Frequency
Lyme disease is the most common tick-borne illness in the United States. An estimated 300,000 new cases occur every year. Lyme disease occurs in areas in which blacklegged ticks are found, primarily the northeastern states (from Virginia to Maine), the upper Midwest (Wisconsin, Minnesota, and Michigan), and parts of California and Oregon. In these regions of the United States, the incidence of Lyme disease is 10 to 100 cases per 100,000 people each year.
Lyme disease is also common in Europe, China, and Japan.
Causes
Lyme disease is caused by infection with bacteria rather than by genetic changes. The risk of developing Lyme disease is influenced by a variety of lifestyle and environmental factors that reflect how likely a person is to get bitten by an infected tick, such as where a person lives, how much time is spent outdoors, and the time of year. While there is no evidence that genetic factors play a role in susceptibility to Lyme disease, such factors may affect the severity of the disease, particularly whether antibiotic-refractory Lyme arthritis develops.
The signs and symptoms of Lyme disease result from the body's immune response to the bacteria. When the body recognizes foreign invaders, such as bacteria, it stimulates inflammation to help fight the infection. This inflammation causes the skin irritation; flu-like symptoms; and neurological, cardiac, and joint problems that characterize Lyme disease.
Certain genes that help mediate the body's immune response have been associated with the development of antibiotic-refractory Lyme arthritis. Particular variants in these genes are found more often in people with this complication than in those who do not develop it.
Some of the genes thought to be associated with the development of antibiotic-refractory Lyme arthritis provide instructions for making proteins called Toll-like receptors. As one of the first lines of defense against infection, Toll-like receptors recognize patterns that are common to many foreign invaders, rather than recognizing a specific invader, and stimulate a quick immune response that triggers inflammation. Some variants of certain Toll-like receptor genes are thought to overstimulate the body's immune response to the Lyme disease bacteria, contributing to the joint inflammation of antibiotic-resistant Lyme arthritis.
Other genes thought to be associated with antibiotic-resistant Lyme arthritis belong to a gene family called the human leukocyte antigen (HLA) complex. The HLA complex helps the immune system distinguish the body's own proteins from proteins made by foreign invaders. Each HLA gene has many different variations, allowing each person's immune system to react to a wide range of proteins. The proteins produced from HLA genes attach to protein fragments and display them to the immune system. If the immune system recognizes the fragment as foreign or abnormal, it triggers an immune response. Some evidence suggests that certain variations of HLA genes contribute to an inappropriate immune response that causes the body to react to one of its own normal proteins. The resulting inflammation may contribute to development of antibiotic-refractory Lyme arthritis.
Inheritance
Lyme disease cannot be inherited. The risk of certain complications of the condition may be influenced by inherited genetic factors, but the inheritance pattern is unknown.
Other Names for This Condition
- B. burgdorferi infection
- Borrelia burgdorferi infection
- Borreliosis, Lyme
- Infection by Borrelia burgdorferi
- Infection due to Borrelia burgdorferi sensu lato
- Lyme borreliosis
Additional Information & Resources
Patient Support and Advocacy Resources
Clinical Trials
Scientific Articles on PubMed
References
- Bush LM, Vazquez-Pertejo MT. Tick borne illness-Lyme disease. Dis Mon. 2018 May;64(5):195-212. doi: 10.1016/j.disamonth.2018.01.007. Citation on PubMed
- Drouin EE, Seward RJ, Strle K, McHugh G, Katchar K, Londono D, Yao C, Costello CE, Steere AC. A novel human autoantigen, endothelial cell growth factor, is a target of T and B cell responses in patients with Lyme disease. Arthritis Rheum. 2013 Jan;65(1):186-96. doi: 10.1002/art.37732. Citation on PubMed or Free article on PubMed Central
- Rahman S, Shering M, Ogden NH, Lindsay R, Badawi A. Toll-like receptor cascade and gene polymorphism in host-pathogen interaction in Lyme disease. J Inflamm Res. 2016 May 31;9:91-102. doi: 10.2147/JIR.S104790. eCollection 2016. Citation on PubMed or Free article on PubMed Central
- Steere AC, Dwyer E, Winchester R. Association of chronic Lyme arthritis with HLA-DR4 and HLA-DR2 alleles. N Engl J Med. 1990 Jul 26;323(4):219-23. doi: 10.1056/NEJM199007263230402. Erratum In: N Engl J Med 1991 Jan 10;324(2):129. Citation on PubMed
- Steere AC, Klitz W, Drouin EE, Falk BA, Kwok WW, Nepom GT, Baxter-Lowe LA. Antibiotic-refractory Lyme arthritis is associated with HLA-DR molecules that bind a Borrelia burgdorferi peptide. J Exp Med. 2006 Apr 17;203(4):961-71. doi: 10.1084/jem.20052471. Epub 2006 Apr 3. Citation on PubMed or Free article on PubMed Central
- Steere AC, Strle F, Wormser GP, Hu LT, Branda JA, Hovius JW, Li X, Mead PS. Lyme borreliosis. Nat Rev Dis Primers. 2016 Dec 15;2:16090. doi: 10.1038/nrdp.2016.90. Erratum In: Nat Rev Dis Primers. 2017 Aug 03;3:17062. doi: 10.1038/nrdp.2017.62. Citation on PubMed or Free article on PubMed Central
- Strle K, Shin JJ, Glickstein LJ, Steere AC. Association of a Toll-like receptor 1 polymorphism with heightened Th1 inflammatory responses and antibiotic-refractory Lyme arthritis. Arthritis Rheum. 2012 May;64(5):1497-507. doi: 10.1002/art.34383. Citation on PubMed or Free article on PubMed Central
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