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 Here are some important information for your kind consideration, which will give you additional information to diagnose

 

 1.               Coronary Heart Disease (CAD)

 2.               Ischemic heart disease  (IHD)

 3.               Assessment of the effectiveness of pharmacological             treatment with lipid lowering Drugs

 

using latest diagnostic techniques available in laboratory medicine.  The information provided will be useful for your reference.


  Diagnostic Relevance of Apo A1 and Apo B Measurement:

 

·        Apolipoproteins A1 is the major protein of HDL and Apolipoprotein B is the main part of LDL, but also present on VLDL and Intermediate Density Lipoproteins (IDL).  Each of the three particle classes LDL, IDL and VLDL carries exactly one molecule of Apo B per particle, the latter is a measure for the total number of LDL, IDL and VLDL.

 

·        The liver secrets a Triglyceride rich lipoprotein, VLDL, which by the removal of the most of its Triglycerides is converted to a smaller Cholesterol rich Lipoprotein, LDL.  The biological Half Life of an LDL particle is at least 9 times longer than that of a VLDL particle and, therefore, there are always 9 times more LDL particles than VLDL  particles.  Because each VLDL and LDL particles contains one molecule of Apo B, measuring plasma Apo B measures exactly the total number of VLDL and LDL particles, that is 90%  of which is LDL.    

 

·        As LDL particles differ substantially from one another in the amount of cholesterol they contain, Total and LDL cholesterol are imprecise measure the number of Apo B particles.  Therefore measuring Apo B, provides a direct estimate of the total number of atherogenic particles

 

·        Apo B measurement can be performed on non-fasting samples.

 

·         Elevated Apo B levels were associated with an increased risk, independent of the LDL particle size as per the study conducted by Dr. Benoit Lamarche, Dr.Ande Tchernof and Dr. Bernard Cantin  on 2103 men initially free of IHD, among whom 114developed IHD during a 5 years follow up period.  These 114 case patients were matched with health control subjects for age, body mass index, smoking habits and alcohol intake.  The study found that individuals having both elevated Apo B levels and Small LDL particles showed the increase in IHD risk by 6 folds. The study found that among lipids, lipoproteins and apolipoprotein variables, Apo B individually and Apo B:Apo A1 ratio is the best and only significant predictor of IHD.

 

·        The Quebec Cardiovascular study found that Apo B concentration was the best metabolic predictor of IHD risk.

 

·        The study suggests that prevention and treatment of IHD should only be focused on reducing the number of LDL+VLDL+IDL particles, that is Apo B concentration rather than altering the size of the particles.

 

·        The study by Dr. Judith F Lynch and Dr. Michella D Marshell in Australian children, of 6992 (3501 boys and 3491 girls) aged 5-13 years, between 1991-1995 showed that Indian children had the highest levels of Apo B and Apo B:Apo A1 ratio.  This suggests that, when the food habits and life style is altered or changes the Apo B gets elevated and Indians are prone to retain additional Cholesterol in their body.

 

·        As per Dr. N. Sahi and Dr. G. S. Salinani, Apo A1 and Apo B ratio has emerged as a better predictor of angiographically assessed coronary artery disease.  In 17.3% of cardiac population, the levels of HDL cholesterol and LDL cholesterol were considered to be normal, the Apo B:ApoA1 ratio was increased, as per the study conducted in Jeslok Hospital, Mumbai.       

 


Suggestions:

 

 1.                  Why should we not measure Apo A1 and Apo B in routine practice if it improves the prediction of risk and the outcome?

 2.                If statin therapy is chosen, the evidence described, suggests that only Apo B need to be measured in follow up.  That is, care would be simpler for the patient, in that, fasting is not necessary and simpler for the physician in that only one result, and not all the 5, need to be considered and tested on.  Simpler care would translate into more cost effective care.

 3.                Please note, we would emphasize that we are proposing modification, not abolition, of the present system.  Apo A1 and Apo B should not be the only parameter measured in the initial assessment of the risk of disease due too lipids.

 


 Conclusion:

 

                Given the importance that has been assigned to Cholesterol, change will not be easy in the initial periods.  But however, we shall have the regular Cholesterol testing for a period of time with Apo A1 and Apo B in the lipid profile.  Change is the price of progress.

                Given the potential for benefit for our patients and our society, we hope the Apo A1 and Apo B testing will prove the case.  

 


 How to introduce these tests for your patients?

 

a      Apo A1 and Apo B testing reagents costs only Rs 20/- each in your Hospital’s Laboratory.

 

a      You shall ask your laboratory to add Rs 100/- extra for the lipoid profile and ask your laboratory to do Apo A1 and Apo B in the lipid profile.

That is: If the charges for Lipid Profile is Rs 350/- you shall make it to Rs  450/- including Apo A1 and Apo B.


As discussed in detail for the past 5 minutes we believe that Apo A1 and Apo B testing will be a better marker of the risk due to the atherogenic lipoproteins namely LDL, IDL and VLDL.

 

Your Hospital Laboratory, as you are very much aware, is fully equipped to include these tests for your patients.

 

Please leave your comments below, about the change – the progress – you believe to make and mail back to [email protected]

 

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