2016
DOI: 10.1111/ajt.13443
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Serum Calcification Propensity Is a Strong and Independent Determinant of Cardiac and All-Cause Mortality in Kidney Transplant Recipients

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Cited by 78 publications
(85 citation statements)
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“…Secondary calciprotein particles (but not primary calciprotein particles) have been shown to induce vascular calcification in vitro (5), and low T 50 has been shown to be associated with cardiovascular events and all-cause mortality in ESKD (6), CKD stages 3 and 4 (7), and kidney transplant recipients (8,9). Increasing T 50 might, therefore, prevent calcification and reduce the incidence of cardiovascular events.…”
Section: Introductionmentioning
confidence: 99%
“…Secondary calciprotein particles (but not primary calciprotein particles) have been shown to induce vascular calcification in vitro (5), and low T 50 has been shown to be associated with cardiovascular events and all-cause mortality in ESKD (6), CKD stages 3 and 4 (7), and kidney transplant recipients (8,9). Increasing T 50 might, therefore, prevent calcification and reduce the incidence of cardiovascular events.…”
Section: Introductionmentioning
confidence: 99%
“…The half-maximum time for this conversion is called “T 50 ” and is given in minutes (min) [15]. Low T 50 -time (i.e., low resistance towards calcification) is associated with progressive aortic stiffening and with all-cause mortality in non-dialysis CKD [16], dialysis [17], and transplant patients [18, 19]. …”
Section: Introductionmentioning
confidence: 99%
“…The transformation time point reflects the ability of a given serum to delay the crystallization cascade and is specific for individual patient sera. Excitingly, the transformation time point has to date been shown to correlate with prognosis many years in advance in various large cohorts [59][60][61][62] including more than 5,000 patients. This indicates a considerable intraindividual and technical stability of the test result.…”
mentioning
confidence: 99%
“…While the precise mechanistic link between test result and outcome has not been firmly elucidated in detail yet, it appears reasonable that they might be based at least in part on the development of vascular calcification/soft tissue calcification, oxidative stress, and inflammatory events, which may all be triggered alone or in combination by circulating nanocrystals. The occurrence of naturally occurring CPPs in the circulation has of note been demonstrated both indirectly (by measuring sedimentable fetuin-A) [59,63] and directly (using cryo-TEM imaging) [64] .…”
mentioning
confidence: 99%