Fatima Cody Stanford

Dr. Fatima Cody Stanford

Massachusetts General Hospital, Boston, Massachusetts, USA
orcid

Research Focus & Metrics

Academic Career Length

52Years (1975-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2018 in Surgery for Obesity and Related Diseases
Verified
Journal Article
Open access
JPJaney S.A. Pratt
Janey S.A. Pratt
ABAllen Browne
Allen Browne
NBNancy T. Browne
Nancy T. Browne
MBMatias Bruzoni
Matias Bruzoni
MCMegan Cohen
Megan Cohen
JZJeffrey Zitsman
Jeffrey Zitsman
The American Society for Metabolic and Bariatric Surgery Pediatric Committee updated their evidence-based guidelines published in 2012, performing a comprehensive literature search (2009-2017) with 1387 articles and other supporting evidence through February 2018. The significant increase in data supporting the use of metabolic and bariatric surgery (MBS) in adolescents since 2012 strengthens these guidelines from prior reports. Obesity is recognized as a disease; treatment of severe obesity requires a life-long multidisciplinary approach with combinations of lifestyle changes, nutrition, medications, and MBS. We recommend using modern definitions of severe obesity in children with the Centers for Disease Control and Prevention age- and sex-matched growth charts defining class II obesity as 120% of the 95th percentile and class III obesity as 140% of the 95th percentile. Adolescents with class II obesity and a co-morbidity (listed in the guidelines), or with class III obesity should be considered for MBS. Adolescents with cognitive disabilities, a history of mental illness or eating disorders that are treated, immature bone growth, or low Tanner stage should not be denied treatment. MBS is safe and effective in adolescents; given the higher risk of adult obesity that develops in childhood, MBS should not be withheld from adolescents when severe co-morbidities, such as depressed health-related quality of life score, type 2 diabetes, obstructive sleep apnea, and nonalcoholic steatohepatitis exist. Early intervention can reduce the risk of persistent obesity as well as end organ damage from long standing co-morbidities.

6 December 2011 in Circulation
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Journal Article
Closed access
PDF file
DLDuck-Chul Lee
Duck-Chul Lee
XSXuemei Sui
Xuemei Sui
Enrique G. ArteroEnrique G. Artero
Enrique G. Artero
ILI-Min Lee
I-Min Lee
TCTimothy S. Church
Timothy S. Church
SBSteven N. Blair
Steven N. Blair
Background—: The combined associations of changes in cardiorespiratory fitness and body mass index (BMI) with mortality remain controversial and uncertain. Methods and Results—: We examined the independent and combined associations of changes in fitness and BMI with all-cause and cardiovascular disease (CVD) mortality in 14 345 men (mean age 44 years) with at least 2 medical examinations. Fitness, in metabolic equivalents (METs), was estimated from a maximal treadmill test. BMI was calculated using measured weight and height. Changes in fitness and BMI between the baseline and last examinations over 6.3 years were classified into loss, stable, or gain groups. During 11.4 years of follow-up after the last examination, 914 all-cause and 300 CVD deaths occurred. The hazard ratios (95% confidence intervals) of all-cause and CVD mortality were 0.70 (0.59–0.83) and 0.73 (0.54–0.98) for stable fitness, and 0.61 (0.51–0.73) and 0.58 (0.42–0.80) for fitness gain, respectively, compared with fitness loss in multivariable analyses including BMI change. Every 1-MET improvement was associated with 15% and 19% lower risk of all-cause and CVD mortality, respectively. BMI change was not associated with all-cause or CVD mortality after adjusting for possible confounders and fitness change. In the combined analyses, men who lost fitness had higher all-cause and CVD mortality risks regardless of BMI change. Conclusions—: Maintaining or improving fitness is associated with a lower risk of all-cause and CVD mortality in men. Preventing age-associated fitness loss is important for longevity regardless of BMI change.

1 September 2020 in Current Obesity Reports
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Journal Article
Closed access
PDF file
CAChika Vera Anekwe
Chika Vera Anekwe
AJAmber R. Jarrell
Amber R. Jarrell
MTMatthew J. Townsend
Matthew J. Townsend
GGGabriela I. Gaudier
Gabriela I. Gaudier
JHJulia M. Hiserodt
Julia M. Hiserodt
Fatima Cody StanfordFatima Cody Stanford
Fatima Cody Stanford

23 April 2020 in Journal of the National Medical Association
Verified
Journal Article
Closed access
Fatima Cody StanfordFatima Cody Stanford
Fatima Cody Stanford

4 February 2021 in New England Journal of Medicine
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Journal Article
Closed access
PDF file
SBSimar Singh Bajaj
Simar Singh Bajaj
Fatima Cody StanfordFatima Cody Stanford
Fatima Cody Stanford
J. Marion Sims. Henrietta Lacks. The Tuskegee Syphilis Study.

30 August 2024 in eClinicalMedicine
Verified
Journal Article
Open access
NANasreen Alfaris
Nasreen Alfaris
SWStephanie Waldrop
Stephanie Waldrop
VJVeronica Johnson
Veronica Johnson
Brunna BoaventuraBrunna Boaventura
Brunna Boaventura
KKKarla Kendrick
Karla Kendrick
Fatima Cody StanfordFatima Cody Stanford
Fatima Cody Stanford
Obesity and type 2 diabetes mellitus (T2DM) present major global health challenges, with an increasing prevalence worldwide. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have emerged as a pivotal treatment option for both conditions, demonstrating efficacy in blood glucose management, weight reduction, cardiovascular disease prevention, and kidney health improvement. GLP-1, an incretin hormone, plays a crucial role in glucose metabolism and appetite regulation, influencing insulin secretion, insulin sensitivity, and gastric emptying. The therapeutic use of GLP-1RAs has evolved significantly, offering various formulations that provide different efficacy, routes of administration, and flexibility in dosing. These agents reduce HbA1c levels, facilitate weight loss, and exhibit cardiovascular protective effects, making them an integral component of T2DM and obesity management. This review will discuss the currently approved medication for T2DM and obesity, and will also highlight the advent of novel agents which are dual and triple hormonal agonists which represent the future direction of incretin-based therapy. National Institutes of HealthNIDDKU24 DK132733 (FCS), UE5 DK137285 (FCS), and P30 DK040561 (FCS).