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Reference intervals for bone turnover markers in Spanish premenopausal women

  • Núria Guañabens EMAIL logo , Xavier Filella , Ana Monegal , Carmen Gómez-Vaquero , María Bonet , Dolors Buquet , Enrique Casado , Dacia Cerdá , Alba Erra , Silvia Martinez , Núria Montalá , Concepción Pitarch , Eduardo Kanterewicz , Miquel Sala , Xavier Surís , Ferran Torres and on behalf of the LabOscat Study Group
Published/Copyright: June 18, 2015

Abstract

Background: The aims of this study were to establish robust reference intervals and to investigate the factors influencing bone turnover markers (BTMs) in healthy premenopausal Spanish women.

Methods: A total of 184 women (35–45 years) from 13 centers in Catalonia were analyzed. Blood and second void urine samples were collected between 8 a.m. and 10 a.m. after an overnight fast. Serum procollagen type I amino-terminal propeptide (PINP) and serum cross-linked C-terminal telopeptide of type I collagen (CTX-I) were measured by two automated assays (Roche and IDS), bone alkaline phosphatase (bone ALP) by ELISA, osteocalcin (OC) by IRMA and urinary NTX-I by ELISA. PTH and 25-hydroxyvitamin D (25OHD) levels were measured. All participants completed a questionnaire on lifestyle factors.

Results: Reference intervals were: PINP: 22.7–63.1 and 21.8–65.5 μg/L, bone ALP: 6.0–13.6 μg/L, OC: 8.0–23.0 μg/L, CTX-I: 137–484 and 109–544 ng/L and NTX-I: 19.6–68.9 nM/mM. Oral contraceptive pills (OCPs) influenced PINP (p=0.007), and low body mass index (BMI) was associated with higher BTMs except for bone ALP. Women under 40 had higher median values of most BTMs. CTX-I was influenced by calcium intake (p=0.010) and PTH (p=0.007). 25OHD levels did not influence BTMs. Concordance between the two automated assays for PINP and particularly CTX-I was poor.

Conclusions: Robust reference intervals for BTMs in a Southern European country are provided. The effects of OCPs and BMI on their levels are significant, whilst serum 25OHD levels did not influence BTMs. Age, calcium intake, BMI and PTH influenced CTX-I. The two automated assays for measuring PINP and CTX-I are not interchangeable.


Corresponding author: Núria Guañabens, Service of Rheumatology, Hospital Clínic, IDIBAPS, CIBERehd, University of Barcelona, C/Villarroel 170, 08036 Barcelona, Spain, Phone: +34 93 2275400 ext 2236, E-mail:

Acknowledgments

This study was funded by a research grant from the Catalan Society of Rheumatology. The kits were generously provided by Roche Diagnostics and by Immunodiagnostic Systems, Spain.

Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

Research funding: None declared.

Employment or leadership: None declared.

Honorarium: None declared.

Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

LabOscat Study group

Marta Larrosa, Rheumatology Department, University Institute Parc Taulí, Sabadell; Joan Miquel Nolla, Rheumatology Department, IDIBELL, Hospital Universitari de Bellvitge, L’Hospitalet, Barcelona; Pilar Peris, Rheumatology Department, Hospital Clinic, IDIBAPS, CIBERehd, Barcelona; Daniel Roig-Vilaseca, Rheumatology Department, Hospital Moisés Broggi, Barcelona.

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Received: 2015-2-16
Accepted: 2015-5-18
Published Online: 2015-6-18
Published in Print: 2016-2-1

©2016 by De Gruyter

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