Searched for: department:Medicine. General Internal Medicine
recentyears:2
school:SOM
Vascular endothelium as a target for perfluroalkyl substances (PFAs)
Wittkopp, Sharine; Wu, Fen; Windheim, Joseph; Robinson, Morgan; Kannan, Kurunthachalam; Katz, Stuart D; Chen, Yu; Newman, Jonathan D; [Levy, Natalie]
INTRODUCTION/BACKGROUND:Perfluoroalkyl substances (PFAs) are ubiquitous, anthropogenic organic compounds that have been linked with cardiovascular disease and cardiovascular risk factors. Older, long-chain PFAs have been phased out due to adverse cardiometabolic health effect and replaced by newer short-chain PFAs. However, emerging research suggests that short-chain PFAs may also have adverse cardiovascular effects. Non-invasive measures of vascular function can detect preclinical cardiovascular disease and serve as a useful surrogate for early CVD risk. We hypothesized that serum concentrations of PFAs would be associated with noninvasive measures of vascular function, carotid-femoral pulse wave velocity (PWV) and brachial artery reactivity testing (BART), in adults with non-occupational exposure to PFAs. METHODS:We measured serum concentrations of 14 PFAs with hybrid solid-phase extraction and ultrahigh-performance liquid chromatography-tandem mass spectrometry in 94 adult outpatients with no known cardiovascular disease. We collected clinical and demographic data; and measured vascular function, PWV and BART, using standard protocols. We assessed associations of individual PFAs with log-transformed BART and PWV using linear regression. We used weighted quantile sum regression to assess effects of correlated PFA mixtures on BART and PWV. RESULTS:Ten PFAs were measured above the limit of detection in >50% of participants. Each standard deviation increase in concentration of perfluoroheptanoic acid (PFHpA) was associated with 15% decrease in BART (95% CI: -28.5, -0.17). The weighted index of a mixture of PFAs with correlated concentrations was inversely associated with BART: each tertile increase in the weighted PFA mixture was associated with 25% lower BART, with 73% of the effect driven by PFHpA. In contrast, no PFAs or mixtures were associated with PWV. CONCLUSIONS:Serum concentration of PFHpA, a new, short-chain PFA, was associated with impaired vascular function among outpatients without CVD. Our findings support a potential adverse cardiovascular effect of newer, short-chain PFAs.
PMID: 35447152
ISSN: 1096-0953
CID: 5428772
Homotypic fibrillization of TMEM106B across diverse neurodegenerative diseases
Chang, Andrew; Xiang, Xinyu; Wang, Jing; Lee, Carolyn; Arakhamia, Tamta; Simjanoska, Marija; Wang, Chi; Carlomagno, Yari; Zhang, Guoan; Dhingra, Shikhar; Thierry, Manon; Perneel, Jolien; Heeman, Bavo; Forgrave, Lauren M; DeTure, Michael; DeMarco, Mari L; Cook, Casey N; Rademakers, Rosa; Dickson, Dennis W; Petrucelli, Leonard; Stowell, Michael H B; Mackenzie, Ian R A; Fitzpatrick, Anthony W P
Misfolding and aggregation of disease-specific proteins, resulting in the formation of filamentous cellular inclusions, is a hallmark of neurodegenerative disease with characteristic filament structures, or conformers, defining each proteinopathy. Here we show that a previously unsolved amyloid fibril composed of a 135 amino acid C-terminal fragment of TMEM106B is a common finding in distinct human neurodegenerative diseases, including cases characterized by abnormal aggregation of TDP-43, tau, or α-synuclein protein. A combination of cryoelectron microscopy and mass spectrometry was used to solve the structures of TMEM106B fibrils at a resolution of 2.7 Å from postmortem human brain tissue afflicted with frontotemporal lobar degeneration with TDP-43 pathology (FTLD-TDP, n = 8), progressive supranuclear palsy (PSP, n = 2), or dementia with Lewy bodies (DLB, n = 1). The commonality of abundant amyloid fibrils composed of TMEM106B, a lysosomal/endosomal protein, to a broad range of debilitating human disorders indicates a shared fibrillization pathway that may initiate or accelerate neurodegeneration.
PMID: 35247328
ISSN: 1097-4172
CID: 5174822
Temporal reproducibility of IgG and IgM autoantibodies in serum from healthy women
Clendenen, T V; Hu, S; Afanasyeva, Y; Askenazi, M; Koenig, K L; Hulett, T; Liu, M; Liu, S; Wu, F; Zeleniuch-Jacquotte, A; Chen, Y
Autoantibodies are present in healthy individuals and altered in chronic diseases. We used repeated samples collected from participants in the NYU Women's Health Study to assess autoantibody reproducibility and repertoire stability over a one-year period using the HuProt array. We included two samples collected one year apart from each of 46 healthy women (92 samples). We also included eight blinded replicate samples to assess laboratory reproducibility. A total of 21,211 IgG and IgM autoantibodies were interrogated. Of those, 86% of IgG (n = 18,303) and 34% of IgM (n = 7,242) autoantibodies showed adequate lab reproducibility (coefficient of variation [CV] < 20%). Intraclass correlation coefficients (ICCs) were estimated to assess temporal reproducibility. A high proportion of both IgG and IgM autoantibodies with CV < 20% (76% and 98%, respectively) showed excellent temporal reproducibility (ICC > 0.8). Temporal reproducibility was lower after using quantile normalization suggesting that batch variability was not an important source of error, and that normalization removed some informative biological information. To our knowledge this study is the largest in terms of sample size and autoantibody numbers to assess autoantibody reproducibility in healthy women. The results suggest that for many autoantibodies a single measurement may be used to rank individuals in studies of autoantibodies as etiologic markers of disease.
PMCID:9008031
PMID: 35418192
ISSN: 2045-2322
CID: 5201972
A Novel Needleless Delivery System for Scalp Platelet-Rich Plasma: Pilot Study
Linkov, Gary; Sukhdeo, Kumar; Grand, Elizabeth
PMID: 35066548
ISSN: 1524-4725
CID: 5241982
Mentoring Underrepresented Minority Physician-Scientists to Success
Kalet, Adina; Libby, Anne M; Jagsi, Reshma; Brady, Kathleen; Chavis-Keeling, Deborah; Pillinger, Michael H; Daumit, Gail L; Drake, Amelia F; Drake, Wonder Puryear; Fraser, Victoria; Ford, Daniel; Hochman, Judith S; Jones, Rochelle D; Mangurian, Christina; Meagher, Emma A; McGuinness, Georgeann; Regensteiner, Judith G; Rubin, Deborah C; Yaffe, Kristine; Ravenell, Joseph E
As the nation seeks to recruit and retain physician-scientists, gaps remain in understanding and addressing mitigatable challenges to the success of faculty from underrepresented minority (URM) backgrounds. The Doris Duke Charitable Foundation Fund to Retain Clinical Scientists program, implemented in 2015 at 10 academic medical centers in the United States, seeks to retain physician-scientists at risk of leaving science because of periods of extraordinary family caregiving needs, hardships that URM faculty-especially those who identify as female-are more likely to experience. At the annual Fund to Retain Clinical Scientists program directors conference in 2018, program directors-21% of whom identify as URM individuals and 13% as male-addressed issues that affect URM physician-scientists in particular. Key issues that threaten the retention of URM physician-scientists were identified through focused literature reviews; institutional environmental scans; and structured small- and large-group discussions with program directors, staff, and participants. These issues include bias and discrimination, personal wealth differential, the minority tax (i.e., service burdens placed on URM faculty who represent URM perspectives on committees and at conferences), lack of mentorship training, intersectionality and isolation, concerns about confirming stereotypes, and institutional-level factors. The authors present recommendations for how to create an environment in which URM physician-scientists can expect equitable opportunities to thrive, as institutions demonstrate proactive allyship and remove structural barriers to success. Recommendations include providing universal training to reduce interpersonal bias and discrimination, addressing the consequences of the personal wealth gap through financial counseling and benefits, measuring the service faculty members provide to the institution as advocates for URM faculty issues and compensating them appropriately, supporting URM faculty who wish to engage in national leadership programs, and sustaining institutional policies that address structural and interpersonal barriers to inclusive excellence.
PMID: 34495889
ISSN: 1938-808x
CID: 5200092
Things We Do for No Reason: Tumor Markers CA125, CA19-9, and CEA in the Initial Diagnosis of Malignancy
Israilov, Sigal; Cho, Hyung J; Krouss, Mona
PMID: 34424189
ISSN: 1553-5606
CID: 5006632
Healthcare Professionals' Perspectives on Adapting a Community Health Worker Model to Facilitate Lung Cancer Screening for Chinese For-Hire Vehicle Drivers
Leng, Jennifer; Li, Randall; Lui, Florence; Gany, Francesca
Chinese immigrant for-hire vehicle (FHV) drivers who smoke or smoked are at high risk for lung cancer due to the combined impact of tobacco use and air pollution exposure yet underutilize lung cancer screening (LCS). Community Health Worker (CHW) programs have been effective at improving cancer screening rates. This study describes a community needs assessment to inform the adaptation of an existing CHW intervention to facilitate LCS among Chinese FHV drivers. Interviews were conducted until saturation with 13 Chinese-serving health professionals to determine the community's needs, priorities, and preferences. Transcripts were qualitatively analyzed using Atlas.ti. Seven frequently occurring themes were identified: knowledge of guidelines/access to LCS, acceptability of CHW program, CHW role in screening process, qualities of an ideal CHW, barriers to LCS, challenges to implementing a CHW program, and adaptations to CHW program. The adapted CHW intervention should include culturally tailored health education to increase LCS knowledge for patients and providers.
PMCID:7759596
PMID: 32583351
ISSN: 1543-0154
CID: 5937342
Effects of Reduced Sodium Consumption on Interdialytic Weight Gain and Blood Pressure in Maintenance Hemodialysis Patients [Meeting Abstract]
Clark-Cutaia, M; Aryal, S; Yu, G; Townsend, R; Rivera, E; Compher, C
Dietary sodium (Na) restriction is universally prescribedfor hemodialysis patients to decrease adverse outcomes.1 However, few studies have investigated the impact of Na restriction on volume status and blood pressure (BP), and none in American community-dwelling populations in prospective, randomized controlled trial (RCT). The purpose of this feasibility RCT was to assess the effects of three levels of Na intake (unrestricted [control group; CG], 1.5G, 2.4G) on interdialytic weight gain (IDWG) and BP in patients undergoing hemodialysis. We conducted a three-group, double-blinded, RCT of 42 individuals living with end stage kidney disease in a domiciled feeding study. We examined the effects of 5 days of unrestricted Na in the control group (CG, n=14) and Na restriction to 1.5G (n=11) or 2.4G (n=14) per day on IDWG and BP. Our sample was overwhelmingly African American (85%), male (52.2%), with hypertension as the primary etiology of kidney disease (45%). The mean IDWG on Day 1 was 2.62kg (SD=1.54) and BP was 143/75.44 (SD=29.77/17.74). There were no significant differences in the change in IDWG regardless of group membership, although the trend demonstrated a decrease by Day 5. Decreases in BP were also not statistically significant across the groups, but there were potentially meaningful differences in systolic BP of 7mmHg and 11mmHg in the 1.5G and 2.4G groups respectfully, and diastolic BP in the 2.4G group of 7.31mmHg Our small pilot study suggests that Na restriction can reduce IDWG and systolic and diastolic BP in potentially clinically meaningful amounts. The optimal Na intake prescription and the long-term impact on hemodialysis-specific variables and cardiovascular disease remains unclear. A prospective, longitudinal study, with a sample sufficient to achieve adequate power is needed to gain a better understanding of the interplay between dietary sodium and outcomes.
Copyright
EMBASE:2017310594
ISSN: 1523-6838
CID: 5378032
Sexuality and Intimacy Needs Within a Hospitalized Palliative Care Population: Results From a Qualitative Study
Kelemen, Anne; Van Gerven, Clara; Mullins, Katherine; Groninger, Hunter
BACKGROUND:Palliative care (PC) clinicians are well trained to address physical, psychosocial and spiritual needs of patients who have a serious illness. However, one area that is often overlooked is intimacy and sexuality. OBJECTIVE:To explore patient concerns regarding intimacy as it relates to illness, family reactions, physician conversations, and coping strategies and challenges. METHODS:Eligible subjects (at least 18 years old, capacitated, receiving PC consultation at the lead author's institution) participated in semi-structured interviews between November and December 2017. Transcripts were open-coded and analyzed using Dedoose 3.5.35 software. A constant comparative method was used to identify patterns in the data. RESULTS:21 interviews were analyzed and several themes emerged. Participants described the effect of physical and mental/emotional changes on their relationships. Family relationships, romantic relationships, and sexuality were prominent in patients' experiences of intimacy and how it changed as the illness progressed. Relationships were often noted to strengthen during the course of illness, while sexual activity was frequently reported to be negatively impacted. Patients consistently reported little provider communication on the impact of illness on intimacy beyond instructions about what sexual activities they could or could not engage in. CONCLUSION/CONCLUSIONS:This study underlines the significant impact of serious, progressive illness on relationships, sexuality, and physical and emotional intimacy. It highlights that these topics continue to be priorities for patients with serious illness, and that medical teams frequently fail to address them at all. Future research should further explore these issues across diverse patient populations.
PMID: 34372687
ISSN: 1938-2715
CID: 5297172
Antihypertensive drugs reduced risk for new-onset type 2 diabetes; effect varies by antihypertensive class [Comment]
Tanner, Michael
SOURCE CITATION:Lancet. 2021;398:1803-10. 34774144.
PMID: 35377716
ISSN: 1539-3704
CID: 5216822