Pilot Project: The Amplicon and Metatranscriptomic Study of Intra and Extra Intestinal Microbiome in Non-infectious Uveitis Disease

University of Indonesia (UI)

Status: Unknown

Conditions: Vogt-Koyanagi-Harada Disease; Posterior Uveitis; Behçet Disease; Noninfectious Panuveitis; Intermediate Uveitis; Autoimmune Uveitis; Anterior Uveitis Idiopathic; Idiopathic Uveitis

Study type: Observational

Funder types: Other

Identifiers

NCT04126850

19-05-0624

Details and patient eligibility

About

This study aimed to discover the composition on the microbiome in several sites of the human body; and to find out the difference in microbiome composition on ocular fluid, blood, and feces before and after therapy in uveitis patient with history of autoimmune disease (Behcet and Vogt-Koyanagi-Harada) and idiopathic uveitis

Full description

Gut microbiome has been widely studied around the globe, and it is convinced that the gut microbiome plays an essential role in many human diseases. In a published review showed the presence of microbes in blood from a patient who suffered from non-communicable disease. The microbes present in dormant or not-immediately-culturable states as if blood is a 'sterile' environment. It was argued that the difficulty of culturing microbes from the blood was coming from the limited understanding of suitable growth/isolation media for the microbes to be cultured. This limitation can be overcome by the sequenced-based methods for detecting non-proliferating microbes. The presence of microbes in blood also can be observed by ultrastructural (microscopic) methods. Through the microscopic observations, it was witnessing the presence of coccus and bacillus shaped bacteria that present proximity to (Red Blood Cell) RBCs in sample blood patients with Alzheimer's or Parkinson's Disease. The presence of microbes in the places other than their normal location state by term 'atopobiosis'. The presence of microbes in blood suspected as a result of translocation between the gut to the blood.

Therefore, according to the current knowledge of microbiome association and the human diseases, we are eager to conduct a pilot project that gives a comprehensive picture of the association between the microbiome and uveitis disease partially non-infectious and idiopathic uveitis. We will investigate microbiome profiling in the intestinal and extra-intestinal of uveitis patients before and after treatment to see whether any alteration of microbial abundance at two distinct clinical conditions partially in uveitis patients with history of autoimmune disease (Behcet and Vogt-Koyanagi-Harada) and idiopathic uveitis. Another objective of this study is to explore any pathogenic microorganism that present in uveitis patients samples conducted by a sequenced-based method.

Enrollment: 10 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• New patient registered at Cipto Mangunkusumo Hospital since November 2019

• Patient diagnosed with non-infectious uveitis (with Behcet, VKH history)

• Patient idiopathic uveitis (proven to have negative result by available etiological uveitis work-ups)

• Minimum age: 18 years old

• Experience active inflammation in the past 180 days and or during patient registration following Standard Uveitis Nomenclature (SUN) guidelines, in at least:

  • equal and or more than 2+ anterior chamber cells
  • equal and or more than 2+ vitreous haze and/or
  • active retinal/choroidal lesions

Exclusion criteria

• patients had taken probiotics supplement or antibiotics 3 months before sample collection
• or who experience prolonged diarrhea or constipation
• or undergone gastrointestinal surgery
• having any form of malignancy
• having a systemic disease such as hypertension, obesity, inflammatory bowel disease, or diabetes.
• Disagree to sign informed consent
• Uveitis is proven to be an infectious origin
• Pregnant patient
• Loss to follow up patient

Healthy volunteers are recruited for this study after giving consent with the following inclusion criteria:

• age: 18-50 years old (Man/Woman)
• having no health complaints or symptoms
• not in any long term medications
• having no history of allergy
• willing to cooperate in the study
• state of complete physical, mental and social well being