“Purpose Our intent was to identify whether cerebrovascula


“Purpose Our intent was to identify whether cerebrovascular CO(2) reactivity in diabetic patients is a risk factor for postoperative cognitive dysfunction after coronary artery bypass graft (CABG) surgery.

Methods One hundred twenty-four diabetic patients undergoing elective CABG were studied and analyzed. Diabetic patients were divided into three groups: normal CO(2) reactivity group (above 5%/mmHg), medium CO(2) reactivity group (between

5 and 3%/mmHg), or Selleckchem IPI145 impaired CO(2) reactivity group (below 3%/mmHg). After the induction of anesthesia and before the start of surgery, cerebrovascular CO(2) reactivity was measured for all patients. Hemodynamic parameters (arterial and jugular venous blood gas values) were measured during cardiopulmonary bypass. All patients underwent a battery of neurological and neuropsychological tests the day before surgery, 7 days after surgery, and 6 months after surgery.

Results At 7 days, the rate of cognitive dysfunction in the impaired CO(2) group was higher than in the other three groups (normal, 30%; medium,

25%; impaired, 57%; *P < 0.01 compared with the other groups). In contrast, at 6 months postoperatively, no significant difference in the rate of cognitive dysfunction was found among the three groups. ALK mutation Age, hypertension, CO(2) reactivity, the duration for which jugular venous oxygen saturation (SjvO(2)) was less than 50%, ascending aorta atherosclerosis, diabetic retinopathy, and insulin therapy were independent predictors of short-term cognitive dysfunction in diabetic patients, and HbA1c, diabetic retinopathy, and insulin therapy were independent predictors of long-term cognitive dysfunction in diabetic patients.

Conclusions We found that impaired cerebrovascular CO(2) reactivity was associated with postoperative short-term cognitive dysfunction

in diabetic patients.”
“Dendritic spines form postsynaptic contact sites in the central nervous system. The rapid and spontaneous morphology changes of spines have been widely observed by neurobiologists. Determining the relationship between dendritic spine morphology change and its functional properties such as memory learning is a fundamental yet challenging problem in neurobiology Pfizer Licensed Compound Library high throughput research. In this paper, we propose a novel algorithm to track the morphology change of multiple spines simultaneously in time-lapse neuronal images based on nonrigid registration and integer programming. We also propose a robust scheme to link disappearing-and-reappearing spines. Performance comparisons with other state-of-the-art cell and spine tracking algorithms, and the ground truth show that our approach is more accurate and robust, and it is capable of tracking a large number of neuronal spines in time-lapse confocal microscopy images.

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