Kidney Function in People With Cystic Fibrosis in the Era of HEMT
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 260
- 试验地点
- 6
- 主要终点
- Examine whether trajectories of eGFR (calculated from serum creatinine and cystatin C) correlate with urinary kidney injury signatures detected in different urine fractions, or urinary neutrophil levels/activation.
研究概览
简要总结
The purpose of this study is to find out what causes kidney disease in people with CF. The investigators will study biomarkers in the blood and urine that can either predict who is at risk or detect kidney damage early before it becomes permanent. The study will compare these markers in people with CF over time and during the treatment of lung flare-ups. It will also compare the blood and urine samples obtained from people without CF. The comparison aims to better understand the impact of cystic fibrosis and its treatment on the kidneys, as well as to develop improved methods for preventing, diagnosing, and treating kidney issues associated with CF.
详细描述
The prevalence of chronic kidney disease is significantly increased in patients with cystic fibrosis (PwCF) with a major impact on morbidity and medication tolerance as people age. Although expressed in both the proximal and distal tubules, the specific contribution of CFTR dysfunction to renal disease remains uncertain. PwCF often are exposed to renal toxins such as frequent aminoglycosides, systemic inflammation, and activated leukocytes, but it is unknown if CFTR dysfunction predisposes to amplified tubular injury. Conventional measures of kidney function, such as serum creatinine, are insensitive to detecting early injury, limiting an opportunity to prevent CKD. This study will address the gaps in early detection and mechanisms of renal dysfunction in CF. The investigators will define the triggers and targetable mechanistic pathways of kidney injury in CF and discover novel strategies for renal protection. The central hypothesis of this study is that CFTR dysfunction alters renal development and increases the inflammatory and fibrogenic responses to nephrotoxic stimuli.
The study involves prospective evaluation of biospecimens (blood and urine) and clinical data. The study analyzes biospecimens in CF outpatients (n=110), CF inpatients (n=110), and healthy subjects (n=40). In the outpatient cohort, biospecimens will be collected at the time of each routine care visit every 3 months for 24 months. PwCF admitted for intravenous (IV) antibiotics will have biospecimens collected on admission and 2/week thereafter during the admission, and then after hospital discharge at each subsequent clinical encounter for 24 months.
These biospecimens will be analyzed for biomarkers, fibrogenic analysis, inflammatory signals, and extracellular vesicles. Clinical data will be examined from chart review and correlated with biospecimen result.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 7 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Outpatient CF Cohort
- •Diagnoses of Cystic Fibrosis
- •Age > 30 years old
- •Able to provide informed consent
- •Inpatient CF Cohort
- •Diagnoses of Cystic Fibrosis
- •Age > 7 years old
- •Able to provide informed consent and assent (where applicable)
- •55 PwCF frequently hospitalized for a pulmonary exacerbation (>1 hospital admission in the prior 12 months)
- •55 PwCF sporadically hospitalized for a pulmonary exacerbation (no hospital admissions in the prior 12 months)
- •Able to provide urine sample independently
- •Healthy Controls
- •Healthy, as per participant self-report
- •Age between 30-50 years
- •Able to provide informed consent
排除标准
- •Outpatient CF Cohort
- •History of any organ transplant
- •History of immunodeficiency
- •Previous or current cancer diagnoses
- •Pregnant or breastfeeding
- •On chronic dialysis
- •Non-compliance (demonstrated by <2 visits during the 12 months before enrollment)
- •Inpatient CF Cohort
- •The initiation of intravenous antibiotic therapy after hospital admission before obtaining the first blood and urine sample
- •History of any organ transplant
- •History of immunodeficiency
- •Previous or current cancer diagnoses
- •Pregnant or breastfeeding
- •On chronic dialysis
- •Healthy Controls
- •History or current kidney disease, organ transplantation, cancer, or any other chronic illness
- •Current use of antibiotics
- •Urinary symptoms or UTI (dysuria, frequency, urgency)
- •Pregnant women
- •Menstruating on the study visit day
- •Blood relatives of PwCF
研究组 & 干预措施
Outpatient CF Cohort
Not hospitalized CF group: Diagnosis of CF, age >30 y, with ongoing care at one of the 3 CF Centers (Dartmouth, UAB, UVA).
Inpatient CF Cohort
Hospitalized CF cohort: Diagnosis of CF, age >7 y, being admitted for intravenous antibiotic treatment of pulmonary exacerbation.
Healthy Controls
Healthy Volunteers without CF
结局指标
主要结局
Examine whether trajectories of eGFR (calculated from serum creatinine and cystatin C) correlate with urinary kidney injury signatures detected in different urine fractions, or urinary neutrophil levels/activation.
时间窗: Enrollment and every 3 months for 24 months
Outpatient CF Cohort
Correlation between recurrent hospitalizations and urinary kidney injury signature.
时间窗: On admission before the initiation of intravenous antibiotic therapy, every 48 hrs during the hospitalization, after discharge at each subsequent routine CF care visit for 24 months.
Inpatient CF Cohort
Relationship between recurrent hospitalization and change in slope of eGFR
时间窗: On admission before the initiation of intravenous antibiotic therapy, every 48 hrs during the hospitalization, after discharge at each subsequent routine CF care visit for 24 months.
Inpatient CF Cohort
次要结局
- The correlation between changes in the urinary protein biomarker panel, neutrophil activation, and extracellular vesicles over time and eGFR.(Enrollment and every 3 months for 24 months.)
- Correlation between %FEV1 at admission or decline in %FEV1 and urinary kidney injury signature.(On admission before the initiation of intravenous antibiotic therapy, every 48 hrs during the hospitalization, after discharge at each subsequent routine CF care visit for 24 months.)
研究者
Agnieszka Swiatecka-Urban
Professor of Pediatrics
University of Virginia