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ABSTRACTS from 16th International COnference on ... - CRRT Online

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<str<strong>on</strong>g>ABSTRACTS</str<strong>on</strong>g> FROM 17 TH INTERNATIONAL CONFERENCE ON <strong>CRRT</strong>,<br />

SAN DIEGO, FEB 14-17, 2012<br />

We isolated MVs <str<strong>on</strong>g>from</str<strong>on</strong>g> EPC<br />

supernatants by uktracentrifugati<strong>on</strong> and<br />

we characterized their RNA c<strong>on</strong>tent<br />

showing the enrichment in microRNAs<br />

that modulate proliferati<strong>on</strong> and<br />

apoptosis. Results: After i.v. injecti<strong>on</strong> in<br />

cisplatin-treated mice, MVs localized in<br />

peritubular capillaries and tubular<br />

epithelial cells, significantly decreased<br />

mortality 7 days after administrati<strong>on</strong> and<br />

c<strong>on</strong>ferred functi<strong>on</strong>al and morphologic<br />

protecti<strong>on</strong> <str<strong>on</strong>g>from</str<strong>on</strong>g> AKI by enhancing<br />

tubular proliferati<strong>on</strong> and reducing<br />

apoptosis. In surviving animals, a<br />

preserved renal functi<strong>on</strong> and histology<br />

was observed also 28 days after<br />

injecti<strong>on</strong>. Evidence for a role of MVmediated<br />

transfer of RNAs in the<br />

renoprotective effect of MVs was<br />

derived <str<strong>on</strong>g>from</str<strong>on</strong>g> the loss of MV activity<br />

after 1) their treatment with RNase, 2)<br />

unspecific microRNA-depleti<strong>on</strong> of MVs<br />

by EPC transfecti<strong>on</strong> with siRNA for<br />

Dicer, the intracellular enzyme essential<br />

for microRNA synthesus and 3) MV<br />

depleti<strong>on</strong> of the anti-apoptotic<br />

microRNA miR-27a by EPC transfecti<strong>on</strong><br />

with a specific antagomiR. In vitro, we<br />

c<strong>on</strong>firmed the role of miR-27a in the<br />

anti-apoptotic effect of MVs in cisplatintreated<br />

human tubular epithelial cells.<br />

Indeed, MVs derived <str<strong>on</strong>g>from</str<strong>on</strong>g> EPCs<br />

significantly reduced apoptosis through<br />

the down-regulati<strong>on</strong> of the death<br />

receptor Fas (CD95), of the<br />

mitoch<strong>on</strong>drial molecules Bcl-XL/Bcl-2<br />

and of caspase-3, -8 and -9 activati<strong>on</strong>.<br />

These effects were not observed after<br />

miR-27a depleti<strong>on</strong>. C<strong>on</strong>clusi<strong>on</strong>s: MVs<br />

derived <str<strong>on</strong>g>from</str<strong>on</strong>g> EPCs protected <str<strong>on</strong>g>from</str<strong>on</strong>g><br />

cisplatin-induced AKI by delivering<br />

their RNA c<strong>on</strong>tent. The miRNA cargo of<br />

MVs and in particular miR-27a<br />

c<strong>on</strong>tributed to reprogramming cisplatininjured<br />

tubular epithelial cells toward a<br />

regenerative program, inhibiting the<br />

death receptor/mitoch<strong>on</strong>drial apopototic<br />

pathways.<br />

35. Classificati<strong>on</strong> Of AKI Using P-<br />

Rifle Score In A Picu In<br />

Fundación Valle Del Lili, Cali,<br />

Colombia<br />

Gastón Castillo, Angie Cañas, María del<br />

Pilar Duque, Fernando Bermúdez,<br />

Eliana Manzi, Teresa Agudelo, Jaime<br />

Restrepo, Magda Cepeda<br />

Fundación Valle del Lili<br />

Introducti<strong>on</strong> and Aim: Acute Kidney<br />

Injury (AKI)\'s incidence in PICU<br />

patient worsen mortality. We used the p-<br />

RIFLE score to estimate the incidence of<br />

AKI in children of PICU in an institute<br />

in of fourth level in Cali. Methods:<br />

Prospective study of patients<br />

hospitalized in PICU between<br />

september/29 and august/211, with AKI,<br />

in whom the p-RIFLE score was applied.<br />

Results: Am<strong>on</strong>g 1891 patients registered<br />

in PICU, 3.86% presented AKI. Half<br />

were under 24 m<strong>on</strong>th age (p25-p75: 6-<br />

18), and 58% were male. At 24 and 72<br />

hours of admissi<strong>on</strong>, 43% and 66% of<br />

patients presented Failure, respectively.<br />

The principal admissi<strong>on</strong> diagnosis were<br />

cardiovascular (34%) and infectious<br />

(18%). 32 (44%) dead. Mortality by p-<br />

RIFLE in 24hrs is similar across strata,<br />

while at 72hrs Failure was higher. The<br />

relati<strong>on</strong> in mortality was invested for<br />

patients classified as Failure am<strong>on</strong>g 24<br />

and 72 hrs, vs. observed in Risk and<br />

Injury (Graphic). The associati<strong>on</strong> of<br />

mortality with p-RIFLE at 72hrs was<br />

significant (p=.), while at 24hrs did not<br />

(p=.712). 4% of patients were classified<br />

as very high of mortality by PRISM, but<br />

was not associated with mortality<br />

(p=.455). 39 (53%) of patients required<br />

RRT, but was not associated neither<br />

mortality (p=.368) nor worsening of<br />

RIFLe (p=.99). C<strong>on</strong>clusi<strong>on</strong>s: The use of<br />

149

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