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Using data from Geisinger electronic medical records, researchers identified 9657 Lyme disease cases diagnosed between 2006 and 2014 in central and northeastern Pennsylvania.
[bctt tweet=”Are African-Americans less likely to be diagnosed with Lyme disease?” username=”DrDanielCameron”]
Moon and colleagues found that more than 97% of the Lyme disease patients were white non-Hispanic. Only 0.9% were Hispanic and 1.4% were black non-Hispanic.
The authors suggest that “The low-density semi-rural and suburban communities close to wooded, brushy, or grassy landscapes favored by ticks are more likely to be white and affluent,” and therefore put this population at a greater risk.
However, different socioeconomic levels, involvement in outdoor leisure activities, access to health care, and awareness of Lyme disease may also play a role. “There is some evidence,” the authors write, “that African-Americans may be at higher risk than whites for delayed diagnosis and treatment of Lyme disease,” writes Moon, citing a study by Fix. [2]
Related Articles:
Lyme disease diagnosis almost missed in patient with Babesia
Lyme disease in children rising in Pennsylvania: An inside look
References:
- Moon KA, Pollak J, Hirsch AG, et al. Epidemiology of Lyme disease in Pennsylvania 2006-2014 using electronic health records. Ticks Tick Borne Dis. 2018.
- Fix AD, Pena CA, Strickland GT. Racial differences in reported Lyme disease incidence. Am J Epidemiol. 2000;152(8):756-759.
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Could being a Southerner affect the diagnosis and treatment of Lyme and other tick-borne diseases?
Yes.
Interesting, however in my case, white female undiagnosed for 20+ years with access to endless doctors who had no clue and treated me horribly, so …
Thanks for sharing your frustration.
I’m african american suffering from Lyme Borreliosis and Candida for a few years. I’ve gone from physician to physician without treatment. I’m tired and weary. I see the disparity of treatment with regards to demographic info. My mother died from the same symptoms I’m experiencing. I just want help. I’ve spent my life savings on life sustaining treatments for my mother and I. In Alabama but willing to travel but require a physician who accepts Medicare/ Medicaid and Igenex results!
Hello sir.
Did you ever get help or diagnosed?
MX Hayes,
You should join the Facebook Lyme groups! I got so much information. The Lyme Support and Wellness is the most helpful, but I’m in about 5-6 groups. I learn something new everyday. I’m so sorry you are going thru this. It took 17 years of misdiagnosis to finally get a Lyme diagnosis for myself. You need a Lyme Literate Dr(LLMD). There is a directory online, if you Google that phrase! I wish you so much luck!
I have met many with darker complexions who couldn’t see the rashes or ticks in their scalps, etc.