Urine Protein/Creatinine Ratio in Thrombotic Microangiopathies: A Simple Test to Facilitate Thrombotic Thrombocytopenic Purpura and Hemolytic and Uremic Syndrome Diagnosis.

diagnosis differential hemolytic-uremic syndrome proteinuria purpura thrombotic microangiopathies thrombotic thrombocytopenic

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
27 Jan 2022
Historique:
received: 06 12 2021
revised: 14 01 2022
accepted: 24 01 2022
entrez: 15 2 2022
pubmed: 16 2 2022
medline: 16 2 2022
Statut: epublish

Résumé

Early diagnosis of thrombotic thrombocytopenic purpura (TTP) versus hemolytic and uremic syndrome (HUS) is critical for the prompt initiation of specific therapies. To evaluate the diagnostic performance of the proteinuria/creatininuria ratio (PU/CU) for TTP versus HUS. In a retrospective study, in association with the "French Score" (FS) (platelets < 30 G/L and serum creatinine level < 200 µmol/L), we assessed PU/CU for the diagnosis of TTP in patients above the age of 15 with thrombotic microangiopathy (TMA). Patients with a history of kidney disease or with on-going cancer, allograft or pregnancy were excluded from the analysis. Between February 2011 and April 2019, we identified 124 TMA. Fifty-six TMA patients for whom PU/CU were available, including 35 TTP and 21 HUS cases, were considered. Using receiver-operating characteristic curves (ROC), those with a threshold of 1.5 g/g for the PU/CU had a 77% sensitivity (95% CI (63, 94)) and a 90% specificity (95% CI (71, 100)) for TTP diagnosis compared with those having an 80% sensitivity (95% CI (66, 92)) and a 90% specificity (95% CI (76, 100) with a FS of 2. In comparison, a composite score, defined as a FS of 2 or a PU/CU ≤ 1.5 g/g, improved sensitivity to 99.6% (95% CI (93, 100)) for TTP diagnosis and enabled us to reclassify seven false-negative TTP patients. The addition of urinary PU/CU upon admission of patients with TMA is a fast and readily available test that can aid in the differential diagnosis of TTP versus HUS alongside traditional scoring.

Sections du résumé

BACKGROUND BACKGROUND
Early diagnosis of thrombotic thrombocytopenic purpura (TTP) versus hemolytic and uremic syndrome (HUS) is critical for the prompt initiation of specific therapies.
OBJECTIVE OBJECTIVE
To evaluate the diagnostic performance of the proteinuria/creatininuria ratio (PU/CU) for TTP versus HUS.
PATIENTS/METHODS METHODS
In a retrospective study, in association with the "French Score" (FS) (platelets < 30 G/L and serum creatinine level < 200 µmol/L), we assessed PU/CU for the diagnosis of TTP in patients above the age of 15 with thrombotic microangiopathy (TMA). Patients with a history of kidney disease or with on-going cancer, allograft or pregnancy were excluded from the analysis.
RESULTS RESULTS
Between February 2011 and April 2019, we identified 124 TMA. Fifty-six TMA patients for whom PU/CU were available, including 35 TTP and 21 HUS cases, were considered. Using receiver-operating characteristic curves (ROC), those with a threshold of 1.5 g/g for the PU/CU had a 77% sensitivity (95% CI (63, 94)) and a 90% specificity (95% CI (71, 100)) for TTP diagnosis compared with those having an 80% sensitivity (95% CI (66, 92)) and a 90% specificity (95% CI (76, 100) with a FS of 2. In comparison, a composite score, defined as a FS of 2 or a PU/CU ≤ 1.5 g/g, improved sensitivity to 99.6% (95% CI (93, 100)) for TTP diagnosis and enabled us to reclassify seven false-negative TTP patients.
CONCLUSIONS CONCLUSIONS
The addition of urinary PU/CU upon admission of patients with TMA is a fast and readily available test that can aid in the differential diagnosis of TTP versus HUS alongside traditional scoring.

Identifiants

pubmed: 35160098
pii: jcm11030648
doi: 10.3390/jcm11030648
pmc: PMC8836555
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Laure Burguet (L)

Service de Néphrologie Transplantation Dialyse Aphérèses, Centre de Référence Maladies Rénales Rares du Sud-Ouest, Centre Hospitalier Universitaire de Bordeaux, 33000 Bordeaux, France.

Benjamin Taton (B)

Service de Néphrologie Transplantation Dialyse Aphérèses, Centre de Référence Maladies Rénales Rares du Sud-Ouest, Centre Hospitalier Universitaire de Bordeaux, 33000 Bordeaux, France.

Mathilde Prezelin-Reydit (M)

Service de Néphrologie Transplantation Dialyse Aphérèses, Centre de Référence Maladies Rénales Rares du Sud-Ouest, Centre Hospitalier Universitaire de Bordeaux, 33000 Bordeaux, France.

Sébastien Rubin (S)

Service de Néphrologie Transplantation Dialyse Aphérèses, Centre de Référence Maladies Rénales Rares du Sud-Ouest, Centre Hospitalier Universitaire de Bordeaux, 33000 Bordeaux, France.

Walter Picard (W)

Service de Réanimation, Centre Hospitalier de PAU, 64000 Pau, France.

Didier Gruson (D)

Service de Réanimation, Centre Hospitalier Universitaire de Bordeaux, 33000 Bordeaux, France.

Anne Ryman (A)

Laboratoire d'hématologie Biologique, Centre Hospitalier Universitaire de Bordeaux, 33000 Bordeaux, France.
Département d'hématologie et Centre de Reference des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, Assistance Publique des Hôpitaux de Paris and Sorbonne Universités, 75651 Paris, France.

Cécile Contin-Bordes (C)

Département d'hématologie et Centre de Reference des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, Assistance Publique des Hôpitaux de Paris and Sorbonne Universités, 75651 Paris, France.
Laboratoire d'Immunologie et Immunogénétique, Centre Hospitalier Universitaire de Bordeaux, 33000 Bordeaux, France.
Immunoconcept, CNRS UMR 5164, Université de Bordeaux, 33076 Bordeaux, France.

Paul Coppo (P)

Département d'hématologie et Centre de Reference des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, Assistance Publique des Hôpitaux de Paris and Sorbonne Universités, 75651 Paris, France.

Christian Combe (C)

Service de Néphrologie Transplantation Dialyse Aphérèses, Centre de Référence Maladies Rénales Rares du Sud-Ouest, Centre Hospitalier Universitaire de Bordeaux, 33000 Bordeaux, France.
Unité INSERM 1026 Biotis, Université de Bordeaux, 33076 Bordeaux, France.

Yahsou Delmas (Y)

Service de Néphrologie Transplantation Dialyse Aphérèses, Centre de Référence Maladies Rénales Rares du Sud-Ouest, Centre Hospitalier Universitaire de Bordeaux, 33000 Bordeaux, France.
Département d'hématologie et Centre de Reference des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, Assistance Publique des Hôpitaux de Paris and Sorbonne Universités, 75651 Paris, France.

Classifications MeSH