What Is Saffron? Pricing, Origin, Health Effects
What You Should Know About Hyperlipidemia
Hyperlipidemia is a medical term for abnormally high levels of fats (lipids) in the blood, which include cholesterol and triglycerides. You can inherit it or develop it from lifestyle factors, including diet and too little physical activity.
The most common type of hyperlipidemia is high cholesterol. Other forms of hyperlipidemia include hypertriglyceridemia and mixed hyperlipidemia, in which both cholesterol and triglyceride levels are high.
Hyperlipidemia is very common, especially in modern developed countries. It's also increasing around the world.
In the United States, 94 million people over age 20 have elevated total cholesterol levels. This amounts to about 50 percent of all U.S. Adults.
People with untreated hyperlipidemia are twice as likely to develop coronary artery disease (CAD) as those with cholesterol levels in the normal range. This can lead to clogged arteries, which can trigger heart attack, stroke, or other serious problems.
Hyperlipidemia is usually quite manageable, though, and these emergency events can often be avoided. The key is an early diagnosis and treatment plan to prevent its progression.
Understanding cholesterolCholesterol is a fatty substance that travels through your bloodstream on proteins called lipoproteins.
When you have too much cholesterol in your blood, it can build up on the walls of your blood vessels and form plaque. Over time, plaque deposits grow larger and begin to clog up your arteries. This may lead to:
There are two types of cholesterol, LDL and HDL. You've probably heard them called "bad" and "good" cholesterol, respectively.
LDL ("bad") cholesterol builds up in your artery walls, making them hard and narrow. HDL ("good") cholesterol cleans up excess "bad" cholesterol and moves it away from the arteries, back to your liver.
Hyperlipidemia is an imbalance of cholesterol in your blood caused by a combination of having too much LDL cholesterol and not enough HDL cholesterol to clear it up.
There are two main classifications of hyperlipidemia: familial and acquired. The familial type stems from genes you inherit from your parents.
The acquired type is the result of:
Acquired hyperlipidemia is most often the result of certain lifestyle factors. It may also result from medications you take or underlying health conditions.
Lifestyle causes of hyperlipidemiaLifestyle factors can raise "bad" cholesterol levels and lower "good" cholesterol levels.
According to the American Heart Association, the main lifestyle choices that raise your chances of developing high cholesterol levels include:
Certain health conditions can also contribute to high cholesterol levels, including:
Other inherited conditions and pregnancy may also contribute to high cholesterol.
Medications that contribute to hyperlipidemiaYour cholesterol levels may sometimes be affected by certain medications, such as:
Beta-blockers rarely affect cholesterol levels, and often not enough to merit stopping the medications.
Familial combined hyperlipidemiaFamilial combined hyperlipidemia (or mixed hyperlipidemia) is a type that you can inherit from your parents or grandparents. It causes high cholesterol and high triglyceride levels.
People with familial combined hyperlipidemia often develop high cholesterol or high triglyceride levels in their teens and receive a diagnosis in their 20s or 30s. This condition increases chances of early coronary artery disease and heart attack.
Unlike people with typical hyperlipidemia, people with familial combined hyperlipidemia may experience symptoms of cardiovascular disease early in life, such as:
Hyperlipidemia usually does not show symptoms until it has advanced to the state where people have emergency complications, such as a heart attack or stroke. These can occur when high cholesterol has led to plaque buildup in your arteries that limits or blocks the flow of blood.
A simple blood test will let you and your doctor know your blood cholesterol levels.
The 2018 guidelines published in the Journal of the American College of Cardiology (JACC) propose that a total blood cholesterol level above 240 milligrams per deciliter (mg/dL) is considered high, while levels above 200 mg/dl are considered elevated. This can vary based on many factors, however.
The CDC recommends that generally, you should get a cholesterol test starting at the age of 20, then:
Sometimes, tests are appropriate for children and adolescents. The CDC points out that 1 in 5 adolescents have high cholesterol in the United States.
Check with your doctor about a cholesterol test for your child if:
Hyperlipidemia has no symptoms, so the only way to detect it is to have your doctor request a blood test called a lipid panel or a lipid profile. Your doctor will use your lipid panel to make a hyperlipidemia diagnosis.
This test determines your cholesterol levels. A healthcare professional will take a sample of your blood and send it to a lab for testing, then get back to you with a full report. Your report will show your levels of:
Your doctor may ask you to fast for 8 to 12 hours before getting your blood drawn. That means you'll need to avoid eating or drinking anything other than water during that time. However, recent studies suggest that fasting isn't always necessary, so follow your doctor's instructions.
Safe levels of cholesterol can vary from person to person depending on health history and current health concerns and are best determined with your doctor.
Lifestyle changes are the first line of treatment for hyperlipidemia. If these are insufficient, your doctor may prescribe medications to help manage your high cholesterol.
Lifestyle changesLifestyle changes are often key to managing hyperlipidemia at home. Even if your hyperlipidemia is inherited (familial combined hyperlipidemia), lifestyle changes are still an essential part of treatment.
These changes alone may be enough to reduce your risk of complications like heart disease and stroke.
If you're already taking medications to manage hyperlipidemia, lifestyle changes can improve their cholesterol-lowering effects.
Eat a heart healthy dietMaking changes to your diet can lower your LDL cholesterol levels and increase your HDL cholesterol levels. Here are a few changes you can make:
If you have high body weight or obesity, losing weight may help lower your total cholesterol levels.
Losing weight starts with figuring out how many calories you're taking in and how many you're burning. For a typical adult, it takes cutting 3,500 calories from your diet to lose about a pound.
You don't have to start this process alone, though. You can work with a doctor or registered dietitian to create an eating plan that works for you, along with increasing physical activity so you're burning more calories than you're eating.
Get active, if you canPhysical activity is important for overall health, weight loss, and cholesterol levels. When you aren't getting enough physical activity, your HDL cholesterol levels go down. This means there isn't enough "good" cholesterol to carry the "bad" cholesterol away from your arteries.
You only need 40 minutes of moderate to vigorous exercise 3 or 4 times a week to lower your total cholesterol levels. The goal should be 150 minutes of total exercise each week.
This can look like anything you enjoy doing, but some of the following can help you add exercise to your daily routine:
Smoking lowers your "good" cholesterol levels and raises your triglycerides. Even if you haven't been diagnosed with hyperlipidemia, smoking can increase your risk of heart disease.
Talk with your doctor about quitting, or try the nicotine patch. Nicotine patches are available at the pharmacy without a prescription.
MedicationsIf lifestyle changes aren't enough to treat your hyperlipidemia, your doctor may prescribe medication.
Statins are the first line medication for hyperlipidemia. If you cannot tolerate statins or if they do not reduce your LDL cholesterol enough, mRNA and monoclonal antibody drugs have been developed recently.
Common cholesterol- and triglyceride-lowering medications include:
New medications for high cholesterolInclisiran
Inclisiran is a new drug using mRNA technology. It has been approved in Europe but not yet in the United States.
Clinical trials in 2020 showed the drug could cut levels of LDL cholesterol by 50 percent in people who are either intolerant or resistant to standard statin medications.
Inclisiran is the pioneer cholesterol drug in what's called "small interfering RNA therapy." This is a type of drug that blocks, or interferes with, the function of an RNA messenger (mRNA). An mRNA is a molecule that carries code for making a particular protein.
In the case of Inclisiran, the drug blocks, or interferes with, the production of an enzyme called PCSK9 (proprotein convertase subtilisin kexin type 9). This enzyme causes problems with the LDL receptors in the liver that are necessary for the uptake of LDL cholesterol by liver cells.
By blocking PCSK9 activity, Inclisiran helps the body reduce the amount of LDL cholesterol. The drug is intended for hyperlipidemia treatment in adults whose high LDL cholesterol persists even while they're on a maximum tolerated dose of statin therapy.
Bempedoic acid (Nexlitol) and ezetimibe (Nexlizet)
The two drugs Nexlitol and Nexlizet, approved by the FDA in 2020, are the first new non-statin cholesterol drugs approved by the FDA since 2002.
Nexlitol contains bempedoic acid, which has been shown in clinical trials to inhibit cholesterol. It's designed to be taken in combination with the maximum tolerable dosage of statins.
Nexlizet contains ezetimibe, which lowers cholesterol by preventing the body from absorbing cholesterol from foods. It's also designed to be taken along with statins.
Both Nexlitol and Nexlizet can cause serious side effects. Your doctor can help you decide if one of these drugs would benefit your treatment plan.
Alirocumab (Praluent)
Praluent (alirocumab) was approved by the FDA in 2021 as an add-on treatment for familial hypercholesterolemia. This is a genetic condition that causes severely high cholesterol.
Praluent was originally approved by the FDA in 2015 for treating heart disease and primary inherited hyperlipidemia. It was then the first PCSK9 inhibitor approved by the FDA.
PCSK9 inhibitor drugs work by attaching to the PCSK9 gene to prevent it from degrading LDL receptors in the liver that help lower LDL cholesterol in the body. This differs from the new mRNA drug Inclirisan, in that inhibitors attach to the PCSK9 gene, whereas the mRNA drug prevents PCSK9 from being produced.
Alirocumab, the active drug in Praluent, is a monoclonal antibody. This is a protein synthesized in a laboratory that behaves like antibodies made by the human body.
Praluent comes as a liquid solution in a prefilled pen. You deliver it as an injection every 2 to 4 weeks, which can be done at home. It has a number of reported possible side effects, so be sure to discuss with your doctor whether it would suit your treatment plan.
You can make changes to your lifestyle to prevent high cholesterol or reduce your risk of developing hyperlipidemia:
You may want to try a heart healthy eating plan like the Mediterranean diet, which includes a lot of the nutritious foods mentioned above.
People with untreated hyperlipidemia have double the risk of developing coronary heart disease as those with normal-range cholesterol levels. Coronary heart disease can lead to heart attack, stroke, or other serious problems.
Hyperlipidemia is very treatable, however, and complications can often be avoided.
You may be able to prevent complications and manage hyperlipidemia by making lifestyle choices, like:
If lifestyle choices are not sufficient, you can talk with your doctor about adding medications such as statins to help bring your cholesterol and triglycerides down to healthy levels.
Hyperlipidemia And Cerebral Small-vessel Disease
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Leys, D. Et al. White matter changes in stroke patients. Relationship with stroke subtype and outcome. Eur. Neurol. 42, 67–75 (1999).
Laloux, P., Galanti, L. & Jamart, J. Lipids in ischemic stroke subtypes. Acta Neurol. Belg. 104, 13–19 (2004).
Bejot, Y. Et al. Ischaemic stroke subtypes and associated risk factors: a French population based study. J. Neurol. Neurosurg. Psychiatry 79, 1344–1348 (2008).
Olsen, T. S., Christensen, R. H., Kammersgaard, L. P. & Andersen, K. K. Higher total serum cholesterol levels are associated with less severe strokes and lower all-cause mortality: ten-year follow-up of ischemic strokes in the Copenhagen Stroke Study. Stroke 38, 2646–2651 (2007).
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White, H. Et al. Ischemic stroke subtype incidence among whites, blacks, and Hispanics: the Northern Manhattan Study. Circulation 111, 1327–1331 (2005).
Pomegranate's Power: Studies Show Promise In Cardiovascular And Diabetic Health
In a recent review published in Nutrients, researchers reviewed existing data on the bio-modulatory effects of pomegranate (Punica granatum l., PG) polyphenols on metabolic disorders.
Study: The Modulatory Bioeffects of Pomegranate (Punica granatum L.) Polyphenols on Metabolic Disorders: Understanding Their Preventive Role against Metabolic Syndrome. Image Credit: azeraijan _stockers/Shutterstock.Com BackgroundPomegranate, a natural nutrient, has long been used to treat bacterial infections, diabetes, obesity, and other metabolic disorders. However, there have been concerns expressed concerning the side effects of pharmacological therapies such as anti-obesity medications and insulin-sensitizing medicines. Modern research supports the health-promoting advantages of polyphenol-rich natural products and diets, including antibacterial, anti-diabetic, anti-obesity, and atheroprotective qualities.
About the reviewIn the present review, researchers examined the pharmacokinetic characteristics, safety, and bioavailability of PG compounds in preventing metabolic disorders such as type 2 diabetes, obesity, dyslipidemia, and cardiovascular-related diseases.
Prevention of metabolic disorders by PG consumptionPG is a plant that can reduce insulin resistance, cytokine levels, redox gene expression, blood pressure increase, vascular damage, and lipoprotein oxidative alterations. PG-ellagitannins have been demonstrated in studies to be beneficial in lowering hyperlipidemia, raising plasma high-density lipoprotein cholesterol (HDL-C), and improving total cholesterol (TC)/HDL-C and low-density lipoprotein cholesterol (LDL-C)/HDL-C ratios. Since obesity is reversible, nutritional interventions can restore metabolic equilibrium and prevent the development of obesity-related diseases.
In C57Bl/J6 mice, dietary treatment with pomegranate seed oil reduced fat mass and body weight while enhancing insulin sensitivity in peripheral tissues. These findings support prior findings of a considerable decrease in lipid indicators, including plasma TC concentration, triglyceride content, and total cholesterol/high-density lipoprotein cholesterol ratio. Lipid metabolism-associated enzymes, such as carnitine palmitoyltransferase-1 (CPT 1) and acyl-CoA oxidase (AOX), and nuclear receptors like the peroxisome proliferator-activated receptor-alpha (PPAR-α) favorably affect PG floral components.
Studies have reported weight reductions after consuming PG extracts for 30 days. However, contradicting results concerning food intake and gain in weight have been documented. The reported discrepancies may be explained by altered physiologic responses to phytochemicals resulting from genetic variances.
Traditional medicine is considering PG polyphenols for their anti-diabetic properties. PG may exert its effects via a variety of mechanisms, including PPAR-γ activity modulation, protein degradation resistance, adiponectin gene expression, inhibition of β-glucosidase enzymatic activities, glucose transporter protein type-4 (Glut-4) messenger ribonucleic acid (mRNA) expression, and β-mass regeneration.
Short-term therapy with PG peel extract can lower α-amylase activity, blood glucose levels, and lipid peroxidation. Studies have indicated that PG intake can improve plasma HDL-C concentrations in hyperlipidemia patients and control lipid parameters in dyslipidemic individuals with type 2 diabetes.
Pharmacokinetics, pharmacodynamics, and safety of ellagitannin constituents of PG compoundsPunicic acid, a PG compound, has been found to have potential health advantages. Several factors, including the physicochemical properties of the molecules and individual-specific factors, including microbiota makeup and gut pH, regulate the bioavailability and absorption capacities of the compound. The ability of urolithins to produce and absorb urolithins varies greatly, with punicalagin being detected at a maximum concentration (C-max) of 30 g/mL in rats fed a diet containing six percent punicalagin.
In body tissues, urolithin accumulates in the colon and prostate, with a restricted ability to reach organs such as the liver and kidney. The biochemical qualities of organ cells, such as their selective properties and permeability, the overall structure of the ellagitannins (ET) molecule, and individual variances in blood transport efficiency, may all impact the dispersion and deposition capacities of PG ellagitannins.
Although traditional medicine literature supports the use of PG and its potential to improve health outcomes, several toxicological studies have revealed cellular component modification and nuclear damage following PG administration.
In vitro and in vivo toxicological studies of PG seed oil, a high source of punicic acid, found that it is neither mutagenic nor clastogenic. The post-mortem examinations revealed no cellular abnormalities, and 4.3 g/kg/day of PG intake produced no harm. The use of PG or pure PG compounds appears safe, with adverse effects predicted at dosages far higher than those seen in traditional ethnomedicine treatments and now employed for therapeutic purposes.
ConclusionOverall, the review findings showed that PG consumption may help prevent metabolic disorders such as hyperglycemia and hyperlipidemia; however, clinical and pharmacokinetic studies are inconsistent due to factors like plant part selection, cultivar, geographical region, bioclimatic and soil characteristics, plasma bioavailability, organ accessibility, and nutrigenomics considerations. Irrespective of these variations, the medicinal efficacy of PG in treating metabolic syndrome components necessitates multifaceted treatment approaches.
Journal reference:
Alami, M.; Boumezough, K.; Khalil, A.; Ramchoun, M.; Boulbaroud, S.; Fulop, T.; Morvaridzadeh, M.; Berrougui, H. The Modulatory Bioeffects of Pomegranate (Punica granatum L.) Polyphenols on Metabolic Disorders: Understanding Their Preventive Role against Metabolic Syndrome, Nutrients, 2023, 15, 4879. Doi:https:// doi.Org/10.3390/nu15234879 https://www.Mdpi.Com/2072-6643/15/23/4879
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