Proximal renal tubular acidosis is a condition that occurs when the kidneys don't properly remove acids in the urine, leaving the blood too acidic.
Alternative NamesRenal tubular acidosis - proximal; Type II RTA; RTA - proximal; Renal tubular acidosis type II
Causes, incidence, and risk factorsYour kidneys help regulate your body's acid-base balance (pH). Acidic substances in the body are buffered (counteracted) by alkaline substances, primarily bicarbonate.
The kidneys contain more than a million filtering units, called nephrons. Bicarbonate is reabsorbed into the blood in the initial (proximal) part of the tubule of each nephron. Proximal renal tubular acidosis (Type II RTA) occurs when bicarbonate is not properly reabsorbed by the proximal tubules, leaving the body in an acidic state (called acidosis).
Type II RTA is less common than Type I RTA. It most often occurs during infancy, and may go away by itself.
Causes of type II RTA include:
Other symptoms can include:
Arterial blood gas and blood chemistries may suggest metabolic acidosis and electrolyte imbalances, most often low levels of potassium or bicarbonate.
Other tests that may be done include:
This disease may also change the results of the following tests:
TreatmentThe goal is to restore the normal pH (acid-base level) and electrolyte balance to the body. This will indirectly correct bone disorders and reduce the risk of osteomalacia and osteopenia in adults.
Some adults may need no treatment. All children need alkaline medication to prevent acid-induced bone disease, such as rickets, and to allow normal growth. The underlying cause should be corrected if it can be found.
Alkaline medications include sodium bicarbonate and potassium citrate. They correct the acidic condition of the body and correct low blood potassium levels. Thiazide diuretics may indirectly decrease bicarbonate loss but may worsen the low blood potassium levels.
Vitamin D and calcium supplements may be needed to help reduce skeletal deformities resulting from osteomalacia or rickets.
Expectations (prognosis)Although the underlying cause of proximal renal tubular acidosis may go away by itself, the effects and complications can be permanent or life-threatening. Treatment is usually successful.
ComplicationsCall your health care provider if you have symptoms of proximal renal tubular acidosis.
Get medical help immediately if you develop any of the following emergency symptoms:
Most of the disorders that cause proximal renal tubular acidosis are not preventable.
ReferencesSeifter JL. Acid-base disorders. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier; 2007: chap 119.
Proximal renal tubular acidosis (type 2) is caused by hereditary diseases, such as Fanconi's syndrome, fructose intolerance, and Lowe's syndrome.
Relatives of patients with the possibly hereditary forms of renal tubular acidosis should be tested.
vitamin D deficiency, kidney transplantation, heavy metal poisoning, and treatment with certain drugs.
The prognosis is good for someone who has renal tubular acidosis and they are receiving the right treatments. They will need high doses of bicarbonate and correction of the acidosis and potassium levels are required.
Type 4 renal tubular acidosis is not hereditary, but is associated with diabetes mellitus, sickle cell anemia, an autoimmune disease, or an obstructed urinary tract.
Type I Renal Tubular Acidosis
If the kidneys do not effectively eliminate acid, it builds up in the blood, leading to a condition called metabolic acidosis. These conditions are called renal tubular acidosis.
Paul P. Leyssac has written: 'The regulation of proximal tubular reabsorption in the mammalian kidney' -- subject(s): Absorption (Physiology), Angiotensins, Kidney tubules, Renal tubular transport
These diseases include primary parathyroidism, sarcoidosis, hyperthyroidism , renal tubular acidosis, multiple myeloma, hyperoxaluria, and some types of cancer.
Tubular reabsorption is the movement of filtrate from renal tubules back into blood in response to the body's specific needs.
The main capillaries of the renal cortex which arise from the efferent arteriole after it leaves the renal corpuscle and wrap around the renal tubules, especially the proximal and distal tubules, to supply nutrients and oxygen to the tubules, to carry away wastes from the tubular cells.
1.glomerular filtration by the glomeruli2.tubular reabsorption by the renal tubules3.tubular secretion by the renal tubules