Improving Prevention of Heart Disease in Latinos

BACKGROUND:

While there has been great progress in reducing CVD morbidity and mortality in the United
States over the past 40 years, some minority groups have not shared fully in this progress
and continue to have lower life expectancy and higher CVD morbidity. On average, minorities
have less access to medical care, receive less aggressive care and fewer diagnostic and
therapeutic cardiac procedures, and adhere poorly to prescribed medical regimens. Thus,
research to reduce health disparities by improving CVD outcomes in minorities offers
potential for a substantial positive public heath impact. Academic medical centers and
institutions capable of carrying out such research, however, often lack access to and the
trust of minority patients. Minority patients often receive fragmented care because they
lack access to regular medical care, present to emergency departments rather than primary
care physicians for complications of an advanced chronic CVD condition, and are less likely
to follow medical regimens. Minority communities often harbor distrust of clinical research.
Minority patients report greater satisfaction when receiving care from minority providers
and are reluctant to receive treatment outside their minority health care serving systems.

In general, minorities have high rates of hypertension, elevated cholesterol, cigarette
smoking, obesity, metabolic syndrome, and diabetes as well as other behavioral,
environmental, and occupational risk factors for cardiovascular diseases, such as sleep
problems - all elements that contribute to excess CVD morbidity and mortality. The causes of
minority health disparities are complex and incompletely understood. Although evidence of
genetic, biologic, and environmental factors is well documented, poor outcomes are also
attributed to undertreatment. Such undertreatment may be due to limited access to health
care or, in some cases, breakdown of the medical system, or failure of the physician and/or
patient to allow for optimal health care, even when access is not impaired. The complex
interactions of behavior, socioeconomic status (SES), culture, and ethnicity are important
predictors of health outcomes and sources of health disparities. Despite efforts to
elucidate genetic and environmental risk factors and to promote cardiovascular health in
high-risk populations, trends in CVD outcomes suggest that CVD health disparities continue
to widen.

The Partnerships Program to Reduce Cardiovascular Health Disparities involves collaboration
between research-intensive medical centers (RIMCs) that have a record of NIH-supported
research and patient care and minority health care serving systems (MSSs) that lack a strong
research program. Each Partnership Program will (a) design and carry out multiple
interdisciplinary research projects that investigate complex biological, behavioral, and
societal factors that contribute to CVD health disparities and facilitate clinical research
within the MSS to improve CVD outcomes and reduce health disparities and (b) provide
reciprocal educational and skills development programs so that investigators are able to
conduct research aimed at reducing cardiovascular disparities and thereby enhance research
opportunities and enrich cultural sensitivity and cardiovascular research capabilities at
both institutions.

The Request for Applications for Partnership Programs to Reduce Cardiovascular Disparities
was released in September 2003. The awards were made in September 2004.

DESIGN NARRATIVE:

The study will develop a partnership between Denver Health (DH), an MSS, and the University
of Colorado Health Sciences Center (UCHSC), an RIMC. The first specific aim of the project
is to develop and evaluate an interactive computer-based tool to improve community-based
recognition of cardiovascular risk factors and to improve self-management skills, including
adherence with clinic visits. The tool will be culturally sensitive and bilingual. The
second specific aim is to test the ability of a nurse-based disease management program to
improve control of risk factors. Under this aim, DH's unique computerized information system
will be used to develop a registry of patients with hypertension and to characterize
patients' overall risk for CVD and their risk for nonadherent behavior. A randomized
clinical trial will be used to assess the impact of a nurse-based disease management
intervention in those at highest risk and with a history of nonadherence. The intervention
will be based on programs already in place at DH but will be modified in response to input
from community-based focus groups. Specific aims 3 and 4 will seek to refine current
cardiovascular risk profiling in ways specific to Hispanics. Specific aim 3 will assess
ethnic differences in the relationship between traditional risk factors (diabetes,
hypertension, smoking, and hyperlipidemia) and preclinical markers of cardiovascular disease
(left ventricular mass, carotid intima media thickness, and brachial artery reactivity) over
time. Specific aim 4 will assess the relationship among the traditional risk factors,
preclinical markers, and a panel of circulating inflammatory markers. Also under specific
aim 4, a randomized, placebo-controlled trial will assess the efficacy of "statin"
medications to reduce circulating levels of these inflammatory markers. Specific aims 5 and
6 will develop educational programs to increase the cultural proficiency of clinical
researchers, increase minority researcher participation in cardiovascular prevention
research, and assist junior DH physicians in developing research careers in cardiovascular
prevention.

Eligibility Criteria vary with each study.