Searched for: Department/Unit:Population Health
Discordance in Creatinine- and Cystatin C-Based eGFR and Clinical Outcomes: A Meta-Analysis
Estrella, Michelle M; Ballew, Shoshana H; Sang, Yingying; Grams, Morgan E; Coresh, Josef; Surapaneni, Aditya; Alencar de Pinho, Natalia; Ärnlöv, Johan; Brenner, Hermann; Carrero, Juan-Jesus; Chen, Teresa K; Cohen, Debbie L; Cushman, Mary; Gansevoort, Ron T; Hwang, Shih-Jen; Inker, Lesley A; Ix, Joachim H; Kabasawa, Keiko; Konta, Tsuneo; Lees, Jennifer S; Polkinghorne, Kevan R; Shlipak, Michael G; Vernooij, Robin W M; Wheeler, David C; Yadav, Ashok Kumar; Levey, Andrew S; Eckardt, Kai-Uwe; ,
IMPORTANCE/UNASSIGNED:Estimated glomerular filtration rates (eGFRs) can differ according to whether creatinine or cystatin C is used for the eGFR calculation, but the prevalence and importance of these differences remain unclear. OBJECTIVES/UNASSIGNED:To evaluate the prevalence of a discordance between cystatin C-based eGFR (eGFRcys) and creatinine-based eGFR (eGFRcr), identify characteristics associated with greater discordance, and evaluate associations of discordance with adverse outcomes. DATA SOURCES/UNASSIGNED:Participants in the Chronic Kidney Disease Prognosis Consortium (CKD-PC). STUDY SELECTION/UNASSIGNED:Participants with concurrent cystatin C and creatinine measurements and clinical outcome measurement. DATA EXTRACTION AND SYNTHESIS/UNASSIGNED:Between April 2024 and August 2025, data were synthesized using individual-level meta-analysis. MAIN OUTCOMES AND MEASURES/UNASSIGNED:The primary independent measurement was a large negative eGFR difference (eGFRdiff), defined as an eGFRcys that was at least 30% lower than eGFRcr. Secondary (dependent) outcomes included all-cause and cardiovascular mortality, atherosclerotic cardiovascular disease, heart failure, and kidney failure with replacement therapy. RESULTS/UNASSIGNED:A total of 821 327 individuals from 23 outpatient cohorts (mean [SD] age, 59 [12] years; 48% female; 13.5% with diabetes; 40% with hypertension) and 39 639 individuals from 2 inpatient cohorts (mean [SD] age, 67 [16] years; 31% female; 30% with diabetes; 72% with hypertension) were included. Among outpatient participants, 11% had a large negative eGFRdiff (range, 3%-50%). Among inpatients, 35% had a large negative eGFRdiff. Among outpatient participants, at a mean (SD) follow-up of 11 (4) years, a large negative eGFRdiff, compared with an eGFRdiff between -30% and 30%, was associated with higher rates of all-cause mortality (28.4 vs 16.8 per 1000 person-years [PY]; hazard ratio [HR], 1.69 [95% CI, 1.57-1.82]), cardiovascular mortality (6.1 vs 3.8 per 1000 PY; HR, 1.61 [95% CI, 1.48-1.76]), atherosclerotic cardiovascular disease (13.3 vs 9.8 per 1000 PY; HR, 1.35 [95% CI, 1.27-1.44]), heart failure (13.2 vs 8.6 per 1000 PY; HR, 1.54 [95% CI, 1.40-1.68]), and kidney failure with replacement therapy (2.7 vs 2.1 per 1000 PY; HR, 1.29 [95% CI, 1.13-1.47]). CONCLUSIONS AND RELEVANCE/UNASSIGNED:In the CKD-PC, 11% of outpatient participants and 35% of hospitalized patients had an eGFRcys that was at least 30% lower than their eGFRcr. In the outpatient setting, presence of eGFRcys at least 30% lower than eGFRcr was associated with significantly higher rates of all-cause mortality, cardiovascular events, and kidney failure.
PMID: 41202182
ISSN: 1538-3598
CID: 5960402
A Culturally and Linguistically Tailored Intervention to Improve Diabetes-Related Outcomes in Chinese Americans With Type 2 Diabetes: Pilot Randomized Controlled Trial
Liu, Jing; Cao, Jiepin; Shi, Yun; Sevick, Mary Ann; Islam, Nadia; Feldman, Naumi; Li, Huilin; Wang, Chan; Zhao, Yanan; Tamura, Kosuke; Levy, Natalie; Jiang, Nan; Zhu, Ziqiang; Wang, Yulin; Hong, Jia; Hu, Lu
BACKGROUND:levels. However, it remains unclear whether the CARE program also improves diabetes self-efficacy and psychosocial outcomes in the same study sample. OBJECTIVE:This is a secondary analysis to examine the potential efficacy of the CARE program on secondary outcomes, including diabetes self-efficacy, self-care activities, beliefs in diabetes self-care activities, and diabetes distress among Chinese Americans with T2D. METHODS:level of 7% or higher. Participants were recruited from various health care settings in New York City, including community health centers, private primary care providers, and NYU Langone Health and its affiliates, and were randomly assigned to either the CARE intervention group (n=30) or a waitlist control group (n=30). The intervention consisted of 2 culturally and linguistically tailored educational videos per week for 12 weeks, covering diabetes self-care topics such as healthy eating, physical activity, and medication adherence. These videos were delivered via the WeChat app. In addition, community health workers provided support calls to assist them in setting goals, problem-solving, and addressing social determinants of health barriers every 2 weeks. Secondary outcomes included patient self-reported diabetes self-efficacy, self-care activities, beliefs in diabetes self-care activities, and diabetes distress. Outcomes were assessed at baseline, 3 months, and 6 months. RESULTS:Participants had a mean age of 54.3 (SD 11.5) years and 62% (37/60) were male, 78% (47/60) were married, 58% (35/60) were employed, 70% (42/60) had a high school education or lower, and 88% (53/60) reported limited English proficiency. Intervention participants demonstrated statistically significant improvements in self-efficacy at 3 months (estimated difference in change: 8.47; 95% CI 2.44-14.5; adjusted P=.02), diabetes distress at 6 months (estimated difference in change: -0.43; 95% CI -0.71 to -0.15; adjusted P=.009), and adherence to a healthy diet at both 3 months (estimated difference in change: 1.61; 95% CI 0.46-2.75; adjusted P=.02) and 6 months (estimated difference in change: 1.64; 95% CI 0.48-2.81; adjusted P=.02). CONCLUSIONS:The culturally and linguistically tailored intervention showed promise in improving self-efficacy and diabetes self-care activities among Chinese Americans with T2D, warranting validation through a large-scale randomized controlled trial. TRIAL REGISTRATION/BACKGROUND:ClinicalTrials.gov NCT03557697; https://clinicaltrials.gov/study/NCT03557697.
PMID: 41144955
ISSN: 2291-5222
CID: 5960992
Air-Noise Pollution Linkages: Testing Innovative Community-Based Adaptation and Mitigation Strategies in Kenya
Kumar, Manasi; Danube, Ngongang Wandji; Nyongesa, Vincent; Kalama, Lucas; Ngunu, Carol; Leli, Hassan; Tele, Albert; Apondi, Edith; Asande, Josphat; Warfa, Osman; Macharia, Ayub; Madeghe, Beatrice; Yator, Obadia; Nyamai, Darius; Osano, Philip
PMCID:12577548
PMID: 41179854
ISSN: 2214-9996
CID: 5959312
Organophosphate Pesticide Exposure and Semen Quality in Healthy Young Men: A Pilot Study
Stapleton, Jenisha L; Adelman, Sarah; Najari, Bobby B; Kannan, Kurunthachalam; Albergamo, Vittorio; Kahn, Linda G
This cross-sectional pilot study aimed to examine associations between urinary metabolites of organophosphate (OP) pesticides and semen quality in 42 healthy young men. Participants answered questionnaires, provided semen and urine samples, and had anthropometric measures taken. Urine and seminal plasma were assayed for dialkylphosphate (DAP) metabolites of OP pesticides using high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry. Semen quality parameters were analyzed according to the World Health Organization protocol, and seminal oxidative stress was assayed using MiOXSYS, a galvanic cell-based technology that yields an integrated measure of oxidants and antioxidants. Associations of OP pesticide metabolites with continuous and dichotomous sperm concentration, percent motility, and percent normal morphology, and with seminal oxidative-reduction potential (ORP) were analyzed statistically. OP pesticide exposure was associated with lower overall semen quality. Specifically, ∑DAP metabolites, driven by diethyl metabolites, was inversely associated with percent sperm motility, but this relationship was not mediated by seminal ORP. Seminal ORP was inversely associated with sperm concentration, but OP pesticide exposure was not associated with seminal ORP.
PMCID:12562182
PMID: 41154467
ISSN: 2076-3921
CID: 5961262
Preventive effect of vaccination on long COVID in adolescents with SARS-CoV-2 infection
Thaweethai, Tanayott; Gross, Rachel S; Pant, Deepti B; Rhee, Kyung E; Jernigan, Terry L; Kleinman, Lawrence C; Snowden, Jessica N; Salisbury, Amy L; Kinser, Patricia A; Milner, Joshua D; Tantisira, Kelan; Warburton, David; Mohandas, Sindhu; Wood, John C; Fitzgerald, Megan L; Carmilani, Megan; Krishnamoorthy, Aparna; Reeder, Harrison T; Foulkes, Andrea S; Stockwell, Melissa S; ,
PURPOSE/OBJECTIVE:In adolescents (12-17 years), it is unknown whether COVID-19 vaccination reduces progression from COVID-19 to Long COVID (LC) beyond preventing SARS-CoV-2 infection. We assessed the effect of vaccination among SARS-CoV-2 infected adolescents. METHODS AND RESULTS/RESULTS:Participants were recruited from over 60 US healthcare and community settings. The exposure was any COVID-19 vaccination 6 months prior to infection. The outcome was LC defined using the LC research index. Vaccinated (n = 724) and unvaccinated (n = 507) adolescents were matched on sex, infection date, and enrollment date. The risk of LC was 36 % lower (95 % CI, 17 %, 50 %) in vaccinated compared to unvaccinated participants. CONCLUSIONS:Vaccination reduces the risk of LC. Given the profound impact LC can have on the health and well-being of adolescents and the limited availability of treatments during this developmental stage, this supports vaccination as a strategy for preventing LC by demonstrating an important secondary prevention effect.
PMID: 41176968
ISSN: 1873-2518
CID: 5959202
COVID-19 School Disruptions in Early Childhood Education and Children's Early Elementary School Outcomes: Findings from the Smart Beginnings Randomized Clinical Trial
Miller, Elizabeth B; Canfield, Caitlin F; Aviles, Ashleigh I; Hunter, Leah J; Shaw, Daniel S; Mendelsohn, Alan L; Morris-Perez, Pamela A
The COVID-19 pandemic has significantly impacted families with young children (age 0-5). Using a subset of data from the randomized clinical trial of an integrated, preventive parenting model, Smart Beginnings (SB), this study examined associations between COVID-19-related school disruptions in early childhood education (ECE) and children's early elementary school outcomes. A secondary, exploratory aim sought to determine whether SB attenuated these relations. Path analyses demonstrated that school disruptions in ECE were associated with lower literacy skills at age 6 in letter-word identification (β=-.32, p<.01) and phonemic decoding (β=-.26, p<.05), but not for math or oral language skills. School disruptions in ECE were also related to increased internalizing behavior in children (β=.34, p<.01), with a trend for increased externalizing behavior (β=.22, p<.10). There was no significant moderation by SB intervention group. Implications for future school disruptions and acute stressors more broadly, as well as the role of preventive interventions, are discussed.
PMCID:12574550
PMID: 41179929
ISSN: 0300-4430
CID: 5959322
Environmental and social injustices impact dementia risk among older adults with end-stage kidney disease: a national registry study
Li, Yiting; Menon, Gayathri; Long, Jane J; Wilson, Malika; Kim, Byoungjun; Bae, Sunjae; DeMarco, Mario P; Wu, Wenbo; Orandi, Babak J; Gordon, Terry; Thurston, George D; Purnell, Tanjala S; Thorpe, Roland J; Szanton, Sarah L; Segev, Dorry L; McAdams-DeMarco, Mara A
BACKGROUND/UNASSIGNED:; environmental injustice) by racial/ethnic segregation (social injustice) on dementia diagnosis in ESKD. METHODS/UNASSIGNED:concentrations (annualized and matched to older adults' residential ZIP code at dialysis initiation) and by segregation scores (Theil's H method). FINDINGS/UNASSIGNED:and segregation. INTERPRETATION/UNASSIGNED:experienced an increased risk of dementia; this risk was particularly pronounced among individuals in high segregation and predominantly minority neighborhoods. Environmental and social injustices likely drive racial and ethnic disparities in dementia for older adults with ESKD, underscoring the need for interventions and policies to mitigate these injustices. FUNDING/UNASSIGNED:National Institutes of Health.
PMCID:12550583
PMID: 41141567
ISSN: 2667-193x
CID: 5960892
Predicted Risk, Preclinical Heart Failure Measures, and Incident Heart Failure: The ARIC Study
Grant, Jelani K; Zhang, Sui; Khan, Sadiya S; Ozkan, Bige; Blumer, Vanessa; Nambi, Vijay; Echouffo-Tcheugui, Justin B; Pandey, Ambarish; Blumenthal, Roger S; Ballantyne, Christie M; Selvin, Elizabeth; Matsushita, Kunihiro; Shah, Amil; Coresh, Josef; Ndumele, Chiadi E
BACKGROUND:The association of PREVENT-HF (Predicting Risk of Cardiovascular Events-Heart Failure) risk estimates with preclinical heart failure (HF) and whether preclinical HF measures add to the predictive utility of PREVENT-HF remain undefined. OBJECTIVES/OBJECTIVE:The aims of this study were to evaluate the association between PREVENT-HF risk estimates and preclinical HF, to examine how preclinical HF measures correspond to absolute HF risk within PREVENT-HF categories, and to determine whether they provide predictive value beyond the PREVENT-HF score. METHODS:The authors performed a prospective analysis of 2,714 ARIC (Atherosclerosis Risk In Communities) Visit 5 participants <80 years of age, without baseline cardiovascular disease. Preclinical HF was defined by elevated cardiac biomarkers (N-terminal of pro-b-type natriuretic peptide ≥125 pg/mL or high-sensitivity cardiac troponin T ≥22 ng/L/≥14 ng/L in men/women) and/or abnormal echocardiographic findings. Within PREVENT-HF 10-year risk categories (<7.5%, ≥7.5% to <10%, ≥10% to <15%, ≥15% to <20%, and ≥20%), we assessed preclinical HF prevalence and compared 10-year HF incidence rates for those with and without preclinical HF. We assessed changes in predictive utility by adding preclinical HF measures to PREVENT-HF. RESULTS:The mean age was 74 years, with 63% women, and 22% Black adults. Higher PREVENT-HF risk was associated with higher preclinical HF prevalence, with the highest prevalence of combined elevated biomarkers plus abnormal echocardiograms (37%) in those with PREVENT-HF ≥20%. Over a median follow-up of 9.9 years, 262 HF events occurred. Within PREVENT-HF categories, preclinical HF measures were strongly associated with absolute HF risk: among those with PREVENT-HF ≥20%, HF incidence rates (per 1,000 person-years) were 9.5 with no preclinical HF and 51.5 with elevated biomarkers plus abnormal echocardiography. Adding cardiac biomarkers to PREVENT-HF improved risk discrimination (C statistic change 0.69 to 0.75; P < 0.001) and reclassification (categorical Net Reclassification Index: 0.17; 95% CI: 0.09-0.26), with modest further improvement from adding echocardiographic measures. CONCLUSIONS:Preclinical HF measures indicate higher absolute HF risk within PREVENT-HF categories and enhance HF risk prediction.
PMID: 41045906
ISSN: 2213-1787
CID: 5959172
Using longitudinal, multi-partner qualitative data to evaluate the implementation of a diabetes prevention and management intervention among South Asians Americans
Ali, Shahmir H; Onakomaiya, Deborah; Saif, Nabeel I; Rahman, Fardin; Mohsin, Farhan M; Mohaimin, Sadia; Rakhra, Ashlin; Mammen, Shinu; Hussain, Sarah; Zanowiak, Jennifer; Lim, Sahnah; Shelley, Donna; Islam, Nadia S
BACKGROUND:Community-clinical linkage models (CCLM) display significant potential to address the unique, multi-level type 2 diabetes risk factors facing minoritized communities, such as South Asian Americans. However, there lacks a systematic, longitudinal evaluation of how such tailored CCLMs can be better implemented in dynamic, real-world settings. This study aims to leverage multi-partner insights, collected in real time, to explore the barriers and facilitators to implement a South Asian American diabetes management and prevention intervention (the DREAM intervention). METHODS:The DREAM intervention, a two-arm randomized controlled trial, was implemented from 2019-2022; partners involved in its implementation were interviewed annually to understand their experiences of the program. Implementation partners included community health workers (CHWs), participating healthcare providers, community advisory board (CAB) partners, and research staff. The interview guide and subsequent deductive qualitative analysis was informed by the Consolidated Framework for Implementation Research (CFIR). RESULTS:Overall, 78 interviews were conducted across four waves (2019-2022) with 5 research staff, 8 CHWs, 18 providers/clinic staff, and 12 CAB partners. CHWs adapted intervention characteristics by tailoring curriculum and implementation to patient needs, including personalized goal setting and shifting to remote delivery with COVID-19-related content. At the individual level, participants' occupations, family dynamics, and technological capacity shaped engagement, while changing social, financial, and health contexts over time required CHWs to continually adjust support. Within the inner setting, partner roles and resource availability fluctuated, yet structured and consistent meetings facilitated communication and problem-solving. Outer setting influences, including shifting government and universities policies and the COVID-19 pandemic, required repeated adaptations, while CAB partnerships expanded community connections and services over time. Process-related findings underscored the evolving role of CHWs and research staff in planning and fidelity, with training shifting toward peer mentorship to build capacity. CONCLUSION/CONCLUSIONS:Findings revealed the pivotal role of programmatic adaptability and robust partner engagement in navigating dynamic contexts to support the diabetes needs of minoritized communities. The real-time, longitudinal approach taken for data collection and analysis was crucial in understanding how intervention changes were implemented and experienced, providing a model for similar implementation assessments.
PMCID:12574163
PMID: 41168908
ISSN: 2662-2211
CID: 5961692
Development of a core outcome set for clinical trials of interventions to improve sleep in people with cognitive impairment-the Sleep in Cognitive Impairment Core Outcome Set (SCICOS)
Crowley, Patrick; Henry, Alasdair L; Flanagan, Evelyn; Antonsdottir, Inga; Bentley, Alison; Blackman, Jonathan; Bliwise, Donald L; Bubu, Omonigho M; Buysse, Daniel J; Camargos, Einstein F; Cassidy-Eagle, Erin; Cote, Kimberly; Coulthard, Elizabeth; D'Rozario, Angela L; Espie, Colin A; Falck, Ryan S; Gabb, Victoria G; Harvey, Allison G; Hmwe, Nant Thin Thin; Hoyos, Camilla M; Jobbins, Lucy; Kennelly, Seán; Kent, Brianne A; Köpke, Sascha; Krystal, Andrew; Leroi, Iracema; Liguori, Claudio; Lim, Yen Ying; Lorenz, Rebecca; Lucey, Brendan P; Mander, Bryce; Moline, Margaret; Naismith, Sharon L; Ogunniyi, Adesola; Rapaport, Penny; Reynolds, Charles F; Richards, Kathy; Siengsukon, Catherine F; Sindi, Shireen; Singer, Clifford M; Wirz-Justice, Anna; Yaffe, Kristine; O'Caoimh, Rónán
INTRODUCTION/BACKGROUND:Sleep disturbances are common in older people with cognitive impairment, potentially contributing to negative outcomes. A core outcome set (COS) is required to reduce heterogeneity in clinical trials and promote the development of high-quality evidence to support clinical management. METHODS:A multi-stage mixed methods study was conducted in accordance with The Core Outcome Set Standards for Development. RESULTS:A systematic review identified 287 sleep outcomes from previous clinical trials. Qualitative interviews ensured the COS was informed by what matters most to people with cognitive impairment and their caregivers. A modified Delphi process identified nine outcomes for the COS: total sleep time, sleep onset latency, wakefulness after sleep onset, number of night-time awakenings, sleep efficiency, and measures of sleep quality, daytime sleepiness, cognition, and mood. DISCUSSION/CONCLUSIONS:This COS will support researchers to produce more reliable and coherent trial data to guide the management of sleep disturbances in people with neurodegenerative cognitive impairment. HIGHLIGHTS/CONCLUSIONS:Evidence is lacking regarding the treatment of sleep disturbances in people with cognitive impairment. Heterogeneity of reported outcomes in clinical trials limits data synthesis. A qualitative analysis established what matters most to people with cognitive impairment and their caregivers when determining treatment effectiveness. A Delphi panel of experts agreed upon a core outcome set. This core outcome set will improve the reliability and comparability of data from future trials.
PMCID:12591993
PMID: 41198603
ISSN: 1552-5279
CID: 5960172