TY - JOUR
T1 - Focus on increased serum angiotensin-converting enzyme level
T2 - From granulomatous diseases to genetic mutations
AU - Lopez-Sublet, Marilucy
AU - Caratti di Lanzacco, Lorenzo
AU - Danser, A. H.Jan
AU - Lambert, Michel
AU - Elourimi, Ghassan
AU - Persu, Alexandre
N1 - Publisher Copyright:
© 2018 The Canadian Society of Clinical Chemists
PY - 2018/9
Y1 - 2018/9
N2 - Angiotensin I-converting enzyme (ACE) is a well-known zinc-metallopeptidase that converts angiotensin I to the potent vasoconstrictor angiotensin II and degrades bradykinin, a powerful vasodilator, and as such plays a key role in the regulation of vascular tone and cardiac function. Increased circulating ACE (cACE) activity has been reported in multiple diseases, including but not limited to granulomatous disorders. Since 2001, genetic mutations leading to cACE elevation have also been described. This review takes advantage of the identification of a novel ACE mutation (25-IVS25 + 1G > A) in two Belgian pedigrees to summarize current knowledge about the differential diagnosis of cACE elevation, based on literature review and the experience of our centre. Furthermore, we propose a practical approach for the evaluation and management of patients with elevated cACE and discuss in which cases search for genetic mutations should be considered.
AB - Angiotensin I-converting enzyme (ACE) is a well-known zinc-metallopeptidase that converts angiotensin I to the potent vasoconstrictor angiotensin II and degrades bradykinin, a powerful vasodilator, and as such plays a key role in the regulation of vascular tone and cardiac function. Increased circulating ACE (cACE) activity has been reported in multiple diseases, including but not limited to granulomatous disorders. Since 2001, genetic mutations leading to cACE elevation have also been described. This review takes advantage of the identification of a novel ACE mutation (25-IVS25 + 1G > A) in two Belgian pedigrees to summarize current knowledge about the differential diagnosis of cACE elevation, based on literature review and the experience of our centre. Furthermore, we propose a practical approach for the evaluation and management of patients with elevated cACE and discuss in which cases search for genetic mutations should be considered.
UR - http://www.scopus.com/inward/record.url?scp=85049347185&partnerID=8YFLogxK
U2 - 10.1016/j.clinbiochem.2018.06.010
DO - 10.1016/j.clinbiochem.2018.06.010
M3 - Review article
C2 - 29928904
AN - SCOPUS:85049347185
SN - 0009-9120
VL - 59
SP - 1
EP - 8
JO - Clinical Biochemistry
JF - Clinical Biochemistry
ER -