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Cited by 285

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Refined Geographic Distribution of the Oriental ALDH2*504Lys (nee 487Lys) Variant

Open access
Li, Hui, Borinskaya, Svetlana, Yoshimura, Kimio, Kal’ina, Nina, Marusin, Andrey, Stepanov, Vadim A., Qin, Zhendong, Khaliq, Shagufta, Lee, Mi‐Young, Yang, Yajun, Mohyuddin, Aisha, Gurwitz, David, Mehdi, Syed Qasim, Rogaev, Evgeny, Jin, Li, Yankovsky, Nikolay K., Kidd, Judith R., Kidd, Kenneth K.·2009·Annals of Human Genetics

Abstract

Summary: Mitochondrial aldehyde dehydrogenase (ALDH2) is one of the most important enzymes in human alcohol metabolism. The oriental ALDH2*504Lys variant functions as a dominant negative, greatly reducing activity in heterozygotes and abolishing activity in homozygotes. This allele is associated with serious disorders such as alcohol liver disease, late onset Alzheimer disease, colorectal cancer, and esophageal cancer, and is best known for protection against alcoholism. Many hundreds of papers in various languages have been published on this variant, providing allele frequency data for many different populations. To develop a highly refined global geographic distribution of ALDH2*504Lys, we have collected new data on 4,091 individuals from 86 population samples and assembled published data on a total of 80,691 individuals from 366 population samples. The allele is essentially absent in all parts of the world except East Asia. The ALDH2*504Lys allele has its highest frequency in Southeast China, and occurs in most areas of China, Japan, Korea, Mongolia, and Indochina with frequencies gradually declining radially from Southeast China. As the indigenous populations in South China have much lower frequencies than the southern Han migrants from Central China, we conclude that ALDH2*504Lys was carried by Han Chinese as they spread throughout East Asia. Esophageal cancer, with its highest incidence in East Asia, may be associated with ALDH2*504Lys because of a toxic effect of increased acetaldehyde in the tissue where ingested ethanol has its highest concentration. While the distributions of esophageal cancer and ALDH2*504Lys do not precisely correlate, that does not disprove the hypothesis. In general the study of fine scale geographic distributions of ALDH2*504Lys and diseases may help in understanding the multiple relationships among genes, diseases, environments, and cultures.

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Metadata

Authors
Li, H., Borinskaya, S., Yoshimura, K., Kal’ina, N., Marusin, A., Stepanov, V. A., Qin, Z., Khaliq, S., Lee, M., Yang, Y., Mohyuddin, A., Gurwitz, D., Mehdi, S. Q., Rogaev, E., Jin, L., Yankovsky, N. K., Kidd, J. R., & Kidd, K. K.
Venue
Annals of Human Genetics
Publisher
Wiley
Published
2009-04-28
Volume
73
Issue
3
Pages
335-345
ISSN
  • 0003-4800 (ISSN-L)
  • 1469-1809
OpenAlex
W2149623954
Cited by
285
References
1
FWCI
5.26
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Refined Geographic Distribution of the Oriental ALDH2*504Lys (nee 487Lys) Variant. https://app.cochat.ai/papers/10.1111/j.1469-1809.2009.00517.x
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Li, H., Borinskaya, S., Yoshimura, K., Kal’ina, N., Marusin, A., Stepanov, V. A., Qin, Z., Khaliq, S., Lee, M., Yang, Y., Mohyuddin, A., Gurwitz, D., Mehdi, S. Q., Rogaev, E., Jin, L., Yankovsky, N. K., Kidd, J. R., & Kidd, K. K. (2009). Refined Geographic Distribution of the Oriental ALDH2*504Lys (nee 487Lys) Variant. Annals of Human Genetics. https://doi.org/10.1111/j.1469-1809.2009.00517.x

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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