ACE gene codes for Angiotensin-Converting Enzyme.
This enzyme is a part of the Renin-Angiotensin System, which is responsible for maintaining blood pressure, and fluid and salt balance in the body.
The enzyme cleaves the protein angiotensin I at a particular site, converting it into angiotensin II.
This angiotensin II brings about constriction of blood vessels, thereby increasing the blood pressure.
ACE gene is located on the long arm of chromosome 17.
Mutations in the ACE gene have been associated with a severe form of the renal disease called renal tubular dysgenesis.
As the name goes, ACE inhibitors are medications that slow down or inhibit the effects of angiotensin-converting enzyme (ACE).
Such medications are involved in relaxing the blood vessels and reducing blood pressure levels.
They are primarily used as anti-hypertensive drugs.
The ACE inhibitors prevent the angiotensin-converting enzyme from producing angiotensin II.
This reduces blood pressure and makes it easier for the heart to pump blood, thereby improving the functioning of the heart.
ACE inhibitors can be used to treat the following conditions:
Common examples of ACE inhibitors are:
Like any other medication, ACE inhibitors too, have a few side effects. But, most of them are not a cause of worry.
According to a study conducted by researchers in Australia, it was observed that ACE deficient mice weighed 20% lesser than the mice with ACE activity. It was also observed that the ACE deficient mice had 50% less body fat, especially around the belly area.
The results from this study have suggested that ACE inhibitors might help in weight loss around the mid-section in humans.
This, along with the other effects of ACE inhibitors, might be cardio-protective.
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ACE inhibitors are cardio and renoprotective.
They reduce systemic vascular resistance in patients with hypertension, chronic renal disease, and heart failure.
ACE inhibitors as we know by now cause a fall in the blood pressure.
Intrarenal efferent vasodilation is also observed along with a fall in the glomerular filtration pressure.
These events are said to be renoprotective.
However, when the glomerular filtration is critically dependent on the angiotensin II-mediated efferent vascular tone, giving ACE inhibitors to the patient can induce acute renal failure.
The systemic and renal hemodynamic consequences, both benefits and adverse effects, are brought about by the depletion of sodium.
Treating such patients with diuretics and ACE inhibitors, along with some sodium intake restrictions, can improve their therapeutic efficiency.
So, if the patients have a high risk of adverse renal effects to ACE inhibitors, their dosages should be titrated appropriately, and renal function and potassium levels should be closely monitored.
ACE inhibitors and beta-blockers are both classes of drugs that are used to treat hypertension.
Though their goal is the same, their mechanism of action is entirely different.
ACE inhibitors work by preventing the conversion of angiotensin I to angiotensin II.
Thus, they cause the relaxation of blood vessels and lower the blood pressure.
Beta-blockers, on the other hand, block epinephrine (adrenaline) and norepinephrine (noradrenaline) from binding to beta receptors on the nerves.
This reduces the heart rate and subsequently lowers blood pressure.
Both these classes of drugs have their side effects and drawbacks.
In most cases, a combination of one or more anti-hypertensive drugs is used to treat high blood pressure.
Hypertension is a widespread and highly prevalent lifestyle disease.
It is a medical term given for consistently high blood pressure over 120mm Hg systolic and 80mm Hg diastolic.
Hypertension is characterized by the flow of blood at high pressure against the walls of the blood vessels.
As a result, the workload of the blood vessels and the heart increases substantially.
Over a period of time, this force and friction on these tissues end up damaging them, and this can precipitate many conditions.
Some of them include:
Hypertension can be of two types: Primary and secondary.
When the rise in blood pressure levels is due to a non-identifiable cause, it is known as primary hypertension.
However, when there is an increase in the blood pressure levels due to an underlying condition, it is called secondary hypertension.
Some common causes of hypertension include:
Though hypertension is often silent, in some cases, the patient does show some symptoms. Like:
Individuals who are in the prehypertension stage can progress to the other stages if immediate action is not taken.
Untreated cases of hypertension can even be fatal.
One of the primary causes that result in hypertension is poor lifestyle choices, which includes an unhealthy diet.
So, to reduce the blood pressure levels and maintain it under the limit, certain dietary recommendations should be followed.
DASH diet is an acronym for Dietary Approaches to Hypertension diet.
The plan includes adopting a diet which includes fruits, vegetables, whole grains, low-fat dairy, nuts and seeds, legumes, fish, and poultry.
The most important aspect is to eat foods that are rich in potassium, calcium, magnesium, protein, and fiber and avoiding foods rich in sodium.
DASH diet is low salt and low sugar diet that does not allow the intake of desserts, sweetened drinks and beverages, red meat, and processed meats and fats.
The diet allows a maximum of 2000 calories a day, which includes:
In most cases of primary hypertension, blood pressure levels can be brought down by a combination of medications, dietary changes, regular exercise, and lifestyle modifications.
Once the blood pressure has been controlled, the individual can maintain his/her blood pressure levels within a reasonable range by living and eating healthy.
In many cases, a precautionary medication is advised to prevent the blood pressure from shooting up.
Our kidneys are responsible for water and salt regulation.
More the salt we consume, more the kidneys tend to retain water.
The increased water retention results in an increase in our systemic blood pressure.
This leads to increased pressure on the walls of many blood vessels, which may result in organ damage.
Of the many factors that can cause hypertension, the ACE gene also plays a role.
We know that the blood pressure in the body is controlled by the kidneys.
But, to be more specific, the Renin-Angiotensin System or RAS system is responsible for regulating it.
Some genetic variations are related to the RAS system, the most common one being the insertion/deletion polymorphism of the ACE gene.
So, essentially, the interactions between the ACE I/D polymorphism, sodium intake the RAS system determine your blood pressure and influence the risk of developing hypertension.
It was observed that the DD genotype of ACE and the TT genotype of ACE2 were significantly high in female hypertensives and the T allele of ACE2 was also linked to male hypertensives.[table “123” not found /]
SNP rs4308 is located on chromosome 17.
Presence of the A allele is responsible for the increase in the diastolic blood pressure.
This SNP locus also features as a target of anti-hypertensive drugs.
The ACE gene has been linked to athletic performance.
A genetic variation consisting of 287 DNA bases when inserted into the ACE gene causes a decrease in the ACE enzyme activity.
This version of the gene is called the ‘I’ version.
This variation is shown to be present in athletes, especially sprinters.
The presence of this insertion has been seen in many athletes who perform well in endurance sports such as wrestling, swimming, triathlons, etc.
Though the exact mechanism of how the ACE I gene contributes to fitness and athleticism is unknown, it probably has something to do with an increase in the heart rate, blood pressure, and muscle growth during training.
SNP rs4343 of the ACE gene has the ‘A’ and ‘G’ allele.
The A allele is associated with the insertion or I variation, whereas the G allele of the gene is associated with deletion or the D variation.
The G allele results in an increased risk of heart disease (GG) whereas, the minor A allele shows an increased association with endurance-based athletes.
SNP rs4343 has also recently been linked to susceptibility to migraine, where a G/G polymorphism was seen in patients with migraine with aura as compared to patients of migraine without aura.
|CHIP Version||VDR SNPs|
|23andMe (Use your 23andme raw data to know your ACE Variant)|
|V5 23andme (current chip)||Present|
|AncestryDNA (Use your ancestry DNA raw data to know your ACE Variant)|
|v1 ancestry DNA||Present|
|V2 ancestry DNA (current chip)||Present|
|Family Tree DNA (Use your FTDNA raw data to know your ACE Variant)|
|OmniExpress microarray chip||Present|