Nicole M. Ali
· MDVerifiedNew York University · Transplant
Active 2005–2025
About
As a transplant nephrologist and the medical director of the Kidney Transplant Program at NYU Langone, Nicole M. Ali, MD, is dedicated to providing personalized treatment plans that emphasize patient wellbeing. Her role involves leading a team committed to helping patients navigate their path to transplantation and thrive as kidney transplant recipients. The program is nationally recognized for achieving the best outcomes, and she takes pride in offering transplants to all patients who will benefit, including those who are medically, surgically, or immunologically complex. She specializes in the care of transplant candidates and recipients, focusing on a personalized approach that recognizes each patient’s unique journey. Dr. Ali emphasizes education as a cornerstone of her care, helping patients understand the complexities of the waiting list, organ allocation, and both living and deceased donation. She aims to build trust and rapport with her patients and their referring physicians to ensure seamless transition and continuity of care. Throughout her career, she has been passionate about fostering strong partnerships within the nephrology community across Manhattan, Brooklyn, Queens, The Bronx, Staten Island, and Long Island, ensuring comprehensive care through collaboration with nephrologists, surgeons, nurses, and advanced practice providers. Inspired by her grandmother’s struggles with diabetes and lack of access to reliable medical care, Dr. Ali is committed to helping those in similar situations and leading a team dedicated to advancing transplantation care with compassion and the most advanced treatments.
Research topics
- Medicine
- Andrology
- Internal medicine
- Urology
Selected publications
Frailty in Kidney Transplant Candidates: The Role of Social Determinants
American Journal of Transplantation · 2025-08-01
articleOpen accessAmerican Journal of Transplantation · 2025-08-01
articleOpen access1st authorCorrespondingPhysical Domains, Access to Kidney Transplantation, and Waitlist Mortality
Clinical Transplantation · 2025-11-01
articleBACKGROUND: Frail kidney transplant (KT) candidates, characterized by low physical activity/function, have decreased chances of listing and increased risk of waitlist mortality. Impairments in these physical domains contribute to perceived physical burden and may exacerbate one another. Further, understanding the association of each domain individually with adverse outcomes may improve pre-KT risk stratification. METHODS: We leveraged 2708 KT candidates (age ≥ 18) from a two-center prospective cohort study (2014-2024). We assessed physical activity (Minnesota Leisure Time Physical Activity Questionnaire), physical function (gait speed), and physical burden (10 questions from the Kidney Disease Quality of Life Short Form) at evaluation. We quantified the association of these three physical domains with listing (Cox proportional hazards) and waitlist mortality (competing risks, Harrell's C-statistic). RESULTS: Among 2708 candidates, 40% had low physical activity, 16% had low physical function, and 54% had high physical burden. Candidates with impairment in these three physical domains were less likely to be listed (activity: adjusted hazard ratio [aHR] = 0.86, 95% confidence interval [CI]: 0.75-0.99; function: aHR = 0.54, 95%CI: 0.45-0.64; burden: aHR = 0.75, 95%CI: 0.67-0.83) and had a higher risk of waitlist mortality (activity: adjusted sub-hazard ratio [aSHR] = 1.51, 95%CI: 1.11-2.04; function: aSHR = 1.83, 95%CI: 1.30-2.58; burden: aSHR = 1.40, 95%CI: 1.09-1.82). Physical burden showed the best discrimination in predicting mortality after adjustment (Harrell's C-statistic = 0.6899). CONCLUSION: Although impairment in physical activity, function, and burden was all associated with KT listing and waitlist mortality, physical burden was the strongest predictor of waitlist mortality. KT centers should consider measuring physical burden - a simple, low-cost tool to help identify high-risk candidates for prehabilitation.
Physiology and immunology of a pig-to-human decedent kidney xenotransplant
Nature · 2025-11-13 · 16 citations
articleAmerican Journal of Transplantation · 2025-06-18 · 1 citations
articleOpen accessClinical Transplantation · 2025-11-01
articleOpen accessABSTRACT Background Older patients who are evaluated for kidney transplantation (KT) experience an earlier onset of cognitive impairment due to dialysis, comorbidities, and inactivity. Ambient fine particulate matter (PM 2.5 ) is a modifiable risk factor for dementia among community‐dwelling older adults. Inflammatory responses and oxidative stress caused by inactivity in older patients evaluated for KT may heighten vulnerability to PM 2.5 . Thus, the impact of PM 2.5 on dementia may be more severe in this population. Methods We leveraged a prospective cohort (2009–2019) of older (age ≥ 50) patients evaluated for KT ( n = 2073) with Modified Mini‐Mental State Examination (3MS). We derived annual PM 2.5 from residential ZIP codes (high: PM 2.5 > 9 µg/m 3 ), quantifying its association with global cognitive function (linear regression), impairment (logistic regression), and risk of dementia (Cox proportional hazards model). We tested the interaction between PM 2.5 and dementia risk factors using a Wald test. Models were adjusted for confounders, including social determinants of health. Results High PM 2.5 was associated with worse global cognitive function (difference = −3.00 points [3MS score], 95% CI: −3.93 to −2.07), with a stronger association among patients with low physical activity ( p [interaction] < 0.001). High PM 2.5 was associated with 1.90‐fold higher odds of global cognitive impairment (95% CI: 1.48–2.46), and 3.29‐fold higher risk of dementia (95% CI: 1.14–9.55). Conclusion High PM 2.5 was associated with worse cognitive function among older patients evaluated for KT, particularly those with low physical activity. The association was stronger than prior findings among community‐dwelling older adults. Clinicians may counsel patients to monitor air quality. Patients in high PM 2.5 neighborhoods should discuss cognitive assessments and ways to increase physical activity with providers.
Clinical Journal of the American Society of Nephrology · 2025-06-17 · 26 citations
articleKey Points GLP-1 receptor agonists (GLP-1 RAs) in diabetes and dialysis are associated with 23% lower mortality and 66% higher chance of transplant waitlisting. GLP-1 RAs are not associated with increased risk of acute pancreatitis, biliary complications, or medullary thyroid cancer. GLP-1 RAs are associated with a 32% increased risk of diabetic retinopathy in patients with diabetes on dialysis. Background Of the 808,000 US patients on dialysis, 60% have diabetes and are eligible for glucagon-like peptide-1 receptor agonists (GLP-1 RAs). Safety and outcomes in this population are unknown. We sought to examine GLP-1 RA real-world safety, efficacy, and weight loss in people with diabetes on dialysis. Methods In this observational national cohort study (2013–2021), we identified adults with type 2 diabetes on dialysis. The exposure of interest was GLP-1 RA use. Body mass index (BMI) change after dialysis initiation was quantified among patients with two measurements ( N =6474). Extended Cox models with inverse probability of treatment weights (censoring for kidney transplant waitlisting) were used to quantify all-cause mortality associated with GLP-1 RAs. Specific safety outcomes (acute pancreatitis, biliary complications, medullary thyroid cancer, and diabetic retinopathy) were assessed. Results The study included 151,649 patients on incident dialysis with type 2 diabetes. Mean BMI and weight change among GLP-1 RA users were greater than those among nonusers (−1.47 versus −0.61 kg/m 2 ; −4.03 versus −1.47 kg; P < 0.001 for both). The mortality incidence rate was lower among GLP-1 RA users (219.0 versus 279.5 patients/1000 person-years; P < 0.001). GLP-1 RA use was associated with a 23% lower risk of mortality (adjusted hazard ratio [aHR], 0.77; 95% confidence interval [CI], 0.70 to 0.85; P < 0.001); results were consistent among initiates with BMI ≥30 kg/m 2 . GLP-1 RA use was associated with a 66% higher chance of waitlisting (aHR, 1.66; 95% CI, 1.28 to 2.13; P < 0.001). There was an increased association with diabetic retinopathy (aHR, 1.32; 95% CI, 1.12 to 1.56; P = 0.001), but not with any other safety outcomes. Inferences were consistent across multiple sensitivity analyses. Conclusions GLP-1 RA use in patients with type 2 diabetes on dialysis was associated with weight loss, reduced mortality risk, and increased likelihood of kidney transplant waitlisting. These real-world data are the strongest evidence to date supporting GLP-1 RA use in this population.
American Journal of Transplantation · 2025-08-01 · 4 citations
articleOpen accessGLP-1 Receptor Agonists in Kidney Transplant Recipients with Pre-Existing Diabetes
American Journal of Transplantation · 2025-01-01
articleOpen accessDosing of Pegcetacoplan with Plasmapheresis for Treatment of Xenoantibody Mediated Rejection
American Journal of Transplantation · 2025-08-01 · 1 citations
articleOpen access
Frequent coauthors
- 27 shared
Ernesto P. Molmenti
Renown Health
- 23 shared
Amit Basu
Tata Institute of Fundamental Research
- 23 shared
Bonnie E. Lonze
New York University
- 19 shared
Sameer Mehta
- 19 shared
Zoe A. Stewart
National Jewish Health
- 17 shared
Madhu Bhaskaran
- 17 shared
Asha Alex
- 16 shared
Vasishta Tatapudi
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