Objective:To evaluate the value of ultra-widefield scanning laser ophthalmoscopy (UWFSLO) for screening diabetic retinopathy (DR).Methods:A cross-sectional study was conducted.A total of 1 288 patients (2 304 eyes) with type 2 diabetes who underwent the screening of DR were selected in Kailuan Rehabilitation Hospital in Tangshan City, Hebei Province from October 2016 to December 2016.The general information and medical records were collected.Patients completed fundus inspection by both UWFSLO and two-field 45° horizontal digital color fundus photography.The effective retinal images of the two methods were analyzed and the detection and grading of DR were compared between the two methods.This study adhered to the Declaration of Helsinki.The study protocol was approved by the Ethics Committee of Kailuan (Group) Co., Ltd.Hospital (No.2006-5).Written informed consent was obtained from each subject.Results:After excluding the unclear and missing images, 1 857 eyes were finally included in this study.The detection rates of DR by color fundus photo, UWFSLO pseudocolor image and green channel image were 31.3%(581/1 857), 44.5%(826/1 857), and 43.4%(807/1 857), respectively, with a statistically significant difference ( χ2=85.547, P<0.001).The detection rates of DR by UWFSLO pseudocolor image and green channel image were higher than that by color fundus photo, and the differences were statistically significant (both at P<0.001).The agreement between UWFSLO and two-field 45° horizontal digital color fundus photography for grading DR severity was moderate with a Kappa value of 0.375 ( P<0.001) and a complete agreement of 64.08%.The UWFSLO green channel image and pseudocolor images had excellent consistency for grading DR severity with a Kappa value of 0.953( P=0.008) and complete agreement of 98.17%.The detection rates of microaneurysm (MA), intraretinal microvascular abnormalitie (IRMA) and neovascularization (NV) by UWFSLO pseudocolor images were lower than that by green channel images, showing statistically significant differences ( Z=-16.489, -4.198, -2.111; all at P<0.05). Conclusions:UWFSLO has better detection and grading of DR than two-field 45° horizontal digital color fundus photography, and green channel images are better at detecting MA, IRMA, and small NV lesions.UWFSLO has good application value in the screening and diagnosis of DR in large populations.

Background: Diabetes-related neuropathic pain frequently occurs, and the underpinning mechanism remains elusive. The periaqueductal gray (PAG) exhibits descending inhibitory effects on central pain transmission. The current work aimed to examine whether inflammatory cytokines regulate mechanical allodynia and thermal hyperalgesia induced by diabetes through the phosphoinositide 3-kinase (PI3K)-mammalian target of rapamycin (mTOR) pathway in the PAG. Methods: Streptozotocin (STZ) was administered intraperitoneally to mimic allodynia and hyperalgesia evoked by diabetes in rats. Behavioral assays were carried out for determining mechanical pain and thermal hypersensitivity. Immunoblot and ELISA were performed to examine PAG protein amounts of interleukin-1β (IL-1β), IL-6, and tumor necrosis factor-α (TNF-α), as well as their corresponding receptors in STZ rats, and the expression of PI3K/protein kinase B (Akt)/mTOR signaling effectors. Results: Increased PAG p-PI3K/p-Akt/p-mTOR protein amounts were observed in STZ-induced animals, a PI3K-mTOR pathway inhibition in the PAG attenuated neuropathic pain responses. Moreover, the PAG concentrations of IL-1β, IL-6, and TNF-α and their receptors (namely, IL-1R, IL-6R, and tumor necrosis factor receptor [TNFR] subtype TNFR1, respectively) were increased in the STZ rats. Additionally, inhibiting IL-1R, IL-6R, and TNFR1 ameliorated mechanical allodynia and thermal hyperalgesia in STZ rats, alongside the downregulation of PI3K-mTOR signaling. Conclusions Overall, the current study suggests that upregulated proinflammatory cytokines and their receptors in the PAG activate PI3K-mTOR signaling, thereby producing a de-inhibition effect on descending pathways in modulating pain transmission, and eventually contributing to neuropathic pain.

Background: Diabetes-related neuropathic pain frequently occurs, and the underpinning mechanism remains elusive. The periaqueductal gray (PAG) exhibits descending inhibitory effects on central pain transmission. The current work aimed to examine whether inflammatory cytokines regulate mechanical allodynia and thermal hyperalgesia induced by diabetes through the phosphoinositide 3-kinase (PI3K)-mammalian target of rapamycin (mTOR) pathway in the PAG. Methods: Streptozotocin (STZ) was administered intraperitoneally to mimic allodynia and hyperalgesia evoked by diabetes in rats. Behavioral assays were carried out for determining mechanical pain and thermal hypersensitivity. Immunoblot and ELISA were performed to examine PAG protein amounts of interleukin-1β (IL-1β), IL-6, and tumor necrosis factor-α (TNF-α), as well as their corresponding receptors in STZ rats, and the expression of PI3K/protein kinase B (Akt)/mTOR signaling effectors. Results: Increased PAG p-PI3K/p-Akt/p-mTOR protein amounts were observed in STZ-induced animals, a PI3K-mTOR pathway inhibition in the PAG attenuated neuropathic pain responses. Moreover, the PAG concentrations of IL-1β, IL-6, and TNF-α and their receptors (namely, IL-1R, IL-6R, and tumor necrosis factor receptor [TNFR] subtype TNFR1, respectively) were increased in the STZ rats. Additionally, inhibiting IL-1R, IL-6R, and TNFR1 ameliorated mechanical allodynia and thermal hyperalgesia in STZ rats, alongside the downregulation of PI3K-mTOR signaling. Conclusions Overall, the current study suggests that upregulated proinflammatory cytokines and their receptors in the PAG activate PI3K-mTOR signaling, thereby producing a de-inhibition effect on descending pathways in modulating pain transmission, and eventually contributing to neuropathic pain.

Lung transplantation is an effective treatment for various end-stage lung diseases. Optimizing perioperative fluid management can reduce the incidence of postoperative pulmonary edema and improve the prognosis of lung transplant recipients. Excessive fluid administration may lead to pulmonary edema, ischemia-reperfusion injury of the transplant lung, and increased cardiac burden, which can induce heart failure. On the other hand, overly strict fluid restriction may lead to hypovolemia, affecting tissue perfusion and causing organ dysfunction. Therefore, precise regulation of fluid balance is crucial for the postoperative recovery of lung transplant recipients. This article reviews the physiological characteristics of lung transplant recipients, types of infused fluids, fluid therapy regimens, and hemodynamic monitoring, aiming to elucidate the particularities of perioperative fluid management in lung transplantation and provide new ideas and directions for individualized fluid management.