The Role of Complement in Diabetic Kidney Disease
试验速览
- 阶段
- 不适用
- 状态
- Enrolling By Invitation
- 入组人数
- 90
- 试验地点
- 1
- 主要终点
- Level of complement system activation
研究概览
简要总结
Diabetes is a chronic condition marked by long-term elevated blood glucose levels. There are more types of diabetes; the majority of patients have type 1 or type 2 diabetes. Over long period of time, high blood sugar damages blood vessels and organs. One of the most common complications is diabetic kidney disease, which can slowly lead to kidney failure. People with this condition also have a much higher risk of heart and blood vessel diseases.
Newer research shows that the immune system, especially the complement system (a group of proteins that help defend the body), may also play a role in worsening kidney disease in diabetes. High blood sugar can activate these proteins, and they have been found in kidney tissue of patients with diabetic kidney disease.
The goal of this study is to find out how much the complement system contributes to kidney damage in diabetes, whether it affects different groups of patients differently, and whether it is linked to blood vessel health or the stage of kidney disease. The study will also assess if improved diabetes control is linked to reduced complement system activity.
详细描述
Diabetes is a chronic disease characterized by long-term elevated blood glucose levels. Several types of diabetes are known, with most affected individuals having type 1 or type 2 diabetes. Long-term elevation of blood glucose affects various organs in the body, a condition referred to as chronic complications of diabetes. Since elevated blood glucose damages both small and large blood vessels, complications are classified as microvascular (damage to small vessels) and macrovascular (damage to large vessels). Diabetic kidney disease is the main microvascular complication in both type 1 and type 2 diabetes and is also the leading cause of kidney failure.
Changes in the kidneys develop over many years. Gradual deterioration of kidney function is monitored using laboratory parameters. Along with declining kidney function, blood pressure also increases, and cardiovascular diseases begin to develop- the risk of these rises exponentially with worsening kidney function. Cardiovascular diseases represent the leading cause of mortality among people with diabetes.
Traditionally, diabetic kidney disease was considered as non-inflammatory condition. Its development was attributed to impaired glucose metabolism and elevated blood pressure. Consequently, achieving optimal blood glucose and blood pressure values has been regarded as key to preventing chronic complications. However, diabetes itself represents an additional risk factor for cardiovascular disease compared with individuals without diabetes. Thus, individuals with diabetic kidney disease are even more prone to cardiovascular events. In these patients it is especially important to follow treatment guidelines and to treat elevated blood glucose and blood pressure as intensively as possible. For individuals with diabetic kidney disease, medications from the group of angiotensin-converting enzyme inhibitors or angiotensin receptor blockers are prescribed for the treatment of high blood pressure. Both medication groups also have a protective effect on the kidneys and slow the decline of kidney function. Angiotensin is a substance in the body responsible for raising blood pressure-when its action is inhibited, blood pressure decreases.
The investigators now know that inflammation and the immune system also play a role in the development of chronic diabetic complications. The complement system (a group of proteins in the blood involved in immune responses) is becoming recognized for its importance. Current studies do not suggest that the complement system plays a key role in the onset of the disease; however, its role in the progression of diabetic kidney disease and possibly in the occurrence of different forms of the disease has become evident. Hyperglycaemia increases the activity of certain complement proteins and activates specific pathways, while the hyperglycaemic environment also impairs the regulation of some proteins. Kidney biopsies of individuals with diabetic kidney disease have shown the presence of complement proteins in kidney tissue, and gene expression analyses have identified activation of complement-related genes.
The purpose of this study is to determine whether and to what extent activation of the complement system contributes to diabetic kidney disease and to define potential differences among different groups of individuals with diabetes. Additionally, the investigators aim to determine whether there is a connection between complement system activation and arterial function, as well as between complement system activation and the stage of kidney disease. The investigators will also investigate whether diabetes control influences complement system activation and whether previous kidney biopsy findings correspond with laboratory results.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 40 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •body mass index below 30 kg/m²
- •unknown macrovascular complications
- •treated with angiotensin-converting enzyme inhibitors or angiotensin receptor blockers at the highest tolerated dose
排除标准
- •a body mass index above 30 kg/m²
- •macrovascular complications
研究组 & 干预措施
Patients with type 1 diabetes without chronic kidney disease
The investigators will include male and female patients aged between 40 and 65 years, who have diagnosis of diabetes for at least 10 years and no more than 25 years, with a body mass index below 30 kg/m², and without known macrovascular complications (coronary artery, peripheral arterial, or cerebrovascular disease). All participants must be treated with angiotensin-converting enzyme inhibitors or angiotensin receptor blockers at the highest tolerated dose. Individuals without known chronic kidney disease must meet kidney function criteria with an estimated glomerular filtration rate (eGFR) ≥ 60 ml/min and a urine albumin-to-creatinine ratio (UACR) < 3 g/mol.
Patients with type 1 diabetes and chronic kidney disease
The investigators will include male and female patients aged between 40 and 65 years, who have diagnosis of diabetes for at least 10 years and no more than 25 years, with a body mass index below 30 kg/m², and without known macrovascular complications (coronary artery, peripheral arterial, or cerebrovascular disease). All participants must be treated with angiotensin-converting enzyme inhibitors or angiotensin receptor blockers at the highest tolerated dose. Individuals diagnosed with chronic kidney disease must meet the criteria of kidney function eGFR < 60 ml/min and UACR > 3 g/mol, or UACR > 30 g/mol regardless of eGFR.
Patients with type 2 diabetes and chronic kidney disease
The investigators will include male and female patients aged between 40 and 65 years, who have diagnosis of diabetes for at least 10 years and no more than 25 years, with a body mass index below 30 kg/m², and without known macrovascular complications (coronary artery, peripheral arterial, or cerebrovascular disease). All participants must be treated with angiotensin-converting enzyme inhibitors or angiotensin receptor blockers at the highest tolerated dose. Individuals diagnosed with chronic kidney disease must meet the criteria of kidney function eGFR < 60 ml/min and UACR > 3 g/mol, or UACR > 30 g/mol regardless of eGFR.
结局指标
主要结局
Level of complement system activation
时间窗: An additional visit to the diabetes outpatient clinic is planned within one year, where this will be determined.
The investigators will determine components of the complement system in blood and urine samples. * Blood parameters: * S compl. component C3: 0.6-1.3 g/L, ↓ consumpt.; ↑ inflam., * S compl. component C4: 0.1-0.3 g/L,↓ classical/lectin \| ↑ inflam., * S fact. B: 166-399 mg/L, ↓ AP (alter. path.) consumpt. \| ↑ AP act., * S fact. H: 380.6-674.9 mg/L, ↓ regul. \| ↑ compensation, * S fact. I: 21.2-42.1 mg/L, ↓ regul. \| ↑ compensation, * S soluble C5b-9 lytic complex (sC5b-9): 127-303 ng/mL, ↑ terminal compl., * S fact. B fragment Bb: 0.49-1.42 µg/mL, ↑ AP act., * S fact. H antibodies (anti-FH): \< 10 U/mL, ↑ AP dysreg., * S C1q antibodies (anti-C1q): \< 10 U/mL, ↑ classical pathway, * S C3a: man.ref., ↑ compl. act., * S C3c: man. ref., ↑ C3 breakdown, * S C5a: man. ref., ↑ strong act. * Urine parameter : * Urinary soluble C5b-9 lytic complex (sC5b-9): \< 30 ng/mL, ↑ renal compl. act. Expressed in different mass units (mg,g,µg,ng) or activity units (U) per volume units of blood serum (mL,L).
次要结局
- IMT thickness(An additional visit to the diabetes outpatient clinic is planned within one year, where the examination will be performed.)
- Carotid-femoral pulse wave velocity (PWV)(An additional visit to the diabetes outpatient clinic is planned within one year, where the examination will be performed.)
- Endothelial Function(An additional visit to the diabetes outpatient clinic is planned within one year, where the examination will be performed.)