期刊论文详细信息
Immunity & Ageing
Low heart-type fatty acid binding protein level during aging may protect down syndrome people against atherosclerosis
Massimiliano Marco Corsi Romanelli1  Elena Dozio2  Giada Dogliotti2  Elena Vianello2 
[1] U.O.C. di Patologia Clinica, Dipartimento dei Servizi Sanitari di Diagnosi e Cura – Medicina di Laboratorio, IRCCS Policlinico San Donato, Piazza E. Malan, 20097 San Donato Milanese, Milan, Italy;Dipartimento di Scienze Biomediche per la Salute, Cattedra di Patologia Clinica, Università degli Studi di Milano, Via Mangiagalli 31, Milan, 20133, Italy
关键词: Heart-type fatty acid binding protein;    Down syndrome;    Atherosclerosis;    Aging;   
Others  :  815154
DOI  :  10.1186/1742-4933-10-2
 received in 2012-10-30, accepted in 2013-01-17,  发布年份 2013
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【 摘 要 】

Background

Aging is considered an important independent risk factor for atherosclerosis. Down syndrome people (DS) display an accelerated aging process compared to healthy subjects, anyway they are relatively resistant to developing atherosclerosis. The mechanisms involved in such protective effect are not well known. Since heart-type fatty acid binding protein (H-FABP) is a protein involved in the transport of fatty acids and it has been recently correlated with the presence of atherosclerosis, we aimed to measure H-FABP level both in DS and in healthy subjects during aging to evaluate the association between this molecule, aging and atherosclerosis.

Findings

We quantified plasmatic H-FABP level in three groups of male DS and age-matched healthy subjects (children, age 2–14 years; adults, age 20–50 years; elderly, > 60 years) using a biochip array analyzer. We observed that aging is associated with increased H-FABP level in healthy subjects but not in DS which display both the same protein level in the different ages of life and have also lower level compared to their age-matched healthy subjects.

Conclusion

Reduced H-FABP level during aging in DS may play a protective role against atherosclerosis. The potential involvement of H-FABP in the relationship between aging, atherosclerosis and development of coronary artery disease needs further investigations.

【 授权许可】

   
2013 Vianello et al.; licensee BioMed Central Ltd.

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