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1.
Commun Med (Lond) ; 4(1): 183, 2024 Sep 30.
Artículo en Inglés | MEDLINE | ID: mdl-39349936

RESUMEN

BACKGROUND: Transgender patients face a higher burden of cardiovascular morbidity due to structural and biological stressors, particularly in low-resource settings. No studies exist comparing machine learning model development strategies for this unique patient cohort and limited literature exists comparing data/outcomes between transgender and cisgender populations. METHODS: We compare machine learning models trained solely on transgender patients against models developed on a size-matched and ratio-matched cohort of cisgender patients and a 300-fold larger, ratio-matched cohort of cisgender patients undergoing obstetric/gynecologic procedures in the National Surgical Quality Improvement Program from January 1, 2005 through December 31, 2019. All models were developed to predict the outcome of hypertension. Statistical significance between models was calculated using 5-by-2 fold cross validation hypothesis testing. RESULTS: Among 626,102 patients having an obstetric/gynecologic surgery, there are 1959 transgender patients of which 85,405 (13.7%) have hypertension requiring medication. Saliently, the logistic regression machine learning models trained selectively on the transgender cohort have an AUC of 0.865 (95% CI: 0.83-0.90), with an accuracy of 85% (95% CI: 0.80-0.87) compared to (p < 0.05) the logistic regression model trained on the 300-fold larger combined cohort which has an AUC of 0.861 (95% CI: 0.82-0.90), with an accuracy of 83% (95% CI: 0.80-0.87). CONCLUSION: Machine learning models can be trained on smaller, selectively transgender populations and may perform similarly or better to predict cardiovascular outcomes in transgender patients, than models developed on predominantly cisgender patients; this can be useful in lower-resource settings with smaller-volume transgender patients.


Transgender patients face a higher burden of cardiovascular disease. Statistical models that predict cardiovascular disease-related outcomes, such as high blood pressure (hypertension), may be useful to clinicians to guide treatment, but existing models are mainly developed in cisgender populations. Here, we developed models to predict hypertension in patients undergoing surgery, and compared models developed using data from cisgender patients, transgender patients, or mixed populations to see if this affected how well these models could predict hypertension in the transgender population. We ultimately found that one of our models trained on a much smaller cohort of solely transgender patients outperformed the same model trained on a 300-times larger population of mixed cisgender and transgender patients. These findings might help to guide future efforts to develop statistical approaches to accurately predict health outcomes in transgender patients.

2.
Cell ; 187(17): 4690-4712.e30, 2024 Aug 22.
Artículo en Inglés | MEDLINE | ID: mdl-39142281

RESUMEN

Electrical excitability-the ability to fire and propagate action potentials-is a signature feature of neurons. How neurons become excitable during development and whether excitability is an intrinsic property of neurons remain unclear. Here, we demonstrate that Schwann cells, the most abundant glia in the peripheral nervous system, promote somatosensory neuron excitability during development. We find that Schwann cells secrete prostaglandin E2, which is necessary and sufficient to induce developing somatosensory neurons to express normal levels of genes required for neuronal function, including voltage-gated sodium channels, and to fire action potential trains. Inactivating this signaling pathway in Schwann cells impairs somatosensory neuron maturation, causing multimodal sensory defects that persist into adulthood. Collectively, our studies uncover a neurodevelopmental role for prostaglandin E2 distinct from its established role in inflammation, revealing a cell non-autonomous mechanism by which glia regulate neuronal excitability to enable the development of normal sensory functions.


Asunto(s)
Potenciales de Acción , Dinoprostona , Células de Schwann , Células Receptoras Sensoriales , Animales , Células de Schwann/metabolismo , Dinoprostona/metabolismo , Ratones , Células Receptoras Sensoriales/metabolismo , Transducción de Señal
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