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Potential protein biomarkers in saliva for detection of frailty syndrome by targeted proteomics. | LitMetric

AI Article Synopsis

  • Frailty is a syndrome in older adults linked to immune decline and inflammation, and it's assessed using the Frailty-VIG index.
  • This study aimed to find out if saliva could serve as a non-invasive source for identifying protein biomarkers related to frailty, using a proteomics technique on a Spanish rural population.
  • Eight proteins (e.g., CYTC, CYTD) were identified in saliva that correlate with frailty characteristics, such as cardiovascular health, obesity, and cognitive impairment, highlighting their potential role in diagnosing and understanding frailty syndrome.

Article Abstract

Frailty is a physiological geriatric syndrome, caused by immunosenescence, inflammation and alterations at the protein level leading to metabolic and microbiota changes. Currently, this syndrome is evaluated clinically with the Frailty-VIG index. The aim of the study was therefore to investigate the potential suitability of saliva as a non-invasive proximal biological fluid for the characterisation and identification of possible protein-level biomarkers in frailty syndrome. This cross-sectional study was conducted in a rural population of older Spanish adults using the SMR proteomics technique. A differential protein profile of eight potential and surrogate proteins (CYTC, CYTD, CYTS, CYTB, MIF, ALBU, CD44 and B2MG) was detected in saliva, all of which correlated with factors characterising frailty syndrome, such as vascular ageing (arterial stiffness and cardiovascular disease), obesity, mood problems, global cognitive impairment, changes in gait and hand pressure strength. The proteins CYTD (r = 0.415, p = 0.013) and CYTC (r = 0.280, p = 0.026), which were detected differentially in the protein profile, were associated with the Frailty-VIG index. All analysed proteins are associated not only with the clinical symptoms of frailty syndrome, but also with an acute inflammatory response, endothelial cell proliferation and the complement system, among others.

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Source
http://dx.doi.org/10.1016/j.mad.2024.111974DOI Listing

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