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Impaired Urine Dilution Capability in HIV Stable Patients
Author(s) -
Waldo Belloso,
Mariana de Paz Sierra,
Matilde Navarro,
Marisa Sánchez,
Ariel Perelsztein,
Carlos G. Musso
Publication year - 2014
Publication title -
international journal of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.551
H-Index - 29
eISSN - 2090-2158
pISSN - 2090-214X
DOI - 10.1155/2014/381985
Subject(s) - medicine , renal function , urine , urine osmolality , reabsorption , osmotic concentration , free water clearance , sodium , tenofovir , human immunodeficiency virus (hiv) , renal tubule , kidney , urology , endocrinology , physiology , immunology , chemistry , organic chemistry
Renal disease is a well-recognized complication among patients with HIV infection. Viral infection itself and the use of some antiretroviral drugs contribute to this condition. The thick ascending limb of Henle's loop (TALH) is the tubule segment where free water clearance is generated, determining along with glomerular filtration rate the kidney's ability to dilute urine. Objective . We analyzed the function of the proximal tubule and TALH in patients with HIV infection receiving or not tenofovir-containing antiretroviral treatment in comparison with healthy seronegative controls, by applying a tubular physiological test, hyposaline infusion test (Chaimowitz' test). Material & Methods . Chaimowitz' test was performed on 20 HIV positive volunteers who had normal renal functional parameters. The control group included 10 healthy volunteers. Results . After the test, both HIV groups had a significant reduction of serum sodium and osmolarity compared with the control group. Free water clearance was lower and urine osmolarity was higher in both HIV+ groups. Proximal tubular function was normal in both studied groups. Conclusion . The present study documented that proximal tubule sodium reabsorption was preserved while free water clearance and maximal urine dilution capability were reduced in stable HIV patients treated or not with tenofovir.

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