CARDIOVASCULAR JOURNAL OF AFRICA • Volume 28, No 1, January/February 2017
46
AFRICA
Adropin is synthesised in the intercalated duct, mucous acinus
and interlobular cells of human salivary glands, and this could
contribute to the high concentrations in saliva. Saliva adropin
levels could also be more useful than serum levels for diagnosing
some metabolic conditions.
Saliva offers advantages over blood, including that collection
is non-invasive and therefore stress free for patients, especially
children,
21
making it a more suitable choice than serum for
measuring adropin in diagnosing EPACS. However there are
some limitations and difficulties in using ELISA on saliva, since
inhibitors and/or binding proteins could be present and could
negatively affect the quantitative determination of peptides/
proteins.
Overall, four and six hours after EPACS, ROC curve analysis
demonstrated that the saliva adropin concentration reflected
EPACS with 91.7% (at four hours) and 91.7% (at six hours)
sensitivity and 57% (at four hours) and 57% (at six hours)
specificity. Therefore, four and six hours after EPACS, the saliva
adropin concentration showed the same sensitvity and specifity
for diagnosing EPACS as the serum level. All these data promise
new possibilities for the diagnosis of EPACS, besides measuring
other cardiac enzymes and proteins (troponins).
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