14 results on '"Myers, Kristopher"'
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2. New York State, New York City, New Jersey, Puerto Rico, and the US Virgin Islands' Health Department Experiences Promoting Health Equity During the Initial COVID-19 Omicron Variant Period, 2021-2022
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Cox, Heidi, primary, Gebru, Yonathan, additional, Horter, Libby, additional, Palomeque, Francisco S., additional, Myers, Kristopher, additional, Stowell, Daniel, additional, Easterling, Torian, additional, de Noguera, Nayeli Salazar, additional, Medina-Forrester, Amanda, additional, Bravo, Josely, additional, Pérez, Siomara, additional, Chaparro, Jaikiz, additional, Ekpo, Lisa La Place, additional, Cranford, Hannah, additional, Santibañez, Scott, additional, and Valencia, Diana, additional
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- 2023
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3. Missing Data and Systematic Bias
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Myers, Kristopher O
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- 2017
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4. Dependence measures based on hookah smokers’ experiences and context are needed
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Myers, Kristopher, Ward, Kenneth D., and Maziak, Wasim
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- 2016
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5. The individual, interactive, and syndemic effect of substance use, depression, education, and ethnicity on retention in HIV care
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Myers, Kristopher, primary, Li, Tan, additional, Baum, Marianna, additional, Ibanez, Gladys, additional, and Fennie, Kristopher, additional
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- 2020
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6. 2019 Health Equity Summer Research Summit Organized by the Center of Excellence in Health Equity, Training and Research, Baylor College of Medicine, Houston, Texas 77030, USA on June 18th, 2019
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Uribe-Gomez, A, primary, Salinas-Miranda, Abraham A., additional, Turner, Acara E., additional, Strutt, Adriana M., additional, Joseph, Adrienne, additional, Wright, Alex, additional, Martin, Alexander C., additional, Milton, Alexis N., additional, Khoei, Amelia, additional, Kanakamedala, Amritha, additional, Iyinbor, Angie, additional, O, Anna, additional, Morrow, Asha, additional, Butler, Ashley M., additional, Young, Ashley, additional, Shah, Asim, additional, Matin, Asna, additional, Christiansen, Audrey E., additional, Ibrahimou, Boubakari, additional, Alonzo, Breanna, additional, Ossenkop, Chase, additional, O, Carli, additional, Hsu, Chih-Wei, additional, Ikeanyionwu, Charles, additional, Anyanwu, Chinwe, additional, Rivas, Charlotte, additional, Ikedionwu, Chioma A., additional, Anugwom, Chioma, additional, Broda, Christopher R., additional, Bocchini, Claire, additional, Cummins, Claire, additional, Rooney, Cliona M., additional, Keo-Meier, Colton L., additional, Johnson, Connor, additional, Miller-Chism, Courtney, additional, Titus, Courtney, additional, Parker, Crystal L., additional, Bird, Cylaina, additional, Mauck, Daniel, additional, Persse, David, additional, Austin, Deborah A., additional, Dongarwar, Deepa, additional, Cherla, Deepa V., additional, Wolf, Dwayne, additional, Schwartz, Eleanor Bimla, additional, Petrova, Elena, additional, Perli, Elias, additional, Shell, Elisabeth, additional, Tran, Elizabeth U., additional, Baena, Elsa, additional, Lopez, Elyse, additional, Berry, Estrellita, additional, Rodriguez, Evadne, additional, Faustinella, Fabrizia, additional, Ihekweazu, Faith D., additional, Jiwani, Faiz, additional, Chmaitelli, Gabriella P., additional, Chan, Galant, additional, Wang, Haijun, additional, Salihu, Hamisu M., additional, Combs, Hannah L., additional, Rogers, Hayley, additional, Haq, Heather, additional, Sosa, Iberia Romina, additional, Jose, Irene E., additional, Griffin, Isabel, additional, Cao, J., additional, Montealegre, Jane, additional, Salemi, Jason L., additional, Chang, Jennifer, additional, Stinson, Jennifer M., additional, Mills, JL, additional, Schulte, Joann, additional, Thomas, Joel, additional, Prochaska, John, additional, Saunders, John, additional, Go, Jonathan, additional, Lim, Jonathan, additional, Salley, Jordan, additional, Pineda, Josue Estiven, additional, Tabilona, Jules, additional, Holihan, Julie L., additional, Bowen-Jallow, Kanika, additional, Bernardi, Karla, additional, Fredricks, Karla, additional, Salciccioli, Katherine B., additional, Lopez, Keila N., additional, Barning, Kenneth, additional, Vuong, Kevin Dat, additional, Yusuf, Korede K., additional, Myers, Kristopher, additional, Wilson, Kyle, additional, Laufman, Larry E., additional, Love, Latanya J., additional, Nolan, Lauren, additional, Schoen, Lauren, additional, Huang, Lillian, additional, King, Lindsey M., additional, Nunez, Lisa F., additional, Brown, Louis, additional, Hernandez, Luna, additional, Hydod, Lynn, additional, Rossetti, M. Agustina, additional, Allman, Madeleine, additional, Khan, Mahmood, additional, Marty, Makenna, additional, Lee, MaKenzie D., additional, Jaramillo, Maria A., additional, Vigil, Maria, additional, Boyle, Mariaelena, additional, Masciale, Marina, additional, Hilliard, Marisa, additional, Munoz, Marisela, additional, Dickinson, Mary E., additional, Bell, Meishon, additional, York, Michele K., additional, Loor, Michelle, additional, Lopez, Michelle, additional, Liang, Mike K., additional, Aziz, Moez Karim, additional, Karla, Moriel, additional, Osazuma, Nancy, additional, Ramirez, Natalya, additional, Navejar, Natasha, additional, Cort, Nicol, additional, Lyons, Nicole B., additional, Perez, Norma, additional, Barshes, NR, additional, Barron, Olivia A., additional, Olavarria, Oscar A., additional, Constable, Petra, additional, Nwokolo, Phyllis, additional, Omokaro, Precious, additional, Patel, Premal, additional, Vallabh, Prithvi, additional, Shah, Puja, additional, Yusuf, Rafeek A., additional, Rosero, Rebecca A., additional, Lunstroth, Rebecca, additional, Obure, Renice, additional, Beach, Robert, additional, Goin-Kochel, Robin, additional, Parihar, Robin, additional, Zoorob, Roger, additional, Wilson, Ronee E., additional, Schmidt, Rosa Michelle, additional, Pettit, Rowland, additional, Udoetuk, Sade C., additional, Tasnim, Sadia, additional, Khan, Sara, additional, Adnan, Sareema, additional, Rodriguez, Sean, additional, Anandasabapathy, Sharmila, additional, Nesbitt, Shawna, additional, Bhushan, Sheena, additional, Sharath, Sherene, additional, Rogers, SO, additional, Dinh, Son, additional, Banu, Sophia, additional, Rose, Stacey, additional, Drake, Stacy, additional, Morain, Stephanie, additional, McCauley, Stephen R., additional, Abdelaziz, Sue, additional, Malik, Tahir, additional, Rasmussen, Tara L., additional, Shum, Thomas, additional, Raphel, Tiana, additional, Ko, Tien C., additional, Harris, Toi, additional, Hadley, Trevor, additional, Akoma, Uchechukwu, additional, Eduok, Uwem Bridgette, additional, Armendariz, Victoria, additional, Cole-Lewis, Yasmin C., additional, Al-Mohtaseb, Zaina, additional, and Yusuf, Zenab, additional
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- 2020
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7. Maternal Caffeine Consumption and Racial Disparities in Fetal Telomere Length
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Griffin, Isabel, primary, Ibrahimou, Boubakari, additional, Navejar, Natasha, additional, Aggarwal, Anjali, additional, Myers, Kristopher, additional, Mauck, Daniel, additional, Yusuf, Korede K., additional, Wudil, Usman J., additional, Aliyu, Muktar H., additional, and Salihu, Hamisu M., additional
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- 2019
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8. The effect of maternal vitamin C intake on fetal telomere length.
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Myers, Kristopher O., Ibrahimou, Boubakari, Yusuf, Korede K., Mauck, Daniel E., and Salihu, Hamisu M.
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VITAMIN C , *TELOMERES , *POLYMERASE chain reaction , *UMBILICAL cord , *DNA analysis - Abstract
A telomere is a nucleoprotein structure that is located at the end of a chromosome. Reduced telomere length manifests as physical ailments such as the increased risk of age-related illnesses. These age-related illnesses include heart disease and failure. Telomere length has been studied extensively in adults; however, limited information exists regarding maternal dietary influences on fetal telomere length. The objective of this study is to investigate the relationship between maternal vitamin C intake and fetal telomere length. Data for this analysis were collected as part of a prospective cohort study that recruited pregnant women upon admission into labor and delivery. Umbilical cord serum was collected for 96 maternal–fetal dyads, and DNA analysis was performed using a quantitative polymerase chain reaction. The telomere to single copy gene ratio method was used to determine telomere length, and maternal vitamin C intake was measured using the Dietary History Questionnaire (DHQ). Statistical analysis was conducted using generalized linear modeling-based analyses. The linear model indicates that maternal vitamin C intake (OR = 1.0032, 95%CI: 1.0014–1.0052, p ≤.05) was positively associated with fetal telomere length. BMI (OR = 1.1096, 95%CI: 1.0619–1.1660, p ≤.05) had a significant positive association with fetal telomere length while sodium intake was negatively associated with this outcome (OR = 0.9997, 95%CI: 0.9995–0.9998, p ≤.05). Black ethnicity had a significant negative association with fetal telomere length (OR = 0.0186, 95%CI: 0.0031–0.0824, p ≤.05). Our study shows a positive association between maternal vitamin C intake and fetal telomere length. These findings may provide a method of understanding and preventing adult-onset disease and mortality through intrauterine reprograming. [ABSTRACT FROM AUTHOR]
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- 2021
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9. The effect of maternal vitamin C intake on fetal telomere length
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Myers, Kristopher O., primary, Ibrahimou, Boubakari, additional, Yusuf, Korede K., additional, Mauck, Daniel E., additional, and Salihu, Hamisu M., additional
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- 2019
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10. The individual, interactive, and syndemic effect of substance use, depression, education, and ethnicity on retention in HIV care.
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Myers, Kristopher, Li, Tan, Baum, Marianna, Ibanez, Gladys, and Fennie, Kristopher
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HIV infection epidemiology ,HIV infections ,RESEARCH ,SUBSTANCE abuse ,RESEARCH methodology ,MEDICAL cooperation ,EVALUATION research ,HIGHLY active antiretroviral therapy ,COMPARATIVE studies ,MENTAL depression ,HEALTH attitudes ,RESEARCH funding ,ETHNIC groups ,EDUCATIONAL attainment ,DISEASE complications - Abstract
In this study, we sought to assess the individual, syndemic, and interactive associations between individual-level factors and retention in care. The sample was derived from the Miami Adult Studies on human immunodeficiency virus (HIV)/ acquired immune deficiency syndrome (AIDS) cohort from 2009 to 2014. The variables were entered into a multiple logistic regression with retention as the outcome. Backward regression, adjusting for all main effects, was conducted to determine which two-way interactions were associated with retention. Multivariable logistic regression was used to test which number of factors were associated with retention. Non-Hispanic Black race/ethnicity was associated with improved retention (odds ratio [OR] = 2.44, 95% confidence interval [CI]: 1.06-5.75, p ≤ 0.05) when compared to Non-Hispanic White persons. Black-Hispanic and Other racial/ethnic identities were associated with increased retention (OR = 4.84, 95%CI: 1.16-25.79, p ≤ 0.05 and OR = 7.24, 95%CI: 1.54-54.05, p ≤ 0.05, respectively) when compared to Non-Hispanic White persons. The interaction between depressive symptoms and Alcohol Use Disorder Identification Test (AUDIT, a test that assesses alcohol use disorder) score was significantly and negatively associated with retention in HIV care (OR = 0.14, 95%CI: 0.01-1.11, p ≤ 0.10). The interaction between age and male gender was also negatively associated with retention (OR = 0.95, 95%CI: 0.88-1.01, p ≤ 0.10), and the interaction between male gender and depression was positively associated with retention (OR = 7.17, 95%CI: 0.84-98.49, p ≤ 0.10). In conclusion, multiple races/ethnicities, specifically Non-Hispanic Black, Black-Hispanic, and Other racial/ethnic identification, were associated with increased odds of retention. Multiple interactions, specifically depressive symptoms * alcohol use disorder and male gender * age, were negatively associated with retention. The male gender * depression interaction was positively associated with retention in HIV care. [ABSTRACT FROM AUTHOR]
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- 2021
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11. Errors in Assessing Race and Ethnicity in Clinical Trial Enrollment
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Myers, Kristopher, primary, Osibogun, Olatokunbo, additional, and Madhivanan, Purnima, additional
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- 2016
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12. The Role of HIV in the Progression through the Stages of the Human Papillomavirus to Cervical Cancer Pathway.
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Myers, Kristopher O. and Ahmed, Nasar U.
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UTERINE tumors ,PAPILLOMAVIRUSES ,HUMAN papillomavirus vaccines ,CERVICAL cancer ,CARCINOGENESIS ,HIV infections - Abstract
Globally, an estimated 36.9 million persons are living with HIV/AIDS, and approximately 291 million women worldwide are carriers of human papillomavirus (HPV). A large number of women currently infected with either or both viruses constitute a large burden on the national health care system. Women with HIV have significantly higher rates of HPV infections than women without HIV. Approximately 77% of women with HIV are carriers of HPV. While research has established a linkage between HIV and progression to cervical cancer in general, there are currently no review articles exploring the role HIV has in the progression from HPV to each stage of carcinogenesis that leads to cervical cancer. The objective of this review is to examine the relationship between HIV and progression from HPV to each stage of carcinogenesis related to cervical cancer. The findings of the review support the conclusion that HIV infection increases the likelihood of progression to each stage of the HPV to cervical cancer pathway. [ABSTRACT FROM AUTHOR]
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- 2018
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13. Economic Costs Attributed to Diagnosed Diabetes in Each U.S. State and the District of Columbia: 2021.
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Khavjou OA, Sun M, D'Angelo SR, Neuwahl SJ, Hoerger TJ, Cho P, Myers K, and Zhang P
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Objective: To update state-specific estimates of diabetes-attributable costs in the U.S. and assess changes in spending from 2013 to 2021., Research Design and Methods: We used an attributable fraction approach to estimate direct medical costs of diagnosed diabetes using the 2021 State Health Expenditure Accounts, the 2021 Behavioral Risk Factor Surveillance System, and the Centers for Medicare and Medicaid Services 2018-2019 Minimum Data Set. We estimated diabetes-attributable productivity losses from morbidity and mortality using the 2016-2021 National Health Interview Survey and the 2021 mortality data from the Centers for Disease Control and Prevention. Costs were adjusted to 2021 U.S. dollars., Results: Total diabetes-attributable cost in 2021 was $640 billion ($335 billion in direct medical costs and $305 billion in indirect costs). The median state-level total diabetes-attributable cost was $8.2 billion (range $842 million to $81 billion). The median state-level per-person cost was $21,082, ranging from $17,452 to $37,090. Total diabetes-attributable cost increased by a median of 33% between 2013 and 2021, ranging from 16 to 68% across states. Medical costs increased by 50% overall (range 33-79%) and by 27% (range 15-41%) for per person with diabetes. Costs paid by Medicaid experienced the highest increase between 2013 and 2021 (median 153%; range 41-483%)., Conclusions: State economic costs of diagnosed diabetes are substantial and increased over the last decade. These costs and their growth vary considerably across states. These findings may help state policy makers in developing evidenced-based public health interventions in their respective states to prevent and control the prevalence of diabetes., (© 2024 by the American Diabetes Association.)
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- 2024
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14. Maternal Caffeine Consumption and Racial Disparities in Fetal Telomere Length.
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Griffin I, Ibrahimou B, Navejar N, Aggarwal A, Myers K, Mauck D, Yusuf KK, Wudil UJ, Aliyu MH, and Salihu HM
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Background and Objectives: The identification of risk factors for shorter telomere length, especially during fetal development, would be important towards caffeine consumption recommendations for pregnant women on a global scale. The purpose of this study was to evaluate the association between caffeine intake and fetal telomere length as well as racial/ethnic differences in telomere length regardless of maternal caffeine consumption status., Methods: Caffeine intake was measured using a food frequency questionnaire (FFQ). Three generalized linear models (GLM) were compared based on binary categorical variables of caffeine levels using data mean value of 117.3 mg as cut-off; the World Health Organization (WHO) recommendations of 300 mg; and the American College of Obstetricians and Gynecologists (ACOG) recommendations of 200 mg. The association between caffeine consumption and telomere length (telomere to single-copy [T/S] ratio) was then assessed., Results: Among 57 maternal-fetal dyads, 77.2% reported less than 200 mg of caffeine (ACOG) and 89.5% less than 300 mg (WHO). Both WHO and ACOG models found that caffeine intake was significantly and positively associated with longer telomere length (p<0.05); and sodium (p<0.05). Other" race (p<0.001) and "white" race (p<0.001) were also significantly and positively associated with longer telomere length in the same models. Increasing maternal age shortened telomere length significantly in all models (p<0.001)., Conclusion and Global Health Implications: Caffeine intake, maternal age, and race may be associated with alterations in fetal telomere length. This indicates that caffeine consumption during pregnancy may have long-term implications for fetal development. The racial/ethnic differences in telomere length found in this study warrant larger studies to further confirm these associations., Competing Interests: Conflicts of Interest: The authors have no conflicts of interest to report., (Copyright © 2020 Griffin et al.)
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- 2020
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