Abstract
ABO blood type is an inherited characteristic. The associations between ABO blood type and risk of all cancer and specific cancers were examined in a prospective cohort study of 18,244 Chinese men enrolled in 1986. During the 25 years of follow-up, 3,973 men developed cancer including 964 lung cancers, 624 colorectal cancers, 560 gastric cancers, 353 liver cancers, and 172 urinary bladder cancers. Hazard ratios (HR) for all cancer and specific cancers by ABO blood type were calculated using Cox proportional hazards models. Compared with blood type A, blood type B was associated with statistically significant reduced risk of all cancers (HR, 0.91, 95% CI:0.84, 0.99). Both blood types B and AB were associated with significantly lower risk of gastrointestinal cancer and colorectal cancer, respectively. Blood type B was also associated with significantly lower risk of stomach cancer and bladder cancer, while blood type AB was associated with significantly increased risk of liver cancer. By histological type, blood types B and AB were associated with lower risk of epidermoid carcinoma and adenocarcinoma, but were not associated with risk of sarcoma, lymphoma, leukemia or other cell types of cancer. The findings of this study support a role of genetic traits related to ABO blood type in the development of cancers in the gastrointestinal and urinary tracts.
Introduction
The ABO blood types, discovered by Karl Landsteiner in 1901, are medically the most important blood types. The ABO blood types are defined by carbohydrate moieties displayed on the surface of red blood cells and attached to a protein backbone, known as the H antigen [1]. A simple test for the presence or absence of antigen A or antigen B in the blood can determine an individual’s ABO blood type [2]. Individuals with blood type A have antigen A present but absence of antigen B in their red blood cells whereas those with blood type B have antigen B but no antigen A. People with blood type AB have both antigens A and B present in the red blood cells. In contrast, individuals with blood type O have neither antigen A nor antigen B expressed in their red blood cells [3]. In addition to their expression on the surface of red blood cells, the ABO antigens are highly expressed on the surface of epithelial cells of the gastrointestinal, bronchopulmonary, and urogenital tracts [1]. Alterations in surface glycoconjugates may lead to modifications in intercellular adhesion, membrane signaling, and immunosurveillance, which could have important implications for the development of cancer [1, 4].
Aird et al in 1953 discovered a statistically significant association between blood type A and risk of gastric cancer [5]. This finding has stimulated an immense amount of research that examined the relationship between ABO blood type and risk of cancer, other chronic diseases, and infectious diseases. The results of those early studies drew severe criticisms. The critiques included (1) the use of hospital-based case series that were not representative for the patient population under study, (2) the inappropriate use of a comparison group that comprised blood donors (blood type O could be overrepresented due to the universal donor status), relatives of patients (the similar genetic traits) or other patients who were admitted to the same hospitals for other diseases, and (3) uncontrolled for potential confounding effects on the association between ABO blood type and disease risk. Results from well designed and well executed prospective cohort studies would be required to confirm those early observations [6]. A recent epidemiological study in two large cohorts in the United States found that self-reported ABO blood types were statistically significantly associated with risk of pancreatic cancer [7]. Given that ABO blood types are inherited through genes on chromosome 9q34 [8], a genome-wide association study also noted an association between DNA sequence variants in the ABO locus and susceptibility to pancreatic cancer. These findings further support a role of ABO blood type as a risk marker for pancreatic cancer [9].
Epidemiologic data in Asian populations, in particular from population-based prospective cohort studies, are sparse. Most of previous prospective studies only examined the ABO blood type with risk of single cancer site. In the present study, we utilized the data set of a prospective cohort of more than 18,000 men with up to 25 years of follow-up to examine the association between ABO blood type and the risk of all cancer and specific cancers by site or histology. The determination of ABO blood type for each study participant at baseline provided an unique opportunity to test the hypothesis that ABO blood type contributes to subsequent risk of cancer development.
Materials and methods
Study population
The Shanghai Cohort Study began in 1986. The study design and subject recruitment has been previously described in details [10, 11]. Briefly, the cohort consisted of 18,244 men (constituting 80% of eligible subjects) enrolled from January 1, 1986 through September 30, 1989, who were between 45 and 64 years of age and resided in one of four small geographically defined communities in Shanghai, China. At enrollment, each participant was interviewed in person by a trained research nurse using a structured questionnaire asking for information on demographic characteristics, history of tobacco and alcohol use, adult dietary habits, and medical history. Following the completion of the interview, participants were asked to provide a 10-mL blood sample and a single-void urine specimen. The Institutional Review Boards at the Shanghai Cancer Institute and the University of Pittsburgh had approved the Shanghai Cohort Study. All procedures performed were in accordance with the ethical standards of these IRBs and with the 1964 Helsinki declaration and its later amendments.
The ABO blood type was determined at the time of baseline blood draw using a standard test for the presence of ABO antigens in subject’s whole blood at the blood draw station (i.e., ABO forward grouping method) [2]. The test result of the ABO blood type was recorded in the study questionnaire at baseline.
Identification of outcome events
Follow-up of the cohort for incident cancers and deaths has been ongoing through multiple means that were previously described [10]. In addition to annual in-person follow-up interviews to all surviving cohort members, we performed periodically record linkage analysis of all study participants with the databases of the Shanghai Cancer Registry and Shanghai Municipal Vital Statistics Office, respectively. As of December 31, 2013, the cut-off date for the present analysis, only 670 (3.7%) original cohort members were lost to follow-up and additional 598 (3.3%) refused to our annual follow-up interviews since the beginning of this cohort study. For these subjects, we searched the cancer registry and death index databases to ascertain their cancer diagnosis and vital status, and cause and date of death. Therefore, the follow-up for incident cancer and death for the entire cohort was virtually completed.
When we identified a new cancer patient by self-reports or reports of the-next-of-kin of the study participants who died, or through linkage analysis with the cancer registry database, we already had the permission granted by the study subject to review his medical records and pathology reports. During the review of these records, a research nurse completed a medical record abstract form that recorded information on cancer diagnosis including site, date of initial diagnosis, basis of diagnosis, and histology of cancer, if available. Both topography (site) and morphology (histology) of all cancer cases were coded according to the World Health Organization’s International Classification of Diseases 9th version (ICD-9) and ICD for Oncology (ICD-O), respectively. Besides groups of cancer cases by system (i.e., digestive or respiratory system) or individual site, we further classified cases by histology in a standard way according to the previous description [12]. This system classifies histological diagnoses of cancers into carcinoma (ICD-O: 801–867), lymphoma (ICD-O: 959–971), sarcoma and other soft tissue tumors (ICD-O: 868–871, 880–892, 899, 904, 912–934, 937, 954–958), leukemia (ICD-O: 980–994), and other specified or unspecified types of cancer. For carcinoma, this system further classified cancer cases into epidermoid carcinomas (ICD-O: 805–813), adenocarcinoma (ICD-O: 814, 816, 818–822, 825–850, 952–855, 857), other specified (ICD-O: 803–804, 815, 817, 823, 824, 851, 856, 867) and unspecified carcinomas (ICD-O: 801–802) [12].
Statistical analysis
The present analysis included 18,069 individuals after we excluded 146 subjects with a history of cancer at baseline, 5 cancer cases with missing information on diagnosis date (2 lung cancer, 1 esophagus cancer, 1 colon cancer, and 1 gallbladder cancer), and 24 with unknown ABO blood type. The χ2 test and the analysis of variance (ANOVA) methods were used to compare the distributions of selected demographic characteristics and lifestyle factors at baseline by ABO blood type.
For each individual, person-years of follow-up were calculated from the date of recruitment to the date of cancer diagnosis or death, the date of last known vital status for those lost to follow-up, or the date of the last annual follow-up interview, whichever occurred first. The Cox proportional hazards regression models were used to examine the associations between ABO blood type and risk of all cancer combined or groups of common cancers by site or histology. The magnitude of the association was assessed by the hazard ratio (HR) and its 95% confidence interval (CI) and P value. All Cox regression models were adjusted for age at baseline interview, year of baseline interview, level of education (no formal school or primary school, junior middle school, senior middle school, or college or above), body mass index (kg/m2), cigarette smoking status (never, former, or current smokers), and alcohol intake (nondrinkers, <3 drinks, or 3 or more drinks per day).
Statistical analyses were carried out using SAS software version 9.3 (SAS Institute, Cary, NC). All P-values reported are two-sided. P’s less than 0.05 were considered to be statistically significant.
Results
Among 18,069 original cohort participants with available ABO blood types, 32% were blood type O, 31% type A, 27% type B, and 10% type AB. The distributions of age, body mass index, level of education, smoking status and the number of cigarettes consumed per day or over lifetime, and alcohol intake were comparable across different ABO blood types (Table 1).
Table 1. Baseline demographic and lifestyle characteristics by ABO blood type, Shanghai Cohort Study 1986–2013.
| ABO blood type | Pa | ||||
|---|---|---|---|---|---|
| A | B | AB | O | ||
| No. of persons | 5,586 | 4,891 | 1,890 | 5,702 | |
| Age at interview (year), mean (SD) | 55.7(5.7) | 55.7 (5.8) | 55.9 (5.7) | 55.8 (5.8) | 0.329 |
| Body mass index (kg/m2), mean (SD) | 22.2 (3.0) | 22.2 (3.0) | 22.2 (3.0) | 22.1 (2.9) | 0.496 |
| Level of education, n (%) | |||||
| Primary school or below | 1596 (28.6) | 1390 (28.4) | 557 (29.5) | 1599 (28.0) | |
| Secondary school | 2622 (46.9) | 2266 (46.3) | 898 (47.5) | 2673 (46.9) | 0.581 |
| College or above | 1368 (24.5) | 1235 (25.3) | 435 (23.0) | 1430 (25.1) | |
| Smoking status, n (%) | |||||
| Never smokers | 2369 (42.4) | 2078 (42.5) | 794 (42.0) | 2497 (43.5) | |
| Former smokers | 372 (6.7) | 323 (6.6) | 151 (8.0) | 368 (6.5) | 0.312 |
| Current smokers | 2845 (50.9) | 2490 (50.9) | 945 (50.0) | 2855 (50.0) | |
| Among ever smokers | |||||
| No. of cigarettes/day, mean (SD) | 16.1 (8.2) | 16.3 (8.3) | 16.1 (8.2) | 16.3 (8.3) | 0.764 |
| No. of years of smoking, mean (SD) | 29.7 (10.8) | 29.3 (10.6) | 29.7 (10.7) | 29.7 (10.6) | 0.543 |
| No. of pack-years of smoking, mean (SD) | 25.0 (16.7) | 25.0 (16.6) | 25.0 (16.6) | 25.5 (16.9) | 0.827 |
| Alcohol drinking status (%) | |||||
| Non-drinkers | 3178 (56.9) | 2783 (56.9) | 1070 (56.6) | 3338 (58.5) | 0.204 |
| Drinkers | 2408 (43.1) | 2108 (43.1) | 820 (43.4) | 2364 (41.5) | |
| Among drinkers | |||||
| No. of drinks/day, mean (SD) | 2.4 (2.4) | 2.4 (2.4) | 2.4 (2.4) | 2.3 (2.6) | 0.579 |
| No. of years of drinking, mean (SD) | 26.3 (13.0) | 25.6 (13.2) | 26.2 (13.0) | 25.3 (13.3) | 0.115 |
| Ethanol intake over lifetime (kg), mean (SD) | 329 (423) | 323 (420) | 326 (411) | 306 (483) | 0.597 |
| H. pylori antibody serologic status, n (%)b | |||||
| Negative | 45 (14.1) | 55 (19.2) | 17 (18.3) | 53 (16.9) | 0.390 |
| Positive | 274 (85.9) | 231 (80.8) | 76 (81.7) | 261 (83.1) | |
| HBsAg serologic status, n (%)c | |||||
| Negative | 338 (89.9) | 295 (91.1) | 110 (90.2) | 398 (90.3) | 0.964 |
| Positive | 38 (10.1) | 29 (9.0) | 12 (9.8) | 43 (9.8) | |
Abbreviations: n, number; No., number; SD, standard deviation
a Two-sided P’s were derived from analysis of variance (ANOVA) for continuous values or chi-square test for categorical or nominal values.
b Based on 1,012 cohort members with available measurement of Helicobactor pylori (H. pylori) who remained free of cancer by the latest follow-up.
c Based on 1,263 cohort members with available measurement of hepatitis B surface antigen (HBsAg) who remained free of cancer by the latest follow-up.
After 25 years of follow-up, the cohort accumulated a total of 355,797 person-years and 3,973 incident cancer cases by the end of 2013. The cancer of digestive system was the most frequent diagnosis that accounted for 51% of total cancer cases, followed by respiratory system (26%), and genitourinary system (13%). Lymphoma, leukemia and sarcoma combined together accounted for 4% of total malignancies. Cancer of the skin, bone and connective tissue were relatively rare (accounting for only 2%). The remaining 4% malignancies belonged to other or unspecified sites. By individual sites, cancer of the lung was the most common cancer diagnosis (accounting for 24% of total cancers), followed by colorectum (16%), stomach (14%) and liver (9%). The esophageal, pancreas, prostate and urinary bladder cancer each accounted for approximately 6% of total cancer cases (Table 2). By histology, carcinoma accounted for 60% of total histologically confirmed cancer cases while sarcomas, lymphoma and leukemia altogether accounted for 4%. The remaining 36% of cancer cases consisted of cases with other histology types or no histological confirmation. Among carcinomas, 66% were adenocarcinomas, 25% were epidermoid carcinomas, and the remaining 9% were other or unspecified carcinomas (Table 2).
Table 2. Number of cancer cases by ABO blood type, Shanghai Cohort Study 1986–2013.
| ABO blood type | Total | ||||
|---|---|---|---|---|---|
| A | B | AB | O | ||
| No. of person-years | 109,201 | 96,975 | 36,925 | 112,696 | 355,797 |
| No. of all cancer cases | 1,284 | 1,036 | 406 | 1,247 | 3,973 |
| By cancer site (ICD-9 codes) | |||||
| Digestive system (140–159) | 668 | 519 | 204 | 625 | 2,016 |
| Gastrointestinal tract (140–154) | 486 | 351 | 126 | 442 | 1,405 |
| Esophagus (150) | 44 | 43 | 10 | 40 | 137 |
| Stomach (151) | 199 | 131 | 58 | 172 | 560 |
| Colorectum (153–154) | 221 | 155 | 51 | 197 | 624 |
| Liver (155) | 101 | 87 | 50 | 115 | 353 |
| Pancreas (157) | 53 | 47 | 15 | 47 | 162 |
| Respiratory system (160–165) | 320 | 278 | 112 | 323 | 1,033 |
| Lung and trachea (162) | 302 | 256 | 104 | 302 | 964 |
| Bone/connective tissue/skin (170–173) | 24 | 24 | 3 | 18 | 69 |
| Genitourinary organs (185–189) | 172 | 125 | 51 | 160 | 508 |
| Prostate (185) | 86 | 69 | 25 | 72 | 252 |
| Urinary bladder (188) | 59 | 34 | 19 | 60 | 172 |
| Lymphoma/multiple myeloma/leukemia (200–208) | 54 | 45 | 15 | 57 | 171 |
| All other or unspecified sites | 46 | 45 | 21 | 64 | 176 |
| By cancer histology a | |||||
| Carcinoma | 802 | 595 | 227 | 767 | 2,391 |
| Epidermoid carcinoma | 201 | 160 | 52 | 195 | 608 |
| Adenocarcinoma | 537 | 397 | 155 | 494 | 1,583 |
| Sarcoma/lymphoma/leukemia | 58 | 51 | 14 | 46 | 169 |
| All other/unspecified neoplasm | 424 | 390 | 165 | 434 | 1,413 |
Abbreviations: ICD, International Classification of Diseases; No., number
a See the ICD-O codes in the Materials and Methods section.
Compared with blood type A, blood type B was associated with a statistically significant lower risk of all cancers (Table 3). The incidence of cancers of the gastrointestinal tract was statistically significantly different among different ABO blood types. Compared with blood type A, individuals with non-A blood types were at an approximately 20% lower risk of cancer of the gastrointestinal tract (HR = 0.83, 95% CI = 0.75–0.93, P = 0.001), stomach cancer (HR = 0.80, 95% CI = 0.67–0.95, P = 0.013), and colorectum cancer (HR = 0.80, 95% CI = 0.68–0.94, P = 0.008). For blood type B, the hazard ratio of developing stomach and colorectal cancer was 0.75 (95% CI = 0.76–0.94, P = 0.009) and 0.78 (95% CI = 0.64–0.96, P = 0.020), respectively. Blood type AB was also associated with significantly reduced risk of cancers in the gastrointestinal tract (HR = 0.76, 95%CI = 0.63–0.93, P = 0.007) or the large intestine (HR = 0.68, 95%CI = 0.50–0.92, P = 0.013). Conversely, when compared with blood type O, individuals with blood type A had a statistically borderline significant higher risk of stomach cancer (HR = 1.21, 95% CI = 0.98–1.48, P = 0.070) and colorectal cancer (HR = 1.18, 95% CI = 0.97–1.43, P = 0.097) (Table 3).
Table 3. Hazard ratios (95% confidence intervals) for cancer associated with ABO blood type Shanghai Cohort Study 1986–2013.a.
| ABO blood type | ||||
|---|---|---|---|---|
| A | B | AB | O | |
| All cancer | 1.00 (referent) | 0.91 (0.84–0.99) b | 0.93 (0.83–1.04) | 0.93 (0.86–1.01) |
| By cancer site | ||||
| Digestive system | 1.00 (referent) | 0.88 (0.78–0.98) b | 0.90 (0.77–1.05) | 0.90 (0.81–1.00) |
| Gastrointestinal tract | 1.00 (referent) | 0.81 (0.71–0.93) b | 0.76 (0.63–0.93) b | 0.88 (0.77–1.00) |
| Esophagus | 1.00 (referent) | 1.13 (0.74–1.72) | 0.67 (0.34–1.33) | 0.90 (0.58–1.37) |
| Stomach | 1.00 (referent) | 0.75 (0.60–0.93) b | 0.86 (0.64–1.15) | 0.83 (0.68–1.02) |
| Colorectum | 1.00 (referent) | 0.78 (0.64–0.96) b | 0.68 (0.50–0.92) b | 0.85 (0.70–1.03) |
| Liver | 1.00 (referent) | 0.98 (0.73–1.30) | 1.45 (1.04–2.04) b | 1.10 (0.84–1.43) |
| Pancreas | 1.00 (referent) | 1.00 (0.67–1.47) | 0.83 (0.47–1.47) | 0.85 (0.57–1.26) |
| Respiratory system | 1.00 (referent) | 1.00 (0.85–1.17) | 1.03 (0.83–1.27) | 0.97 (0.83–1.14) |
| Lung and trachea | 1.00 (referent) | 0.97 (0.82–1.15) | 1.01 (0.81–1.26) | 0.96 (0.82–1.13) |
| Bone/connective tissue/skin | 1.00 (referent) | 1.12 (0.63–1.97) | 0.37 (0.11–1.24) | 0.72 (0.39–1.33) |
| Genitourinary organs | 1.00 (referent) | 0.80 (0.64–1.01) | 0.88 (0.71–1.09) | 0.88 (0.64–1.20) |
| Prostate | 1.00 (referent) | 0.87 (0.64–1.20) | 0.86 (0.55–1.34) | 0.79 (0.58–1.08) |
| Urinary bladder | 1.00 (referent) | 0.64 (0.42–0.98) b | 0.95 (0.57–1.59) | 0.96 (0.67–1.38) |
| Lymphoma/multiple myeloma/leukemia | 1.00 (referent) | 0.93 (0.63–1.38) | 0.82 (0.46–1.46) | 1.01 (0.69–1.46) |
| All other or unspecified sites | 1.00 (referent) | 1.10 (0.73–1.66) | 1.36 (0.81–2.27) | 1.35 (0.92–1.97) |
| By cancer histology | ||||
| Carcinoma | 1.00 (referent) | 0.84 (0.75–0.93) b | 0.83 (0.72–0.97) b | 0.92 (0.83–1.02) |
| Epidermoid carcinoma | 1.00 (referent) | 0.91 (0.74–1.12) | 0.76 (0.56–1.03) | 0.94 (0.77–1.14) |
| Adenocarcinoma | 1.00 (referent) | 0.83 (0.73–0.94) b | 0.85 (0.71–1.02) | 0.88 (0.78–1.00) |
| Sarcoma/lymphoma/leukemia | 1.00 (referent) | 0.98 (0.67–1.43) | 0.72 (0.40–1.28) | 0.76 (0.51–1.11) |
| All other/unspecified neoplasm | 1.00 (referent) | 1.04 (0.91–1.20) | 0.98 (0.86–1.12) | 1.14 (0.95–1.36) |
a Adjusted for age at baseline, body mass index, year of interview, level of education, smoking status (never, former, current), and alcohol intake (nondrinker, <3 drinks/day, 3+ drinks/day).
b Two-sided P < 0.05.
Subjects with blood type AB were at increased risk of liver cancer with a statistically significant 42–45% higher risk of liver cancer (Table 3). HR for liver cancer for individuals with blood type AB was 1.45 (95% CI = 1.04–2.04, P = 0.028) when comparing with blood type A or 1.42, (95% CI = 1.05–1.91, P = 0.023) when comparing with non-AB blood type (i.e., blood types A, B, and O combined).
In the present study, blood type AB and O were associated with reduced risk of developing pancreatic cancer compared with blood type A. Compared with blood type A, individuals with blood types AB and blood type O experienced a 17% and 15% lower risk of pancreatic cancer, respectively, but none of them reached statistical significance (Table 3).
Blood type B was associated with reduced risk of urinary bladder cancer. Compared with blood type A, subjects with blood type B had a statistically significant 36% lower risk of urinary bladder cancer (HR = 0.64, 95% CI = 0.42–0.98, P = 0.040). Individuals with blood type AB or O had bladder cancer risk comparable with blood type A (Table 3). ABO blood type was not associated with risk of cancer of the lung, prostate, skin, bone, and connective tissue (Table 3).
When cancer cases were classified by histological type, blood type B and AB were associated with a statistically significant 15~17% lower risk of carcinoma or adenocarcinoma compared with blood type A (Table 3). Similarly, compared with blood type A, hazard ratio for carcinoma were 0.84 (95% CI = 0.75–0.93, P <0.001) for blood type B. When compared with blood type A and O combined (i.e., absence of antigen B), individuals with blood type B and AB (i.e., presence of blood antigen B) experienced a statistically significant 13% lower risk of carcinoma (HR = 0.87, 95% CI = 0.80–0.95, P = 0.001) and a 11% lower risk of adenocarcinoma (HR = 0.89, 95% CI = 0.80–0.98, P = 0.025). Blood types AB and O were associated with statistically non-significant 24~28% lower risk of sarcoma, lymphoma, or leukemia combined compared with blood type A.
Analyses were repeated after excluding individuals who developed cancer within the first two years of blood draw and the corresponding person-years of follow-up. In general, the results remained unchanged except for that the inverse association between blood type AB and risk of adenocarcinoma became stronger and statistically significant (HR = 0.81, 95% CI = 0.67–0.98, P = 0.028) (S1 Table). Further adjustment for history of diabetes and high blood pressure did not materially change the association between ABO blood type and cancer risk (data not shown).
Discussion
This prospective study of a cohort of middle-aged or older Chinese men demonstrates a lower risk of all cancer for blood type B, as well as lower risk for gastrointestinal cancers including stomach and colorectal cancer for blood types B and AB than blood type A. In contrast, the present study showed a higher risk of liver cancer for blood type AB and lower risk of urinary bladder cancer for blood type B. These findings are consistent with the notion that besides red blood cells, the ABO blood type antigens are expressed in epithelial cells of gastrointestinal and urinary tract, and suggesting a role of ABO blood type in the development of epithelial cancers in the gastrointestinal and urinary tracts.
For several decades, a role of ABO blood type antigens in the development of cancer has been suspected. Since the initial reports of Aird et al of the association of peptic ulcer and gastric carcinoma with ABO blood types [5, 13], a voluminous literature has accumulated on these topics, and it has been summarized previously [6, 14]. Those previous studies, mostly conducted in Western populations, consistently showed an approximately 20% excess risk of gastric cancer in individuals with blood type A. Data from Chinese population are sparse. A cross-sectional study in northern China found that blood type A was associated with statistically significant 30–40% higher risk of intestinal metaplasia or gastric dysplasia, the most advanced pre-malignant lesions in the stomach, in people with blood type A than in those with other blood types [15]. A recent prospective cohort study in a Taiwanese population showed that blood type A was associated with a 38% increased risk of stomach cancer [16]. The present study found a 26% increased risk of gastric cancer for blood type A as compared with blood types B and O (HR = 1.26, 95% CI = 1.06–1.51, P = 0.011), consistent with findings of earlier studies in Chinese as well as in Western populations.
The mechanism for the association between ABO blood type and gastric cancer is not completely understood. Experimental studies have found that the specific blood type antigen (e.g., Lewisb), the product of blood type genes at 19q13, mediates the attachment to human gastric mucosa of H. pylori, a causative agent in chronic active gastritis, gastric and duodenal ulcers, and gastric adenocarcinoma [17]. Human epithelial cells of type O individuals bound significantly more H. pylori and had greater inflammatory responses to H. pylori than did cells of persons with other blood types [18, 19]. H. pylori bacteria could not bind to gastric tissue that lacks the Lewisb antigen [17, 20]. These data suggest that the availability of H. pylori receptors might be reduced in people with blood type B and AB phenotype as compared with blood type O. These experimental studies have provided strong biological explanations for the higher prevalence of peptic ulcer among individuals with blood type O than type A [6]. In contrast, an excessive risk of gastric cancer associated with blood type A in the present study as well as many previous studies strongly implicates a different mechanism. The controversy of increased risk of gastric cancer among individuals with blood type A while a high peptic ulcer risk among those with blood type O was also observed in another cohort study among Scandinavian populations [21]. Further studies are warranted to delineate the mechanism between ABO blood type and risk of gastric cancer.
In addition to the stomach, we extended our analysis to the entire gastrointestinal tract. Similar to gastric cancer, blood type A individuals experienced statistically significantly increased risk of colorectal cancer compared to those with non-A blood type. These findings are consistent with previous summary report in Western populations [6] and a prospective study in Taiwan [22]. Experimental studies have demonstrated that the expression of ABO blood type antigens on colon tumor cells, and the cell proliferation and motility are highly associated with the expression of blood type antigen A [23, 24]. These data suggest a direct involvement of ABO blood type antigens in the development and metastasis of colorectal cancer.
The present study also showed an increased incidence of pancreatic cancer among subjects with blood type antigen A or B compared with those who were lack of these antigens (i.e., blood type O). Although none of these associations reached statistical significance due to relatively small number of pancreatic cancer cases, these findings were consistent with findings of the Nurses’ Health Study and Health Professionals Follow-up Study [7].
The present study noted several novel associations between ABO blood type and risk of cancer of the liver and urinary bladder. Subjects with blood type AB had a statistically significant 45% increased risk of liver cancer. In laboratory investigations, patient-derived hepatocellular tumor cells express blood type antigens on their cell surface and have different patterns of expression than cells in adjacent nontumorous liver tissues [25, 26], indicating a potential role of the ABO blood type antigens in the malignant transformation of hepatocytes. A strong association between plasma alkaline phosphatase, a liver enzyme, and genetic polymorphisms within the ABO locus on chromosome 9q34[8], further supports the biologic link for ABO blood type to the liver function [27]. Alternations in the host inflammatory state due to ABO blood type antigens may provide a further mechanism to explain an association between blood type and liver cancer risk. Chronic infection with hepatitis B is a primary causal factor for liver cancer in this population [28]. A genome-wide association study has noted a direct link of single nucleotide polymorphisms at the ABO locus to serum levels of tumor necrosis factor-alpha [29], an inflammatory cytokine known to modulate risk of liver cancer [30]. Although biologic evidence is strong, this novel statistical association between blood type AB and liver cancer risk needs to be replicated and confirmed in other populations.
Another novel observation of the present study is the reduced risk of urinary bladder cancer for men with blood type B relative to type A. ABO blood type antigens are constitutively expressed on urothelial cells. Studies have found that large proportion of transitional epithelia of bladder carcinoma had either reduced expression of blood type antigen A or loss of A allele [31, 32]. A reduction in the expression of antigen A was correlated with the invasiveness of the malignancies [33]. These pathological findings suggest that the determinants of ABO blood type antigens may play a critical role in the development of urinary bladder cancer. Future studies are warranted to examine the role of the determinants of ABO type antigens or closely linked genetic variations in the development of bladder cancer.
In the present study population of men aged 45–64 years at blood draw, 32% were blood type O, 31% blood type A, 27% blood type B, and 10% blood type AB. The corresponding frequencies in southern Chinese (n = 76,039) were 26%, 34%, 30%, and 10% [34]. In American Chinese (n = 37,822), most immigrants originated from southern China, the prevalence of blood types O, A, B, and AB were 42%, 27%, 25%, and 6%, respectively [35]. Both sets of ABO phenotype frequencies were derived from blood donors, which may explain the difference in the blood type prevalence between the populations of our study and of earlier studies.
The present study has several strengths. The blood type was determined using a standard agglutinin assay for all study participants at recruitment, which avoided inaccurate ABO blood type by self-reports. The prospective design of the study minimized potential selection bias on the inclusion of study subjects due to disease status. A comprehensive questionnaire for collection of potential confounders and demographic information at baseline allowed for controlling for potential confounding effect on the association between the ABO blood type and cancer risk. The follow-up of the cohort participants for incidence of cancer and death was virtually complete, minimizing the potential selection bias due to the loss of follow-up. Relatively large number of incident cancer cases provided sufficient statistical power to examine the association between the ABO blood type and risk of cancer by sites and histology. Our post hoc analysis revealed that the present study had an 80% statistical power to detect a minimal hazard ratios of 1.13 for total cancer, 1.16 for total carcinoma, 1.22 for gastrointestinal cancer, 1.37 for stomach cancer, and 1.34 for colorectal cancer associated with blood type B comparing blood type A. The present study shows higher HRs that these values, suggesting a sufficient statistical power.
The main limitation of the present study is the relatively small sample size of certain specific cancers including pancreatic cancer, which otherwise would provide more definitive results. Another drawback of the present study was multiple comparisons, which could inflate the false positive rate for the observed association. If we applied the most stringent Bonferroni correction method to control for multiple comparisons, the critical P value would be 0.002 if we counted all different cancer sites (n = 21). Under such an assumption of two-sided type I error rate P value, the association between blood type B and risk of carcinoma reached statistical significance level. However, our hypothesis that the blood type A is associated with high risk of cancer in gastrointestinal tract is supported by potential biological mechanisms and previous studies, thus it may not require for such a stringent criterion. Another limitation is only male participants with a narrow age range, thus the findings may not be directly applicable to the general population. Studies conducted among other populations, e.g., women and/or younger age groups, are needed to replicate the study findings.
In summary, the present study demonstrates the variation in risk of carcinoma and adenocarcinoma by different ABO blood types. Compared with blood type A, Chinese men with blood type B were at statistically significantly lower risk of gastrointestinal cancers and bladder cancer while those with blood type AB were at increased risk of liver cancer.
Supporting information
(DOCX)
(SAS7BDAT)
Acknowledgments
We thank Xue-Li Wang of the Shanghai Cancer Institute for supervising the field work of the Shanghai Cohort Study. We also thank the Shanghai Cancer Registry for assistance with the identification of lung cancer cases via database linkage.
Abbreviations
- CI
confidence interval
- HR
hazard ratio
- ICD-O
International Classification of Diseases for Oncology
Data Availability
All relevant data are within the paper and its Supporting Information files.
Funding Statement
This work was supported by the United States National Institutes of Health (R01CA144034, R01 CA043092, and UM1 CA182876) to J.-M.Y. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
References
- 1.Hakomori S. Antigen structure and genetic basis of histo-blood groups A, B and O: their changes associated with human cancer. Biochim Biophys Acta. 1999;1473(1):247–66. . [DOI] [PubMed] [Google Scholar]
- 2.Whitlock SA. Chapter 5. ABO blood group System In: Whitlock SA, editor. Immunohematology for medical laboratory technicians. New York: Delmar, Gengage Learning; 2010. p. 87–108. [Google Scholar]
- 3.Harmening DM, Firestone D. The ABO blood group system In: Harmening DM, editor. Modern blood bank and transfusion practices. Third ed. Philadelphia: F. A. Davis Company; 1994. p. 86–115. [Google Scholar]
- 4.Zhang S, Zhang HS, Cordon-Cardo C, Reuter VE, Singhal AK, Lloyd KO, et al. Selection of tumor antigens as targets for immune attack using immunohistochemistry: II. Blood group-related antigens. International journal of cancer. 1997;73(1):50–6. . [DOI] [PubMed] [Google Scholar]
- 5.Aird I, Bentall HH, Roberts JA. A relationship between cancer of stomach and the ABO blood groups. Br Med J. 1953;1(4814):799–801. . [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Vogel F. Controversy in human genetics. ABO blood groups and disease. Am J Hum Genet. 1970;22(4):464–75. . [PMC free article] [PubMed] [Google Scholar]
- 7.Wolpin BM, Chan AT, Hartge P, Chanock SJ, Kraft P, Hunter DJ, et al. ABO blood group and the risk of pancreatic cancer. J Natl Cancer Inst. 2009;101(6):424–31. doi: 10.1093/jnci/djp020 . [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Reid ME, Mohandas N. Red blood cell blood group antigens: structure and function. Semin Hematol. 2004;41(2):93–117. . [DOI] [PubMed] [Google Scholar]
- 9.Amundadottir L, Kraft P, Stolzenberg-Solomon RZ, Fuchs CS, Petersen GM, Arslan AA, et al. Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. Nat Genet. 2009;41(9):986–90. doi: 10.1038/ng.429 . [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Ross RK, Yuan JM, Yu MC, Wogan GN, Qian GS, Tu JT, et al. Urinary aflatoxin biomarkers and risk of hepatocellular carcinoma. Lancet. 1992;339(8799):943–6. . [DOI] [PubMed] [Google Scholar]
- 11.Yuan JM, Ross RK, Wang XL, Gao YT, Henderson BE, Yu MC. Morbidity and mortality in relation to cigarette smoking in Shanghai, China. A prospective male cohort study. JAMA. 1996;275(21):1646–50. [PubMed] [Google Scholar]
- 12.Berg JW. Morphologic classification of human cancer In: Schottenfeld D, Fraumeni JF Jr., editors. Cancer Epidemiology and Prevention. 2nd ed. New York: Oxford University Press; 1996. p. 28–44. [Google Scholar]
- 13.Aird I, Bentall HH, Mehigan JA, Roberts JA. The blood groups in relation to peptic ulceration and carcinoma of colon, rectum, breast, and bronchus; an association between the ABO groups and peptic ulceration. Br Med J. 1954;2(4883):315–21. . [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Newman E, Naifeh GS, Auer JE, Buckwalter JA. Secretion of ABH antigens in peptic ulceration and gastric carcinoma. Br Med J. 1961;1(5219):92–4. . [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.You WC, Ma JL, Liu W, Gail MH, Chang YS, Zhang L, et al. Blood type and family cancer history in relation to precancerous gastric lesions. Int J Epidemiol. 2000;29(3):405–7. . [PubMed] [Google Scholar]
- 16.Sun W, Wen CP, Lin J, Wen C, Pu X, Huang M, et al. ABO blood types and cancer risk—a cohort study of 339,432 subjects in Taiwan. Cancer epidemiology. 2015;39(2):150–6. doi: 10.1016/j.canep.2014.12.006 ; PubMed Central PMCID: PMC4993100. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Boren T, Falk P, Roth KA, Larson G, Normark S. Attachment of Helicobacter pylori to human gastric epithelium mediated by blood group antigens. Science. 1993;262(5141):1892–5. . [DOI] [PubMed] [Google Scholar]
- 18.Alkout AM, Blackwell CC, Weir DM, Poxton IR, Elton RA, Luman W, et al. Isolation of a cell surface component of Helicobacter pylori that binds H type 2, Lewis(a), and Lewis(b) antigens. Gastroenterology. 1997;112(4):1179–87. . [DOI] [PubMed] [Google Scholar]
- 19.Alkout AM, Blackwell CC, Weir DM. Increased inflammatory responses of persons of blood group O to Helicobacter pylori. J Infect Dis. 2000;181(4):1364–9. doi: 10.1086/315375 . [DOI] [PubMed] [Google Scholar]
- 20.Falk P, Roth KA, Boren T, Westblom TU, Gordon JI, Normark S. An in vitro adherence assay reveals that Helicobacter pylori exhibits cell lineage-specific tropism in the human gastric epithelium. Proc Natl Acad Sci U S A. 1993;90(5):2035–9. . [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Edgren G, Hjalgrim H, Rostgaard K, Norda R, Wikman A, Melbye M, et al. Risk of gastric cancer and peptic ulcers in relation to ABO blood type: a cohort study. Am J Epidemiol. 2010;172(11):1280–5. doi: 10.1093/aje/kwq299 . [DOI] [PubMed] [Google Scholar]
- 22.Hsiao LT, Liu NJ, You SL, Hwang LC. ABO blood group and the risk of cancer among middle-aged people in Taiwan. Asia-Pacific journal of clinical oncology. 2015;11(4):e31–6. doi: 10.1111/ajco.12253 . [DOI] [PubMed] [Google Scholar]
- 23.Labarriere N, Piau JP, Otry C, Denis M, Lustenberger P, Meflah K, et al. H blood group antigen carried by CD44V modulates tumorigenicity of rat colon carcinoma cells. Cancer Res. 1994;54(23):6275–81. . [PubMed] [Google Scholar]
- 24.Iwamoto S, Withers DA, Handa K, Hakomori S. Deletion of A-antigen in a human cancer cell line is associated with reduced promoter activity of CBF/NF-Y binding region, and possibly with enhanced DNA methylation of A transferase promoter. Glycoconj J. 1999;16(10):659–66. . [DOI] [PubMed] [Google Scholar]
- 25.Okada Y, Arima T, Togawa K, Nagashima H, Jinno K, Moriwaki S, et al. Neoexpression of ABH and Lewis blood group antigens in human hepatocellular carcinomas. J Natl Cancer Inst. 1987;78(1):19–28. . [DOI] [PubMed] [Google Scholar]
- 26.Okada Y, Jinno K, Moriwaki S, Morichika S, Torigoe S, Arima T, et al. Expression of ABH and Lewis blood group antigens in combined hepatocellular-cholangiocarcinoma. Possible evidence for the hepatocellular origin of combined hepatocellular-cholangiocarcinoma. Cancer. 1987;60(3):345–52. . [DOI] [PubMed] [Google Scholar]
- 27.Yuan X, Waterworth D, Perry JR, Lim N, Song K, Chambers JC, et al. Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. Am J Hum Genet. 2008;83(4):520–8. doi: 10.1016/j.ajhg.2008.09.012 . [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Yuan JM, Gao YT, Ong CN, Ross RK, Yu MC. Prediagnostic level of serum retinol in relation to reduced risk of hepatocellular carcinoma. J Natl Cancer Inst. 2006;98(7):482–90. doi: 10.1093/jnci/djj104 . [DOI] [PubMed] [Google Scholar]
- 29.Melzer D, Perry JR, Hernandez D, Corsi AM, Stevens K, Rafferty I, et al. A genome-wide association study identifies protein quantitative trait loci (pQTLs). PLoS Genet. 2008;4(5):e1000072 doi: 10.1371/journal.pgen.1000072 . [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Nieters A, Yuan JM, Sun CL, Zhang ZQ, Stoehlmacher J, Govindarajan S, et al. Effect of cytokine genotypes on the hepatitis B virus-hepatocellular carcinoma association. Cancer. 2005;103(4):740–8. doi: 10.1002/cncr.20842 . [DOI] [PubMed] [Google Scholar]
- 31.Meldgaard P, Johnson PH, Langkilde NC, Wolf H, Orntoft TF. Loss of ABH antigen expression in bladder cancer is not caused by loss of heterozygosity of the ABO locus. International journal of cancer. 1995;63(3):341–4. . [DOI] [PubMed] [Google Scholar]
- 32.Orlow I, Lacombe L, Pellicer I, Rabbani F, Delgado R, Zhang ZF, et al. Genotypic and phenotypic characterization of the histoblood group ABO(H) in primary bladder tumors. International journal of cancer. 1998;75(6):819–24. . [DOI] [PubMed] [Google Scholar]
- 33.Yamada T, Fukui I, Kobayashi T, Sekine H, Yokogawa M, Yamada T, et al. The relationship of ABH(O) blood group antigen expression in intraepithelial dysplastic lesions to clinicopathologic properties of associated transitional cell carcinoma of the bladder. Cancer. 1991;67(6):1661–6. . [DOI] [PubMed] [Google Scholar]
- 34.Su M, Lu SM, Tian DP, Zhao H, Li XY, Li DR, et al. Relationship between ABO blood groups and carcinoma of esophagus and cardia in Chaoshan inhabitants of China. World J Gastroenterol. 2001;7(5):657–61. doi: 10.3748/wjg.v7.i5.657 . [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Garratty G, Glynn SA, McEntire R. ABO and Rh(D) phenotype frequencies of different racial/ethnic groups in the United States. Transfusion. 2004;44(5):703–6. doi: 10.1111/j.1537-2995.2004.03338.x . [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
(DOCX)
(SAS7BDAT)
Data Availability Statement
All relevant data are within the paper and its Supporting Information files.