Macrocytosis, a new predictor for esophageal squamous cell carcinoma in Japanese alcoholic men

Akira Yokoyama, Tetsuji Yokoyama, Taro Muramatsu, Tai Omori, Sachio Matsushita, Susumu Higuchi, Katsuya Maruyama, Hiromasa Ishii

Research output: Contribution to journalArticle

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Abstract

Early esophageal squamous cell carcinoma detected by esophageal iodine staining can be easily treated by endoscopic mucosectomy, and identifying its predictors is important in better selecting candidates to screen for this high-mortality cancer. The common etiologies of elevated mean corpuscular volume (MCV) and esophageal cancer, including folate deficiency, smoking, drinking and high acetaldehyde exposure, suggest testing MCV as such a predictor. Japanese alcoholic men with (n = 65) and without (n =206) esophageal squamous cell carcinomas, excluding those with liver cirrhosis, were assessed for MCV within 7 days of their last drink, alone or in combination with findings from either the alcohol flushing questionnaire or genotyping to identify inactive aldehyde dehydrogenase-2 (ALDH2*1/2*2) and the less-active form of alcohol dehydrogenase-2 (ADH2*1/2*1), which pose risks for esophageal squamous cell carcinoma. MCV was higher in cancer patients than in the control group. MCV was higher in both groups in those who were heavier smokers, had lower body mass index (BMI), experienced alcohol flushing, and had ALDH2*1/2*2. After adjusting for age, drinking and smoking habits, BMI and ALDH2/ADH2 genotypes, macrocytosis of MCV ≥106 f1 was associated with increased risk for esophageal cancer (OR = 2.75). Men with both MCV 2>106 f1 and alcohol flushing had an even higher cancer risk (OR = 5.51). The combinations of MCV ≥106 f1 with ALDH2*1/2*2 or ADH2*1/2*1 alone, and both ALDH2*1/2*2 and ADH2*1/2*1 (ORs = 11.44, 21.22 and 319.7, respectively) showed consistently higher risk than the corresponding group with MCV < 106 fl (ORs = 7.24, 4.71 and 27.01, respectively). In conclusion, MCV measurement, alone or in combination with the markers of alcohol sensitivity, provides a new means of predicting risk for esophageal squamous cell carcinoma in Japanese alcoholic men.

Original languageEnglish
Pages (from-to)1773-1778
Number of pages6
JournalCarcinogenesis
Volume24
Issue number11
DOIs
Publication statusPublished - 2003 Nov

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Erythrocyte Indices
Alcoholics
Alcohols
Esophageal Neoplasms
Drinking
Body Mass Index
Smoking
Esophageal Squamous Cell Carcinoma
Neoplasms
Aldehyde Dehydrogenase
Acetaldehyde
Alcohol Dehydrogenase
Folic Acid
Iodine
Liver Cirrhosis
Habits
Genotype
Staining and Labeling
Control Groups

ASJC Scopus subject areas

  • Cancer Research

Cite this

Yokoyama, A., Yokoyama, T., Muramatsu, T., Omori, T., Matsushita, S., Higuchi, S., ... Ishii, H. (2003). Macrocytosis, a new predictor for esophageal squamous cell carcinoma in Japanese alcoholic men. Carcinogenesis, 24(11), 1773-1778. https://doi.org/10.1093/carcin/bgg142

Macrocytosis, a new predictor for esophageal squamous cell carcinoma in Japanese alcoholic men. / Yokoyama, Akira; Yokoyama, Tetsuji; Muramatsu, Taro; Omori, Tai; Matsushita, Sachio; Higuchi, Susumu; Maruyama, Katsuya; Ishii, Hiromasa.

In: Carcinogenesis, Vol. 24, No. 11, 11.2003, p. 1773-1778.

Research output: Contribution to journalArticle

Yokoyama, A, Yokoyama, T, Muramatsu, T, Omori, T, Matsushita, S, Higuchi, S, Maruyama, K & Ishii, H 2003, 'Macrocytosis, a new predictor for esophageal squamous cell carcinoma in Japanese alcoholic men', Carcinogenesis, vol. 24, no. 11, pp. 1773-1778. https://doi.org/10.1093/carcin/bgg142
Yokoyama, Akira ; Yokoyama, Tetsuji ; Muramatsu, Taro ; Omori, Tai ; Matsushita, Sachio ; Higuchi, Susumu ; Maruyama, Katsuya ; Ishii, Hiromasa. / Macrocytosis, a new predictor for esophageal squamous cell carcinoma in Japanese alcoholic men. In: Carcinogenesis. 2003 ; Vol. 24, No. 11. pp. 1773-1778.
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abstract = "Early esophageal squamous cell carcinoma detected by esophageal iodine staining can be easily treated by endoscopic mucosectomy, and identifying its predictors is important in better selecting candidates to screen for this high-mortality cancer. The common etiologies of elevated mean corpuscular volume (MCV) and esophageal cancer, including folate deficiency, smoking, drinking and high acetaldehyde exposure, suggest testing MCV as such a predictor. Japanese alcoholic men with (n = 65) and without (n =206) esophageal squamous cell carcinomas, excluding those with liver cirrhosis, were assessed for MCV within 7 days of their last drink, alone or in combination with findings from either the alcohol flushing questionnaire or genotyping to identify inactive aldehyde dehydrogenase-2 (ALDH2*1/2*2) and the less-active form of alcohol dehydrogenase-2 (ADH2*1/2*1), which pose risks for esophageal squamous cell carcinoma. MCV was higher in cancer patients than in the control group. MCV was higher in both groups in those who were heavier smokers, had lower body mass index (BMI), experienced alcohol flushing, and had ALDH2*1/2*2. After adjusting for age, drinking and smoking habits, BMI and ALDH2/ADH2 genotypes, macrocytosis of MCV ≥106 f1 was associated with increased risk for esophageal cancer (OR = 2.75). Men with both MCV 2>106 f1 and alcohol flushing had an even higher cancer risk (OR = 5.51). The combinations of MCV ≥106 f1 with ALDH2*1/2*2 or ADH2*1/2*1 alone, and both ALDH2*1/2*2 and ADH2*1/2*1 (ORs = 11.44, 21.22 and 319.7, respectively) showed consistently higher risk than the corresponding group with MCV < 106 fl (ORs = 7.24, 4.71 and 27.01, respectively). In conclusion, MCV measurement, alone or in combination with the markers of alcohol sensitivity, provides a new means of predicting risk for esophageal squamous cell carcinoma in Japanese alcoholic men.",
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N2 - Early esophageal squamous cell carcinoma detected by esophageal iodine staining can be easily treated by endoscopic mucosectomy, and identifying its predictors is important in better selecting candidates to screen for this high-mortality cancer. The common etiologies of elevated mean corpuscular volume (MCV) and esophageal cancer, including folate deficiency, smoking, drinking and high acetaldehyde exposure, suggest testing MCV as such a predictor. Japanese alcoholic men with (n = 65) and without (n =206) esophageal squamous cell carcinomas, excluding those with liver cirrhosis, were assessed for MCV within 7 days of their last drink, alone or in combination with findings from either the alcohol flushing questionnaire or genotyping to identify inactive aldehyde dehydrogenase-2 (ALDH2*1/2*2) and the less-active form of alcohol dehydrogenase-2 (ADH2*1/2*1), which pose risks for esophageal squamous cell carcinoma. MCV was higher in cancer patients than in the control group. MCV was higher in both groups in those who were heavier smokers, had lower body mass index (BMI), experienced alcohol flushing, and had ALDH2*1/2*2. After adjusting for age, drinking and smoking habits, BMI and ALDH2/ADH2 genotypes, macrocytosis of MCV ≥106 f1 was associated with increased risk for esophageal cancer (OR = 2.75). Men with both MCV 2>106 f1 and alcohol flushing had an even higher cancer risk (OR = 5.51). The combinations of MCV ≥106 f1 with ALDH2*1/2*2 or ADH2*1/2*1 alone, and both ALDH2*1/2*2 and ADH2*1/2*1 (ORs = 11.44, 21.22 and 319.7, respectively) showed consistently higher risk than the corresponding group with MCV < 106 fl (ORs = 7.24, 4.71 and 27.01, respectively). In conclusion, MCV measurement, alone or in combination with the markers of alcohol sensitivity, provides a new means of predicting risk for esophageal squamous cell carcinoma in Japanese alcoholic men.

AB - Early esophageal squamous cell carcinoma detected by esophageal iodine staining can be easily treated by endoscopic mucosectomy, and identifying its predictors is important in better selecting candidates to screen for this high-mortality cancer. The common etiologies of elevated mean corpuscular volume (MCV) and esophageal cancer, including folate deficiency, smoking, drinking and high acetaldehyde exposure, suggest testing MCV as such a predictor. Japanese alcoholic men with (n = 65) and without (n =206) esophageal squamous cell carcinomas, excluding those with liver cirrhosis, were assessed for MCV within 7 days of their last drink, alone or in combination with findings from either the alcohol flushing questionnaire or genotyping to identify inactive aldehyde dehydrogenase-2 (ALDH2*1/2*2) and the less-active form of alcohol dehydrogenase-2 (ADH2*1/2*1), which pose risks for esophageal squamous cell carcinoma. MCV was higher in cancer patients than in the control group. MCV was higher in both groups in those who were heavier smokers, had lower body mass index (BMI), experienced alcohol flushing, and had ALDH2*1/2*2. After adjusting for age, drinking and smoking habits, BMI and ALDH2/ADH2 genotypes, macrocytosis of MCV ≥106 f1 was associated with increased risk for esophageal cancer (OR = 2.75). Men with both MCV 2>106 f1 and alcohol flushing had an even higher cancer risk (OR = 5.51). The combinations of MCV ≥106 f1 with ALDH2*1/2*2 or ADH2*1/2*1 alone, and both ALDH2*1/2*2 and ADH2*1/2*1 (ORs = 11.44, 21.22 and 319.7, respectively) showed consistently higher risk than the corresponding group with MCV < 106 fl (ORs = 7.24, 4.71 and 27.01, respectively). In conclusion, MCV measurement, alone or in combination with the markers of alcohol sensitivity, provides a new means of predicting risk for esophageal squamous cell carcinoma in Japanese alcoholic men.

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