Jump to content

Isosthenuria

From Wikipedia, the free encyclopedia

This is the current revision of this page, as edited by Anupam (talk | contribs) at 08:52, 2 February 2022 (Clinical significance: added wikilink to chronic kidney disease). The present address (URL) is a permanent link to this version.

(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)

Isosthenuria refers to the excretion of urine whose specific gravity (concentration) is neither greater (more concentrated) nor less (more diluted) than that of protein-free plasma, typically 1.008-1.012.[1] Isosthenuria reflects damage to the kidney's tubules or the renal medulla.

A closely related term is hyposthenuria, where the urine has a relatively low specific gravity "due to inability of the kidney to concentrate the urine normally".[2][3] This specific gravity is not necessarily equal to that of plasma. Therefore, unlike isosthenuria, this condition is not associated with kidney failure as the kidney tubules have altered the glomerular filtrate.

Clinical significance

[edit]

Isosthenuria may be seen in disease states as chronic kidney disease and acute kidney injury in which the kidneys lack the ability to concentrate or dilute the urine and so the initial filtrate of the blood remains unchanged despite the need to conserve or excrete water based on the body's hydration status.[4]

Sickle-cell trait, the heterozygous form of sickle-cell disease, presents with a normal hematological picture but is associated with hyposthenuria.[5]

See also

[edit]

References

[edit]
  1. ^ "isosthenuria" at Dorland's Medical Dictionary
  2. ^ "hyposthenuria" at Dorland's Medical Dictionary
  3. ^ "Medical Definition of HYPOSTHENURIA". Merriam-Webster. Retrieved 2 February 2022.
  4. ^ De Mais, Daniel. ASCP Quick Compendium of Clinical Pathology, 2nd Ed. ASCP Press, Chicago, 2009.
  5. ^ Gupta AK, Kirchner KA, Nicholson R, et al. Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell trait and increased frequency of urinary tract infections J. Clin. Invest. Vol 88, Issue 6, pgs 1963-8. Dec 1991. PMID 1752955 PMC = 295777. DOI = 10.1172/JCI115521