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1.
Health Res Policy Syst ; 22(1): 57, 2024 May 13.
Article in English | MEDLINE | ID: mdl-38741196

ABSTRACT

BACKGROUND: Indigenous populations have increased risk of developing diabetes and experience poorer treatment outcomes than the general population. The FORGE AHEAD program partnered with First Nations communities across Canada to improve access to resources by developing community-driven primary healthcare models. METHODS: This was an economic assessment of FORGE AHEAD using a payer perspective. Costs of diabetes management and complications during the 18-month intervention were compared to the costs prior to intervention implementation. Cost-effectiveness of the program assessed incremental differences in cost and number of resources utilization events (pre and post). Primary outcome was all-cause hospitalizations. Secondary outcomes were specialist visits, clinic visits and community resource use. Data were obtained from a diabetes registry and published literature. Costs are expressed in 2023 Can$. RESULTS: Study population was ~ 60.5 years old; 57.2% female; median duration of diabetes of 8 years; 87.5% residing in non-isolated communities; 75% residing in communities < 5000 members. Total cost of implementation was $1,221,413.60 and cost/person $27.89. There was increase in the number and cost of hospitalizations visits from 8/$68,765.85 (pre period) to 243/$2,735,612.37. Specialist visits, clinic visits and community resource use followed this trend. CONCLUSION: Considering the low cost of intervention and increased care access, FORGE AHEAD represents a successful community-driven partnership resulting in improved access to resources.


Subject(s)
Cost-Benefit Analysis , Diabetes Mellitus , Health Services, Indigenous , Hospitalization , Primary Health Care , Humans , Primary Health Care/economics , Female , Male , Middle Aged , Hospitalization/economics , Canada , Health Services, Indigenous/economics , Diabetes Mellitus/therapy , Delivery of Health Care/economics , Aged , Health Services Accessibility , Health Care Costs , Indians, North American , Indigenous Peoples , Adult , Diabetes Complications/therapy , Diabetes Complications/economics
2.
Int Braz J Urol ; 50(4): 386-397, 2024.
Article in English | MEDLINE | ID: mdl-38701187

ABSTRACT

Erectile dysfunction is observed in about 50% of men. It has been found that diabetes mellitus increases its prevalence to 19-86.3%, necessitating attention to a therapeutic strategy. Among the available treatment methods, intracavernosal injections of mesenchymal stem cells have proven to be particularly effective. OBJECTIVE: The purpose of study is to assess and analyse the effectiveness of their use in the treatment of erectile dysfunction in patients with diabetes mellitus. MATERIALS AND METHODS: The literature search was conducted using systematic methods and analysis in databases such as Web of Science, Scopus, PubMed, Elsevier, and Springer, with 41 sources included for further review. RESULTS: The study highlights microangiopathic and neuropathic links as key factors in erectile dysfunction development in diabetic patients, stemming from endothelial dysfunction and conductivity disturbances. Mesenchymal stem cell therapy from bone marrow, adipose tissue, and umbilical cord mitigates pathogenic impact through regenerative and anti-apoptotic effects. Due to this, most studies indicate high efficacy of the treatment and rapid therapeutic action through intracavernosal administration. Some studies suggest an increase in the body's receptor sensitivity to other drugs, such as sildenafil. CONCLUSION: From the perspective of further research on this issue, standardising the preparation of stem cells and the treatment method using a large sample size is essential to introduce such a method as an extremely promising therapy for this delicate issue in men into practical medicine. The practical value of the study lies in the systematisation of information on different sources of mesenchymal stem cells for treating erectile dysfunction.


Subject(s)
Erectile Dysfunction , Mesenchymal Stem Cell Transplantation , Humans , Male , Erectile Dysfunction/therapy , Erectile Dysfunction/etiology , Mesenchymal Stem Cell Transplantation/methods , Treatment Outcome , Diabetes Complications/therapy , Penis , Reproducibility of Results
3.
Int J Nanomedicine ; 19: 4357-4375, 2024.
Article in English | MEDLINE | ID: mdl-38774027

ABSTRACT

Wound healing is a sophisticated and orderly process of cellular interactions in which the body restores tissue architecture and functionality following injury. Healing of chronic diabetic wounds is difficult due to impaired blood circulation, a reduced immune response, and disrupted cellular repair mechanisms, which are often associated with diabetes. Stem cell-derived extracellular vesicles (SC-EVs) hold the regenerative potential, encapsulating a diverse cargo of proteins, RNAs, and cytokines, presenting a safe, bioactivity, and less ethical issues than other treatments. SC-EVs orchestrate multiple regenerative processes by modulating cellular communication, increasing angiogenesis, and promoting the recruitment and differentiation of progenitor cells, thereby potentiating the reparative milieu for diabetic wound healing. Therefore, this review investigated the effects and mechanisms of EVs from various stem cells in diabetic wound healing, as well as their limitations and challenges. Continued exploration of SC-EVs has the potential to revolutionize diabetic wound care.


Subject(s)
Diabetes Mellitus , Extracellular Vesicles , Stem Cells , Wound Healing , Humans , Wound Healing/drug effects , Extracellular Vesicles/chemistry , Animals , Diabetes Mellitus/therapy , Cell Differentiation , Cell Communication/physiology , Neovascularization, Physiologic , Diabetes Complications/therapy
4.
Front Endocrinol (Lausanne) ; 15: 1343255, 2024.
Article in English | MEDLINE | ID: mdl-38681772

ABSTRACT

Stem cell-based therapies exhibit considerable promise in the treatment of diabetes and its complications. Extensive research has been dedicated to elucidate the characteristics and potential applications of adipose-derived stromal/stem cells (ASCs). Three-dimensional (3D) culture, characterized by rapid advancements, holds promise for efficacious treatment of diabetes and its complications. Notably, 3D cultured ASCs manifest enhanced cellular properties and functions compared to traditional monolayer-culture. In this review, the factors influencing the biological functions of ASCs during culture are summarized. Additionally, the effects of 3D cultured techniques on cellular properties compared to two-dimensional culture is described. Furthermore, the therapeutic potential of 3D cultured ASCs in diabetes and its complications are discussed to provide insights for future research.


Subject(s)
Adipose Tissue , Diabetes Mellitus , Humans , Adipose Tissue/cytology , Diabetes Mellitus/therapy , Animals , Cell Culture Techniques/methods , Mesenchymal Stem Cells/cytology , Diabetes Complications/therapy , Cell Differentiation , Cell Culture Techniques, Three Dimensional/methods
5.
Diabetes Metab Syndr ; 18(3): 102994, 2024 Mar.
Article in English | MEDLINE | ID: mdl-38579489

ABSTRACT

BACKGROUND AND AIMS: Diabetic gastroparesis (DGp) is a common and preventable complication of uncontrolled diabetes mellitus (D.M.) and significantly affects the Quality of Life of patients. Diagnosis and management present as a clinical challenge due to the disease's complexity and limited effective therapeutic options. This review aims to comprehensively outline the pathogenesis, diagnosis, and management of diabetic gastroparesis, evaluating evolving approaches to guide clinicians and provide future recommendations. METHODS: A literature review was conducted on scholarly databases of PubMed, Google Scholar, Scopus and Web of Science encompassing published articles, gray literature and relevant clinical guidelines. Data were synthesized and analyzed to provide a comprehensive overview of diabetic gastroparesis, focusing on pathogenesis, diagnosis, and management. RESULTS: The review intricately explores the pathogenesis contributing to diabetic gastroparesis, emphasizing autonomic neuropathy, oxidative stress, inflammation, hormonal dysregulation, microbiota alterations, and gastrointestinal neuropathy. Primary management strategies are underscored, including lifestyle modifications, symptom relief, and glycemic control. The discussion encompasses pharmacological and surgical options, highlighting the importance of a multidisciplinary approach involving various healthcare professionals for comprehensive patient care. CONCLUSION: This review offers a thorough understanding of pathogenesis, diagnosis, and management of diabetic gastroparesis, underlining evolving approaches for clinicians. A multidisciplinary approach is crucial to address both the physical and mental health aspects of diabetes and its complications.


Subject(s)
Diabetes Complications , Gastroparesis , Humans , Gastroparesis/therapy , Gastroparesis/etiology , Gastroparesis/diagnosis , Diabetes Complications/therapy , Disease Management , Quality of Life , Prognosis
6.
Prog Mol Biol Transl Sci ; 203: 287-300, 2024.
Article in English | MEDLINE | ID: mdl-38360004

ABSTRACT

Diabetes is an ongoing global problem as it affects health of more than 537 million people around the world. Diabetes leaves many serious complications that affect patients and can cause death if not detected and treated promptly. Some of the complications of diabetes include impaired vascular system, increased risk of stroke, neurological diseases that cause pain and numbness, diseases related to the retina leading to blindness, and other complications affecting kidneys, heart failure, muscle weakness, muscle atrophy. All complications of diabetes seriously affect the health of patients. Recently, gene therapy has emerged as a viable treatment strategy for various diseases. DNA and RNA are among the target molecules that can change the structure and function of proteins and are effective methods of treating diseases, especially genetically inherited diseases. RNA therapeutics has attracted deep interest as it has been approved for application in the treatment of functional system disorders such as spinal muscular atrophy, and muscular dystrophy. In this review, we cover the types of RNA therapies considered for treatment of diabetes. In particular, we delve into the mechanism of action of RNA therapies for diabetes, and studies involving testing of these RNA therapies. Finally, we have highlighted the limitations of the current understanding in the mechanism of action of RNA therapies.


Subject(s)
Diabetes Complications , Diabetes Mellitus , Muscular Atrophy, Spinal , Humans , RNA , Muscular Atrophy, Spinal/genetics , Genetic Therapy/methods , Diabetes Complications/therapy
7.
Adv Sci (Weinh) ; 11(13): e2307761, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38286650

ABSTRACT

Delayed wound healing is a major complication of diabetes, and is associated with impaired cellular functions. Current treatments are unsatisfactory. Based on the previous reports on microRNA expression in small extracellular vesicles (sEVs), miR-17-5p-engineered sEVs (sEVs17-OE) and encapsulated them in gelatin methacryloyl (GelMA) hydrogel for diabetic wounds treatment are fabricated. SEVs17-OE are successfully fabricated with a 16-fold increase in miR-17-5p expression. SEVs17-OE inhibited senescence and promoted the proliferation, migration, and tube formation of high glucose-induced human umbilical vein endothelial cells (HG-HUVECs). Additionally, sEVs17-OE also performs a promotive effect on high glucose-induced human dermal fibroblasts (HG-HDFs). Mechanism analysis showed the expressions of p21 and phosphatase and tensin homolog (PTEN), as the target genes of miR-17-5p, are downregulated significantly by sEVs17-OE. Accordingly, the downstream genes and pathways of p21 and PTEN, are activated. Next, sEVs17-OE are loaded in GelMA hydrogel to fabricate a novel bioactive wound dressing and to evaluate their effects on diabetic wound healing. Gel-sEVs17-OE effectively accelerated wound healing by promoting angiogenesis and collagen deposition. The cellular mechanism may be associated with local cell proliferation. Therefore, a novel bioactive wound dressing by loading sEVs17-OE in GelMA hydrogel, offering an option for chronic wound management is successfully fabricated.


Subject(s)
Diabetes Mellitus , Extracellular Vesicles , Gelatin , Methacrylates , MicroRNAs , Wound Healing , Humans , Diabetes Mellitus/genetics , Diabetes Mellitus/metabolism , Endothelial Cells , Extracellular Vesicles/genetics , Glucose , Hydrogels , MicroRNAs/pharmacology , MicroRNAs/therapeutic use , PTEN Phosphohydrolase/antagonists & inhibitors , PTEN Phosphohydrolase/genetics , Wound Healing/genetics , Diabetes Complications/therapy , Proto-Oncogene Proteins p21(ras)/antagonists & inhibitors , Proto-Oncogene Proteins p21(ras)/genetics
8.
Diabet Med ; 41(5): e15255, 2024 May.
Article in English | MEDLINE | ID: mdl-37915229

ABSTRACT

AIM: People with coexisting severe mental illness (SMI) and type 2 diabetes have a shorter life expectancy and poorer diabetes outcomes than those without SMI. This is partly explained by the separate treatment of diabetes and SMI, which occurs in parallel silos in many healthcare systems. The Steno Diabetes Center Sjaelland and Region Zealand established the Fusion Clinic to offer combined psychiatric and diabetes care delivered by both diabetes and mental healthcare professionals. This study describes how the clinic was established and the initial diabetes outcomes. METHODS: The Fusion Clinic was co-designed by people with diabetes and SMI and healthcare professionals to improve the care of adults with diabetes and SMI. The clinic approach utilised the F-ACT model. The 63 people referred to the Fusion Clinic between 01.02.2020 and 01.01.2022 who attended the clinic for more than 6 months were included in this study. Diabetes outcomes were recorded in the electronic medical records (Sundhedsplatformen EPIC). RESULTS: There was a high prevalence of diabetes complications at baseline. Furthermore, 70% had one or more additional concomitant diseases, as well as SMI and diabetes. Assessment of diabetes complications and measurements of HbA1c and lipid profile improved after referral to the clinic. HbA1c declined during the first 6 months of attendance at the clinic. CONCLUSIONS: This model of service delivery has the potential to improve the quality of care for people with SMI and type 2 diabetes.


Subject(s)
Diabetes Complications , Diabetes Mellitus, Type 2 , Mental Disorders , Adult , Humans , Diabetes Mellitus, Type 2/complications , Diabetes Mellitus, Type 2/epidemiology , Diabetes Mellitus, Type 2/therapy , Mental Disorders/epidemiology , Mental Disorders/therapy , Mental Disorders/psychology , Delivery of Health Care , Ambulatory Care Facilities , Diabetes Complications/epidemiology , Diabetes Complications/therapy , Diabetes Complications/complications
9.
Medicine (Baltimore) ; 102(50): e36370, 2023 Dec 15.
Article in English | MEDLINE | ID: mdl-38115358

ABSTRACT

INTRODUCTION: A systematic review and meta-analysis were conducted to evaluate the efficacy and the overall safety of Faricimab compared with other anti-vascular endothelial growth factors (VEGF) therapy for neovascular age-related macular degeneration (AMD) and diabetic macular edema (DME). MATERIALS AND METHODS: A systematic literature search of a comprehensive electronic database was performed to identify randomized clinical trials published from January 2013 to January 2023 for Faricimab in AMD and DME. Weighted mean differences and risk ratios were used to integrate the different studies. RESULTS: A total of 4 randomized controlled trials (RCTs) with 1678 AMD patients and 3 RCTs with 20 DME patients were included in the meta-analysis.In patients with AMD, a significant difference was found in the number of injections between Faricimab and other anti-VEGF therapy (MD = -2.42, 95% CI [-3.93 to -0.90], P = .002).No significant difference was found for the change in best corrected visual acuity (BVCA), central subfoveal thickness (CST), and gaining 15 or more letters. Similarly, no significant difference was found for adverse events.In patients with DME, a significant difference was observed for CST (MD = -22.41, 95% CI [-29.95 to -14.86], P < .00001) and the number of injections(MD = -0.93, 95% CI [-1.33 to -0.54], P < .00001). No significant difference was found for BVCA and gaining 15 or more letters, and no significant difference was found for adverse events. CONCLUSIONS: Comprehensive evidence confirms that Faricimab achieves non-inferior or even better CST improvement than other anti-VEGF therapies with extended dosing intervals, but more long-term follow-up studies are needed to support our conclusions.


Subject(s)
Antibodies, Bispecific , Diabetes Complications , Macular Degeneration , Macular Edema , Vascular Endothelial Growth Factor A , Antibodies, Bispecific/therapeutic use , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Macular Degeneration/therapy , Humans , Randomized Controlled Trials as Topic , Macular Edema/etiology , Macular Edema/therapy , Diabetes Complications/therapy , Treatment Outcome
10.
Tissue Cell ; 85: 102225, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37801960

ABSTRACT

Diabetes mellitus (DM) is a chronic metabolic disorder characterized by high blood glucose and is associated with high morbidity and mortality among the diabetic population. Uncontrolled chronic hyperglycaemia causes increased formation and accumulation of different oxidative and nitrosative stress markers, resulting in microvascular and macrovascular complications, which might seriously affect the quality of a patient's life. Conventional treatment strategies are confined to controlling blood glucose by regulating the insulin level and are not involved in attenuating the life-threatening complications of diabetes mellitus. Thus, there is an unmet need to develop a viable treatment strategy that could target the multi-etiological factors involved in the pathogenesis of diabetic complications. Stem cell therapy, a regenerative medicine approach, has been investigated in diabetic complications owing to their unique characteristic features of self-renewal, multilineage differentiation and regeneration potential. The present review is focused on potential therapeutic applications of stem cells in the treatment of microvascular diabetic complications such as nephropathy, retinopathy, and polyneuropathy.


Subject(s)
Diabetes Complications , Diabetes Mellitus , Hyperglycemia , Humans , Blood Glucose/metabolism , Regenerative Medicine , Diabetes Complications/therapy , Hyperglycemia/complications , Hyperglycemia/therapy , Stem Cells/metabolism , Diabetes Mellitus/therapy
12.
Acta Pharmacol Sin ; 44(12): 2455-2468, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37596398

ABSTRACT

Renal tubulointerstitial fibrosis (TIF) is considered as the final convergent pathway of diabetic nephropathy (DN) without effective therapies currently. MiRNAs play a key role in fibrotic diseases and become promising therapeutic targets for kidney diseases, while miRNA clusters, formed by the cluster arrangement of miRNAs on chromosomes, can regulate diverse biological functions alone or synergistically. In this study, we developed clustered miR-23a/27a/26a-loaded skeletal muscle satellite cells-derived exosomes (Exos) engineered with RVG peptide, and investigated their therapeutic efficacy in a murine model of DN. Firstly, we showed that miR-23a-3p, miR-26a-5p and miR-27a-3p were markedly decreased in serum samples of DN patients using miRNA sequencing. Meanwhile, we confirmed that miR-23a-3p, miR-26a-5p and miR-27a-3p were primarily located in proximal renal tubules and highly negatively correlated with TIF in db/db mice at 20 weeks of age. We then engineered RVG-miR-23a/27a/26a cluster loaded Exos derived from muscle satellite cells, which not only enhanced the stability of miR-23a/27a/26a cluster, but also efficiently delivered more miR-23a/27a/26a cluster homing to the injured kidney. More importantly, administration of RVG-miR-23a/27a/26a-Exos (100 µg, i.v., once a week for 8 weeks) significantly ameliorated tubular injury and TIF in db/db mice at 20 weeks of age. We revealed that miR-23a/27a/26a-Exos enhanced antifibrotic effects by repressing miRNA cluster-targeting Lpp simultaneously, as well as miR-27a-3p-targeting Zbtb20 and miR-26a-5p-targeting Klhl42, respectively. Knockdown of Lpp by injection of AAV-Lpp-RNAi effectively ameliorated the progression of TIF in DN mice. Taken together, we established a novel kidney-targeting Exo-based delivery system by manipulating the miRNA-23a/27a/26a cluster to ameliorate TIF in DN, thus providing a promising therapeutic strategy for DN.


Subject(s)
Diabetic Nephropathies , Exosomes , MicroRNAs , Satellite Cells, Skeletal Muscle , Animals , Humans , Mice , Diabetes Mellitus/therapy , Diabetic Nephropathies/genetics , Diabetic Nephropathies/pathology , Diabetic Nephropathies/therapy , Exosomes/metabolism , Fibrosis , MicroRNAs/metabolism , MicroRNAs/pharmacology , MicroRNAs/therapeutic use , Satellite Cells, Skeletal Muscle/metabolism , Diabetes Complications/therapy
13.
Zhonghua Kou Qiang Yi Xue Za Zhi ; 58(6): 615-620, 2023 Jun 09.
Article in Chinese | MEDLINE | ID: mdl-37272009

ABSTRACT

The number of diabetic patients visiting stomatology for periodontal disease is increasing, and the symptoms are relatively severe, and often complications increase the complexity of periodontal treatment. This article briefly describes the research progress and clinical manifestations of the epidemiology and related pathological mechanisms of periodontitis with diabetes, focusing on the treatment and providing reference for stomatologists in the clinical diagnosis and treatment of patients with diabetic periodontitis.


Subject(s)
Diabetes Complications , Diabetes Mellitus, Type 2 , Diabetes Mellitus , Periodontal Diseases , Periodontitis , Humans , Periodontitis/complications , Periodontitis/diagnosis , Periodontitis/therapy , Diabetes Mellitus/diagnosis , Diabetes Mellitus/therapy , Dental Care , Diabetes Complications/diagnosis , Diabetes Complications/therapy , Diabetes Complications/complications
14.
Tissue Cell ; 81: 102014, 2023 Apr.
Article in English | MEDLINE | ID: mdl-36621294

ABSTRACT

AIMS: Oxidative stress also plays an important role in the pathogenesis of diabetic neuropathy (DN). Both resveratrol (RES) and exercise (EX) have potent anti-oxidative benefits. Low levels of nerve growth factor (NGF) and SIRT1 (a member of sirtuin family) have been reported in patients with DN. The current study has been designed to investigate the role of serum NGF and SIRT1 on DN-induced hyperalgesia and motor incoordination and to evaluate the possible protective role of RES and/or EX. MAIN METHODS: A total of 40 male adult albino rats divided into five groups; control, DN, DN + RES, DN + EX, and DN + RES and EX. DN was confirmed by sensorimotor disturbance and diminished nerve conduction velocity (NCV). NGF and SIRT1 levels were measured by western blot. Calcitonin gene-related peptide (CGRP) was measured by PCR. Myofibrillar degeneration and inflammation scores were revealed via H&E microscopic analysis of the gastrocnemius muscle. Immunohistochemical evaluation of caspase3 and TNF-α was performed in the lumber segment of spinal cord and gastrocnemius muscle sections. Ultrastructural evaluation of sciatic nerve axonal degeneration has also been assessed. KEY FINDINGS: DN group showed decreased SIRT1 level, decreased NGF level and correlated with CGRP level and Na+/K+ ATPase. Treatment with RES and/or EX resulted in improvement of sensorimotor disturbance. DN characterized by reduced SOD level, whereas RES and/or EX could limit oxidative damage by up-regulation Bcl2, Akt and GAP-43 and down-regulation of caspase3 and TNF-α. In conclusion, increased level of SIRT1and NGF by incorporation of RES (natural supplementation) and EX (life style modification) could improve the neuroinflammatory state in DN.


Subject(s)
Diabetic Neuropathies , Exercise , Muscular Diseases , Resveratrol , Male , Calcitonin Gene-Related Peptide , Diabetic Neuropathies/drug therapy , Diabetic Neuropathies/metabolism , Diabetic Neuropathies/therapy , Muscular Diseases/drug therapy , Muscular Diseases/therapy , Nerve Growth Factor/metabolism , Resveratrol/pharmacology , Sirtuin 1/metabolism , Tumor Necrosis Factor-alpha , Rats , Diabetes Complications/drug therapy , Diabetes Complications/metabolism , Diabetes Complications/therapy , GAP-43 Protein/metabolism , Animals
15.
Cardiovasc Diabetol ; 22(1): 18, 2023 01 30.
Article in English | MEDLINE | ID: mdl-36717853

ABSTRACT

BACKGROUND: Patients with concurrent atrial fibrillation (AF) and diabetes mellitus (DM) [AF-DM] have a high risk of cardiovascular and diabetes-related complications, but are less engaged in a comprehensive treatment approach. We evaluated the association of early rhythm control (ERC), lifestyle modification (LSM), and a combination of ERC and LSM with cardiovascular or diabetes-related complication risk in patients with AF-DM (type 2). METHODS: From the National Health Information Database, 47,940 patients diagnosed with AF-DM in 2009-2016 were included. We defined ERC as rhythm control therapy within two years of AF diagnosis and LSM as adherence to ≥ 2 of the healthy behaviors among non-current smoking, non-drinking, and regular exercise. We compared the primary (ischemic stroke) and secondary (macro- and microvascular complications, glycemic emergency, and all-cause death) outcomes in four groups: non-ERC and non-LSM (group 1), LSM only (group 2), ERC only (group 3), and both ERC and LSM (group 4). RESULTS: Of total, 10,617 (22%), 26,730 (55.8%), 2,903 (6.1%), and 7,690 (16.0%) were classified into groups 1 to 4, in sequence. The mean duration from AF diagnosis to ERC was 25.6 ± 75.5 days. During 4.0 (interquartile range: 2.5-6.2) years' follow-up, groups 2 and 3 were associated with 23% and 33% lower risks of stroke than group 1, respectively. Group 4 was associated with the lowest risk of stroke: hazard ratio (HR) 0.58, 95% confidence interval (CI) 0.51-0.67, p < 0.001. Regarding secondary outcomes, the lowest risks were also observed in group 4; macro- and microvascular complications, glycemic emergency, and all-cause death had HRs (95% CIs) of 0.63 (0.56-0.70), 0.88 (0.82-0.94), 0.72 (0.62-0.84), and 0.80 (0.73-0.87), respectively, all p < 0.001. CONCLUSIONS: For AF-DM patients, ERC and LSM exert a synergistic effect in preventing cardiovascular and diabetes-related complications with the greatest lowered risk of stroke. A comprehensive treatment approach should be pursued in AF-DM patients.


Subject(s)
Atrial Fibrillation , Delivery of Health Care, Integrated , Diabetes Complications , Diabetes Mellitus, Type 2 , Diabetes Mellitus , Stroke , Humans , Atrial Fibrillation/diagnosis , Atrial Fibrillation/epidemiology , Atrial Fibrillation/therapy , Cohort Studies , Risk Factors , Prognosis , Diabetes Mellitus, Type 2/complications , Stroke/diagnosis , Stroke/epidemiology , Stroke/prevention & control , Diabetes Complications/diagnosis , Diabetes Complications/epidemiology , Diabetes Complications/therapy , Healthy Lifestyle , Diabetes Mellitus/diagnosis , Diabetes Mellitus/epidemiology , Diabetes Mellitus/therapy
16.
Int Wound J ; 20(6): 2346-2359, 2023 Aug.
Article in English | MEDLINE | ID: mdl-36564054

ABSTRACT

Diabetic chronic wounds cause massive levels of patient suffering and economic problems worldwide. The state of chronic inflammation arises in response to a complex combination of diabetes mellitus-related pathophysiologies. Advanced treatment options are available; however, many wounds still fail to heal, exacerbating morbidity and mortality. This review describes the chronic inflammation pathophysiologies in diabetic ulcers and treatment options that may help address this dysfunction either directly or indirectly. We suggest that treatments to reduce inflammation within these complex wounds may help trigger healing.


Subject(s)
Diabetes Complications , Diabetes Mellitus , Diabetic Foot , Skin Diseases , Humans , Diabetes Complications/therapy , Inflammation/therapy , Wound Healing/physiology , Diabetic Foot/therapy
17.
Diabetes Care ; 46(1): 149-155, 2023 01 01.
Article in English | MEDLINE | ID: mdl-36399714

ABSTRACT

OBJECTIVE: To estimate medical costs associated with 17 diabetes complications and treatment procedures among Medicare beneficiaries aged ≥65 years with type 1 diabetes. RESEARCH DESIGN AND METHODS: With use of the 2006-2017 100% Medicare claims database for beneficiaries enrolled in fee-for-service plans and Part D, we estimated the annual cost of 17 diabetes complications and treatment procedures. Type 1 diabetes and its complications and procedures were identified using ICD-9/ICD-10, procedure, and diagnosis-related group codes. Individuals with type 1 diabetes were followed from the year when their diabetes was initially identified in Medicare (2006-2015) until death, discontinuing plan coverage, or 31 December 2017. Fixed-effects regression was used to estimate costs in the complication occurrence year and subsequent years. The cost proportion of a complication was equal to the total cost of the complication, calculated by multiplying prevalence by the per-person cost divided by the total cost for all complications. All costs were standardized to 2017 U.S. dollars. RESULTS: Our study included 114,879 people with type 1 diabetes with lengths of follow-up from 3 to 10 years. The costliest complications per person were kidney failure treated by transplant ($77,809 in the occurrence year and $13,556 in subsequent years), kidney failure treated by dialysis ($56,469 and $41,429), and neuropathy treated by lower-extremity amputation ($40,698 and $7,380). Sixteen percent of the total medical cost for diabetes complications was for treating congestive heart failure. CONCLUSIONS: Costs of diabetes complications were large and varied by complications. Our results can assist in cost-effectiveness analysis of treatments and interventions for preventing or delaying diabetes complications in Medicare beneficiaries aged ≥65 years with type 1 diabetes.


Subject(s)
Diabetes Complications , Diabetes Mellitus, Type 1 , Aged , Humans , United States/epidemiology , Medicare , Diabetes Mellitus, Type 1/complications , Diabetes Mellitus, Type 1/therapy , Diabetes Complications/epidemiology , Diabetes Complications/therapy , Diabetes Complications/complications , Retrospective Studies
18.
Gerokomos (Madr., Ed. impr.) ; 34(2): 150-153, 2023. tab, ilus
Article in Spanish | IBECS | ID: ibc-221849

ABSTRACT

En la actualidad, el cuidado de las heridas que deben curar por segunda intención se realiza en ambiente húmedo y empleando la estrategia TIME, las personas que las padecen sufren una disminución de la calidad de vida. El objetivo de este trabajo es presentar un abordaje y tratamiento del borde epitelial con vitamina E acetato nebulizada. Se trata de un paciente de 74 años y con diabetes mellitus tipo 2, que presenta una herida en la cara anterior de la pierna izquierda. El principal diagnóstico de enfermería fue integridad tisular. Como principales resultados se han establecido la hidratación de los bordes perilesionales y la disminución del tamaño de la herida. Como conclusión, la vitamina E acetato ha permitido la conservación y mejora del estado del tejido perilesional y del nuevo formado, así como el ahorro de tiempos de exposición de la lesión al ambiente (AU)


At present, the care of wounds that must heal by secondary intention is carried out in a humid environment and using the TIME strategy, the people who suffer from them suffer a decrease in quality of life. The objective of this work is to present an approach and management of the epithelial border with nebulized vitamin E acetate. The case deals with a 74-year-old patient with type 2 diabetes mellitus who presented a wound on the front of his left leg. The main nursing diagnosis has been tissue integrity. As main results, the hydration of the peri-lesion edges and the reduction in the size of the wound have been established. In conclusion, vitamin E acetate has allowed the conservation and improvement of the state of the peri-injury tissue and of the newly formed tissue, as well as the saving of exposure times of the injury to the environment (AU)


Subject(s)
Humans , Male , Aged , Diabetes Complications/therapy , Diabetes Mellitus, Type 2 , Acetates/administration & dosage , Vitamin E/administration & dosage , Leg Ulcer/therapy , Nursing Care , Treatment Outcome
20.
Biomed Pharmacother ; 151: 113165, 2022 Jul.
Article in English | MEDLINE | ID: mdl-35609370

ABSTRACT

OBJECTIVE: To investigate the efficacy of a paeoniflorin-sodium alginate (SA)-gelatin skin scaffold for treating diabetic wound in a rat model. METHODS: Bioinks were prepared using various percentages of paeoniflorin in the total weight of a solution containing SA and gelatin. Skin scaffolds containing 0%, 1%, 3%, 5%, and 10% paeoniflorin were printed using 3D bioprinting technology, and scaffold microstructure was observed with scanning electron microscopy. Skin scaffolds were then used in rats with diabetic wounds. H&E staining, Masson staining, and immunohistochemical staining for IL-1ß and CD31 were performed on days 7 and 14. RESULTS: All skin scaffolds had a mesh-like structure with uniform pore distribution. Wounds healed well in each group, with the 1% and 3% groups demonstrating the most complete healing. H&E staining showed that skin accessory organs had appeared in each group. On day 7, collagen deposition in the 3% group was higher than in the other groups (P<0.05), and IL-1ß infiltration was lower in the 10% group than in the 3% group (P = 0.002). On day 14, IL-1ß infiltration was not significantly different between the 10% and 3% groups (P = 0.078). The CD31 level was higher in the 3% group than in the other groups on days 7 and 14 (P<0.05). CONCLUSION: A 3% paeoniflorin-SA-gelatin skin scaffold promoted the healing of diabetic wounds in rats. This scaffold promoted collagen deposition and microvascular regeneration and demonstrated anti-inflammatory properties, suggesting that this scaffold type could be used to treat diabetic wounds.


Subject(s)
Alginates , Diabetes Complications , Gelatin , Glucosides , Skin , Tissue Scaffolds , Alginates/administration & dosage , Alginates/therapeutic use , Animals , Collagen/metabolism , Diabetes Complications/complications , Diabetes Complications/therapy , Diabetes Mellitus , Disease Models, Animal , Gelatin/administration & dosage , Gelatin/therapeutic use , Glucosides/administration & dosage , Glucosides/therapeutic use , Microvessels/drug effects , Microvessels/physiology , Monoterpenes/administration & dosage , Monoterpenes/therapeutic use , Printing, Three-Dimensional , Rats , Skin/blood supply , Skin/drug effects , Skin/injuries , Wound Healing/drug effects , Wound Healing/physiology , Wounds and Injuries/complications , Wounds and Injuries/physiopathology , Wounds and Injuries/therapy
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