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Assays / Hormones
/ Adiponectin (serum)
Introduction
White adipose tissue can elaborate a variety of molecules with
paracrine and endocrine actions of proven or potential relevance
to body weight and fuel metabolism. Most abundant of these secreted
proteins is adiponectin, a multimeric hormone with homology to complement
factor 1q that circulates in adults at levels that are inversely
related to the total WAT mass. Circulating levels of adiponectin
have been shown to correlate negatively with insulin sensitivity
in a wide range of human populations and to be elevated on treatment
with thiazolidinediones, and low adiponectin levels have been shown
to identify those at future risk of type 2 diabetes and vascular
disease.
Because of the stability and long half life of adiponectin it may
be used as a marker of insulin resistance in situations where assay
of insulin is impossible or difficult to interpret (e.g. in the
non fasting state).
In severe insulin resistance adiponectin is generally very low.
An exception is states of acquired or genetic loss of insulin receptor
function, in which adiponectin is high. This can be used to direct
subsequent investigations.
Clinical Indications
1. Diagnosis of Insulin Receptor Dysfunction in Severe Insulin
Resistance.
Genetic defects of the insulin receptor, or antibodies directed
against the insulin receptor, give rise to a minority of cases of
severe insulin resistance. Identification of causative mutations
in the insulin receptor gene permits pre-emptive screening of other
family members, and also allows antenatal diagnosis where desired,
while detection of anti-insulin receptor antibodies permits specific
immunomodulatory treatments directed against the causative antibodies.
However the insulin receptor gene is a large gene, and detection
of insulin receptor antibodies is onerous, making screening of all
severely insulin resistant patients impossible. Use of serum adiponectin
to refine the pre-test probability of loss of insulin receptor function
(an adiponectin level below 5 mg/l in the context of severe insulin
resistance has a 97% negative predictive value for insulin receptor
mutation or antibodies, while a level above 5mg/l has an 82% positive
predictive value for insulin receptor dysfunction) permits directed
screening with a high likelihood of a positive result, and should
be part of the routine work up of patients with severe insulin resistance.
2. Use as a marker of insulin resistance and vascular risk
The long half life of adiponectin and its strong correlation with
insulin sensitivity means that it is a useful marker of insulin
resistance as well as vascular risk. This is likely to be increasingly
exploited in routine clinical practice.
Method Information
2-site time resolved fluorescence immunoassay (DELFIA)
Patient Preparation
No special requirements
Sample Requirements
0.5mls of serum, EDTA or Lithium heparin anti-coagulated plasma
Sample Handling
Separate with 1 hour and freeze. Send frozen.
Interpretation
Appropriate Gender, Age and BMI related Reference range data will
be provided
Reference Ranges:
| 90TH CENTILE / (mg/L) |
MALE |
FEMALE |
| BMI <25 |
2.6-12.6 |
4.4-17.7 |
| BMI 25-30 |
2.4-10.6 |
3.5-15.5 |
| BMI 30-35 |
2.8-9.9 |
2.6-14.9 |
Quality Assessment
No EQA scheme available
Centres offering this assay
Cambridge
References
Lara-Castro C, Fu Y, Chung BH, Garvey WT. Adiponectin and the metabolic
syndrome: mechanisms mediating risk for metabolic and cardiovascular
disease. Curr Opin Lipidol. 2007 Jun;18(3):263-70.
Semple RK, Halberg NH, Burling K, Soos MA, Schraw T, Luan J, Cochran
EK, Dunger DB, Wareham NJ, Scherer PE, Gorden P, O'Rahilly S. Paradoxical
elevation of high-molecular weight adiponectin in acquired extreme
insulin resistance due to insulin receptor antibodies. Diabetes.
2007 Jun;56(6):1712-7.
Hemmila I, Dakubu S, Mukkala V-M, Siitari H & Lovgren T: Europium
as a label in time-resolved immunofluoroimmunometric assay. Anal.
Biochem. 137, 335-343 (1984)
Suonpaa M, Merkela E, Stahlberg T & Hemmila I: Europium-labelled
Streptavidin as a highly sensitive universal label. J. Immunol.
Meth. 149, 247-253 (1992)
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