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The Impact of Concomitant Hypothyroid Disease on the Course of Inflammatory Bowel Disease
Ahsan, Maaz; Udaikumar, Jahnavi; Hong, Simon; Faye, Adam S; Katz, Seymour; Delau, Olivia; Axelrad, Jordan
BACKGROUND:Inflammatory bowel disease (IBD) is a chronic, immune-mediated inflammatory disorder of the gastrointestinal tract. In IBD, systemic inflammation and immune dysregulation may also impact extraintestinal organs, such as the thyroid gland. Despite this, little is known about the influence of concomitant hypothyroidism on the clinical course of IBD. METHODS:A retrospective analysis was conducted among adult patients with IBD and at least one thyroid stimulating hormone (TSH) measurement within a large healthcare network. Patient charts were reviewed, and baseline demographics, disease characteristics, biomarkers, healthcare utilization, medication use, and other comorbidities were extracted. Patients were stratified by those with IBD only and those with concomitant IBD and hypothyroidism. Multivariable logistic regression was used to identify factors associated with concomitant hypothyroidism. Concomitant disease as an independent predictor for lab abnormalities and increased healthcare utilization was also assessed using multivariable logistic and negative binomial regression. RESULTS:IRR: 1.89, 95% CI 1.08, 3.32). CONCLUSION/CONCLUSIONS:Patients with both IBD and hypothyroidism have an increased likelihood of other extraintestinal manifestations compared to individuals who have IBD without hypothyroidism. Furthermore, patients with concomitant disease exhibited greater healthcare utilization, specifically, increased rates of RBAI studies. The presence of concomitant hypothyroidism may be associated with a more severe course of IBD.
PMID: 40025310
ISSN: 1573-2568
CID: 5842572
Author's Reply: Is Sarcopenia More Than Just Low Body Mass? [Comment]
Minawala, Ria; Faye, Adam S
PMID: 39607851
ISSN: 1536-4844
CID: 5804032
Severe Polypharmacy Increases Risk of Hospitalization Among Older Adults with IBD
Drittel, Darren; Schreiber-Stainthorp, William; Delau, Olivia; Gurunathan, Sakteesh V; Chodosh, Joshua; Segev, Dorry L; McAdams-DeMarco, Mara; Katz, Seymour; Dodson, John; Shaukat, Aasma; Faye, Adam S
BACKGROUND:As the inflammatory bowel disease (IBD) patient population is aging, the prevalence of polypharmacy is rising. However, data exploring the prevalence, risk factors, and clinical outcomes associated with polypharmacy among older adults with IBD are limited. AIMS/OBJECTIVE:To determine (i) prevalence of polypharmacy (≥5 medications) and potentially inappropriate medication (PIM) utilization in older adults with IBD, (ii) changes in medications over time (iii) predictors of polypharmacy, and (iv) the impact of polypharmacy/PIMs on one-year hospitalization rates. METHODS:We conducted a retrospective single-center study of older adults with IBD from September 1st 2011 to December 31st 2022. Wilcoxon-signed rank and McNemar's tests were used to assess changes in polypharmacy between visits, with ordinal logistic regression and Cox proportional hazards models used to determine risk factors for polypharmacy and time to hospitalization, respectively. RESULTS:Among 512 older adults with IBD, 74.0% experienced polypharmacy at initial visit, with 42.6% receiving at least one PIM. Additionally, severe polypharmacy (≥10 medications) was present among 28.6% individuals at index visit and increased to 38.6% by last visit (p<0.01). Multivariable analysis revealed that age ≥70 years, BMI ≥30.0 kg/m2, prior IBD-related surgery, and the presence of comorbidities were associated with polypharmacy. Moreover, severe polypharmacy (adjHR 1.95, 95%CI 1.29-2.92), as well as PIM use (adjHR 2.16, 95%CI 1.37-3.43) among those with polypharmacy, were significantly associated with all-cause hospitalization within a year of index visit. DISCUSSION/CONCLUSIONS:Severe polypharmacy was initially present in more than 25% of older adults with IBD and increased to 34% within 4 years of index visit. Severe polypharmacy, as well as PIM utilization among those with polypharmacy, were also associated with an increased risk of hospitalization at one-year, highlighting the need for deprescribing efforts in this population.
PMID: 39162710
ISSN: 1572-0241
CID: 5680582
Frailty integration in medical specialties: Current evidence and suggested strategies from the Clin-STAR frailty interest group
Singh, Namrata; Faye, Adam S; Abidi, Maheen Z; Grant, Shakira J; DuMontier, Clark; Iyer, Anand S; Jain, Nelia; Kochar, Bharati; Lieber, Sarah B; Litke, Rachel; Loewenthal, Julia V; Masters, Mary Clare; Nanna, Michael G; Robison, Raele Donetha; Sattui, Sebastian E; Sheshadri, Anoop; Shi, Sandra M; Sherman, Andrea N; Walston, Jeremy D; Wysham, Katherine D; Orkaby, Ariela R
Frailty is a syndrome that can inform clinical treatments and interventions for older adults. Although implementation of frailty across medical subspecialties has the potential to improve care for the aging population, its uptake has been heterogenous. While frailty assessment is highly integrated into certain medical subspecialties, other subspecialties have only recently begun to consider frailty in the context of patient care. In order to advance the field of frailty-informed care, we aim to detail what is known about frailty within the subspecialties of internal medicine. In doing so, we highlight cross-disciplinary approaches that can enhance our understanding of frailty, focusing on ways to improve the implementation of frailty measures, as well as develop potential interventional strategies to mitigate frailty within these subspecialties. This has important implications for the clinical care of the aging population and can help guide future research.
PMID: 39584362
ISSN: 1532-5415
CID: 5803822
Inflammation and aging-related disease: A transdisciplinary inflammaging framework
Andonian, Brian J; Hippensteel, Joseph A; Abuabara, Katrina; Boyle, Eileen M; Colbert, James F; Devinney, Michael J; Faye, Adam S; Kochar, Bharati; Lee, Jiha; Litke, Rachel; Nair, Devika; Sattui, Sebastian E; Sheshadri, Anoop; Sherman, Andrea N; Singh, Namrata; Zhang, Yinan; LaHue, Sara C
Inflammaging, a state of chronic, progressive low-grade inflammation during aging, is associated with several adverse clinical outcomes, including frailty, disability, and death. Chronic inflammation is a hallmark of aging and is linked to the pathogenesis of many aging-related diseases. Anti-inflammatory therapies are also increasingly being studied as potential anti-aging treatments, and clinical trials have shown benefits in selected aging-related diseases. Despite promising advances, significant gaps remain in defining, measuring, treating, and integrating inflammaging into clinical geroscience research. The Clin-STAR Inflammation Research Interest Group was formed by a group of transdisciplinary clinician-scientists with the goal of advancing inflammaging-related clinical research and improving patient-centered care for older adults. Here, we integrate insights from nine medical subspecialties to illustrate the widespread impact of inflammaging on diseases linked to aging, highlighting the extensive opportunities for targeted interventions. We then propose a transdisciplinary approach to enhance understanding and treatment of inflammaging that aims to improve comprehensive care for our aging patients.
PMCID:11872841
PMID: 39352664
ISSN: 2509-2723
CID: 5803212
Editorial: Disentangling Early-Life Antibiotics and Infections as Risk Factors for the Development of Childhood IBD [Editorial]
Stone, Katherine L; Faye, Adam S
PMID: 39495055
ISSN: 1365-2036
CID: 5803522
Intravenous Steroids Do Not Improve Short-Term Outcomes of Patients With Crohn's Disease Presenting With an Acute Small Bowel Obstruction
Garcia, Mariely; Debebe, Anketse; Mahmood, Farhan; Nirenberg, Sharon; Rendon, Alexa; Yang, Eunyoung; Xiang, Jiani; Colombel, Jean-Frédéric; Kahan, Tamara; Ghiasian, Ghoncheh; Faye, Adam S; Levine, Irving; Farber, Michael; Ramada, Michael; Omoakhe, Tisor; Sultan, Keith; Sachar, David B
BACKGROUND/UNASSIGNED:Intravenous (IV) steroids are commonly used to treat acute flares of Crohn's disease (CD). However, it is unclear if they are beneficial in the setting of uncomplicated small bowel obstruction (SBO). We sought to examine if IV steroid administration improved short-term outcomes in patients with CD hospitalized for acute, uncomplicated SBO across three New York City hospital systems. METHODS/UNASSIGNED:This retrospective study included patients ≥ 18 years old admitted between January 1, 2011, and December 31, 2019, with Crohn's disease and an admission diagnosis of uncomplicated acute SBO, defined as cases without adhesions, fistula, phlegmon, and sepsis. Primary endpoints (length of stay and frequency of surgery) were compared between patients who received IV steroids upon admission and those who did not. RESULTS/UNASSIGNED: = .85). Sex, age, disease duration, concomitant biologic therapy, and NG tube placement did not independently contribute to either outcome. CONCLUSIONS/UNASSIGNED:These findings suggest that IV steroid administration for uncomplicated SBO in CD patients does not decrease hospital length of stay or need for surgery. Further research may help identify specific obstruction patterns or other therapies associated with different outcomes.
PMCID:11744190
PMID: 39834354
ISSN: 2631-827x
CID: 5802142
Clinical trials and young adults with inflammatory bowel disease
Dave, Sneha; Reed, Sydney; Shapiro, Mara; Taye, Yeabsira; Hernandez, Isabela; Kariyawasam, Navin; Mehes, Ildiko; Agrawal, Manasi; Regueiro, Miguel; Faye, Adam; Adler, Jeremy
Young adults (approximately 18-35 years) with inflammatory bowel disease (IBD) represent a distinct demographic with unique developmental and physiological characteristics, yet they are underrepresented in clinical trials. This commentary synthesizes insights from a roundtable discussion facilitated by the Crohn's and Colitis Young Adults Network (CCYAN) between young adult patients with IBD and medical professionals, including physicians, nurses, psychologists, and trainees/medical students. Themes include defining young adults as a distinct demographic in research, improving outcomes for young adults with IBD through age-specific data disaggregation, barriers for participation and post-trial responsibilities, as well as regulatory and legislative policy opportunities to enhance young adult representation in clinical trials.
PMCID:11997387
PMID: 40236624
ISSN: 2949-9232
CID: 5828032
Risk of malnutrition increases in the year prior to surgery among patients with inflammatory bowel disease
Chaudhary, Vasantham; Chung, Frank R; Delau, Olivia; Dane, Bari; Levine, Irving; Meng, Xucong; Chodosh, Joshua; da Luz Moreira, Andre; Simon, Jessica N; Axelrad, Jordan E; Katz, Seymour; Dodson, John; Shaukat, Aasma; Faye, Adam S
BACKGROUND/UNASSIGNED:In patients with inflammatory bowel disease (IBD) who need intestinal resection, prior data suggest that earlier surgical intervention may be associated with improved outcomes. However, surgery is often deferred for additional trials of advanced therapies, which potentially shifts patients from a fit to a frail preoperative state. OBJECTIVES/UNASSIGNED:This study aimed to evaluate clinical changes that occur in the year prior to intestinal resection in patients with IBD. DESIGN/UNASSIGNED:Retrospective cohort study. METHODS/UNASSIGNED:This was a multi-hospital retrospective study of patients ⩾18 years old who underwent initial IBD-related intestinal resection between January 1, 2018 and May 31, 2023. Clinical characteristics and radiographical skeletal muscle mass were compared using the Wilcoxon Signed-Rank test for continuous variables and McNemar's test for categorical variables. RESULTS/UNASSIGNED: = 0.06). CONCLUSION/UNASSIGNED:In the 6-12 months prior to an IBD-related intestinal resection, as compared to the month prior, individuals were less likely to be malnourished, have an infection, or need hospitalization for IBD. This suggests that minimizing delays to surgery may lead to improved outcomes.
PMCID:12365438
PMID: 40842457
ISSN: 1756-283x
CID: 5909332
Older Adults With Inflammatory Bowel Disease Are at Higher Risk of Developing Antibodies to Infliximab
Faye, Adam S; Lee, Kate E; Hudesman, David; Dervieux, Thierry
PMID: 38170900
ISSN: 1536-4844
CID: 5737102