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Kidney microRNA-21 Expression and Kidney Function in IgA Nephropathy.
Szeto, Cheuk-Chun; Ng, Jack Kit-Chung; Fung, Winston Wing-Shing; Luk, Cathy Choi-Wan; Wang, Gang; Chow, Kai-Ming; Lai, Ka-Bik; Li, Philip Kam-Tao; Lai, Fernand Mac-Moune.
Afiliação
  • Szeto CC; Department of Medicine & Therapeutics, Prince of Wales Hospital, Hong Kong, China.
  • Ng JK; Li Ka Shing Institute of Health Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, China.
  • Fung WW; Department of Medicine & Therapeutics, Prince of Wales Hospital, Hong Kong, China.
  • Luk CC; Department of Medicine & Therapeutics, Prince of Wales Hospital, Hong Kong, China.
  • Wang G; Department of Medicine & Therapeutics, Prince of Wales Hospital, Hong Kong, China.
  • Chow KM; Li Ka Shing Institute of Health Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, China.
  • Lai KB; Department of Medicine & Therapeutics, Prince of Wales Hospital, Hong Kong, China.
  • Li PK; Department of Medicine & Therapeutics, Prince of Wales Hospital, Hong Kong, China.
  • Lai FM; Department of Medicine & Therapeutics, Prince of Wales Hospital, Hong Kong, China.
Kidney Med ; 3(1): 76-82.e1, 2021.
Article em En | MEDLINE | ID: mdl-33604541
ABSTRACT
RATIONALE &

OBJECTIVE:

Previous studies have suggested that microRNA-21 (miR-21) plays an important role in kidney fibrosis. We examined the relationship between intrarenal miR-21 level and rate of kidney function loss in immunoglobulin A nephropathy (IgAN). STUDY

DESIGN:

Prospective cohort study. SETTING &

PARTICIPANTS:

40 patients with IgAN and 10 with hypertensive nephrosclerosis as controls. PREDICTORS miR-21 levels in kidney biopsy specimen and urinary sediment, quantified as ratio to the housekeeping gene.

OUTCOMES:

Kidney event-free survival and rate of kidney function decline. ANALYTIC

APPROACH:

Time-to-event and correlation analysis.

RESULTS:

The IgAN group had significantly higher intrarenal miR-21 expression compared with the hypertensive nephrosclerosis group (1.71 [IQR, 0.99-2.77] vs 0.31 [IQR, 0.25-1.32]; P < 0.0001), but urinary miR-21 levels were similar. Intrarenal miR-21 expression had significant but modest correlation with severity of glomerulosclerosis (r = 0.293; P = 0.05) and tubulointerstitial fibrosis (r = 0.341; P = 0.03). Patients with high intrarenal miR-21 expression had significantly higher risk for developing kidney end points compared with those with low expression (log-rank test, P = 0.017). Univariate Cox analysis showed that intrarenal miR-21 expression significantly predicted the development of kidney end points (unadjusted HR, 1.586; 95% CI, 1.179-2.134; P = 0.002). However, the result was just short of statistical significance after adjusting for the severity of histologic damage (P = 0.06). There was also a significant correlation between intrarenal miR-21 expression and the slope of kidney function decline by univariate analysis (r = -0.399; P = 0.02).

LIMITATIONS:

Small sample size; uncertain cellular origin of miR-21.

CONCLUSIONS:

We found that intrarenal miR-21 expression is increased in patients with IgAN, modestly correlated with the severity of histologic damage, and predictive of subsequent kidney function loss.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article