Previous Page  7 / 9 Next Page
Information
Show Menu
Previous Page 7 / 9 Next Page
Page Background

allied

academies

Page 48

September 05-06, 2019 | London, UK

7

th

International Conference on

2

nd

International Conference on

Otolaryngology: ENT Surgery

Dental Health and Oral Hygiene

Joint Event

&

Saliva as a diagnostic fluid

Hawra Al Janobi

Imam Abdul Rahman Bin Faisal University, Saudi Arabia

I

n humans, the normal biological role of salivary gland is to

produce saliva. Saliva is a clear, slightly acidic mucoserous

exocrine secretion. The saliva provides an important role in

the host defense mechanism of the upper gastrointestinal

tract, which is controlled by variable secretory molecules like

proteins and growth factors.

Saliva has many components, and each one has a specific

function. One of the main components is the electrolytes,

including sodium, potassium, calcium, magnesium,

bicarbonate, and phosphates. Other components of saliva

include immunoglobulins, proteins, enzymes, mucins and

nitrogen products (urea and ammonia). Saliva contains a

high concentration of calcium and phosphate ions. Saliva

is supplied by blood; therefore, biomarkers present in

blood could be also present in saliva. Saliva is emerging

as a diagnostic fluid, as it is easy to collect, noninvasive,

inexpensive, safe, and contains valuable diagnostic material.

It has been used to detect several different diseases including

cystic fibrosis, cardiovascular diseases, diabetes, HIV, oral

and systemic cancer, caries, periodontal disease, and auto-

immune connective tissue diseases like rheumatoid arthritis,

systemic lupus erythematosus, and Sjogren syndrome (SS).

Our study: Our objective was to determine whether saliva

from patients with SS has higher levels of inflammatory

mediators as compared to healthy controls. Moreover, we

sought to establish whether a novel collection device was

superior to a conventional saliva collection method for

detection of inflammatory cytokines. We recruited SS (n = 9)

and healthy controls (n = 8) and collected saliva from them

using a conventional method and a novel collection device

termed the RNAPro SAL. We analyzed saliva using a cytokine

multiplex array. Our results showed that the conventional

method is superior to the RNAPro SAL for the detection IL-1α

and IL-1β. In contrast, the RNAPro SAL was superior to the

conventional method in detecting IL-2, IL-5, TNFβ, and IL-23.

Saliva collected with the RNAPro SAL device revealed that SS

patients showed higher levels of TNFβ and lower levels of IL-5

compared to healthy controls. Therefore, cytokines in saliva

may be useful in distinguishing SS patients, and the RNAPro

SAL may be a valuable novel collection device for salivary

diagnostics.

e

:

haaljanobi@iau.edu.sa

J Clin Dentistry Oral Health

Volume: 3

Journal of Clinical Dentistry and Oral Health | Volume 3