12 research outputs found

    “Family before Anyone Else”: A Qualitative Study on Family, Marginalization, and HIV among Hispanic or Latino/a/x Mexican Sexual Minority Males

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    This study explored the influence family relationships have on HIV-related factors among Hispanic or Latino/a/x Mexican sexual minority cisgender males in San Antonio, TX, US. A total of 15 young adults (7 people living with HIV; PLWH) ages 21–30 completed a semi-structured interview. Data were transcribed verbatim and analyzed using thematic analysis. The following themes emerged: (1) family support; (2) mother-son relationships; (3) father-son relationships; (4) sibling support; (5) family marginalization of sexual minorities; and (6) internalized homophobia. People who reported being HIV negative were more likely to have a prominent mother-son relationship, strong sense of family, supportive siblings, and family acceptance as a sexual minority. PLWH were more likely to report a weak sense of family, being raised in a maternal-led household, and less likely to have a relationship with their father and siblings. Marginalization among participants regardless of HIV status included exposure to religious rhetoric stigmatizing sexual minorities and fathers’ reinforcing Mexican traditional gender norms. In addition to encountering homophobia, PLWH were further marginalized by family members due to their HIV status. The findings suggest a need for greater attention to examining the impact of familial support of Hispanic or Latino/a/x Mexican sexual minority cisgender males as young adults with or at risk of HIV

    Lung Cancer Screening and Epigenetics in African Americans: The Role of the Socioecological Framework

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    Lung cancer is the leading cause of cancer morbidity and mortality in the U.S. and racial/ethnic minorities carry the greatest burden of lung cancer disparities with African Americans (AAs) impacted disproportionately. Inequities in lung cancer health disparities are often associated with multiple bio-behavioral and socio-cultural factors among racial/ethnic minorities. Epigenetic research has advanced the understanding of the intersectionality between biological and socio-cultural factors in lung cancer disparities among AAs. However, gaps exist in the engagement of diverse populations in epigenetic lung cancer research, which poses a challenge in ensuring the generalizability and implementation of epigenetic research in populations that carry an unequal cancer burden. Grounding epigenetic lung cancer research within a socio-ecological framework may prove promising in implementing a multi-level approach to community engagement, screening, navigation, and research participation among AAs. The University of Illinois Cancer Center (UI Cancer Center) is employing an evidence–based (EB) model of community/patient engagement utilizing the socio-ecological model (SEM) to develop a culturally sensitive epigenetic lung cancer research program that addresses multiple factors that impact lung cancer outcomes in AAs. By implementing epigenetic research within a group of Federally Qualified Health Centers (FQHCs) guided by the SEM, the UI Cancer Center is proposing a new pathway in mitigating lung cancer disparities in underserved communities. At the individual level, the framework examines tobacco use among patients at FQHCs (the organizational level) and also tailors epigenetic research to explore innovative biomarkers in high risk populations. Interpersonal interventions use Patient Navigators to support navigation to EB tobacco cessation resources and lung cancer screening. Community level support within the SEM is developed by ongoing partnerships with local and national partners such as the American Lung Association (ALA) and the American Cancer Society (ACS). Lastly, at the policy level, the UI Cancer Center acknowledges the role of policy implications in lung cancer screening and advocates for policies and screening recommendations that examine the current guidelines from the United States Preventive Services Task Force (USPTF)

    The Impact of Puerto Rican Maternal-feeding Practices on Child Obesity Prevention and Development

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    Childhood obesity impacts a third of all American children. Racial and ethnic minority groups in the United States have higher prevalence rates of obesity in comparison to their White counterparts. Specifically, Puerto Rican children in the Chicago Humboldt Park community are disproportionately affected by obesity, which manifests in poorer health outcomes. Researchers have found that parental sociocultural and socioeconomic factors play an important role in shaping early childhood health behavior and are among the noted contributors predisposing children to obesity risk. However, research assessing Latina child-feeding strategies in relation to child obesity is primarily centered on the experiences of Mexican Americans, which is not generalizable across Latino subgroups. Namely, the impact of Puerto Rican child-feeding styles on obesity risk is poorly understood. As the second largest Latino subgroup in the United States, it is important to understand the different experiences, perceptions, and beliefs of Puerto Ricans in relation to acculturation and engagement in risky behavior. Thus, this study employed a descriptive cross-sectional survey to assess the relationship of Puerto Rican maternal child-feeding practices to child obesity, dietary intake, and acculturation. A purposive sample of 100 mother-child pairs recruited from six early childhood centers in Humboldt Park participated between May 2011 and December 2011. Data analyses were performed using SPSS v.20 and SAS v.9.2. Girls (33% body mass index; 62% waist circumference) had a higher risk for obesity than boys (22% body mass index; 51% waist circumference). Maternal encouragement of food restriction and child control may increase the risk for child obesity. Dietary intake may mediate the relationship between child-feeding and child weight status, particularly, the consumption of sweet snacks. Acculturation strengthened the relationship between child-feeding practices and child obesity when waist circumference was used as a measure rather than body mass index. Findings will inform policy development and best practices for structuring and implementing future obesity prevention intervention programs tailored to Puerto Rican populations

    Systematic Review on Tobacco Marketing in Vulnerable Populations

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    Introduction: Tobacco use is the most common preventable cause of death and it increases one’s risk for numerous diseases, associated illness, and death. Unfortunately, certain populations are disproportionality burdened by tobacco-related morbidity and death. These populations consist of individuals from low-income areas, people with mental illnesses, lesbians, gays, bisexuals, transsexuals, African-Americans, and Hispanics/Latinos. Methods: Articles were retrieved using Google Scholar, University of Illinois at Chicago Library (UIC) search engine, and PubMed. The Centers for Disease Control and Prevention (CDC) website was used as source to find information about certain demographics. Articles were chosen if they were published between the years of 2008-2018. Articles were searched using the terms “tobacco,”, “marketing”, “vulnerable populations”, “low-income”, “mental illnesses”, “LGBT” and “minorities”. Overall, a total of 12 articles and one weblink from the CDC was used. Findings: African-Americans, Hispanics/Latinos, and individuals from low-income communities are exposed more to tobacco products and marketing. Findings showed that transgender adults use tobacco a much higher rates than cisgender adults, menthol cigarettes were originally marketed as being healthier than non-menthol cigarettes, mental health and addiction treatment providers have rationalized that their failure to treat tobacco dependence is a form of harm reduction in that it is viewed as a healthier alternative, and the tobacco industry targeted low SES women as early as the 1970s. Conclusion: Tobacco companies have been targeting these vulnerable populations for years. There still needs to be more research done on “healthier” alternatives to smoking cigarettes

    Community–academic partnerships to reduce cancer inequities: The chicagoCHEC community engagement core

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    Background: In 2015, Chicago Cancer Health Equity Collaborative (ChicagoCHEC) was formed to address cancer inequities. The Community Engagement Core (CEC) is one of the key components aimed at establishing meaningful partnerships between the academic institutions and the community. Herein, we describe ChicagoCHEC CEC processes, challenges, opportunities, successes, and preliminary evaluation results. Methods: CEC stresses participatory and empowerment approaches in all aspects of ChicagoCHEC work. Evaluation processes were conducted to assess, report back, and respond to community needs and to evaluate the strength of the partnership. Results: CEC has facilitated meaningful community integration and involvement in all ChicagoCHEC work. The partnership resulted in annual cancer symposium; more than 50 outreach and education activities, including cancer screening and referrals; the development of health resources; and providing expertise in culturally and health literacy appropriate research targeting minorities. Preliminary partnership evaluation results show that ChicagoCHEC researchers and community partners have developed trust and cohesiveness and value the community benefits resulting from the partnership. Conclusions: CEC is essential in achieving research objectives following community participatory action research (CPAR) approaches. Some key lessons learned include 1) the need for clear, honest, and open channels of communication not only among the three participating academic institutions, but also among the community partners, 2) transparent operational processes, and 3) mutual trust and understanding regarding the different cultures, structure, foci and processes, expectations at each institution and partnering organization

    Researching COVID to Enhance Recovery (RECOVER) adult study protocol: Rationale, objectives, and design

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    IMPORTANCE: SARS-CoV-2 infection can result in ongoing, relapsing, or new symptoms or other health effects after the acute phase of infection; termed post-acute sequelae of SARS-CoV-2 infection (PASC), or long COVID. The characteristics, prevalence, trajectory and mechanisms of PASC are ill-defined. The objectives of the Researching COVID to Enhance Recovery (RECOVER) Multi-site Observational Study of PASC in Adults (RECOVER-Adult) are to: (1) characterize PASC prevalence; (2) characterize the symptoms, organ dysfunction, natural history, and distinct phenotypes of PASC; (3) identify demographic, social and clinical risk factors for PASC onset and recovery; and (4) define the biological mechanisms underlying PASC pathogenesis. METHODS: RECOVER-Adult is a combined prospective/retrospective cohort currently planned to enroll 14,880 adults aged ≄18 years. Eligible participants either must meet WHO criteria for suspected, probable, or confirmed infection; or must have evidence of no prior infection. Recruitment occurs at 86 sites in 33 U.S. states, Washington, DC and Puerto Rico, via facility- and community-based outreach. Participants complete quarterly questionnaires about symptoms, social determinants, vaccination status, and interim SARS-CoV-2 infections. In addition, participants contribute biospecimens and undergo physical and laboratory examinations at approximately 0, 90 and 180 days from infection or negative test date, and yearly thereafter. Some participants undergo additional testing based on specific criteria or random sampling. Patient representatives provide input on all study processes. The primary study outcome is onset of PASC, measured by signs and symptoms. A paradigm for identifying PASC cases will be defined and updated using supervised and unsupervised learning approaches with cross-validation. Logistic regression and proportional hazards regression will be conducted to investigate associations between risk factors, onset, and resolution of PASC symptoms. DISCUSSION: RECOVER-Adult is the first national, prospective, longitudinal cohort of PASC among US adults. Results of this study are intended to inform public health, spur clinical trials, and expand treatment options. REGISTRATION: NCT05172024
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