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Effectiveness and safety of insulin glargine U-300 as compared to insulin glargine U-100 in oral antidiabetic (OAD) failure cases—record-based observational study 在口服抗糖尿病药物(OAD)失败病例中,格列卫胰岛素 U-300 与格列卫胰岛素 U-100 的有效性和安全性对比--基于记录的观察性研究
IF 0.9 4区 医学 Q3 Medicine Pub Date : 2024-02-07 DOI: 10.1007/s13410-024-01317-5
Shambo S. Samajdar, Shashank R. Joshi, Sougata Sarkar, Santanu K. Tripathi, Satyabrata Sahoo, Nandini Chatterjee, Jyotirmoy Pal, Rutul A. Gokalani

Background

Type 2 diabetes is a significant public health concern that affects over 537 million adults worldwide. Oral antidiabetic (OAD) failure can be a complex management issue in patients with type 2 diabetes. Insulin glargine U-300 is a newer type of basal insulin with more consistent pharmacological effects than traditional insulin glargine.

Objective

This study aimed to assess the safety and effectiveness of insulin glargine U-300 as compared to insulin glargine U-100 in Indian type 2 diabetes patients who had experienced OAD failure.

Methods

This is a record-based observational study conducted on type 2 diabetes patients who had experienced OAD failure.

Results

The study involved 389 cases (189 on insulin glargine U-300 and 200 on insulin glargine U-100). It was found that 56.6% and 58.1% of patients had reduced fasting glucose levels below 130 mg/dl after 1 month of treatment, and 78.8% and 76.1% had a reduction after 3 months following the use of insulin glargine U-300 and insulin glargine U-100, respectively. In patients on glargine U-300 and insulin glargine U-100, the mean fasting plasma glucose decreased from 241.05 ± 65.93 mg/dl at baseline to 142.61 ± 55.19 mg/dl (p < 0.05) and similarly from 250.68 ± 61.41 to 140.27 ± 48.29 mg/dl (p < 0.05) at the end of the first month, respectively. The incidence of hypoglycemia was comparatively fewer in patients using insulin glargine U-300 as compared to those using insulin glargine U-100 (8.1% vs. 6.7%, p < 0.05).

Conclusion

The results suggest that insulin glargine U-300 is an effective and safer treatment option than insulin glargine U-100 for Indian patients with OAD failure. These findings have the potential to improve the management of type 2 diabetes patients with OAD failure globally.

背景 2 型糖尿病是一个重大的公共卫生问题,影响着全球超过 5.37 亿成年人。口服抗糖尿病药物(OAD)失效可能是 2 型糖尿病患者的一个复杂管理问题。与传统的格列美脲胰岛素相比,格列美脲 U-300 是一种新型基础胰岛素,具有更稳定的药理作用。本研究旨在评估与格列美脲 U-100 相比,格列美脲 U-300 在经历过口服抗糖尿病药失败的印度 2 型糖尿病患者中的安全性和有效性。结果研究涉及 389 例患者(189 例使用格列美脲 U-300 型胰岛素,200 例使用格列美脲 U-100 型胰岛素)。结果发现,使用格列美脲 U-300 和格列美脲 U-100 治疗 1 个月后,分别有 56.6% 和 58.1% 的患者空腹血糖水平降至 130 毫克/分升以下;使用格列美脲 U-300 和格列美脲 U-100 治疗 3 个月后,分别有 78.8% 和 76.1% 的患者空腹血糖水平降至 130 毫克/分升以下。使用格列美脲 U-300 和格列美脲 U-100 的患者的平均空腹血浆葡萄糖分别从基线时的 241.05 ± 65.93 mg/dl 降至 142.61 ± 55.19 mg/dl (p <0.05),第一个月结束时同样从 250.68 ± 61.41 mg/dl 降至 140.27 ± 48.29 mg/dl (p <0.05)。与使用格列美脲 U-100 的患者相比,使用格列美脲 U-300 的患者低血糖发生率相对较低(8.1% 对 6.7%,p <;0.05)。这些研究结果有可能在全球范围内改善对 OAD 治疗失败的 2 型糖尿病患者的管理。
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引用次数: 0
The HNF1B mutations and deletion associated with diabetes and their resulting diabetic phenotypes: a systematic review 与糖尿病相关的 HNF1B 基因突变和缺失及其导致的糖尿病表型:系统综述
IF 0.9 4区 医学 Q3 Medicine Pub Date : 2024-02-07 DOI: 10.1007/s13410-024-01319-3

Abstract

Objective

Mutations or deletion in HNF1B gene has been found to be related to a special type of monogenetic diabetes (HNF1B-DM). However, the phenotypic features of HNF1B-DM and the related gene abnormalities remain unclear.

Methods

We systemically reviewed the literature associated with HNF1B-DM in PubMed, China National Knowledge Infrastructure (CNKI), and Wanfang databases. The mutations and clinical data of HNF1B-DM were recorded. The phenotypes between mutations and deletion in HNF1B were analyzed.

Results

In total, 261 eligible individuals were included. 64 mutations were reported in 134 patients, and another 127 patients carried a large deletion in HNF1B gene. The mutations were distributed throughout from exons 1 to 7, including missense, nonsense, frameshift, and splice site mutation. Body weight index (BMI) was available for 69 patients; 55 patients (79.7%) were normal or underweight. Of the 131 patients with available family history, 105 (80.2%) reported a family history of diabetes. Data on age at diagnosis of diabetes was recorded in 210 patients with a mean of 23.7 years. Estimated glomerular filtration rate was recorded in 52 patients with a median of 47.00 ml/min per 1.73 m2. Renal cysts were in 78.9%, pancreatic dysplasia in 78.6%, and hypomagnesemia in 64.3% of the patients. The patients with HNF1B deletion had different diabetic phenotypes from the patients with HNF1B point mutation.

Conclusions

HNF1B-DM patients were with younger onset age, normal or low BMI, renal cyst, pancreatic dysplasia, and hypomagnesemia. The patients should be recommended for genetic testing to differentiate HNF1BDM from other young-onset diabetes earlier.

摘要 目的 发现 HNF1B 基因突变或缺失与一种特殊的单基因糖尿病(HNF1B-DM)有关。然而,HNF1B-DM 的表型特征及相关基因异常仍不清楚。 方法 我们在PubMed、中国知网(CNKI)和万方数据库中系统查阅了与HNF1B-DM相关的文献。记录了HNF1B-DM的基因突变和临床数据。分析HNF1B突变和缺失之间的表型。 结果 共纳入了 261 名符合条件的患者。134名患者中报告了64个基因突变,另有127名患者的HNF1B基因存在较大缺失。这些基因突变分布在 1 至 7 号外显子中,包括错义突变、无义突变、框架移位突变和剪接位点突变。69名患者有体重指数(BMI),其中55名患者(79.7%)体重正常或偏轻。在131名有家族史的患者中,105人(80.2%)有糖尿病家族史。210 名患者记录了诊断糖尿病时的年龄,平均为 23.7 岁。52 名患者记录了估计肾小球滤过率,中位数为 47.00 毫升/分钟/1.73 平方米。78.9%的患者患有肾囊肿,78.6%的患者患有胰腺发育不良,64.3%的患者患有低镁血症。HNF1B缺失患者与HNF1B点突变患者的糖尿病表型不同。 结论 HNF1B-DM 患者发病年龄较小、体重指数正常或较低、肾囊肿、胰腺发育不良和低镁血症。应建议患者进行基因检测,以便更早地将 HNF1BDM 与其他年轻发病型糖尿病区分开来。
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引用次数: 0
Advancing the understanding and management of diabetic peripheral neuropathy 促进对糖尿病周围神经病变的了解和管理
IF 0.9 4区 医学 Q3 Medicine Pub Date : 2024-02-06 DOI: 10.1007/s13410-024-01313-9
Vijay Viswanathan, Reshma Mirshad
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引用次数: 0
Advancing the understanding and management of diabetic peripheral neuropathy 促进对糖尿病周围神经病变的了解和管理
IF 0.9 4区 医学 Q3 Medicine Pub Date : 2024-02-06 DOI: 10.1007/s13410-024-01313-9
Vijay Viswanathan, Reshma Mirshad
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引用次数: 0
24-h Glucose profile of patients with gestational diabetes mellitus and comparison with pregnant women with normoglycemia 妊娠糖尿病患者的 24 小时血糖谱以及与血糖正常孕妇的比较
IF 0.9 4区 医学 Q3 Medicine Pub Date : 2024-01-29 DOI: 10.1007/s13410-024-01311-x

Abstract

Objective

To study the 24-h glucose profile of patients with mild GDM using the commercially available Abbot Libre continuous glucose monitoring system (CGMS) and compare them with pregnant women with normoglycemia (gestational age comparable).

Methods

A case control study conducted between 2019-2020 followed eligible pregnant women diagnosed with GDM according to Diabetes in Pregnancy Study Group India criteria, after the placement of a CGMS.

Results

Twenty-one GDM patients whose mean age was 27.1 ± 3.3 years with gestational age 28 weeks (24–32) and thirty pregnant women with normoglycemia whose mean age was 25.7 ± 4.2 years and gestational age 26 weeks (23–34) were enrolled in the study. Fasting, pre-breakfast, 2 h post lunch, day time and lowest nocturnal glucose were significantly higher in the GDM group than in controls. Glycemic variability indices like standard deviation of blood glucose, J index, and mean amplitude of glycemic excursions were also significantly higher in GDM patients. GDM patients spent more time above >140 mg/dl than controls.

Conclusion

GDM patients, who have mild hyperglycemia but not overt diabetes, also have an abnormal 24 h glucose profile as compared to normal pregnancy.

摘要 目的 使用市售的 Abbot Libre 连续血糖监测系统(CGMS)研究轻度 GDM 患者的 24 小时血糖情况,并将其与血糖正常(孕龄相当)的孕妇进行比较。 方法 2019-2020 年间进行的一项病例对照研究,对根据妊娠期糖尿病研究小组印度标准诊断为 GDM 的合格孕妇在安装 CGMS 后的情况进行了跟踪。 结果 21 名 GDM 患者(平均年龄为 27.1±3.3 岁,孕周为 28 周(24-32))和 30 名血糖正常的孕妇(平均年龄为 25.7±4.2 岁,孕周为 26 周(23-34))被纳入研究。GDM 组的空腹血糖、早餐前血糖、午餐后 2 小时血糖、日间血糖和夜间最低血糖均明显高于对照组。GDM 患者的血糖变异性指数,如血糖标准偏差、J 指数和血糖偏移的平均振幅也明显高于对照组。与对照组相比,GDM 患者血糖超过 140 mg/dl 的时间更长。 结论 GDM 患者有轻度高血糖,但不是明显的糖尿病,与正常妊娠相比,他们的 24 小时血糖谱也不正常。
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引用次数: 0
Predictive value of Lp-PLA2 for coronary artery disease in type 2 diabetes mellitus patients: an observational study 2 型糖尿病患者 Lp-PLA2 对冠心病的预测价值:一项观察性研究
IF 0.9 4区 医学 Q3 Medicine Pub Date : 2024-01-24 DOI: 10.1007/s13410-024-01312-w

Abstract

Objective

Type 2 diabetes mellitus (T2DM) is a chronic disease characterized by elevated blood glucose levels, which can result in a variety of complications, including coronary artery disease (CAD). Lp-PLA2 is a proinflammatory enzyme associated with low-density lipoprotein (LDL) particles in the circulation and is thought to be a biomarker for CAD risk.

Methods

The purpose of this investigation was to evaluate the diagnostic utility of serum lipoprotein-associated phospholipase A2 (Lp-PLA2) levels in type 2 diabetes mellitus (T2DM) patients with and without coronary artery disease (CAD). Utilizing receiver operating characteristic (ROC) curves, the diagnostic efficacy of Lp-PLA2 was evaluated.

Results

Lp-PLA2 levels were substantially higher in T2DM patients without cardiovascular disease (146.7 ng/mL 88.4) compared to HC (103.3 ng/mL 21.7) and T2DM + CAD (124.31 ng/mL 11.7). There was no statistically significant correlation between Lp-PLA2 levels and age, Hba1c, LDL, or Lp(a) in T2DM patients without CAD. Lp-PLA2 levels were not significantly associated with age (p = 0.97), HbA1c (p = 0.41), LDL (p = 0.59), or Lp(a) (p = 0.56), as determined by multiple linear regression analysis. The area under the curve (AUC) for Lp-PLA2 in T2DM without CAD was calculated to be 0.76, with a 95% confidence interval (CI). The sensitivity and specificity of a termination point of > 115 ng/mL were 0.70 and 0.68, respectively. For patients with T2DM + CAD, the AUC was 0.73 with a 95% confidence interval, and a threshold point of > 115 ng/mL yielded sensitivity and specificity values of 0.73 and 0.75, respectively.

Conclusions

In T2DM patients with or without CAD, serum Lp-PLA2 concentrations may serve as a diagnostic marker. The cutoff value of > 115 ng/mL exhibited excellent sensitivity and specificity, especially in T2DM patients without CAD. This finding suggests the clinical utility of Lp-PLA2 as a diagnostic tool for identifying those at risk for CAD in the context of T2DM.

摘要 目的 2 型糖尿病(T2DM)是一种以血糖水平升高为特征的慢性疾病,可导致多种并发症,包括冠状动脉疾病(CAD)。Lp-PLA2 是一种与血液循环中的低密度脂蛋白(LDL)颗粒相关的促炎酶,被认为是冠状动脉疾病风险的生物标志物。 方法 本研究旨在评估患有和未患有冠状动脉疾病(CAD)的 2 型糖尿病(T2DM)患者血清脂蛋白相关磷脂酶 A2(Lp-PLA2)水平的诊断效用。利用接收器操作特征曲线(ROC)评估了 Lp-PLA2 的诊断效果。 结果 无心血管疾病的 T2DM 患者的脂蛋白-PLA2 水平(146.7 纳克/毫升 88.4)远高于 HC(103.3 纳克/毫升 21.7)和 T2DM + CAD(124.31 纳克/毫升 11.7)。在无 CAD 的 T2DM 患者中,Lp-PLA2 水平与年龄、Hba1c、低密度脂蛋白或脂蛋白(a)之间没有明显的统计学相关性。经多元线性回归分析确定,Lp-PLA2 水平与年龄(p = 0.97)、HbA1c(p = 0.41)、低密度脂蛋白(p = 0.59)或脂蛋白(a)(p = 0.56)无明显相关性。经计算,无 CAD 的 T2DM 患者 Lp-PLA2 的曲线下面积 (AUC) 为 0.76,置信区间 (CI) 为 95%。115 ng/mL 临界点的灵敏度和特异度分别为 0.70 和 0.68。对于 T2DM + CAD 患者,AUC 为 0.73,置信区间为 95%,阈值点为 115 ng/mL,灵敏度和特异性分别为 0.73 和 0.75。 结论 在患有或不患有 CAD 的 T2DM 患者中,血清 Lp-PLA2 浓度可作为诊断标志物。115纳克/毫升的临界值具有极佳的灵敏度和特异性,尤其是在无 CAD 的 T2DM 患者中。这一发现表明,Lp-PLA2 可作为一种诊断工具,用于识别 T2DM 患者中的 CAD 高危人群。
{"title":"Predictive value of Lp-PLA2 for coronary artery disease in type 2 diabetes mellitus patients: an observational study","authors":"","doi":"10.1007/s13410-024-01312-w","DOIUrl":"https://doi.org/10.1007/s13410-024-01312-w","url":null,"abstract":"<h3>Abstract</h3> <span> <h3>Objective</h3> <p>Type 2 diabetes mellitus (T2DM) is a chronic disease characterized by elevated blood glucose levels, which can result in a variety of complications, including coronary artery disease (CAD). Lp-PLA2 is a proinflammatory enzyme associated with low-density lipoprotein (LDL) particles in the circulation and is thought to be a biomarker for CAD risk.</p> </span> <span> <h3>Methods</h3> <p>The purpose of this investigation was to evaluate the diagnostic utility of serum lipoprotein-associated phospholipase A2 (Lp-PLA2) levels in type 2 diabetes mellitus (T2DM) patients with and without coronary artery disease (CAD). Utilizing receiver operating characteristic (ROC) curves, the diagnostic efficacy of Lp-PLA2 was evaluated.</p> </span> <span> <h3>Results</h3> <p>Lp-PLA2 levels were substantially higher in T2DM patients without cardiovascular disease (146.7 ng/mL 88.4) compared to HC (103.3 ng/mL 21.7) and T2DM + CAD (124.31 ng/mL 11.7). There was no statistically significant correlation between Lp-PLA2 levels and age, Hba1c, LDL, or Lp(a) in T2DM patients without CAD. Lp-PLA2 levels were not significantly associated with age (p = 0.97), HbA1c (<em>p</em> = 0.41), LDL (<em>p</em> = 0.59), or Lp(a) (<em>p</em> = 0.56), as determined by multiple linear regression analysis. The area under the curve (AUC) for Lp-PLA2 in T2DM without CAD was calculated to be 0.76, with a 95% confidence interval (CI). The sensitivity and specificity of a termination point of &gt; 115 ng/mL were 0.70 and 0.68, respectively. For patients with T2DM + CAD, the AUC was 0.73 with a 95% confidence interval, and a threshold point of &gt; 115 ng/mL yielded sensitivity and specificity values of 0.73 and 0.75, respectively.</p> </span> <span> <h3>Conclusions</h3> <p>In T2DM patients with or without CAD, serum Lp-PLA2 concentrations may serve as a diagnostic marker. The cutoff value of &gt; 115 ng/mL exhibited excellent sensitivity and specificity, especially in T2DM patients without CAD. This finding suggests the clinical utility of Lp-PLA2 as a diagnostic tool for identifying those at risk for CAD in the context of T2DM.</p> </span>","PeriodicalId":50328,"journal":{"name":"International Journal of Diabetes in Developing Countries","volume":null,"pages":null},"PeriodicalIF":0.9,"publicationDate":"2024-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139561178","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Biomarkers of endothelial dysfunction (vWF), hypofibrinolysis (PAI-1) and metabolic syndrome components in hypertensive patients with and without thrombotic complications 有血栓并发症和无血栓并发症的高血压患者内皮功能障碍(vWF)、纤溶不足(PAI-1)和代谢综合征成分的生物标志物
IF 0.9 4区 医学 Q3 Medicine Pub Date : 2024-01-22 DOI: 10.1007/s13410-023-01299-w
David Santiago-Germán, Rosa María Jiménez-Alvarado, Alfredo Leaños-Miranda, Irma Isordia-Salas

Background

Essential hypertension is associated with increased risk for atherothrombotic disease.

Objective

The aims were to determine and compared the plasma concentration of von Willebrand Factor (vWF) and Plasminogen Activator Inhibitor type 1 (PAI-1) in hypertensive patients with and without atherothrombotic disease and the influence of antihypertensive treatment on those biomarkers.

Methods

Total of 341 individuals were included, 83 normotensive subjects and 258 hypertensive patients (43 with and 215 without atherothrombotic disease). The vWF and PAI-1 were measured by ELISA technique. Multivariate linear and quantile regression analysis were performed.

Results

There was higher vWF concentration (p < 0.001) and PAI-1 (p < 0.001) in hypertensive compared with normotensive individuals. The vWF level was correlated with hypertension, older age and glucose, explaining 26%, 70% and 86% of vWF variability. Increased PAI-1 levels were correlated with glucose, triglycerides, HbA1c, explaining 66%, 73% and 90% of variability. In contrast, lower PAI-1 concentration was determined by older age.

Conclusions

We found higher levels of vWF and PAI-1 in hypertensive patients, with highest concentration of vWF in patients with hypertension and thrombotic disease and the highest of PAI-1 in hypertensive patients without atherothrombotic disease. The lowest level of vWF was determined in patients with angiotensin II receptor blocker, and for the PAI-1 level in patients with calcium channel blocker medication. The lowest concentration of both biomarkers was present in patients who were treated with 3 or more drugs. Hypertension, older age, disorders in glucose and lipid metabolism were the main determinants of vWF and PAI-1 variability.

Graphical Abstract

背景高血压与动脉粥样硬化血栓性疾病风险增加有关。方法共纳入 341 人,其中 83 人为正常血压受试者,258 人为高血压患者(43 人为动脉粥样硬化血栓性疾病患者,215 人为非动脉粥样硬化血栓性疾病患者)。采用 ELISA 技术测量 vWF 和 PAI-1。结果高血压患者的 vWF 浓度(p < 0.001)和 PAI-1 浓度(p < 0.001)均高于正常血压患者。vWF 水平与高血压、年龄和血糖相关,分别占 vWF 变异的 26%、70% 和 86%。PAI-1 水平升高与血糖、甘油三酯和 HbA1c 相关,分别解释了 66%、73% 和 90% 的变异性。结论我们发现高血压患者体内的 vWF 和 PAI-1 水平较高,其中高血压合并血栓性疾病患者体内的 vWF 浓度最高,而无动脉粥样硬化血栓性疾病的高血压患者体内的 PAI-1 浓度最高。血管紧张素 II 受体阻滞剂患者的 vWF 水平最低,而钙通道阻滞剂患者的 PAI-1 水平最低。使用 3 种或 3 种以上药物治疗的患者体内这两种生物标志物的浓度最低。高血压、高龄、糖和脂代谢紊乱是vWF和PAI-1变化的主要决定因素。
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引用次数: 0
Diabetic retinopathy screening guidelines for Physicians in India: position statement by the Research Society for the Study of Diabetes in India (RSSDI) and the Vitreoretinal Society of India (VRSI)-2023 印度医生糖尿病视网膜病变筛查指南:印度糖尿病研究学会(RSSDI)和印度玻璃体视网膜学会(VRSI)-2023 立场声明
IF 0.9 4区 医学 Q3 Medicine Pub Date : 2024-01-20 DOI: 10.1007/s13410-023-01296-z
Manisha Agarwal, Padmaja Kumari Rani, Rajiv Raman, Raja Narayanan, Sreenivasamurthy L., Anil Virmani, Ramachandan Rajalakshmi, Sudha Chandrashekhar, Brij Mohan Makkar, Sanjay Agarwal, Mahesh Shanmugam Palanivelu, Muralidhar Naveenam Srinivasa, Kim Ramasamy

Diabetic retinopathy (DR) is a leading cause of blindness among working-age adults worldwide. India is the diabetes capital of the world and one in five adults is said to have diabetes in India. With the increase in diabetes, there is an increasing burden of diabetic retinopathy (DR). All patients with diabetes have a risk of losing vision due to DR. The prevalence of diabetic retinopathy is 12.5%; out of which, 4% are said to have vision-threatening diabetic retinopathy (VTDR) The early stages of DR are symptomless, necessitating a proactive screening for an early detection of DR in all people with diabetes before they develop VTDR. This is a position statement jointly developed by RSSDI (Research Society for the Study of Diabetes in India) and VRSI (Vitreo Retinal Society of India) to provide guidelines for Physicians on DR screening in India. These guidelines emphasize the need for regular DR screening of all people with diabetes. It is recommended that the Physicians establish an effective DR screening model in their clinics, eg., a non-mydriatic fundus camera utilizing artificial intelligence (AI) algorithms for fundus photography to identify referral or non-referral DR. This will facilitate early detection and timely referral to an ophthalmologist thereby preventing VTDR. The need to create public awareness regarding blindness due to DR and a collaboration between Physicians and ophthalmologists for the management of diabetes, opportunistic screening of DR, and timely management of DR may play a crucial role in decreasing the burden of blindness secondary to diabetes.

糖尿病视网膜病变(DR)是全球劳动适龄成年人失明的主要原因。印度是世界糖尿病之都,据说印度每五个成年人中就有一人患有糖尿病。随着糖尿病患者的增加,糖尿病视网膜病变(DR)的负担也日益加重。所有糖尿病患者都有可能因糖尿病视网膜病变而丧失视力。糖尿病视网膜病变的发病率为 12.5%,其中 4% 的患者据说患有危及视力的糖尿病视网膜病变 (VTDR)。糖尿病视网膜病变的早期阶段没有症状,因此有必要对所有糖尿病患者进行主动筛查,以便在他们发展成 VTDR 之前及早发现糖尿病视网膜病变。这是一份由印度糖尿病研究学会(RSSDI)和印度玻璃体视网膜学会(VRSI)联合制定的立场声明,旨在为印度医生提供 DR 筛查指南。这些指南强调了对所有糖尿病患者进行定期 DR 筛查的必要性。建议医生在其诊所建立有效的 DR 筛查模式,例如,使用非眼球驱动的眼底照相机,利用人工智能(AI)算法进行眼底摄影,以识别转诊或非转诊 DR。这将有助于早期发现并及时转诊给眼科医生,从而预防 VTDR。需要提高公众对 DR 致盲的认识,医生和眼科医生在糖尿病管理、DR 的机会性筛查和 DR 的及时治疗方面开展合作,这对于减轻糖尿病继发性失明的负担至关重要。
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引用次数: 0
Factors affecting the prolongation of glycemic time in range among children with type 1 diabetes using continuous glucose monitoring systems: A case control study 影响使用连续血糖监测系统的 1 型糖尿病患儿血糖控制时间延长的因素:病例对照研究
IF 0.9 4区 医学 Q3 Medicine Pub Date : 2024-01-19 DOI: 10.1007/s13410-024-01310-y
Kowalczyk-Korcz Emilia, Szypowska Agnieszka

Background

Time in range is a reliable measure of the risk of diabetes complications. High percentage of patients with diabetes fail to achieve the recommended time in range (TIR) target of 70–180 mg/dl (3.9–10 mmol/l) >70%.

Objective

This study aimed to identify factors influencing TIR prolongation.

Methods

Children aged 1–17 years with >1-year type 1 diabetes (T1D) duration, treated with continuous subcutaneous insulin infusion (CSII) ≥3 months, using continuous glucose monitoring (CGM) or intermittently scanned CGM (is-CGM) ≥1 month, and with a registration time >70% were included. Data were collected during routine diabetology visits at an outpatient clinic. Insulin pump and CGM or is-CGM reports in the most recent 14 days were recorded using a dedicated software. Legal caregivers were also asked to complete a questionnaire on how the patients use the insulin pump functions and eating habits.

Results

A sample of 110 patients was categorized into two groups: those with TIR >70% and TIR ≤70%. TIR >70% group presented with repeated hyperglycemia and a high glycemic variability coefficient of variation. We noted an acceptable hypoglycemia rate (3%), regardless of the TIR value. Patients with TIR >70% predominantly used predictive low glucose suspend system, maintained adequate intervals between insulin delivery and meal consumption, used the “bolus calculator” function, and more frequently created electronic reports.

Conclusions

Hyperglycemia and high glycemic variability prevent patients from achieving the target TIR. Advanced features in the CGM systems, premeal insulin bolus, and patients’ involvement in diabetes treatment are the main factors contributing to TIR prolongation.

背景达标时间是衡量糖尿病并发症风险的可靠指标。本研究旨在确定影响血糖控制时间延长的因素。方法纳入年龄为 1-17 岁、病程为 1 年的 1 型糖尿病(T1D)患儿,他们接受持续皮下注射胰岛素(CSII)治疗≥3 个月,使用持续葡萄糖监测(CGM)或间歇扫描 CGM(is-CGM)≥1 个月,且登记时间达到 70%。数据是在门诊进行常规糖尿病检查时收集的。使用专用软件记录最近 14 天的胰岛素泵和 CGM 或 is-CGM 报告。此外,还要求法定护理人员填写一份关于患者如何使用胰岛素泵功能和饮食习惯的调查问卷。结果 110 例患者被分为两组:TIR >70%和TIR ≤70%。TIR>70%组反复出现高血糖,血糖变异系数较高。我们注意到,无论 TIR 值如何,低血糖发生率(3%)都是可以接受的。TIR>70%的患者主要使用预测性低血糖暂停系统,在胰岛素给药和进餐之间保持足够的间隔时间,使用 "胰岛素计算器 "功能,并更频繁地创建电子报告。CGM 系统的先进功能、餐前胰岛素注射以及患者参与糖尿病治疗是导致 TIR 延长的主要因素。
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引用次数: 0
Iranian patients with diabetes and COVID-19-associated mucormycosis: Characteristics, manifestations, and mortality risk factors 伊朗糖尿病患者和 COVID-19 相关黏液瘤病:特征、表现和死亡风险因素
IF 0.9 4区 医学 Q3 Medicine Pub Date : 2024-01-18 DOI: 10.1007/s13410-024-01309-5
Mohammadreza Salehi, Alireza Esteghamati, Sadegh Khodavaisy, Nasim Khajavi Rad, Alireza Abdollahi, Sayyed Amirsina Alemzadeh, Sadaf Nasserisina, Azin Tabari, Farzad Pakdel, Saeed Mohammadi, Neda Joorabloo, Mahsa Abdorahimi, Mehrdad Shavandi, Soghra Rabizadeh

Objective

This study evaluated the mortality risk factors in Iranian patients with diabetes mellitus (DM) and COVID-19-associated mucormycosis (CAM).

Methods

This retrospective study was conducted on confirmed CAM cases with DM. Only patients with a confirmed history of COVID-19 within the last 3 months were included. The patients were divided into the survived and deceased groups, and each group’s characteristics were studied and compared. Patients were also studied according to their DM status (known or unknown case).

Results

A total of 106 patients were included. The mortality rate was 25.5%. The most common underlying disease (hypertension, 41.5%) was significantly higher in the deceased group. Sixty-five patients (62.5%) were known cases of DM. The mean duration of DM was 12.46 years. There was a significant relationship between the DM history and mortality rate (84.6% vs. 15.4%, p = 0.007). The history of ICU admission was 8 times higher in unknown DM patients (p = 0.011, OR = 8.000, CI = 1.60–39.95). The mean HbA1C was significantly different in known DM cases (9.36 ± 2.03 vs. 8.02 ± 2.40, p = 0.004). The mean first day FBS, mean first BS in emergency room, and mean FBS on the first hospitalization week were 171, 202, and 167.2 mg/dL, respectively. Although mortality was significantly related to hyperglycemic state of fasting and non-fasting BS levels (p < 0.05), it was not related to HbA1C.

Conclusion

Patients with diabetes and COVID-19 had uncontrolled fasting and non-fasting glucose levels during mucormycosis episode. Hypertension, history of DM, and the lack of glucose control during recent hospitalization can be associated with a poor outcome.

方法 这项回顾性研究针对患有糖尿病(DM)和 COVID-19 相关粘液瘤病 (CAM)的伊朗 CAM 确诊病例。只有在过去 3 个月内确诊过 COVID-19 的患者才被纳入研究范围。将患者分为存活组和死亡组,研究并比较每组的特征。此外,还根据患者的 DM 状态(已知或未知病例)对其进行了研究。死亡率为 25.5%。死亡组中最常见的基础疾病(高血压,41.5%)明显高于死亡组。65名患者(62.5%)已知患有糖尿病。糖尿病的平均病程为 12.46 年。DM病史与死亡率之间存在明显关系(84.6% vs. 15.4%,P = 0.007)。未知DM患者入住重症监护室的病史高出8倍(P = 0.011,OR = 8.000,CI = 1.60-39.95)。已知糖尿病病例的平均 HbA1C 显著不同(9.36 ± 2.03 vs. 8.02 ± 2.40,p = 0.004)。首日平均 FBS、急诊室首次平均 BS 和住院第一周平均 FBS 分别为 171、202 和 167.2 mg/dL。虽然死亡率与空腹和非空腹 BS 水平的高血糖状态有明显关系(p < 0.05),但与 HbA1C 无关。高血压、糖尿病史和近期住院期间血糖控制不佳可能与不良预后有关。
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International Journal of Diabetes in Developing Countries
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