Creatinine-to-cystatin C ratio and bioelectrical impedance analysis for the assessement of low lean body mass in cancer patients: Comparison to L3-computed tomography scan.


Journal

Nutrition (Burbank, Los Angeles County, Calif.)
ISSN: 1873-1244
Titre abrégé: Nutrition
Pays: United States
ID NLM: 8802712

Informations de publication

Date de publication:
01 2021
Historique:
received: 05 02 2020
revised: 07 05 2020
accepted: 27 05 2020
pubmed: 3 8 2020
medline: 24 6 2021
entrez: 3 8 2020
Statut: ppublish

Résumé

Lean body mass (LBM) is an important prognostic factor in patients with cancer. Although the L3-computed tomography (CT) scan is considered a reference method for assessment, a convenient and easily available method for longitudinal follow-up is required. Although bioelectrical impedance analysis (BIA) is widely used, its accuracy is questioned; plasma creatinine-to-cystatin C (CC) ratio could be an attractive alternative. The aim of this study was to evaluate the ability of the CC ratio and BIA to detect myopenia in patients with cancer compared with the use of the CT scan as a standard. Patients with any kind of cancer had body composition evaluation by CT scan, BIA, and CC. Statistical analysis included correlation test, Bland-Altman, and receiver operating characteristic curve analysis. Forty-four patients (14 women) were included. Of the participants, 59% had myopenia on CT scan. Both BIA LBM and CC ratio were well correlated with CT scan LBM (r = 0.763 and 0.648, respectively) but concordance analysis revealed a 3-kg constant bias toward BIA compared with CT scan. In terms of ability to detect myopenia, areas under the curve (AUC) for BIA were 0.675 and 0.388 for men and women, respectively. For CC ratio, AUCs were 0.813 and 0.673. This study demonstrated that LBM assessed by the CC ratio or BIA is well correlated with that determined by L3-CT scan. The ability of the CC ratio to detect myopenia was better than that of BIA. Findings from the present study demonstrated that CC ratio can be conveniently used in patients with cancer as a reliable biomarker of muscularity.

Identifiants

pubmed: 32739656
pii: S0899-9007(20)30178-7
doi: 10.1016/j.nut.2020.110895
pii:
doi:

Substances chimiques

Cystatin C 0
Creatinine AYI8EX34EU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

110895

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Guillame Ulmann (G)

Clinical Chemistry Department, Hôpital Cochin, AP-HP Centre, Université de Paris, Paris, France; EA 4466 PRETRAM, Faculty of Pharmacy, Université de Paris, Paris, France. Electronic address: guillaume.ulmann@aphp.fr.

Joanna Kaï (J)

Clinical Chemistry Department, Hôpital Cochin, AP-HP Centre, Université de Paris, Paris, France.

Jean-Philippe Durand (JP)

EA 4466 PRETRAM, Faculty of Pharmacy, Université de Paris, Paris, France; Medical Oncology Department, Hôpital Cochin, AP-HP Centre, Université de Paris, Paris, France.

Nathalie Neveux (N)

Clinical Chemistry Department, Hôpital Cochin, AP-HP Centre, Université de Paris, Paris, France; EA 4466 PRETRAM, Faculty of Pharmacy, Université de Paris, Paris, France.

Anne Jouinot (A)

Medical Oncology Department, Hôpital Cochin, AP-HP Centre, Université de Paris, Paris, France.

Jean-Pascal De Bandt (JP)

Clinical Chemistry Department, Hôpital Cochin, AP-HP Centre, Université de Paris, Paris, France; EA 4466 PRETRAM, Faculty of Pharmacy, Université de Paris, Paris, France.

Francois Goldwasser (F)

EA 4466 PRETRAM, Faculty of Pharmacy, Université de Paris, Paris, France; Medical Oncology Department, Hôpital Cochin, AP-HP Centre, Université de Paris, Paris, France.

Luc Cynober (L)

Clinical Chemistry Department, Hôpital Cochin, AP-HP Centre, Université de Paris, Paris, France; EA 4466 PRETRAM, Faculty of Pharmacy, Université de Paris, Paris, France.

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