Calcified Tissue International

, Volume 102, Issue 6, pp 651–656 | Cite as

High Serum Retinol as a Relevant Contributor to Low Bone Mineral Density in Postmenopausal Osteoporotic Women

  • Cristina Navarro-Valverde
  • Javier Caballero-Villarraso
  • José M. Mata-Granados
  • Antonio Casado-Díaz
  • Manuel Sosa-Henríquez
  • Jorge Malouf-Sierra
  • Xavier Nogués-Solán
  • Leocadio Rodríguez-Mañas
  • Xavier Cortés-Gil
  • Joaquín Delgadillo-Duarte
  • José Manuel Quesada-Gómez
Original Research

Abstract

There is controversial information about the impact of vitamin A on bone. Some epidemiological studies show that excessive intake of vitamin A, or an excess of serum vitamin A, has related with adverse impact on bone mass; however, other studies did not find these links, and some authors have proposed that this vitamin might promote a better bone health. The present work aims to contribute to clarify the real role of vitamin A in bone tissue. For this purpose, a cross-sectional study of 154 osteoporotic non-treated postmenopausal women (> 65 years old) was carried out. Bone mineral density (BMD) was measured by dual-energy X-ray absorptiometry. We assessed concentrations of serum retinol, osteocalcin, parathyroid hormone, alkaline phosphatase, calcium, and phosphorus. We also studied demographic and anthropometric parameters. Spearman’s correlations between retinol levels and other variables found negative correlations with BMD in both lumbar spine (R = − 0.162, P < 0.01) and femoral neck (R = − 0.182, P < 0.01), as well as alkaline phosphatase (R = − 0.110; P < 0.05) and phosphorus (R = − 0.110; P < 0.05). A positive correlation between retinol and fertile window was observed (R = 0.158; P < 0.01). After multivariable adjustment, we still found a negative correlation between serum retinol and BMD, both at the lumbar spine (R = − 0.210; P < 0.01) and at the femoral neck (R = − 0.324, P < 0.001). It is concluded that elevated serum-retinol levels are associated with an increased risk of low bone mass and thus with osteoporotic fractures. Therefore, osteoporosis-risk assessment should include quantification of serum metabolite of vitamin A.

Keywords

Vitamin A Retinol Osteoporosis Osteoporotic risk Bone mass Bone health 

Abbreviations

WHO

World Health Organization

BMD

Bone mineral density

DEXA

Dual-energy X-ray absorptiometry

HPLC

High-performance liquid chromatography

BMI

Body mass index

RDA

Recommended dietary allowances

FNB

Food and nutrition board

RXR

Nuclear transcription factor

VDR

Vitamin D receptor

RAR

Retinoic acid receptor

Notes

Acknowledgements

The authors are indebted to all participants and the staff of the “Maimonides Biomedical Research Institute of Cordoba” (IMIBIC) for their dedicated and conscientious collaboration and assistance. Also, we are grateful to the Thematic Network of Corporative Research in Aging and Frailty (RETICEF) and CIBERFES for its scientific aid.

Funding

P06-FQM-01515 Excellence Project from “Consejería de Innovación, Ciencia y Empresa,” “Junta de Andalucía,” CM0010/05 FIS Project from “Instituto de Salud Carlos III,” SAF2005-05254 Project from “Ministerio de Educación y Cultura,” PAIDI group CTS-413 and PAIDI group FQM-227 of “Junta de Andalucía” (Spain). RETICEF & CIBERFES, “Instituto de Salud Carlos III.”

Compliance with Ethical Standards

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be considered as a potential conflict of interest.

Human and Animal Rights and Informed Consent

The study was approved by the regional ‘CEIC’ (Clinical Research Ethics Committee) of Córdoba due to Reina Sofía Univertity of Córdoba was the coordinating center. Other hospitals participating in the study, according to the regulations, subsequently adhered after get the permission from their respective Clinical Research Ethics Committees. They guarantee the clinical research is performed in accordance with the ethical standards as laid down in the 1964 Declaration of Helsinki and its later amendments or comparable ethical standards. Informed consent was obtained from all individual participants included in the study.

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  • Cristina Navarro-Valverde
    • 1
  • Javier Caballero-Villarraso
    • 2
  • José M. Mata-Granados
    • 2
  • Antonio Casado-Díaz
    • 2
  • Manuel Sosa-Henríquez
    • 3
  • Jorge Malouf-Sierra
    • 4
  • Xavier Nogués-Solán
    • 5
  • Leocadio Rodríguez-Mañas
    • 6
  • Xavier Cortés-Gil
    • 7
  • Joaquín Delgadillo-Duarte
    • 8
  • José Manuel Quesada-Gómez
    • 2
  1. 1.UGC CardiologíaHospital Universitario Virgen de ValmeSevilleSpain
  2. 2.IMIBIC (Instituto Maimónides de Investigación Biomédica de Córdoba)/Hospital Universitario Reina Sofía/ Universidad de Córdoba & RETICEF, CIBERFES (ISCIII)CórdobaSpain
  3. 3.Unidad Metabólica ÓseaHospital Universitario Insular & RETICEFLas PalmasSpain
  4. 4.Servicio de Medicina InternaHospital de la Santa Creu i Sant Pau & RETICEF (ISCIII)BarcelonaSpain
  5. 5.Servicio de Medicina Interna (Hospital del Mar Medical Research Institute)Universitat Autònoma de Barcelona & RETICEF, CIBERFES (ISCIII)BarcelonaSpain
  6. 6.Fundación para la Investigación Biomédica, Servicio de GeriatríaHospital Universitario de Getafe & RETICEF, CIBERFES (ISCIII)MadridSpain
  7. 7.Laboratorios AlmirallBarcelonaSpain
  8. 8.Departament de Farmacologia, de Terapèutica i de ToxicologiaUniversitat Autònoma de BarcelonaBarcelonaSpain

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