Cardiovascular Diseases Clinical Trial
To investigate whether traditional risk factors and novel risk factors predict higher risk of atherosclerotic cardiovascular disease (ASCVD) in a prospective study of incident dialysis patients.
BACKGROUND:
There is a very high mortality especially from cardiovascular disease among patients who are
on dialysis. Atherosclerotic cardiovascular disease (ASCVD) is a leading contributor to the
high morbidity and mortality among end-stage renal disease (ESRD) patients, accounting for
36 percent of ESRD deaths (total annual mortality of 23 percent). The high mortality among
dialysis patients is a major public health problem and the ability to identify and treat
risk factors that may reduce morbidity and mortality would be of substantial benefit. There
are well-known risk factors for cardiovascular disease that certainly are related to
morbidity and mortality among dialysis patients, i.e., relationship to hypertension,
diabetes, smoking, etc. However, some of the new risk factors could also contribute to the
excess mortality.
DESIGN NARRATIVE:
The prospective study tested the hypothesis that higher levels of several novel risk factors
(Lp(a) levels and apo(a) isoforms; homocysteine and related vitamins; Chlamydia pneumoniae
and cytomegalovirus; and C-reactive protein and fibrinogen) and traditional risk factors
predicted higher risk of ASCVD in 925 incident dialysis patients recruited within three
months of starting dialysis. Although these factors had been implicated in the etiology of
ASCVD in ESRD patients, little prospective data existed. The cohort had already been
recruited through a collaboration between Johns Hopkins and 80 Dialysis Clinics Incorporated
(DCI) clinics; many of the important predictors and possible confounders had been measured.
Long-term follow-up was obtained by extending mean followup of 2.4 years by four more years.
The investigators 1) extended specimen collection, and follow-up, and instituted
standardized review of ASCVD events; 2) characterized baseline associations of novel and
traditional factors with each other, dialysis modality and dose, nutritional status, and
ASCVD prevalence in the full cohort using a cross-sectional design; 3) determined whether
baseline levels of risk factors predicted subsequent incidence of ASCVD events, and total
mortality using a prospective cohort study design and tested a priori hypothesized
interactions between risk factors and the risk of ASCVD; 4) studied the variability of risk
factors over time using annual measurements in a random subset of 180 patients (subcohort)
using a longitudinal design; and lastly, 5) used a case-cohort design, utilizing the
subcohort, to test whether the most recent level before an ASCVD event, the baseline level,
or the mean level of each risk factor was most predictive of ASCVD risk. Baseline data
collection included a patient health questionnaire and a standardized review of comorbidity
using dialysis chart records. Serum, plasma and DNA were stored at -80 degrees C. from
patient visits at recruitment (month 0), and followup (months 1,2,3,6,12,8,24, etc.). ASCVD
was assessed by review of hospital charts, patients and care providers questionnaires, and
HCFA death forms.
The study completion date listed in this record was obtained from the "End Date" entered in
the Protocol Registration and Results System (PRS) record.
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