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Original Contribution |

Incidence of Amyotrophic Lateral Sclerosis Among American Indians and Alaska Natives

Paul H. Gordon, MD, PhD; Jason M. Mehal, MPH; Robert C. Holman, MS; Lewis P. Rowland, MD; Andrew S. Rowland, PhD; James E. Cheek, MD, MPH
JAMA Neurol. 2013;70(4):476-480. doi:10.1001/jamaneurol.2013.929.
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Importance  More thorough evaluation of amyotrophic lateral sclerosis (ALS) and motor neuron disease in unique populations could provide clues to etiologies for these idiopathic conditions, and educational programs for American Indian and Alaska Native (AI/AN) people and health care professionals on reservations could improve awareness, understanding, diagnosis, and treatment. In the ongoing search for susceptibility genes, studying particular racial groups, such as AI/ANs, might facilitate the identification of new mutations.

Objective  To provide better understanding of ALS and secondarily of motor neuron disease among AI/AN people by estimating the incidence and prevalence among AI/ANs served by the Indian Health Service health care system.

Design and Setting  Analysis of electronic records for AI/ANs with ALS and with motor neuron disease separately for the calendar years 2002-2009 using inpatient and outpatient visit data from the Indian Health Service, which provides health care to eligible AI/ANs nationwide.

Participants  Cases were defined by at least 2 inpatient or outpatient visits with the diagnosis.

Main Outcome Measures  Crude and age-adjusted incidence and prevalence rates were calculated.

Results  Seventy-one AI/ANs were diagnosed with ALS, yielding an average annual crude incidence rate of 0.63 cases per 100 000 and an age-adjusted incidence of 0.92. The median age at onset was 56.0 years and was higher among women than men (62.0 vs 55.0 years; P = .06). Age-specific incidence increased to 70 to 74 years. The crude and age-adjusted point prevalence rates were 2.00 and 4.12, respectively. The crude and age-adjusted incidence rates for motor neuron disease were 1.08 and 1.50, respectively. The annual rates were unchanged across the study period.

Conclusions and Relevance  The incidence of ALS among AI/ANs appears to be lower than that reported for white populations, a finding congruent with reports of other minority populations. Community-based studies are important to confirm these findings and to examine reasons for the low rate of ALS among AI/ANs.

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Figures

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Figure 1. Crude incidence rates of amyotrophic lateral sclerosis by age group and sex for American Indian and Alaska Native people using the Indian Health Service direct and contract health service according to inpatient and outpatient visit data, 2002-2009, United States. Women aged 40 to 49 years were not included in the figure because of low patient numbers.

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Figure 2. Indian Health Service (IHS) geographic regions showing average annual crude incidence and point prevalence of amyotrophic lateral sclerosis among American Indian and Alaska Native people using the IHS direct and contract health service according to inpatient and outpatient visit data, 2002-2009, United States. Rates are per 100 000 persons of corresponding group. Average annual user populations by region for 2002-2009: Alaska: 128 878; East: 40 783; Northern Plains East: 93 355; Northern Plains West: 187 650; Southern Plains: 303 572; Southwest: 489 460; and West: 170 618. Note that Texas is administered by the Nashville, Oklahoma City, and Albuquerque areas.

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Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature

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