Chronic kidney disease

Last updated: February 23, 2023

Chronic kidney disease

PBL MS2 S1 Exam 3

PBL MS2 S1 Exam 3

Alcohol-associated liver disease
Liver anatomy and physiology
Benign liver tumors
Non-alcoholic fatty liver disease
Anatomy of the abdominal viscera: Liver, biliary ducts and gallbladder
Hepatic encephalopathy
Wilson disease
Ischemia
Cirrhosis
Cirrhosis: Pathology review
Jaundice
Portal hypertension
Hemochromatosis
Autoimmune hepatitis
Alpha 1-antitrypsin deficiency
Primary sclerosing cholangitis
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Reye syndrome
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Blood histology
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Role of Vitamin K in coagulation
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Clot retraction and fibrinolysis
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ACE inhibitors, ARBs and direct renin inhibitors
Osmotic diuretics
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Loop diuretics
Thiazide and thiazide-like diuretics
Potassium sparing diuretics
Congenital renal disorders: Pathology review
Renal tubular defects: Pathology review
Renal tubular acidosis: Pathology review
Acid-base disturbances: Pathology review
Electrolyte disturbances: Pathology review
Renal failure: Pathology review
Nephrotic syndromes: Pathology review
Nephritic syndromes: Pathology review
Urinary incontinence: Pathology review
Urinary tract infections: Pathology review
Kidney stones: Pathology review
Renal and urinary tract masses: Pathology review
Posterior urethral valves
Hypospadias and epispadias
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Potter sequence
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Hypernatremia
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Renal tubular acidosis
Minimal change disease
Diabetic nephropathy
Focal segmental glomerulosclerosis (NORD)
Amyloidosis
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Poststreptococcal glomerulonephritis
Rapidly progressive glomerulonephritis
IgA nephropathy (NORD)
Alport syndrome
Kidney stones
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Acute pyelonephritis
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Prerenal azotemia
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Chronic kidney disease
Polycystic kidney disease
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Medullary sponge kidney
Renal artery stenosis
Renal cell carcinoma
Angiomyolipoma
Nephroblastoma (Wilms tumor)
WAGR syndrome
Beckwith-Wiedemann syndrome
Physiologic pH and buffers
Buffering and Henderson-Hasselbalch equation
The role of the kidney in acid-base balance
Acid-base map and compensatory mechanisms
Respiratory acidosis
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Plasma anion gap
Respiratory alkalosis
Metabolic alkalosis
Osmoregulation
Sodium homeostasis
Antidiuretic hormone
Kidney countercurrent multiplication
Free water clearance
Potassium homeostasis
Phosphate, calcium and magnesium homeostasis
Renin-angiotensin-aldosterone system
Proximal convoluted tubule
Loop of Henle
Distal convoluted tubule
Tubular reabsorption and secretion
Tubular secretion of PAH
Tubular reabsorption of glucose
Urea recycling
Tubular reabsorption and secretion of weak acids and bases
Renal clearance
Glomerular filtration
TF/Px ratio and TF/Pinulin
Measuring renal plasma flow and renal blood flow
Regulation of renal blood flow
Hydration
Body fluid compartments
Movement of water between body compartments
Renal system anatomy and physiology
Drug administration and dosing regimens
Ureter, bladder and urethra histology
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Haemophilus ducreyi (Chancroid)
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Long QT syndrome and Torsade de pointes
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Positive inotropic medications
Acute kidney injury: Clinical
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Multiple endocrine neoplasia: Pathology review
Endocrine system anatomy and physiology
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Pancreas histology
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Menopause
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Hypothyroidism
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Adrenal insufficiency: Pathology review
Adrenal hormone synthesis inhibitors
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Adrenal insufficiency: Clinical
Synthesis of adrenocortical hormones
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Cushing syndrome and Cushing disease: Pathology review
Testosterone
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Managing diabetes during the holidays: Information for patients and families
Hypernatremia: Clinical
Acromegaly
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Leg ulcers: Clinical
Chronic kidney disease: Clinical
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Abnormal uterine bleeding: Clinical
Perinatal infections: Clinical
Hypertensive disorders of pregnancy: Clinical
Complications during pregnancy: Pathology review
Ectopic pregnancy
Pregnancy

Transcript

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Chronic kidney disease is a broad term that includes subtle decreases in kidney function that develop over a minimum of three months.

In contrast, acute kidney injury refers to any deterioration in kidney function that happens in less than three months.

Now the kidney’s job is to regulate what’s in the blood, so they might remove waste, or make sure electrolyte levels are steady, or regulate the overall amount of water, and even make hormones - the kidneys do a lot of stuff!

Blood gets into the kidney through the renal artery, and once inside it goes gets into tiny clumps of arterioles called glomeruli where it’s initially filtered, and the filtrate which is the stuff that gets filtered out, moves into the renal tubule.

The rate at which this filtration takes place is known as glomerular filtration rate or GFR. In a normal healthy person, this is somewhere around 100-120 milliliter of fluid filtered per minute per 1.73 m2 of body surface area. The value is slightly less in women than men and it decreases slowly in all of us as we grow older.

One of the most common causes of chronic kidney disease is hypertension.

In hypertension, the walls of arteries supplying the kidney begin to thicken in order to withstand the pressure, and that results in a narrow lumen. A narrow lumen means less blood and oxygen gets delivered to the kidney, resulting in ischemic injury to the nephron’s glomerulus.

Immune cells like macrophages and fat-laden macrophages called foam cells slip into the damage glomerulus and start secreting growth factors like Transforming Growth Factor ß1 or TGF-ß1.

These growth factors cause the mesangial cells to regress back to their more immature stem cell state known as mesangioblasts and secrete extracellular structural matrix. This excessive extracellular matrix leads to glomerulosclerosis, hardening and scarr, and diminishes the nephron’s ability to filter the blood - over time leading to chronic kidney disease.

The most common cause of CKD is diabetes, excess glucose in the blood starts sticking to proteins in the blood — a process called non-enzymatic glycation because no enzymes are involved.

This process of glycation particularly affects the efferent arteriole and causes it to get stiff and more narrow - a process called hyaline arteriosclerosis. This creates an obstruction that makes it difficult for blood to leave the glomerulus, and increases pressure within the glomerulus leading to hyperfiltration.

In response to this high-pressure state, the supportive mesangial cells secrete more and more structural matrix expanding the size of the glomerulus.

Over many years, this process of glomerulosclerosis, once again, diminishes the nephron’s ability to filter the blood and leads to chronic kidney disease.

Although diabetes and hypertension are responsible for the vast majority of CKD cases, there are other systemic diseases like lupus and rheumatoid arthritis, can also cause glomerulosclerosis.

Other causes of chronic kidney disease include infections like HIV, as well as long-term use of medications like NSAIDs, and toxins like the ones in tobacco.

Now, normally urea in the body gets excreted in the urine, but when there’s a decreased glomerular filtration fate, less urea get filtered out, and therefore it accumulates in the blood, a condition called azotemia, which can cause general symptoms like It nausea and a loss of appetite.

As the toxin levels really build up, they can affect the functioning of the central nervous system - causing encephalopathy. This results in asterixis, a tremor of the hand that kind of resembles a bird flapping its wings and is best seen when the person attempts to extend their wrists.

Further accumulation of these toxins in the brain can even progress to coma and death.