Searched for: school:SOM
Department/Unit:Population Health
A descriptive analysis of 2020 California Occupational Safety and Health Administration COVID-19-related complaints
Thomas, Marilyn D; Matthay, Ellicott C; Duchowny, Kate A; Riley, Alicia R; Khela, Harmon; Chen, Yea-Hung; Bibbins-Domingo, Kirsten; Glymour, M Maria
COVID-19 mortality disproportionately affected specific occupations and industries. The Occupational Safety and Health Administration (OSHA) protects the health and safety of workers by setting and enforcing standards for working conditions. Workers may file OSHA complaints about unsafe conditions. Complaints may indicate poor workplace safety during the pandemic. We evaluated COVID-19-related complaints filed with California (Cal)/OSHA between January 1, 2020 and December 14, 2020 across seven industries. To assess whether workers in occupations with high COVID-19-related mortality were also most likely to file Cal/OSHA complaints, we compared industry-specific per-capita COVID-19 confirmed deaths from the California Department of Public Health with COVID-19-related complaints. Although 7,820 COVID-19-related complaints were deemed valid by Cal/OSHA, only 627 onsite inspections occurred and 32 citations were issued. Agricultural workers had the highest per-capita COVID-19 death rates (402 per 100,000 workers) but were least represented among workplace complaints (44 per 100,000 workers). Health Care workers had the highest complaint rates (81 per 100,000 workers) but the second lowest COVID-19 death rate (81 per 100,000 workers). Industries with the highest inspection rates also had high COVID-19 mortality. Our findings suggest complaints are not proportional to COVID-19 risk. Instead, higher complaint rates may reflect worker groups with greater empowerment, resources, or capacity to advocate for better protections. This capacity to advocate for safe workplaces may account for relatively low mortality rates in potentially high-risk occupations. Future research should examine factors determining worker complaints and complaint systems to promote participation of those with the greatest need of protection.
PMID: 34909780
ISSN: n/a
CID: 5273852
Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus
Tin, Adrienne; Schlosser, Pascal; Matias-Garcia, Pamela R; Thio, Chris H L; Joehanes, Roby; Liu, Hongbo; Yu, Zhi; Weihs, Antoine; Hoppmann, Anselm; Grundner-Culemann, Franziska; Min, Josine L; Kuhns, Victoria L Halperin; Adeyemo, Adebowale A; Agyemang, Charles; Ärnlöv, Johan; Aziz, Nasir A; Baccarelli, Andrea; Bochud, Murielle; Brenner, Hermann; Bressler, Jan; Breteler, Monique M B; Carmeli, Cristian; Chaker, Layal; Coresh, Josef; Corre, Tanguy; Correa, Adolfo; Cox, Simon R; Delgado, Graciela E; Eckardt, Kai-Uwe; Ekici, Arif B; Endlich, Karlhans; Floyd, James S; Fraszczyk, Eliza; Gao, Xu; Gà o, Xīn; Gelber, Allan C; Ghanbari, Mohsen; Ghasemi, Sahar; Gieger, Christian; Greenland, Philip; Grove, Megan L; Harris, Sarah E; Hemani, Gibran; Henneman, Peter; Herder, Christian; Horvath, Steve; Hou, Lifang; Hurme, Mikko A; Hwang, Shih-Jen; Kardia, Sharon L R; Kasela, Silva; Kleber, Marcus E; Koenig, Wolfgang; Kooner, Jaspal S; Kronenberg, Florian; Kühnel, Brigitte; Ladd-Acosta, Christine; Lehtimäki, Terho; Lind, Lars; Liu, Dan; Lloyd-Jones, Donald M; Lorkowski, Stefan; Lu, Ake T; Marioni, Riccardo E; März, Winfried; McCartney, Daniel L; Meeks, Karlijn A C; Milani, Lili; Mishra, Pashupati P; Nauck, Matthias; Nowak, Christoph; Peters, Annette; Prokisch, Holger; Psaty, Bruce M; Raitakari, Olli T; Ratliff, Scott M; Reiner, Alex P; Schöttker, Ben; Schwartz, Joel; Sedaghat, Sanaz; Smith, Jennifer A; Sotoodehnia, Nona; Stocker, Hannah R; Stringhini, Silvia; Sundström, Johan; Swenson, Brenton R; van Meurs, Joyce B J; van Vliet-Ostaptchouk, Jana V; Venema, Andrea; Völker, Uwe; Winkelmann, Juliane; Wolffenbuttel, Bruce H R; Zhao, Wei; Zheng, Yinan; ,; ,; Loh, Marie; Snieder, Harold; Waldenberger, Melanie; Levy, Daniel; Akilesh, Shreeram; Woodward, Owen M; Susztak, Katalin; Teumer, Alexander; Köttgen, Anna
Elevated serum urate levels, a complex trait and major risk factor for incident gout, are correlated with cardiometabolic traits via incompletely understood mechanisms. DNA methylation in whole blood captures genetic and environmental influences and is assessed in transethnic meta-analysis of epigenome-wide association studies (EWAS) of serum urate (discovery, n = 12,474, replication, n = 5522). The 100 replicated, epigenome-wide significant (p < 1.1E-7) CpGs explain 11.6% of the serum urate variance. At SLC2A9, the serum urate locus with the largest effect in genome-wide association studies (GWAS), five CpGs are associated with SLC2A9 gene expression. Four CpGs at SLC2A9 have significant causal effects on serum urate levels and/or gout, and two of these partly mediate the effects of urate-associated GWAS variants. In other genes, including SLC7A11 and PHGDH, 17 urate-associated CpGs are associated with conditions defining metabolic syndrome, suggesting that these CpGs may represent a blood DNA methylation signature of cardiometabolic risk factors. This study demonstrates that EWAS can provide new insights into GWAS loci and the correlation of serum urate with other complex traits.
PMCID:8660809
PMID: 34887389
ISSN: 2041-1723
CID: 5586302
Meta-analyses identify DNA methylation associated with kidney function and damage
Schlosser, Pascal; Tin, Adrienne; Matias-Garcia, Pamela R; Thio, Chris H L; Joehanes, Roby; Liu, Hongbo; Weihs, Antoine; Yu, Zhi; Hoppmann, Anselm; Grundner-Culemann, Franziska; Min, Josine L; Adeyemo, Adebowale A; Agyemang, Charles; Ärnlöv, Johan; Aziz, Nasir A; Baccarelli, Andrea; Bochud, Murielle; Brenner, Hermann; Breteler, Monique M B; Carmeli, Cristian; Chaker, Layal; Chambers, John C; Cole, Shelley A; Coresh, Josef; Corre, Tanguy; Correa, Adolfo; Cox, Simon R; de Klein, Niek; Delgado, Graciela E; Domingo-Relloso, Arce; Eckardt, Kai-Uwe; Ekici, Arif B; Endlich, Karlhans; Evans, Kathryn L; Floyd, James S; Fornage, Myriam; Franke, Lude; Fraszczyk, Eliza; Gao, Xu; Gà o, Xīn; Ghanbari, Mohsen; Ghasemi, Sahar; Gieger, Christian; Greenland, Philip; Grove, Megan L; Harris, Sarah E; Hemani, Gibran; Henneman, Peter; Herder, Christian; Horvath, Steve; Hou, Lifang; Hurme, Mikko A; Hwang, Shih-Jen; Jarvelin, Marjo-Riitta; Kardia, Sharon L R; Kasela, Silva; Kleber, Marcus E; Koenig, Wolfgang; Kooner, Jaspal S; Kramer, Holly; Kronenberg, Florian; Kühnel, Brigitte; Lehtimäki, Terho; Lind, Lars; Liu, Dan; Liu, Yongmei; Lloyd-Jones, Donald M; Lohman, Kurt; Lorkowski, Stefan; Lu, Ake T; Marioni, Riccardo E; März, Winfried; McCartney, Daniel L; Meeks, Karlijn A C; Milani, Lili; Mishra, Pashupati P; Nauck, Matthias; Navas-Acien, Ana; Nowak, Christoph; Peters, Annette; Prokisch, Holger; Psaty, Bruce M; Raitakari, Olli T; Ratliff, Scott M; Reiner, Alex P; Rosas, Sylvia E; Schöttker, Ben; Schwartz, Joel; Sedaghat, Sanaz; Smith, Jennifer A; Sotoodehnia, Nona; Stocker, Hannah R; Stringhini, Silvia; Sundström, Johan; Swenson, Brenton R; Tellez-Plaza, Maria; van Meurs, Joyce B J; van Vliet-Ostaptchouk, Jana V; Venema, Andrea; Verweij, Niek; Walker, Rosie M; Wielscher, Matthias; Winkelmann, Juliane; Wolffenbuttel, Bruce H R; Zhao, Wei; Zheng, Yinan; ,; ,; Loh, Marie; Snieder, Harold; Levy, Daniel; Waldenberger, Melanie; Susztak, Katalin; Köttgen, Anna; Teumer, Alexander
Chronic kidney disease is a major public health burden. Elevated urinary albumin-to-creatinine ratio is a measure of kidney damage, and used to diagnose and stage chronic kidney disease. To extend the knowledge on regulatory mechanisms related to kidney function and disease, we conducted a blood-based epigenome-wide association study for estimated glomerular filtration rate (n = 33,605) and urinary albumin-to-creatinine ratio (n = 15,068) and detected 69 and seven CpG sites where DNA methylation was associated with the respective trait. The majority of these findings showed directionally consistent associations with the respective clinical outcomes chronic kidney disease and moderately increased albuminuria. Associations of DNA methylation with kidney function, such as CpGs at JAZF1, PELI1 and CHD2 were validated in kidney tissue. Methylation at PHRF1, LDB2, CSRNP1 and IRF5 indicated causal effects on kidney function. Enrichment analyses revealed pathways related to hemostasis and blood cell migration for estimated glomerular filtration rate, and immune cell activation and response for urinary albumin-to-creatinineratio-associated CpGs.
PMCID:8660832
PMID: 34887417
ISSN: 2041-1723
CID: 5586312
Capturing missed HIV pre-exposure prophylaxis opportunities-sexually transmitted infection diagnoses in the emergency department
Mclaughlin, Stephanie E; Kapadia, Farzana; Greene, Richard E; Pitts, Robert
The United States Centers for Disease Control and Prevention (CDC) recommends HIV pre-exposure prophylaxis (PrEP) be considered for all patients diagnosed with a sexually transmitted infection (STI). Emergency departments (EDs) are an important site for diagnosis and treatment of STIs for under-served populations. Consequently, we identified 377 patients diagnosed with a bacterial sexually transmitted infection (gonorrhea, chlamydia, and/or syphilis) at a major New York City emergency department between 1/1/2014 and 7/30/2017 to examine associations between key sociodemographic characteristics and missed opportunities for PrEP provision. In this sample, 299 (79%) emergency department patients missed their medical follow-up 90 days after STI diagnosis, as recommended. Results from adjusted generalized estimating equation regression models indicate that patients >45Â yo (aOR = 2.2, 95% CI 1.2-3.9) and those with a primary care provider in the hospital system (aOR = 6.8, 95% CI 3.8-12.0) were more likely to return for follow-up visits, whereas Black patients (aOR = 0.44, 95% CI 0.25-0.77) were less likely to return for follow-up visits. These findings indicate that lack of STI treatment follow-up visits are significantly missed opportunities for PrEP provision and comprehensive human immunodeficiency virus prevention care.
PMID: 34879782
ISSN: 1758-1052
CID: 5110312
Psychosexual functioning in cancer survivorship: What the pediatric oncologist needs to know
Frederick, Natasha N; Lehmann, Vicky; Ahler, Astrid; Carpenter, Kristen; Cherven, Brooke; Klosky, James L; Nahata, Leena; Quinn, Gwendolyn P
Sexual health may be disrupted in adolescents and young adults (AYAs) both during and after cancer treatment, irrespective of whether they are diagnosed in childhood, adolescence, or young adulthood. Unfortunately, oncology providers often underestimate the relevance of psychosexual issues for AYAs and underprioritize sexual health throughout treatment and survivorship. The purpose of this narrative review is to provide information on (a) the etiology of psychosexual dysfunction in childhood, adolescent, and young adult cancer patients and young adult survivors of childhood cancer; (b) strategies for communicating and evaluating potential sexual health issues of AYA patients/survivors; and (c) guidance for the practicing pediatric oncologist on how to address sexual health concerns with patients.
PMID: 34873822
ISSN: 1545-5017
CID: 5070182
Racial and weight discrimination associations with pain intensity and pain interference in an ethnically diverse sample of adults with obesity: a baseline analysis of the clustered randomized-controlled clinical trial the goals for eating and moving (GEM) study
Merriwether, Ericka N; Wittleder, Sandra; Cho, Gawon; Bogan, Eushavia; Thomas, Rachel; Bostwick, Naja; Wang, Binhuan; Ravenell, Joseph; Jay, Melanie
BACKGROUND:Everyday experiences with racial (RD) and weight discrimination (WD) are risk factors for chronic pain in ethnically diverse adults with obesity. However, the individual or combined effects of RD and WD on pain in adults with obesity is not well understood. There are gender differences and sexual dimorphisms in nociception and pain, but the effect of gender on relationships between RD, WD, and pain outcomes in ethnically diverse adults with obesity is unclear. Thus, the purposes of this study were to: 1) examine whether RD and WD are associated with pain intensity and interference, and 2) explore gender as a moderator of the associations between RD, WD, and pain. METHODS:with weight-related comorbidity. RD and WD were measured using questions derived from the Experiences of Discrimination questionnaire (EOD). Pain interference and intensity were measured using the PROMIS 29 adult profile V2.1. Linear regression models were performed to determine the associations between WD, RD, gender, and pain outcomes. RESULTS:Participants (n = 483) reported mild pain interference (T-score: 52.65 ± 10.29) and moderate pain intensity (4.23 ± 3.15). RD was more strongly associated with pain interference in women (b = .47, SE = .08, p < 001), compared to men (b = .14, SE = .07, p = .06). Also, there were no significant interaction effects between RD and gender on pain intensity, or between WD and gender on pain interference or pain intensity. CONCLUSIONS:Pain is highly prevalent in adults with obesity, and is impacted by the frequencies of experiences with RD and WD. Further, discrimination against adults with obesity and chronic pain could exacerbate existing racial disparities in pain and weight management. Asking ethnically diverse adults with obesity about their pain and their experiences of RD and WD could help clinicians make culturally informed assessment and intervention decisions that address barriers to pain relief and weight loss. TRIAL REGISTRATION:NCT03006328.
PMID: 34856961
ISSN: 1471-2458
CID: 5065842
Factors influencing intent to receive COVID-19 vaccination among Black and White adults in the southeastern United States, October - December 2020
Cunningham-Erves, Jennifer; Mayer, Carol S; Han, Xijing; Fike, Landon; Yu, Chang; Tousey, Phyllis M; Schlundt, David G; Gupta, Deepak K; Mumma, Michael T; Walkley, David; Steinwandel, Mark D; Edwards, Kathryn M; Lipworth, Loren; Sanderson, Maureen; Shu, Xiao-Ou; Shrubsole, Martha J
Vaccination intent is foundational for effective COVID-19 vaccine campaigns. To understand factors and attitudes influencing COVID-19 vaccination intent in Black and White adults in the US south, we conducted a mixed-methods cross-sectional survey of 4512 adults enrolled in the Southern Community Cohort Study (SCCS), an ongoing study of racial and economic health disparities. Vaccination intent was measured as "If a vaccine to prevent COVID-19 became available to you, how likely are you to choose to get the COVID-19 vaccination?" with options of "very unlikely," "somewhat unlikely," "neither unlikely nor likely," "somewhat likely," and "very likely." Reasons for intent, socio-demographic factors, preventive behaviors, and other factors were collected. 46% of participants had uncertain or low intent. Lower intent was associated with female gender, younger age, Black race, more spiritual/religious, lower perceived COVID-19 susceptibility, living in a greater deprivation area, lower reading ability, and lack of confidence in childhood vaccine safety or COVID-19 vaccine effectiveness or safety (p <Â .05 for all). Most factors were present in all racial/gender groups. Contextual influences, vaccine/vaccination specific issues, and personal/group influences were identified as reasons for low intent. Reasons for higher intent included preventing serious illness, life returning to normal, and recommendation of trusted messengers. Hesitancy was complex, suggesting tailored interventions may be required to address low intent.
PMID: 34847822
ISSN: 2164-554x
CID: 5162862
Loneliness and its predictors among older adults prior to and during the COVID-19 pandemic: cross-sectional and longitudinal survey findings from participants of the Atherosclerosis Risk in Communities (ARIC) Study cohort in the USA
Kucharska-Newton, Anna; Matsushita, Kunihiro; Mok, Yejin; Minotti, Melissa; Oelsner, Elizabeth C; Ring, Kim; Wagenknecht, Lynne; Hughes, Timothy M; Mosley, Thomas; Palta, Priya; Lutsey, Pamela L; Coresh, Joe
OBJECTIVES:We aimed to ascertain the prevalence of perceived loneliness among older adults following the onset of the COVID-19 pandemic and to examine factors contributing to the perception of loneliness. DESIGN:Cross-sectional and longitudinal data from the Atherosclerosis Risk in Communities (ARIC) Study cohort. SETTING:The ARIC Study cohort, a prospective cohort that recruited (1987-1989) participants from four distinct communities in the USA. PARTICIPANTS:2984 ARIC cohort members. PRIMARY AND SECONDARY OUTCOMES:Perceived loneliness assessed using the University of California at Los Angeles (UCLA) UCLA three-item Loneliness Scale telephone interviews conducted May-October 2020 and prior to March 2020. RESULTS:Of the total 5037 participants alive in 2020, 2984 (56.2%) responded to the UCLA three-item questionnaire (mean age 82.6 (SD 4.6) years, 586 (19.6%) black participants, 1081 (36.2%) men), of which 66 (2.2%) reported having had a COVID-19 infection during the observation period. The proportion of participants reporting feeling lonely was 56.3% (n=1680). Among participants with repeat measures of loneliness (n=516), 35.2% (n=182) reported feeling more lonely following pandemic onset. Self-rated health and emotional resilience were strongly associated with self-perceived loneliness. The burden of COVID-19 infections, concern about the pandemic and decreased self-reported physical activity were greater among black as compared with white participants and among those with an educational attainment of less than high school as compared with high school or more. CONCLUSION:Findings from this study document the increase in perceived loneliness among older adults during the COVID-19 pandemic in the USA.
PMCID:8640201
PMID: 34857573
ISSN: 2044-6055
CID: 5586292
Bayesian model comparison for rare-variant association studies
Venkataraman, Guhan Ram; DeBoever, Christopher; Tanigawa, Yosuke; Aguirre, Matthew; Ioannidis, Alexander G; Mostafavi, Hakhamanesh; Spencer, Chris C A; Poterba, Timothy; Bustamante, Carlos D; Daly, Mark J; Pirinen, Matti; Rivas, Manuel A
Whole-genome sequencing studies applied to large populations or biobanks with extensive phenotyping raise new analytic challenges. The need to consider many variants at a locus or group of genes simultaneously and the potential to study many correlated phenotypes with shared genetic architecture provide opportunities for discovery not addressed by the traditional one variant, one phenotype association study. Here, we introduce a Bayesian model comparison approach called MRP (multiple rare variants and phenotypes) for rare-variant association studies that considers correlation, scale, and direction of genetic effects across a group of genetic variants, phenotypes, and studies, requiring only summary statistic data. We apply our method to exome sequencing data (n = 184,698) across 2,019 traits from the UK Biobank, aggregating signals in genes. MRP demonstrates an ability to recover signals such as associations between PCSK9 and LDL cholesterol levels. We additionally find MRP effective in conducting meta-analyses in exome data. Non-biomarker findings include associations between MC1R and red hair color and skin color, IL17RA and monocyte count, and IQGAP2 and mean platelet volume. Finally, we apply MRP in a multi-phenotype setting; after clustering the 35 biomarker phenotypes based on genetic correlation estimates, we find that joint analysis of these phenotypes results in substantial power gains for gene-trait associations, such as in TNFRSF13B in one of the clusters containing diabetes- and lipid-related traits. Overall, we show that the MRP model comparison approach improves upon useful features from widely used meta-analysis approaches for rare-variant association analyses and prioritizes protective modifiers of disease risk.
PMCID:8715195
PMID: 34822764
ISSN: 1537-6605
CID: 5494932
Cytokine-induced liver injury in coronavirus disease-2019 (COVID-19): untangling the knots
Anirvan, Prajna; Narain, Sonali; Hajizadeh, Negin; Aloor, Fuad Z; Singh, Shivaram P; Satapathy, Sanjaya K
Liver dysfunction manifesting as elevated aminotransferase levels has been a common feature of coronavirus disease-2019 (COVID-19) infection. The mechanism of liver injury in COVID-19 infection is unclear. However, it has been hypothesized to be a result of direct cytopathic effects of the virus, immune dysfunction and cytokine storm-related multiorgan damage, hypoxia-reperfusion injury and idiosyncratic drug-induced liver injury due to medications used in the management of COVID-19. The favored hypothesis regarding the pathophysiology of liver injury in the setting of COVID-19 is cytokine storm, an aberrant and unabated inflammatory response leading to hyperproduction of cytokines. In the current review, we have summarized the potential pathophysiologic mechanisms of cytokine-induced liver injury based on the reported literature.
PMID: 33405427
ISSN: 1473-5687
CID: 4738992