
What Is Choline? An Essential Nutrient With Many Benefits
Choline was only acknowledged as a required nutrient by the Institute of Medicine in 1998. Although your body makes some choline naturally, you need to get it from your diet to avoid a deficiency.
Many people are not meeting the recommended intake for this nutrient.
This article provides everything you need to know about choline, including what it is and why you need it.
What is choline?
Choline is an essential nutrient. This means it's required for normal bodily function and human health. Though your liver can make small amounts, you must obtain the majority through your diet.
Choline is an organic, water-soluble compound. It is neither a vitamin nor a mineral.
However, it is often grouped with the vitamin B complex due to its similarities. In fact, this nutrient affects a number of vital bodily functions.
It impacts liver function, healthy brain development, muscle movement, your nervous system and metabolism.
Therefore, adequate amounts are needed for optimal health.
Serves many functions in your body
Choline plays an important part in many processes in your body, including:
Cell structure: It is needed to make fats that support the structural integrity of cell membranes.
Cell messaging: It is involved in the production of compounds that act as cell messengers.
Fat transport and metabolism: It is essential for making a substance required for removing cholesterol from your liver. Inadequate choline may result in fat and cholesterol buildup in your liver.
DNA synthesis: Choline and other vitamins, such as B12 and folate, help with a process that's important for DNA synthesis.
A healthy nervous system: This nutrient is required to make acetylcholine, an important neurotransmitter. It's involved in memory, muscle movement, regulating heartbeat and other basic functions.
How much do you need?
Due to a lack of available evidence, a Reference Daily Allowance (RDA) for choline has not been determined.
However, the Institute of Medicine has set a value for adequate intake (AI).
This value is intended to be sufficient for most healthy people, helping them avoid negative consequences of deficiency, such as liver damage.
Nevertheless, requirements differ according to age, gender, and genetic makeup.
In addition, determining choline intake is difficult because its presence in various foods is relatively unknown.
Here are the recommended AI values of choline for different age groups:
0–6 months: 125 mg per day
7–12 months: 150 mg per day
1–3 years: 200 mg per day
4–8 years: 250 mg per day
9–13 years: 375 mg per day
14–18 years: 400 mg per day for females and 550 mg per day for males
Adult females: 425 mg per day
Adult males: 550 mg per day
People breastfeeding: 550 mg per day
Pregnant people: 430 mg per day
Deficiency is unhealthy but rare
Choline deficiency can cause harm, especially for your liver.
One small, older study in 57 adults found that 77% of men, 80% of postmenopausal women and 44% of premenopausal women developed fatty liver and/or muscle damage after going on a choline-deficient diet.
Another older study noted that when postmenopausal women consumed a diet deficient in choline, 73% developed liver or muscle dysfunction.
However, these symptoms disappeared once they began getting enough choline.
Choline is especially important during pregnancy, as a low intake may raise the risk of neural tube defects in unborn babies.
Another older study determined that a higher dietary intake around the time of conception was associated with a lower risk of neural tube defects.
In addition, low choline intake may raise your risk of other pregnancy complications. These include preeclampsia, premature birth and low birth weight.
Top dietary sources
Choline can be obtained from a variety of foods and supplements.
Food sources
Dietary sources are generally in the form of phosphatidylcholine from lecithin, a type of fat-like molecule found in lecithin.
The richest dietary sources of choline include:
Food Portion Amount of choline contained (mg)
Pan-fried beef liver 1 slice (3 ounces or 85 grams) 356
Hardboiled eggs 1 large egg 147
Lean braised beef top round 3 ounces or 85 grams 117
Roasted soybeans Half a cup 107
Roasted chicken breast 3 ounces or 85 grams 72
Cooked fresh cod 3 ounces or 85 grams 71
Baked red potatoes with skin 1 large potato 57
Canned kidney beans Half a cup 45
Additives and supplements
Soy lecithin is a widely used food additive that contains choline. Therefore, it is likely that extra choline is consumed through the diet via food additives.
Some additive and supplemental forms of chlorine include:
lecithin
phosphatidylcholine
choline chloride
CDP-choline
alpha-GPC
betaine
Some sources claim that choline in nutritional supplements may reduce body fat, but there is little to no evidence supporting these claims.
Impact on heart health
Elevated levels of homocysteine in your blood have been linked to an increased risk of heart disease and strokes, as well as lower blood pressure. However, evidence is mixed, and more studies are needed to confirm any positive link.
Choline helps convert the amino acid homocysteine to methionine. Therefore, a deficiency of choline can result in an accumulation of homocysteine in your blood.
Impact on your brain
Choline is required to produce acetylcholine, a neurotransmitter that plays an important role in regulating memory, mood and intelligence.
It's also needed for the process that synthesizes DNA, which is important for brain function and development.
Therefore, choline intake is associated with improvements in brain function and cognitive performance.
Observational studies link higher choline intake to better brain function and a lower risk of dementia and Alzheimer's disease.
However, further studies on this subject are needed to better understand whether choline supplementation would affect cognitive function.
Too much can be harmful
Consuming too much choline has been associated with unpleasant and potentially harmful side effects.
These include drops in blood pressure, sweating, fishy body odor, diarrhea, nausea and vomiting.
The daily upper limit for adults is 3,500 mg per day. This is the highest level of intake that is unlikely to cause harm.
It is very unlikely that someone could ingest this amount from food alone. It would be almost impossible to reach this level without taking supplements in large doses.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
Yahoo
21 minutes ago
- Yahoo
FDA Approves Insmed's Drug As First Treatment For Type Of Chronic Lung Disease
The U.S. Food and Drug Administration (FDA) on Tuesday approved Insmed Incorporated's (NASDAQ:INSM) Brinsupri (brensocatib 10 mg and 25 mg tablets). It is an oral, once-daily treatment for non-cystic fibrosis bronchiectasis (NCFB) in adults and children 12 years and older. Brinsupri is the first and only FDA-approved treatment for NCFB, a chronic lung condition characterized by permanently widened and damaged airways (bronchi), leading to persistent mucus production, recurrent infections, and difficulty breathing. There are approximately 500,000 people in the U.S. diagnosed with NCFB. The approval is based on data from the Phase 3 ASPEN and Phase 2 WILLOW ASPEN, patients taking Brinsupri 10 mg or 25 mg had a 21.1% and 19.4% reduction in the annual rate of exacerbations, respectively, as compared to placebo. Both dosage strengths of Brinsupri also met several exacerbation-related secondary endpoints, including significantly prolonging the time to first exacerbation and significantly increasing the proportion of patients remaining exacerbation-free over the treatment period. Patients who received Brinsupri 25 mg experienced a statistically significantly less decline in lung function, as measured by forced expiratory volume in one second (FEV₁) after using a bronchodilator, at week 52. The safety profile for adult patients with NCFB in WILLOW was generally similar to ASPEN, except for a higher incidence of gingival and periodontal adverse reactions in WILLOW. In parallel, applications for brensocatib with the European Medicines Agency (EMA) and the Medicines and Healthcare products Regulatory Agency (MHRA) have been accepted, and the company plans to file in Japan in 2025. Commercial launches are anticipated in 2026, pending approval in each territory. Price Action: INSM stock is up 6.20% at $119.89 at the last check on Tuesday. Read Next:Photo: Shutterstock UNLOCKED: 5 NEW TRADES EVERY WEEK. Click now to get top trade ideas daily, plus unlimited access to cutting-edge tools and strategies to gain an edge in the markets. Get the latest stock analysis from Benzinga? INSMED (INSM): Free Stock Analysis Report This article FDA Approves Insmed's Drug As First Treatment For Type Of Chronic Lung Disease originally appeared on © 2025 Benzinga does not provide investment advice. All rights reserved. Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data
Yahoo
21 minutes ago
- Yahoo
What to say and do if your child comes out as trans
"Is it a boy or a girl?" expectant parents are often asked. Some even hold a gender reveal party, where a popped balloon might release blue or pink confetti, depending on the baby's sex. But sex isn't the same as gender. Just because someone is assigned, on the basis of their physical characteristics, the sex of male or female at birth, doesn't mean they'll later identify with their biological status. Their gender identity may be different, as gender is a social construct. A transgender person is someone who doesn't, or doesn't fully, identify with the sex they were assigned at birth. Some identify as male or female, others as non-binary - that is, neither exclusively male nor female, or as no gender at all. If a child comes out as transgender - often shortened to "trans" - or non-binary, parents may be out of their depth and not know how best to handle the situation. Ulrich Ritzer-Sachs, a counsellor with Germany's Federal Conference for Child Guidance Counselling (bke), offers some tips: How should you react on learning your child doesn't identify with their assigned sex? Ritzer-Sachs: Stay calm, listen to your child, take them seriously and give them a hug. Taking your child in your arms is always the best thing you can do. You should also consider whether you're ready and able to talk about the matter right away. You may be flummoxed at first and need some time, in which case it's OK to say, "It's great that you're telling me this. Why don't we find another time so that we can talk about it at length?" But then you really must find the time, since it's such an important issue. You can't just discuss it while, say, you're cooking dinner or have just 10 minutes to spare. How can you help your child's gender identity formation if you're not well informed about the subject or aren't comfortable with it? Ritzer-Sachs: You should take your child really seriously and address the subject together. Find out, educate yourself about it and talk to experts. You can find specialized advice centres that are well versed [in transgenderism]. The current state of research says it's wise to accept children and adolescents in their development, whether or not it's as you envisioned it would be. The thinking is that they'll be able to grow up better having found their true gender identity, and live a much happier life if it's not suppressed. No one has to go through this alone. If you're unsure what to say or how to act, it's sometimes a good idea to get professional advice independently of your child, who, after all, has already grappled with the issue and given it a lot of thought before coming out to you. So it's perfectly all right for you to first get clarity, because no matter how equanimous and liberal-minded you are, it's a big challenge and not easy for anyone. Go to an advice centre and ask all the questions rushing through your mind, including those that may be difficult for your child. One concern of parents is that their child could face problems in school or elsewhere on account of not everyone accepting their gender identity. Are there ways you can protect your child? Ritzer-Sachs: That kind of support starts a lot earlier, namely by raising your child to be as self-confident as possible in all areas. You want to help them be able to deal with setbacks as well as successes. You can prepare them for intolerant people they'll come across who may make fun of them. There will always be people who make stupid comments - you've got to let them bounce off. You can't protect your child from this, as it's fairly certain to happen. But it happens in many areas and is part of life. You always have to look at the situation individually. What does your child need? Can they handle it? Can they steer clear of such people? Do you have to speak with the school or peer group? It is always a balancing act, between how much you can bear your child's difficult confrontations, and how much you get involved yourself. I don't think it's any different from going against other norms. The norm is always what the majority does - that doesn't mean it's right or wrong. You can explain this to your child in a way that is appropriate for their age. I wouldn't say, "If you do this, then expect X, Y or Z," but you can imply it. And when the time comes, you can still work together to see what you can do to get through it. Solve the daily Crossword


Medscape
22 minutes ago
- Medscape
Does This Side Effect Spell Doom for the GLP-1's?
This transcript has been edited for clarity. Welcome to Impact Factor , your weekly dose of commentary on a new medical study. I'm Dr F. Perry Wilson from the Yale School of Medicine. About a year ago, I was talking to one of my friends about the slew of studies showing very broad benefits of the GLP-1 receptor agonists, such as semaglutide (Ozempic) and tirzepatide (Mounjaro). including weight loss and improved diabetes control. But studies also showed improved heart and kidney health, as well as lower overall mortality. Some analyses found reductions in problem drinking, smoking, and even compulsive shopping among people taking these drugs. I told my friend that I thought these drugs were complete game changers, fundamentally 'anticonsumption' agents that are the cure for society's primary ill of overconsumption. 'Yeah, but what about the side effects?' he said. I said, 'Sure, some gastrointestinal issues can come up, but usually it's not that bad.' Still, I demurred, 'It's early days; perhaps after 10 years on the drugs your eyes fall out or something.' This week's study doesn't suggest that GLP-1's cause your eyes to fall out exactly, but, as you'll see in a second, it's not that far off. We're talking about this study, ' Semaglutide or Tirzepatide and Optic Nerve and Visual Pathway Disorders in Type 2 Diabetes,' appearing in JAMA Network Open , which looks at eye problems in people taking the two most potent GLP-1 drugs. This was a huge retrospective cohort study using the TrinetX database, which contains electronic health record data on millions of patients across the United States. Researchers identified more than a million individuals with diabetes in the database who had no history of eye disease. They then identified when they were first prescribed Ozempic, Mounjaro, or a bunch of non-GLP-1 diabetes medications (such as insulin and metformin) which serve as controls here. They were on the lookout for conditions that some smaller studies had suggested might be associated with the weight-loss drugs: disorders of the optic nerve — in particular, a rather rare condition that can occur even outside diabetes, known as non-arteritic anterior ischemic optic neuropathy (NAION). This is a syndrome caused by a decline in blood supply to the optic nerve and is characterized by the sudden and painless loss of eyesight in one eye, which can lead to permanent blindness. It seems straightforward to ask which group — those who got the GLP-1 drugs or those who took other diabetes drugs — had more eye problems. But you probably suspect that these two groups weren't exactly comparable even before they started the drug. People who took weight-loss drugs were younger, more likely to be female, more likely to be on antihypertensive drugs, more likely to have a history of sleep apnea, and much more likely to have obesity. This is a classic apples-vs-oranges problem in observational research, one that was overcome, in this case, through a form of statistical wizardry called propensity score matching. In this process, each patient is assigned a likelihood of being prescribed the weight-loss drug, and then they are matched with someone with similar propensities. Thus, only one of each pair actually received the drug. Naturally, not everyone was matched; the apples and oranges that were just too appley or orangey were dropped from further analysis. After matching, the two groups were much more similar. Now that we have two similar groups — one of orangish apples and the other of appley oranges — we can compare the rates of NAION between them. Of 79,699 individuals started on either Ozempic or Mounjaro, 35 developed NAION within 2 years of follow-up. Of 79,699 started on non-GLP-1 diabetes drugs, 19 developed NAION over a similar duration of follow-up. That's 0.04% compared with 0.02%. There are a couple of ways to look at the data. On the relative scale, we see nearly a doubling of the risk for this eyesight-threatening disorder among people taking GLP-1 drugs. But on the absolute scale, any given individual's chance of actually getting this disorder is vanishingly small; the rate in the GLP-1 group was 462 per million individuals, compared with a baseline rate of about 238 per million individuals. Identifying rare risks like this is still important, especially for drugs that are as widely prescribed as the GLP-1's. Patients and providers need to have this in the back of their minds so that, if an unusual eye symptom does develop, everyone can react quickly. It's still not clear how these drugs could lead to NAION. It's true that the optic nerve has GLP-1 receptors on it, so this could be a direct drug effect. But the researchers suggest other possibilities as well, including the idea that sudden metabolic changes associated with weight loss or glucose effects from the drugs may change the microenvironment of the eye. I hate to fall back on 'more research is necessary,' but the truth is, more research is necessary to figure out how this works and, importantly, who is most at risk. I should remind you that this study shows us correlation, not causation. Even with propensity score matching, there will still be differences between the comparison groups that aren't fully accounted for. Beyond that, the very fact that people may be on alert for eye disorders among those taking GLP-1's may become something of a self-fulfilling prophecy in a study like this. If physicians are primed to think of a rare diagnosis like NAION when they see a patient on a GLP-1 drug, they might be more likely to make the diagnosis than they would if presented with exactly the same symptoms in someone not taking the drug. When the outcome is rare like this, minor biases can drive the results. So, I'm not ready to go back on my statement that these drugs are game changers. They clearly are. But we'd be naive to assume that there wouldn't be some risk. I'm encouraged that this particular risk is not nearly of a magnitude and frequency to counteract the obvious benefits of the drugs. In the end, this is one of those knowledge-is-power things. I don't think we'll see enthusiasm dampen for the GLP-1 drugs because of NAION, but it doesn't hurt for any of us — patients or providers — to be aware of it.