Updated: 3/29/2023
For 30 percent of people with chronic Lyme disease, disulfiram is a game changer. While disulfiram has been historically used to treat people with alcoholism, ground-breaking research from Jayakumar Rajadas, PhD’s Stanford University lab in 2016 showed disulfiram kills persister and growing forms of Lyme germs. Based on Dr. Rajada’s research, disulfiram is being repurposed as a Lyme antibiotic.
In alcoholism, disulfiram prevents the breakdown of a toxic alcohol by-product called acetaldehyde. As acetaldehyde builds up, it makes a person sick with severe abdominal pains and even headaches. In alcoholism, a person takes this medicine daily to prevent them from drinking out of fear it will cause severe illness if they drink alcohol.
In Lyme disease, we do not know the mechanism of how disulfiram works. However, we do know in the laboratory that it kills Lyme persisters and is moderately effective at treating growing Lyme, too. We also theorize that it breaks up biofilm slime layers that protect the germs.
Lyme exists in two growth states. One state is replicating growing Lyme. The other is a hibernating (persister) state. A persister germ slows its metabolism way down and ignores the world around it, including regular antibiotics and the immune system. Also, in a persister state the germ forms cover themselves in biofilms to hide from the immune system.
One reason some people with Lyme do not recover is regular antibiotics may only treat the growth state of Lyme. Experiments published in 2016 from Kim Lewis, PhD’ lab at Northeastern University showed that 20 percent of Lyme spirochetes and 20 percent of Lyme cyst forms assume the persister growth state when they are exposed to continuous antibiotics.
To be clear, Lyme has two extracellular forms and two growth states. The extracellular forms are spirochetes and cysts. These spirochetes and cysts are either growing or hibernating (persisters). Lyme also has an L-form that lives in cells. The L-form does not have a covering. It is not clear if disulfiram works on L-forms inside of cells.
The pioneer of treating Lyme disease with disulfiram is Ken Liegner, MD. In 2019, he published a case study of three patients showing success using disulfiram. In 2020, he went further and published a paper documenting his outcomes treating nearly 70 patients. His data and experience is similar to what I see in my practice. Dr. Liegner’s review of his patients’ charts shows:
The overwhelming majority of Dr. Liegner’s patients use no other antibiotics while they are on disulfiram. It probably goes without saying that his patients had already been on numerous antibiotics in the past.
Even if a person cannot reach the target dose, in my experience many get benefit by staying at a dose they can tolerate for at least four months
I use disulfiram in patients who do not fully recover after using prolonged antibiotics targeting growing Lyme for two years or more. One reason these patients may not recover is that persister forms of the Lyme germ develop that are missed by regular antibiotics. In these patients, I use disulfiram alone. For some of these patients, if they do not respond to disulfiram alone, I am also using antibiotics that target growing forms of the Lyme germ better than disulfiram. You can read about these antibiotics in A Lyme Disease Antibiotic Guide.
Based on my experience and laboratory experiments from Ying Zhang, MD’s lab at Johns Hopkins University, disulfiram does not work for persister Bartonella. Read Kills Bartonella: A Brief Guide for approaches to persister Bartonella.
Disulfiram can treat growing Babesia, but since I find it to be a weaker agent, I prefer other treatment approaches. See Kills Babesia: A Brief Guide for Babesia treatments.
At this point, based on Dr. Liegner’s data and my own clinical experience treating patients, disulfiram should not be used alone as the first antibiotic a patient takes to treat Lyme. There are a number of reasons I say this.
For more information about these other persister options, see How to Treat Persister Lyme & Bartonella.
We have no data to suggest disulfiram is effective for an acute tick bite, and I do not use it in this situation. For more information, see How to Treat Acute Tick Bites.
Intestinal yeast can produce acetaldehyde. As I discussed previously, disulfiram blocks the breakdown of acetaldehyde, which is why it is used to treat alcoholics. If acetaldehyde builds up, it leads to severe abdominal pain, headaches, nausea, and more. Before starting disulfiram, it is important to see if someone has yeast overgrowth in the intestines. If they do, then the yeast should be treated first. For more information about diagnosing and treating yeast, see A Silent Problem - Is It Yeast? and Kills & Prevents Yeast: A Brief Guide.
An average treatment length for disulfiram is eight months. Disulfiram triggers a large Herxheimer reaction in many people. Because of this, the medicine is started low and slow, gradually working to a target dose. It can take up to four months to reach the target dose in many patients. Once a person reaches the target dose, or a lower dose they can tolerate, they stay at that dose for four months.
The target dose for disulfiram is based on your weight. If a person can tolerate it, I try to reach 4-5 mg/kg a day. To figure out how many kilograms you weigh, divide your weight in pounds by 2.2. Here is the calculation of the target dose for a person weighing 150 pounds:
For this weight, I choose a target dose of 312.5 mg which is halfway between 4 and 5 mg/kg. Disulfiram is manufactured as a 250 mg and 500 mg pill. It is also compounded as a 62.5 mg pill. One and ¼ 250 mg pill or five of the 62.5 mg pills equal 312.5 mg.
I usually start patients at 62.5 mg every third day for 10 days, then I advance to 62.5 mg every other day for 10 days, then to 62.5 mg 1 time a day. Based on the response in the first month, I decide how rapidly I will increase the dose from there.
If a person has a very sensitive stomach with symptoms like nausea, I will have the capsule compounded and put into an enteric-coated pill. These pills deliver the disulfiram to the small intestines without breakdown of the medicine in the acid of the stomach. If I use enteric-coated pills, I adjust the above target and starting doses by a factor of 2.6. This means if my target dose is 250 mg for regular disulfiram, I would adjust the target dose to 100mg (250 mg / 2.6). One more note: I do not find any benefit using liposomal forms of this medication over regular forms. Additionally, I only use the enteric-coated form if someone has stomach or nausea issues. I do not find the liposomal or enteric-coated forms prevent any of the disulfiram side-effect issues like headaches or neuropathy.
Disulfiram may cause intense Herxheimer reactions. To prevent this and to manage it, I recommend
For more ideas about how to limit Herxheimer reactions, see Herxheimer Reactions: Inflammation Run Amok.
Disulfiram may also lead to neuropathy. I am finding that neuropathy is permanent in a very small percentage of people. To prevent or treat neuropathy while on disulfiram, I recommend the following supportive supplements:
Alcohol detox is blocked by the disulfiram. Therefore, do not eat or use food, medicines, skin care products, or mouthwash with alcohol. Read labels of anything in a bottle. Foods to avoid include:
If you find yourself reacting to the disulfiram even with these food restrictions, then consider removing sources of polyphenols, which includes coffee and green tea.
For more information about Lyme persisters and treatment options see How to Treat Persister Lyme & Bartonella.
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Marty Ross, MD is a passionate Lyme disease educator and clinical expert. He helps Lyme sufferers and their physicians see what really works based on his review of the science and extensive real-world experience. Dr. Ross is licensed to practice medicine in Washington State (License: MD00033296) where he has treated thousands of Lyme disease patients in his Seattle practice.
Marty Ross, MD is a graduate of Indiana University School of Medicine and Georgetown University Family Medicine Residency. He is a member of the International Lyme and Associated Disease Society (ILADS), The Institute for Functional Medicine, and The American Academy of Anti-Aging Medicine (A4M).
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