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Low serum haemolytic function of the fourth complement component (C4) in insulin dependent diabetes
G Senaldi1, B A Millward, M J Hussain
1Department of Immunology, King's College School of Medicine and Dentistry, London.
Journal of Clinical Pathology
|October 1, 1988
Summary
Low serum concentrations of the fourth component of complement (C4) are linked to insulin-dependent diabetes. Impaired C4 function and concentration in diabetics suggest a potential genetic predisposition to the disease.
Area of Science:
- Immunology
- Endocrinology
- Genetics
Background:
- Low serum concentrations of the fourth component of complement (C4) are observed in insulin-dependent diabetes mellitus (IDDM).
- These low C4 levels may play a role in the disease's etiology.
- The functional capacity of C4 in IDDM requires further investigation.
Purpose of the Study:
- To investigate whether the function of C4 is impaired in individuals with IDDM.
- To compare C4 function and concentration in IDDM patients, non-IDDM patients, and healthy controls.
- To explore the role of C4 in the genetic predisposition to IDDM using discordant monozygotic twins.
Main Methods:
- Radial immune hemolytic assay was used to measure C4 hemolytic activity (function).
- Laser nephelometry was employed to determine C4 concentration.
- Study included 34 IDDM patients, 15 non-IDDM patients, 20 healthy subjects, and 12 discordant monozygotic twin pairs.
Main Results:
- Both C4 function and concentration were significantly lower in IDDM patients compared to non-IDDM patients and healthy controls.
- C4 function and concentration were also reduced in both diabetic and non-diabetic twins compared to controls.
- A strong correlation was observed between C4 function and concentration in both diabetic and non-diabetic twins.
Conclusions:
- Defects in both C4 function and concentration are evident in insulin-dependent diabetes.
- The presence of these defects in non-diabetic co-twins suggests a potential genetic predisposition to IDDM.
- C4 deficiency may represent a heritable risk factor for developing insulin-dependent diabetes.