1997
DOI: 10.1093/clinchem/43.9.1670
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Serum Prostatic Specific-Antigen Concentrations in Acute Myocardial Infarction

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Cited by 19 publications
(6 citation statements)
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“…The rise of tPSA in our four patients did not change the statistical result. In our study when all of our patients' findings were statistically examined we found similar results as did Crook et al (1997). Crook et al (1997) measured tPSA levels 1, 2 and 3 days after AMI and reported tPSA levels significantly lower on the second day than on the first and third days.…”
Section: Discussionsupporting
confidence: 82%
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“…The rise of tPSA in our four patients did not change the statistical result. In our study when all of our patients' findings were statistically examined we found similar results as did Crook et al (1997). Crook et al (1997) measured tPSA levels 1, 2 and 3 days after AMI and reported tPSA levels significantly lower on the second day than on the first and third days.…”
Section: Discussionsupporting
confidence: 82%
“…In our study when all of our patients' findings were statistically examined we found similar results as did Crook et al (1997). Crook et al (1997) measured tPSA levels 1, 2 and 3 days after AMI and reported tPSA levels significantly lower on the second day than on the first and third days. In that study as well as in our study, the maximum reduction was on day 2 and a significant increase was detected on day 3.…”
Section: Discussionsupporting
confidence: 82%
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“…Recently, attention has been focused on the association between PSA levels and the cardiovascular system [21]. PSA variation has been associated with coronary lesions and occurrence of major adverse cardiac events, which intrigued new possible scenarios considering the role of PSA [4]. On the other hand, arterial stiffness is an independent predictor of cardiovascular risk in the general population, in subjects with risk factors, including hypertension, and in various disease states [22–24].…”
Section: Discussionmentioning
confidence: 99%
“…Prostate‐specific antigen (PSA) is a glycoprotein produced primarily from the epithelial cells of the prostate gland and its regulation is under the control of androgens and progestins. The physiological function of PSA is not yet entirely clarified; while it is possibly related to the activity of kallikreins [1–3], it has also other potential functions, such as inhibition of cell growth, procession of anticarcinogenic/antiangiogenic properties, and induction of apoptosis [4]. Although its clinical utility is confined to the detection of prostatic hyperplasia and cancer [5], at lower concentrations it has been detected in many tissues, including the female breast [4].…”
Section: Introductionmentioning
confidence: 99%