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1.
Clin Transl Sci ; 17(5): e13829, 2024 May.
Article in English | MEDLINE | ID: mdl-38769746

ABSTRACT

To investigate the effects of neutrophil elastase inhibitor (sivelestat sodium) on gastrointestinal function in sepsis. A reanalysis of the data from previous clinical trials conducted at our center was performed. Septic patients were divided into either the sivelestat group or the non-sivelestat group. The gastrointestinal dysfunction score (GIDS), feeding intolerance (FI) incidence, serum levels of intestinal barrier function and inflammatory biomarkers were recorded. The clinical severity and outcome variables were also documented. A total of 163 septic patients were included. The proportion of patients with GIDS ≥2 in the sivelestat group was reduced relative to that in the non-sivelestat group (9.6% vs. 22.5%, p = 0.047) on the 7th day of intensive care unit (ICU) admission. The FI incidence was also remarkably reduced in the sivelestat group in contrast to that in the non-sivelestat group (21.2% vs. 37.8%, p = 0.034). Furthermore, the sivelestat group had fewer days of FI [4 (3, 4) vs. 5 (4-6), p = 0.008]. The serum levels of d-lactate (p = 0.033), intestinal fatty acid-binding protein (p = 0.005), interleukin-6 (p = 0.001), white blood cells (p = 0.007), C-reactive protein (p = 0.001), and procalcitonin (p < 0.001) of the sivelestat group were lower than those of the non-sivelestat group. The sivelestat group also demonstrated longer ICU-free days [18 (0-22) vs. 13 (0-17), p = 0.004] and ventilator-free days [22 (1-24) vs. 16 (1-19), p = 0.002] compared with the non-sivelestat group. In conclusion, sivelestat sodium administration appears to improve gastrointestinal dysfunction, mitigate dysregulated inflammation, and reduce disease severity in septic patients.


Subject(s)
Gastrointestinal Diseases , Glycine , Sepsis , Sulfonamides , Humans , Sepsis/drug therapy , Sepsis/complications , Sepsis/blood , Male , Female , Glycine/analogs & derivatives , Glycine/therapeutic use , Middle Aged , Aged , Sulfonamides/therapeutic use , Sulfonamides/administration & dosage , Gastrointestinal Diseases/drug therapy , Proteinase Inhibitory Proteins, Secretory , Biomarkers/blood , Treatment Outcome
2.
Brain Res ; 1838: 148947, 2024 Sep 01.
Article in English | MEDLINE | ID: mdl-38657887

ABSTRACT

Perceived stress is an acknowledged risk factor for subthreshold depression (StD), and fluctuations in perceived stress are thought to disrupt the harmony of brain networks essential for emotional and cognitive functioning. This study aimed to elucidate the relationship between eye-open (EO) and eye-closed (EC) states, perceived stress, and StD. We recruited 27 individuals with StD and 33 healthy controls, collecting resting state fMRI data under both EC and EO conditions. We combined intrinsic connectivity and seed-based functional connectivity analyses to construct the functional network and explore differences between EC and EO conditions. Graph theory analysis revealed weakened connectivity strength in the right superior frontal gyrus (SFG) and right median cingulate and paracingulate gyrus (MCC) among participants with StD, suggesting an important role for these regions in the stress-related emotions dysregulation. Notably, altered SFG connectivity was observed to significantly relate to perceived stress levels in StD, and the SFG connection emerges as a neural mediator potentially influencing the relationship between perceived stress and StD. These findings highlight the role of SFG and MCC in perceived stress and suggest that understanding EC and EO states in relation to these regions is important in the neurobiological framework of StD. This may offer valuable perspectives for early prevention and intervention strategies in mental health disorders.


Subject(s)
Brain , Depression , Magnetic Resonance Imaging , Stress, Psychological , Humans , Male , Female , Magnetic Resonance Imaging/methods , Stress, Psychological/physiopathology , Stress, Psychological/psychology , Depression/physiopathology , Depression/diagnostic imaging , Depression/psychology , Adult , Brain/physiopathology , Brain/diagnostic imaging , Young Adult , Brain Mapping , Neural Pathways/physiopathology , Neural Pathways/diagnostic imaging , Nerve Net/diagnostic imaging , Nerve Net/physiopathology , Emotions/physiology , Connectome/methods
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