ALS (amyotrophic lateral sclerosis), also known as Lou Gehrig's disease, is a progressive neurodegenerative disorder characterized by muscle weakness, difficulty speaking and breathing, and eventual paralysis. While the cause of ALS is unknown, certain factors like age, genetics, and race have been linked to an increased risk of developing the disease.
Race and ALS Risk
Studies have found that certain racial and ethnic groups may be at a higher risk of developing ALS than others. According to the ALS Association, people of Asian descent have the highest risk of developing ALS, followed by Caucasians, Hispanics, and African Americans.
Asian Descent
Studies have found that Asian populations have the highest risk of developing ALS. In Japan, for example, the incidence rate of ALS is 3.3 per 100,000 people, while in the United States, the incidence rate is 1.9 per 100,000 people.
Caucasian Descent
Caucasians, particularly those of Northern European descent, have the second-highest risk of developing ALS. In the United States, the incidence rate is 1.8 per 100,000 people.
Hispanic Descent
Studies have found that the incidence rate of ALS in Hispanic populations is lower than that of Caucasian and Asian populations. The incidence rate in Hispanic populations is 1.5 per 100,000 people.
African American Descent
Studies have found that African American populations have the lowest risk of developing ALS. The incidence rate in African Americans is 1.1 per 100,000 people.
Overall, it is important to note that while certain racial and ethnic groups may be at a higher risk of developing ALS, anyone can develop the disease. It is also important to note that genetics and lifestyle choices may also play a role in the development of ALS.