Platelet Factor 4 Antibodies and Severe AKI.


Journal

Kidney360
ISSN: 2641-7650
Titre abrégé: Kidney360
Pays: United States
ID NLM: 101766381

Informations de publication

Date de publication:
01 Nov 2023
Historique:
received: 13 06 2023
accepted: 19 10 2023
medline: 1 11 2023
pubmed: 1 11 2023
entrez: 1 11 2023
Statut: aheadofprint

Résumé

Heparin-induced thrombocytopenia, which results from production of antibodies that bind to heparin-platelet factor 4 (PF4) complexes, is a hypercoagulable state associated with considerable morbidity and mortality due to thrombotic complications. We investigated whether PF4 antibodies are associated with an increased risk of acute kidney injury (AKI). We conducted a cohort study of hospitalized adults who underwent testing for PF4 antibodies at two large medical centers in Boston between 2015 and 2021. The primary exposure was PF4 test positivity. The primary outcome was severe AKI, defined by KDIGO stage 3 as a ≥3-fold increase in serum creatinine or receipt of kidney replacement therapy within 7 days following the PF4 test. We used multivariable logistic regression to adjust for potential confounders. A total of 4224 patients were included in our analysis, 469 (11.1%) of whom had a positive PF4 test. Severe AKI occurred in 50 of 469 patients (10.7%) with a positive PF4 test and in 235 of 3755 (6.3%) with a negative test (unadjusted odds ratio [OR] 1.79 [95% CI, 1.30-2.47]). In multivariable analyses adjusted for demographics, comorbidities, laboratory values, and severity-of-illness characteristics, PF4 test positivity remained associated with a higher risk of severe AKI (adjusted OR 1.56 [95% CI 1.10-2.20]). Among hospitalized adults, the presence of PF4 antibodies is independently associated with a 56% higher odds of developing severe AKI. Additional studies are needed to investigate potential mechanisms that may underlie these findings, such as pathogenic effects of PF4 antibodies on the microvasculature of the kidneys.

Sections du résumé

BACKGROUND BACKGROUND
Heparin-induced thrombocytopenia, which results from production of antibodies that bind to heparin-platelet factor 4 (PF4) complexes, is a hypercoagulable state associated with considerable morbidity and mortality due to thrombotic complications. We investigated whether PF4 antibodies are associated with an increased risk of acute kidney injury (AKI).
METHODS METHODS
We conducted a cohort study of hospitalized adults who underwent testing for PF4 antibodies at two large medical centers in Boston between 2015 and 2021. The primary exposure was PF4 test positivity. The primary outcome was severe AKI, defined by KDIGO stage 3 as a ≥3-fold increase in serum creatinine or receipt of kidney replacement therapy within 7 days following the PF4 test. We used multivariable logistic regression to adjust for potential confounders.
RESULTS RESULTS
A total of 4224 patients were included in our analysis, 469 (11.1%) of whom had a positive PF4 test. Severe AKI occurred in 50 of 469 patients (10.7%) with a positive PF4 test and in 235 of 3755 (6.3%) with a negative test (unadjusted odds ratio [OR] 1.79 [95% CI, 1.30-2.47]). In multivariable analyses adjusted for demographics, comorbidities, laboratory values, and severity-of-illness characteristics, PF4 test positivity remained associated with a higher risk of severe AKI (adjusted OR 1.56 [95% CI 1.10-2.20]).
CONCLUSIONS CONCLUSIONS
Among hospitalized adults, the presence of PF4 antibodies is independently associated with a 56% higher odds of developing severe AKI. Additional studies are needed to investigate potential mechanisms that may underlie these findings, such as pathogenic effects of PF4 antibodies on the microvasculature of the kidneys.

Identifiants

pubmed: 37907435
doi: 10.34067/KID.0000000000000287
pii: 02200512-990000000-00257
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NHLBI NIH HHS
ID : K23HL159313
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01HL144566
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01DK125786, R01DK126685
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23HL159313
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01HL144566
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01DK125786, R01DK126685
Pays : United States

Informations de copyright

Copyright © 2023 by the American Society of Nephrology.

Auteurs

Charlotte Thomas (C)

Harvard Medical School, Boston, MA.
Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA.

Rafia Ali (R)

Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA.

Isabel Park (I)

Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA.

Helena Kim (H)

Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA.

Samuel Short (S)

Larner College of Medicine, University of Vermont, Burlington, VT.

Sarah Kaunfer (S)

Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA.

Lavanya Durai (L)

Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA.

Osman A Yilmam (OA)

Harvard Medical School, Boston, MA.
Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA.

Tushar Shenoy (T)

Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA.

Elisabeth M Battinelli (EM)

Harvard Medical School, Boston, MA.
Division of Hematology, Brigham and Women's Hospital, Boston, MA.

Hanny Al-Samkari (H)

Harvard Medical School, Boston, MA.
Division of Hematology, Massachusetts General Hospital, Boston, MA.

David E Leaf (DE)

Harvard Medical School, Boston, MA.
Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA.

Classifications MeSH