The Urinary Angiotensinogen to Urinary Albumin Ratio Reflects Whether the Renin-angiotensin System in the Kidney Is Activated due to Filtration of Plasma Angiotensinogen through the Damaged Glomeruli or the Production of Angiotensinogen in the Proximal Tubules.


Journal

Internal medicine (Tokyo, Japan)
ISSN: 1349-7235
Titre abrégé: Intern Med
Pays: Japan
ID NLM: 9204241

Informations de publication

Date de publication:
01 Feb 2020
Historique:
pubmed: 20 9 2019
medline: 5 6 2020
entrez: 20 9 2019
Statut: ppublish

Résumé

Objective Urinary angiotensinogen (AGT) is a surrogate marker for intrarenal renin-angiotensin system (RAS) activity that plays an important role in the development of renal damage. Urinary AGT levels are determined by the filtration of plasma AGT through the damaged glomeruli and production of AGT in the proximal tubules. However, the relative merits of the filtration and production of urinary AGT levels in chronic kidney diseases (CKD) have not been clarified. Therefore, we investigated them in CKD patients. Methods We recruited 41 biopsy-proven patients diagnosed with IgA nephropathy (IgAN) in 31, membranous nephropathy (MN) in 5, and tubulointerstitial nephritis (TIN) in 5. The patients taking RAS blockers were excluded. Results The urinary albumin levels in MN patients were significantly higher and those in TIN patients significantly lower than in IgAN patients, and the urinary AGT levels in the MN and TIN patients were significantly higher than those in IgAN patients. Conversely, the urinary AGT-to-urinary albumin (urinary AGT/Alb) ratios were the same for IgAN and MN patients, and those of TIN patients were significantly higher than those of IgAN and MN patients. A multiple linear regression analysis revealed that the urinary AGT/Alb ratios had a significant positive association with IgAN and TIN after adjustments (β=0.75, and p<0.01). Conclusion These data suggest that the origins of urinary AGT may differ according to the etiology of renal damage [i.e. glomerular damage (such as IgAN and MN) or tubulointerstitial damage (such as TIN)], and a higher urinary AGT/Alb ratio, as in TIN, may reflect AGT production in the kidney.

Identifiants

pubmed: 31534091
doi: 10.2169/internalmedicine.3624-19
pmc: PMC7028426
doi:

Substances chimiques

Angiotensinogen 11002-13-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

357-364

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Auteurs

Naro Ohashi (N)

Internal Medicine 1, Hamamatsu University School of Medicine, Japan.

Taro Aoki (T)

Internal Medicine 1, Hamamatsu University School of Medicine, Japan.

Takashi Matsuyama (T)

Internal Medicine 1, Hamamatsu University School of Medicine, Japan.

Sayaka Ishigaki (S)

Blood Purification Unit, Hamamatsu University School of Medicine, Japan.

Shinsuke Isobe (S)

Internal Medicine 1, Hamamatsu University School of Medicine, Japan.

Naoko Katahashi (N)

Internal Medicine 1, Hamamatsu University School of Medicine, Japan.

Taichi Sato (T)

Internal Medicine 1, Hamamatsu University School of Medicine, Japan.

Tomoyuki Fujikura (T)

Internal Medicine 1, Hamamatsu University School of Medicine, Japan.

Akihiko Kato (A)

Blood Purification Unit, Hamamatsu University School of Medicine, Japan.

Hideo Yasuda (H)

Internal Medicine 1, Hamamatsu University School of Medicine, Japan.

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Classifications MeSH