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Hypovitaminosis D3, Leukopenia, and Human Serotonin Transporter Polymorphism in Anorexia Nervosa and Bulimia Nervosa

Vitamin D3 has been described to have different extraskeletal roles by acting as parahormone in obesity, diabetes, cancer, cognitive impairment, and dementia and to have important regulatory functions in innate immunity. There are no studies showing extraskeletal changes associated with hypovitamino...

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Autores principales: Tasegian, Anna, Curcio, Francesco, Dalla Ragione, Laura, Rossetti, Francesca, Cataldi, Samuela, Codini, Michela, Ambesi-Impiombato, Francesco Saverio, Beccari, Tommaso, Albi, Elisabetta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745338/
https://www.ncbi.nlm.nih.gov/pubmed/26903713
http://dx.doi.org/10.1155/2016/8046479
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author Tasegian, Anna
Curcio, Francesco
Dalla Ragione, Laura
Rossetti, Francesca
Cataldi, Samuela
Codini, Michela
Ambesi-Impiombato, Francesco Saverio
Beccari, Tommaso
Albi, Elisabetta
author_facet Tasegian, Anna
Curcio, Francesco
Dalla Ragione, Laura
Rossetti, Francesca
Cataldi, Samuela
Codini, Michela
Ambesi-Impiombato, Francesco Saverio
Beccari, Tommaso
Albi, Elisabetta
author_sort Tasegian, Anna
collection PubMed
description Vitamin D3 has been described to have different extraskeletal roles by acting as parahormone in obesity, diabetes, cancer, cognitive impairment, and dementia and to have important regulatory functions in innate immunity. There are no studies showing extraskeletal changes associated with hypovitaminosis D3 in eating disorders. Methods. We have analyzed the blood of 18 patients affected by anorexia nervosa and bulimia nervosa collected over a 15-month period. We performed a panel of chemical and clinical analyses: the assay of vitamin D3, the immunoblotting of vitamin D receptor and peroxisome proliferator-activated receptor gamma, and the genotyping of 5-hydroxytryptamine transporter linked polymorphic region. Results. We choose 18 patients with a normal blood test profile such as thyroid hormones, hepatic and renal parameters, triglycerides, proteins, vitamin B12, and folic acid. Among these emerged the case of a woman with long-term anorexia nervosa and the case of a woman with long-term bulimia nervosa both complicated by anxiety and depression, severe hypovitaminosis D3, decrease of vitamin D receptor, leukopenia, and 5-hydroxytryptamine transporter linked polymorphic region short allele. Conclusion. The results induce hypothesising that the severe hypovitaminosis D3 might be responsible for the lack of the inflammatory response and the depressive symptoms in patients with long-term eating disorders.
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spelling pubmed-47453382016-02-22 Hypovitaminosis D3, Leukopenia, and Human Serotonin Transporter Polymorphism in Anorexia Nervosa and Bulimia Nervosa Tasegian, Anna Curcio, Francesco Dalla Ragione, Laura Rossetti, Francesca Cataldi, Samuela Codini, Michela Ambesi-Impiombato, Francesco Saverio Beccari, Tommaso Albi, Elisabetta Mediators Inflamm Research Article Vitamin D3 has been described to have different extraskeletal roles by acting as parahormone in obesity, diabetes, cancer, cognitive impairment, and dementia and to have important regulatory functions in innate immunity. There are no studies showing extraskeletal changes associated with hypovitaminosis D3 in eating disorders. Methods. We have analyzed the blood of 18 patients affected by anorexia nervosa and bulimia nervosa collected over a 15-month period. We performed a panel of chemical and clinical analyses: the assay of vitamin D3, the immunoblotting of vitamin D receptor and peroxisome proliferator-activated receptor gamma, and the genotyping of 5-hydroxytryptamine transporter linked polymorphic region. Results. We choose 18 patients with a normal blood test profile such as thyroid hormones, hepatic and renal parameters, triglycerides, proteins, vitamin B12, and folic acid. Among these emerged the case of a woman with long-term anorexia nervosa and the case of a woman with long-term bulimia nervosa both complicated by anxiety and depression, severe hypovitaminosis D3, decrease of vitamin D receptor, leukopenia, and 5-hydroxytryptamine transporter linked polymorphic region short allele. Conclusion. The results induce hypothesising that the severe hypovitaminosis D3 might be responsible for the lack of the inflammatory response and the depressive symptoms in patients with long-term eating disorders. Hindawi Publishing Corporation 2016 2016-01-24 /pmc/articles/PMC4745338/ /pubmed/26903713 http://dx.doi.org/10.1155/2016/8046479 Text en Copyright © 2016 Anna Tasegian et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tasegian, Anna
Curcio, Francesco
Dalla Ragione, Laura
Rossetti, Francesca
Cataldi, Samuela
Codini, Michela
Ambesi-Impiombato, Francesco Saverio
Beccari, Tommaso
Albi, Elisabetta
Hypovitaminosis D3, Leukopenia, and Human Serotonin Transporter Polymorphism in Anorexia Nervosa and Bulimia Nervosa
title Hypovitaminosis D3, Leukopenia, and Human Serotonin Transporter Polymorphism in Anorexia Nervosa and Bulimia Nervosa
title_full Hypovitaminosis D3, Leukopenia, and Human Serotonin Transporter Polymorphism in Anorexia Nervosa and Bulimia Nervosa
title_fullStr Hypovitaminosis D3, Leukopenia, and Human Serotonin Transporter Polymorphism in Anorexia Nervosa and Bulimia Nervosa
title_full_unstemmed Hypovitaminosis D3, Leukopenia, and Human Serotonin Transporter Polymorphism in Anorexia Nervosa and Bulimia Nervosa
title_short Hypovitaminosis D3, Leukopenia, and Human Serotonin Transporter Polymorphism in Anorexia Nervosa and Bulimia Nervosa
title_sort hypovitaminosis d3, leukopenia, and human serotonin transporter polymorphism in anorexia nervosa and bulimia nervosa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745338/
https://www.ncbi.nlm.nih.gov/pubmed/26903713
http://dx.doi.org/10.1155/2016/8046479
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