Background: Post-bariatric hypoglycemia (PBH) after Roux-en-Y gastric bypass (RYGB) is a complex complication, often characterized by potentially severe hypoglycemic episodes and reduced hypoglycemia awareness. Recent findings suggest that autonomic dysfunction, preoperative hypoglycemia symptoms, and early dumping syndrome may each contribute to PBH risk.
Objective: To discuss critical insights from the recent study by Grover et al. regarding the clinical characteristics, prevalence, and possible contributing factors of PBH, and to propose avenues for future research, including standardized preoperative screening and targeted dietary interventions.
Discussion: Current evidence underscores a high prevalence of severe (level 3) hypoglycemia episodes among PBH patients, with notable rates of autonomic dysfunction and neuropathy. Dietary strategies (e.g., fermented wheat supplements) hold promise for mitigating PBH-related complications. Emerging data further highlight the significance of preoperative hypoglycemia symptoms and dumping syndrome as early predictors of PBH risk, emphasizing the need for improved risk stratification.
Conclusion: Comprehensive preoperative screening, investigation of autonomic dysfunction in glucose metabolism, and individualized dietary or pharmacological interventions may optimize PBH management. These strategies could refine patient selection, reduce hypoglycemia incidence, and improve long-term outcomes for individuals undergoing RYGB.
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http://dx.doi.org/10.1111/cen.15229 | DOI Listing |
Front Neurol
February 2025
Department of Neurology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Introduction: The aim of this study was to investigate the association between hepatitis B core antibody (HBcAb) positivity and the need of mechanical ventilation (MV) in patients with Guillain-Barré syndrome (GBS).
Methods: We retrospectively analyzed the clinical data of 159 patients who were diagnosed with GBS between December 2014 and April 2023 in the Affiliated Hospital of Xuzhou Medical University. Patients were categorized into two groups according to the need for MV.
J Sleep Res
March 2025
VA Portland Health Care System, Research Service, Portland, Oregon, USA.
Individuals with comorbid rapid eye movement (REM) sleep behaviour disorder (RBD) and neurotrauma (NT; defined by traumatic brain injury and post-traumatic stress disorder) have an earlier age of RBD symptom onset, increased RBD-related symptom severity and more neurological features indicative of prodromal synucleinopathy compared to RBD only. An early sign of neurodegenerative condition is autonomic dysfunction, which we sought to evaluate by examining heart rate variability during sleep. Participants with overnight polysomnography were recruited from the Veterans Affairs Portland Health Care System.
View Article and Find Full Text PDFClin Endocrinol (Oxf)
March 2025
Department of Addiction Psychiatry, Taoyuan Psychiatric Center, Ministry of Health and Welfare, Taoyuan City, Taiwan.
Background: Post-bariatric hypoglycemia (PBH) after Roux-en-Y gastric bypass (RYGB) is a complex complication, often characterized by potentially severe hypoglycemic episodes and reduced hypoglycemia awareness. Recent findings suggest that autonomic dysfunction, preoperative hypoglycemia symptoms, and early dumping syndrome may each contribute to PBH risk.
Objective: To discuss critical insights from the recent study by Grover et al.
Brain Nerve
March 2025
Department of Neurology, Graduate School of Medicine, Chiba University.
Multiple system atrophy (MSA) is a progressive, incurable neurodegenerative disease characterized by the risk of sudden death and various symptoms, including autonomic and cognitive dysfunction, as well as motor symptoms such as cerebellar ataxia and parkinsonism. These clinical features make the diagnosis of MSA challenging for neurologists. Our questionnaire survey on the delivery of an MSA diagnosis revealed that 92.
View Article and Find Full Text PDFEncephalitis
March 2025
Department of Neurology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
Subacute sclerosing panencephalitis (SSPE) is a rare, progressive neurodegenerative disorder caused by persistent aberrant measles virus infection. It is characterized by behavioral changes, cognitive decline with deterioration in academic performance, visual dysfunction, focal or generalized seizures ,myoclonus, spasticity, mutism and akinesia ultimately leading to a vegetative state. Balint's syndrome, characterized by the triad of simultagnosia, optic ataxia, and oculomotor apraxia, as an initial presenting feature of SSPE is rare.
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