Hydroxychloroquine Sulfate Alleviates Persistent Proteinuria in IgA Nephropathy
- Conditions
- Primary IgA Nephropathy
- Interventions
- Registration Number
- NCT02765594
- Lead Sponsor
- Peking Union Medical College Hospital
- Brief Summary
Immunoglobulin A nephropathy (IgAN) is the most common primary glomerulonephritis in the world.There is to date no curative therapy for patients with IgAN.It is considered that dendritic cells, Toll-like receptor (TLR) 9 and cytokines interleukin-6 (IL-6), and interferon-alpha (IFN-a) and tumor necrosis factor-alpha (TNF-α), play an important role in the aberrant mucosal response. Hydroxychloroquine is an antimalarial agent and had a notable impact on immune activation by the reduction of circulating activated immune cells that including decreased TLR-expressing cells, reduced IFN-secreting plasmacytoid dendritic cells, reduced production of inflammatory cytokines including interferon alpha, IL-6 and TNF alpha. Recent studies showed hydroxychloroquine had a benefit for renal remission and could retard the onset of renal damage in patients with lupus nephritis. hydroxychloroquine may have the potential effect in IgA nephropathy, alleviated the proteinuria and had the renal protect effect. This will be a single center, prospective, randomized, controlled study to assess the utility of hydroxychloroquine in IgAN patients.
- Detailed Description
Immunoglobulin A nephropathy (IgAN) is the most common primary glomerulonephritis in the world. Its estimated frequency is at least 2.5 cases per year per 100,000 adults. The glomerulopathy usually progressed slowly leading to end stage renal disease (ESRD). ESRD developed in 20%-40% of patients after 20 years. Given its complex and as yet incompletely understood pathogenetic mechanisms, there is to date no curative therapy for patients with IgAN.
Although pathogenesis of IgAN is still obscure, underglycosylated IgA-containing immune-complex including IgG or IgA antibodies against the hinge region of IgA1 are key factors for IgA nephropathy. Aberrant mucosal immune response might lead to increased production of underglycosylated IgA1. It is considered that dendritic cells, Toll-like receptor (TLR)9, and cytokines interleukin-6 (IL-6), , interferon-alpha (IFN-a) and tumor necrosis factor-alpha (TNF-α), play an important role in the aberrant mucosal response.
Hydroxychloroquine is an antimalarial agent and had a notable impact on immune activation by the reduction of circulating activated immune cells that including decreased TLR-expressing cells, reduced IFN-secreting plasmacytoid dendritic cells, reduced production of inflammatory cytokines including interferon alpha, IL-6 and TNF alpha. Recent studies showed hydroxychloroquine had a benefit for renal remission and could retard the onset of renal damage in patients with lupus nephritis.
Therefore, hydroxychloroquine, targeting dendritic cells, TLR, IL-6, IFN-α and TNF-α，may have the potential effect in IgA nephropathy, alleviated the proteinuria and had the renal protect effect. This will be a single center, prospective, randomized, controlled study to assess the utility of hydroxychloroquine added to valsartan in IgAN patients.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 98
- biopsy proven primary IgA nephropathy
- age 18-60 years
- proteinuria range from 0.5 to 1.5g/d
- serum creatinine ≤132.6μmol/L
- normal blood pressure or blood pressure ≤130/80 mmHg in patients with hypertension
- Hypersensitivity to chloroquine or to hydroxychloroquine
- blood pressure <90/60 mm Hg
- pregnancy and breastfeeding women
- renal artery stenosis
- Rapidly progressive renal insufficiency
- systemic lupus erythematosus or other connective tissue diseases
- Henoch- schoenlein purpura
- other nephritis
- diabetes mellitus
- retinopathy
- other contraindication of hydroxychloroquine
- severe hepatic insufficiency
- G6PD deficiency
- psoriasis or porphyria
- malignant hypertension
- viral hepatitis or other infections
- treatment with steroids or cytotoxic drugs during the previous three months
- psychiatric disorder
- not suitable for the study judged by investigator
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description valsartan only:control group Valsartan valsartan (160mg/d) hydroxychloroquine with valsartan:study group Hydroxychloroquine Sulfate valsartan (160mg/d) and Hydroxychloroquine Sulfate ( 400mg/d, twice daily) hydroxychloroquine with valsartan:study group Valsartan valsartan (160mg/d) and Hydroxychloroquine Sulfate ( 400mg/d, twice daily)
- Primary Outcome Measures
Name Time Method Incidence of Remission (Complete [CR] or Partial [PR]) at Week 24 24 weeks CR: proteinuria \<0.3 g/24 hr with no worsening of renal function (\<15% estimated glomerular filtration rate(eGFR) reduction from Baseline).PR: proteinuria \<3.5g/24 hrs but ≥0.3g/24 hrs and a decrease of \>50% from Baseline based on 24 hours pooled urine, with no worsening of renal function(\<15% eGFR reduction from Baseline). eGFR at Baseline will be defined as the Day 0 values.
- Secondary Outcome Measures
Name Time Method Change from Baseline in Proteinuria Levels at the Indicated Time Points Baseline and Weeks 4, 12, 24 Proteinuria is being assessed at Weeks 0, 4, 12, 24 follow-up visits. Proteinuria is based on 24 hours pooled urine. Baseline is defined as the Day 0 values. The ratio is defined as the post-Baseline value divided by the Baseline value.
Change from Baseline in Serum IgA Levels at the Indicated Time Points Baseline and Weeks 4, 12, 24 IgA levels in serum are being analyzed at Weeks 0, 4, 12, 24 follow-up visits. Baseline is defined as the Day 0 value. The ratio is defined as the post-Baseline value divided by the Baseline value.
Change from Baseline in Serum Creatinine Levels at the Indicated Time Points Baseline and Weeks 4, 12, 24 Serum creatinine is being assessed at Weeks 0, 4, 12, 24 follow-up visits. Baseline is defined as the Day 0 values. The ratio is defined as the post-Baseline value divided by the Baseline value.
Change from Baseline in eGFR at the Indicated Time Points Baseline and Weeks 4, 12, 24 eGFR is being assessed from levels of creatinine using the 4 variable version of the modification of diet in renal disease (MDRD) equation as recommended by national kidney foundation-chronic kidney disease (NKF-CKD) guidelines. eGFR is calculated at Weeks 0, 4, 12, 24 follow-up visits. Baseline is defined as the Day 0 values. The ratio is defined as the post-Baseline value divided by the Baseline value.
Change from Baseline in Serum Interleukin-6 Levels at the Indicated Time Points Baseline and Weeks 4, 12, 24 Interleukin-6 levels in serum are being analyzed at Weeks 0, 4, 12, 24 follow-up visits by means of enzyme linked immunosorbent assay (ELISA). Baseline is defined as the Day 0 value. The ratio is defined as the post-Baseline value divided by the Baseline value.
Change from Baseline in Serum Tumor Necrosis Factor alpha Levels at the Indicated Time Points Baseline and Weeks 4, 12, 24 Tumor necrosis factor alpha levels in serum are being analyzed at Weeks 0, 4, 12, 24 follow-up visits by means of enzyme linked immunosorbent assay (ELISA). Baseline is defined as the Day 0 value. The ratio is defined as the post-Baseline value divided by the Baseline value.
Adverse Effects at the Indicated Time Points Weeks 4, 12, 24 Change from Baseline in Serum Interferon alfa Levels at the Indicated Time Points Baseline and Weeks 4, 12, 24 Interferon alfa levels in serum are being analyzed at Weeks 0, 4, 12, 24 follow-up visits by means of enzyme linked immunosorbent assay (ELISA). Baseline is defined as the Day 0 value. The ratio is defined as the post-Baseline value divided by the Baseline value.
Trial Locations
- Locations (1)
Peing Union Medical College Hospital
🇨🇳Beijing, China