertension on physical exam that occurs because of anxiety experienced by the individual.

Hypertension is classified into primary, or essential hypertension, and secondary hypertension. Primary hypertension occurs without a known secondary cause, and accounts for 90 percent of cases. The pathophysiology of primary hypertension is thought to be related to decreased renal sodium excretion. Reduced sodium excretion increases plasma volume, increasing the stroke volume, and as a result the systolic blood pressure. Also, the increased plasma volume causes decreased renin release from the juxtaglomerular apparatus, producing what’s called low-renin hypertension, and this can be high yield. Additionally, decreased sodium excretion promotes vasoconstriction of the peripheral arterioles, increasing the systemic vascular resistance, which increases diastolic blood pressure.

Okay, so risk factors for primary hypertension include age, physical inactivity, obesity, diabetes mellitus, smoking, family history of hypertension, as well as excess salt or alcohol consumption. It’s thought that in type II diabetes, high levels of insulin promote renal sodium retention.

Okay, before diagnosing an individual with primary hypertension, the causes of secondary hypertension must be ruled out. Your exams will often try to clue you towards this by mentioning that the individuals were on multiple antihypertensives and they didn’t work, or by having a relatively young individual with hypertension. The best approach is to look at different organ systems, starting with the adrenal gland. Important causes include primary hyperaldosteronism, or Conn syndrome, Cushing syndrome and tumors like pheochromocytoma and neuroblastoma. Clues in the question stem will help you identify which one it is. Hypokalemia, metabolic alkalosis and an increase in the aldosterone-to-renin ratio indicate Conn syndrome. Abdominal striae, supraclavicular fat pads, truncal obesity, and hyperglycemia point towards Cushing syndrome. Paroxysmal hypertension, that is hypertension that comes and goes, associated with headaches, palpitations and sweating indicate a pheochromocytoma. Neuroblastomas are common in children, and present with an abdominal mass.

Next is the kidney. Renal artery stenosis, also called renovascular disease is usually caused by an atherosclerotic plaque occluding the renal artery, especially in 60 to 70 year old males. Less commonly, it can be caused by fibromuscular dysplasia, especially in 20 to 30 year old females. This classically causes the “string of beads” appearance of the renal artery. Regardless of the cause, renal artery stenosis decreases renal perfusion. This makes your body think it’s in a hypotensive state. So in response, the renin-angiotensin-aldosterone system, or RAAS, is activated, resulting in vasoconstriction and increased renal sodium and water reabsorption, and eventually hypertension. Decreased renal perfusion causes the affected kidney to shrink, and histologically, there will be glomerular tubulointerstitial atrophy and fibrosis.

A high yield fact to remember for your exams is that unilateral renal artery stenosis does not cause CKD because the contralateral kidney is functioning normally, and in fact it hypertrophies to compensate. However, bilateral renal artery stenosis results in CKD because both kidneys are affected. Also, it’s important to not give ACE inhibitors to people with bilateral renal artery stenosis. This is because angiotensin II constricts the efferent arteriole in the glomerulus, which maintains the GFR. If an ACE inhibitor is given, the efferent arterioles dilate, causing a drop in the GFR.

Okay, renal parenchymal diseases like diabetic nephropathy, glomerulonephritis or polycystic kidney disease can also cause hypertension by retaining sodium.

Moving on, Coarctation of the aorta is also an important cause of hypertension, especially in children. And the mechanism is quite similar to renal artery stenosis, since renal perfusion is decreased, just that the obstruction is more proximal. Speaking of the aorta, aging causes the amount of elastin in the arterial wall to decrease, and the amount of collagen to increase, producing a stiff, non-compliant aorta. This manifests in elderly adults as isolated systolic hypertension, which means an elevated systolic blood pressure, but a normal diastolic.

Moving on, both hyperthyroidism and hypothyroidism can cause hypertension. Hyperthyroidism increases the cardiac output, causing an elevated systolic blood pressure. For some reason, hypothyroidism increases renal retention of sodium, and interestingly causes an isolated elevation of the diastolic blood pressure. The adjacent parathyroid glands are also potential suspects, because primary hyperparathyroidism causes hypercalcemia which increases vasoconstriction of the peripheral arterioles, resulting in an increased total peripheral vascular resistance.

Alright, if the person presents with hypertension, bradycardia and an irregular respiratory pattern, think of an increased intracranial pressure, which triggers a reflex that results in the Cushing’s triad. In pregnancy, it’s crucial to consider preeclampsia and eclampsia.

Finally, always be aware of what medications the individual is taking. Estrogen-containing oral contraceptives are common causes of hypertension, especially in young women. Estrogen works by increasing the synthesis of angiotensinogen in the liver, which is ultimately converted to angiotensin one and two. Cocaine is another potential drug that can cause hypertension by increasing sympathetic activity. Additionally, in people take monoamine-oxidase inhibitors, ingestion of tyramine-containing foods like cheese and wine may initiate an acute hypertension. Remember that sometimes the exam might not mention the medication but simply state that the person has a history of atypical or drug-resistant depression, which is an indication for MAOIs.

Alright, chronic hypertension can result in multiple complications affecting different organ systems. Let’s start with the heart. Hypertension increases the afterload, that is the resistance the heart has to pump against. In response, the left ventricle hypertrophies to overcome that resistance. Concentric hypertrophy increases the myocardial oxygen demand, which means the heart needs more coronary blood supply than usual. Also, concentric hypertrophy makes the heart stiff, which limits diastolic relaxation. This is why heart failure from hypertension is a diastolic heart failure, so the ejection fraction will actually be normal. Hypertension is also a risk factor for atherosclerosis, so there’s an increased risk of coronary artery disease, which is the most common cause of death from hypertension. Aortic dissection is another important complication, and hypertension is the most important risk factor contributing to it.

Sources

  1. "Rapid Review Pathology" Elsevier (2018)
  2. "Fundamentals of Pathology" H.A. Sattar (2017)
  3. "Williams Textbook of Endocrinology" W B Saunders Company (2008)
  4. "Pharmacotherapy for hypertension in adults aged 18 to 59 years" Cochrane Database Syst Rev (2017)
  5. "Hypertensive crisis" Cardiol Rev (2010)