Treatment FAQ

what treatment options exist for fh

by Valentine Sawayn Published 3 years ago Updated 2 years ago
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The most common treatment for FH is statin drug therapy. Statin drugs work by blocking an enzyme that produces cholesterol in the liver and increases your body's ability to remove cholesterol from the blood. They can lower your LDL cholesterol levels by 50 percent or more.

Medication

FH Treatments. Statins. These medications block the production of cholesterol in the liver and make the liver use cholesterol from your bloodstream, thereby reducing ... Cholesterol Absorption Inhibitor (Ezetimibe) Bile Acid Sequestrants. PCSK9 Inhibitors. Bempedoic Acid.

Self-care

Oct 30, 2014 · Treatment Guidelines. Early detection and treatment of FH is recommended to reduce risk of cardiovascular events. The goal of treatment is to reduce LDL-C by 50 % from baseline levels.[] This was based on two trials which showed reduction in CIMT (Carotid Intimal Medial Thickness) in patients who achieved > 50 % reduction of LDL-C on statin therapy.[10,11] …

Nutrition

Dec 29, 2021 · At baseline, the mean LDLc in the homozygous FH patients was 336 mg/dL, and this was reduced 50% after 26 weeks of treatment (P < 0.0001). [ 38 ] A literature review by Liu et al reported that in...

What are the treatment options for homozygous familial hypercholesterolemia (FH)?

Abstract. Even though statins represent the mainstay of treatment of heterozygous familial hypercholesterolemia (FH), their low-density lipoprotein cholesterol (LDL-C) lowering efficacy is finite and most patients with FH will not achieve LDL-C targets with statin monotherapy. Addition of ezetimibe with or without bile acid sequestrants will ...

Why do I need to take statins for FH?

Rosuvastatin (Crestor) Atorvastatin (Lipitor) Pitavastatin (Livalo) Simvastatin (Zocor)

What is the typical US diet for FH?

Nov 08, 2020 · Familial hypercholesterolemia can be inherited from one parent (heterozygous FH), or, in rare instances, from both (homozygous FH). People with this rarer form of FH can have very high LDL cholesterol levels. Some may need bypass surgeries before adulthood. Without treatment, people with homozygous FH rarely live into their 20s. Diagnosing FH

How can I lower my LDL cholesterol with familial hypercholesterolemia?

Apheresis For FH An acute reduction in LDL cholesterol of ≥70% on average during each procedure. An interval mean LDL cholesterol <6.5 mmol/l (or decreases of >65% from baseline values off all treatment). A baseline level of LDL cholesterol <8.5 mmol/l (or decreases of >55%, respectively from baseline values off all treatment).

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What lifestyle changes are recommended for FH?

Eating the right foods to lower cholesterol, exercising regularly, not smoking, controlling your weight and getting medical treatment can help you limit the impact of FH on your heart health.Nov 29, 2014

Can FH be cured?

There isn't a cure for FH but it can be treated. Treatment can reduce your risk of getting heart disease, having a heart attack or stroke, or needing other treatment. If you or your child is diagnosed with FH, speak with your doctor about the best treatment plan.

What is the best treatment for hypercholesterolemia?

Statins are usually the first hypercholesterolemia treatment used. Statins help reduce LDL levels by blocking a specific enzyme that's necessary to produce cholesterol. Along with lowering LDL cholesterol, statins help prevent hardening of the arteries, which reduces the chances of a heart attack or stroke.Jun 30, 2017

Can I live a long life with FH?

Life expectancy with FH is lower without treatment, but the sooner you receive a correct diagnosis and start medication, the better your outlook and life expectancy. FH is inherited from one or both of your parents and requires treatment with medication to lower your LDL cholesterol.Oct 28, 2020

Is hypercholesterolemia reversible?

Hyperlipidemia is treatable, but it's often a life-long condition. You'll need to watch what you eat and also exercise regularly. You might need to take a prescription medication, too.Jul 16, 2020

How do statins help people with FH?

Statins are first line pharmacologic therapy agents in the treatment of FH; they reduce cardiovascular mortality even in receptor-negative patients. [22] Current guidelines recommend maximal statin therapy to reduce LDL-C levels by at least 50 % from baseline.Nov 11, 2014

Are statins the best treatment for hypercholesterolemia?

Statins are the best drugs to lower LDL cholesterol. Statins also have benefits above and beyond cholesterol lowering.Nov 13, 2013

What do fibrates do?

Fibrates are medicines prescribed to help lower high triglyceride levels. Triglycerides are a type of fat in your blood. Fibrates also may help raise your HDL (good) cholesterol. High triglycerides along with low HDL cholesterol increase the risk of heart disease and stroke.Jan 27, 2020

What foods can help with familial hypercholesterolemia?

Good sources include oats, peas, beans, apples, citrus fruits and carrots. Increasing physical activity. Maintaining a healthy body weight. With familial hypercholesterolemia, your doctor likely will also recommend that you take medication to help lower your LDL cholesterol levels.

What is the best treatment for high cholesterol in children?

Diet and exercise are the best initial treatment for children age 2 and older who have high cholesterol, or who are obese. Children age 10 and older might be prescribed cholesterol-lowering drugs, such as statins, if they have extremely high cholesterol levels.

What medications can lower triglycerides?

If you also have high triglycerides, your doctor may prescribe: 1 Fibrates. The medications fenofibrate (Tricor) and gemfibrozil (Lopid) decrease triglycerides by reducing your liver's production of very-low-density lipoprotein (VLDL) cholesterol and by speeding up the removal of triglycerides from your blood. VLDL cholesterol contains mostly triglycerides. 2 Niacin. Niacin (Niaspan) decreases triglycerides by limiting your liver's ability to produce LDL and VLDL cholesterol. But niacin doesn't usually provide any additional benefit than using statins alone. Niacin has also been linked to liver damage and stroke, so most doctors now recommend it only for people who can't take statins. 3 Omega-3 fatty acid supplements. Omega-3 fatty acid supplements can help lower your triglycerides. They are available by prescription or over-the-counter. If you choose to take over-the-counter supplements, get your doctor's OK first. Omega-3 fatty acid supplements could affect other medications you're taking.

What is the best medicine for high triglycerides?

If you also have high triglycerides, your doctor may prescribe: Fibrates. The medications fenofibrate (Tricor) and gemfibrozil (Lopid) decrease triglycerides by reducing your liver's production of very-low-density lipoprotein (VLDL) cholesterol and by speeding up the removal of triglycerides from your blood.

What is the drug that helps reduce cholesterol?

Cholesterol absorption inhibitors. Your small intestine absorbs the cholesterol from your diet and releases it into your bloodstream. The drug ezetimibe (Zetia) helps reduce blood cholesterol by limiting the absorption of dietary cholesterol. Zetia can be used in combination with any of the statin drugs.

When was alirocumab approved?

Alirocumab (Praluent) gained FDA approval in April 2021 for adjunctive use with other LDLc-lowering therapies in the treatment of homozygous FH. Approval was based on the ODYSSEY HoFH trial, which found alirocumab to be associated with significant LDLc reductions in patients with the disease. [ 37] Lomitapide.

Is dietary restriction important for hypercholesterolemia?

The NCEP recommendations for the dietary management of hypercholesterolemia are not highly restrictive, but a more stringent regimen may have a greater impact on lipid levels (see Table 2). Restricting total fat is less important than reducing the intake of saturated fat, trans fat, and cholesterol.

What is the best medication for FH?

The most common type of medication are statins, a class of drugs known as HMG-CoA reductase inhibitors. Statins block a key enzyme in the liver that is responsible for producing cholesterol.

When does a child start treatment for hypercholesterolemia?

Typically children with high LDL cholesterol from FH start treatment at 8 to 10 years of age.

Where is the symptom of FH?

One symptom is cholesterol deposits in the Achilles tendons or the tendons of the hands or elbows. People with FH can also develop cholesterol deposits in other places, such as around the eyes. Familial hypercholesterolemia is often diagnosed based on a combination of physical exam findings and lab results, as well as personal and family history. ...

What is the FH in blood?

Familial hypercholesterolemia (FH) is an inherited defect in how the body recycles LDL (bad) cholesterol. As a result, LDL levels in the blood remain very high – in severe cases, levels can reach above 190 milligrams per deciliter (mg/dL) of blood.

What is the treatment for high LDL cholesterol?

People with extremely high LDL cholesterol, such as those with homozygous familial hypercholesterolemia, may need to undergo a treatment called LDL apheresis.

What is the best way to remove cholesterol from the blood?

This is a dialysis-like procedure that’s done every few weeks to remove cholesterol from the blood. Another class of lipid-lowering medications, bile acid sequestrants (such as cholestyramine or colesevelam), may also be used. These drugs reduce the amount of cholesterol absorbed by the intestines.

How many people have FH?

One in about 200 adults have the FH genetic mutation. Including children, FH affects about 1.3 million in the U.S. But only about 10% are aware they have it. If left untreated, people with FH typically develop coronary heart disease.

How early can you get FH?

Men with FH get coronary heart disease up to 10 to 20 years earlier. Half of men with untreated FH will have a heart attack or angina before they turn 50. For some it will be as early as their 20s. In women, coronary heart disease appears up to 20 to 30 years earlier.

When should a family member get tested for FH?

If one person in a family has FH, all first-degree relatives – parents, siblings, children – should be checked for it. Similarly, if someone in a family has an early heart attack, it’s a good idea for other family members to get tested. Children with increased risk for FH should be screened beginning at age 2.

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