Answer:
Thanks for you question. Your hypothesis suggests a linear relationship between serum Cholesterol levels and MI. This hypothesis seems to ignore the difference in the prevalence and effectiveness of LDL receptors in the FH patient.
FH patients who have inherited the mutation from both parents have very few LDL receptors in their blood and therefore almost no ability to pass the unused Cholesterol through the liver. FH patients who are heterozygous will have more LDL receptors although both will find Cholesterol removal problematic without the addition of a PCSK9 inhibitor.
In short, your hypothesis need to account for other factors that are in play.
Explanation:
Consider my case. I am a 64 year old male who has Heterozygous Familial Hypercholesterolemia. Before treatment at age 12 my Total cholesterol was 510 mg/dl. My genetic testing shows two mutations to the LDL Receptor gene with only one mutation being pathogenic. My first heart attack was at 47 and first stroke at 62. My current LDL is too low to detect with the use of a PCSK9 inhibitor (Repatha®).
Answer:
Yes
Explanation:
Males have two x chromosomes (xx) and females have one x and one y chromosome (xy)
They are thread-like structures on the surfave of roots that absorb water and nutrients.
1. You can build Earthquake resistant buildings- These are built with deep foundations. From rubber absorbers to concrete reinforced with steel.
2.Earthquake drill- They do this in Japan. and they basically practise what to do in the event of an actual earthquake happening
3. you can also be prepared. Have extra food and water.
