2022
DOI: 10.1016/j.cca.2022.07.018
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Proneuropeptide Y and neuropeptide Y metabolites in healthy volunteers and patients with a pheochromocytoma or paraganglioma

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Cited by 5 publications
(4 citation statements)
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“…Blood samples were taken before the CPT, at 30 s and 2 min of the CPT, and 2 min after the end of the CPT. Norepinephrine (NE), epinephrine (E) and neuropeptide Y (NPY) 1–36 and its metabolites, were determined using a liquid chromatography tandem mass spectrometry method as reported previously [ 13 , 14 ]. Plasma renin activity (PRA) and plasma aldosterone concentration (PAC) were determined by a radioimmunoassay kit for the quantitative determination of Angiotensin I in human plasma (REN-CT2, Cisbio Bioassays, Codolet, France) and by a commercial RIA kit (Aldo-Riact, CIS Bio International, Yvette, Cedex, Saclay, France) respectively.…”
Section: Methodsmentioning
confidence: 99%
“…Blood samples were taken before the CPT, at 30 s and 2 min of the CPT, and 2 min after the end of the CPT. Norepinephrine (NE), epinephrine (E) and neuropeptide Y (NPY) 1–36 and its metabolites, were determined using a liquid chromatography tandem mass spectrometry method as reported previously [ 13 , 14 ]. Plasma renin activity (PRA) and plasma aldosterone concentration (PAC) were determined by a radioimmunoassay kit for the quantitative determination of Angiotensin I in human plasma (REN-CT2, Cisbio Bioassays, Codolet, France) and by a commercial RIA kit (Aldo-Riact, CIS Bio International, Yvette, Cedex, Saclay, France) respectively.…”
Section: Methodsmentioning
confidence: 99%
“…As a result, these tumors release NPY into the vascular system. It has been suggested that the plasma NPY level could be used as an early diagnostic marker for pheochromocytomas and paragangliomas in patients who received treatments that interfere with catecholamine reuptake or suffer from severe kidney impairment [ 224 ]. Lower NPY levels were observed in pheochromocytomas from von Hippel-Lindau patients (noradrenergic phenotype) when compared with pheochromocytomas from multiple endocrine neoplasia type 2 patients (adrenergic phenotype) [ 225 ].…”
Section: Involvement Of Neuropeptide Y Peptide Yy and Pancreatic Poly...mentioning
confidence: 99%
“…NPY is a neurotransmitter whose high plasma levels are found in several cancers, including pheochromocytoma, ganglioma, and neuroblastoma, in which it can be used as a marker [59,78]. Despite the measurement of catecholamines displaying a higher sensitivity in pheochromocytoma and paraganglioma, NPY may be a viable alternative in patients suffering from kidney impairment or under treatments that interfere with catecholamine reuptake [79]. However, its clinical use is limited due to the low amount of information available, thus requiring further in-depth studies [79].…”
Section: Other Biomarkersmentioning
confidence: 99%