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Research Article | Volume 15 Issue 10 (October, 2025) | Pages 707 - 709
Investigating a potential correlation between ABO-Rh blood types and the occurrence of Medulloblastoma
 ,
 ,
1
Assistant Professor, Department of Pathology, Shree Narayan Medical Institute and Hospital, Saharsa, Bihar
2
Professor and Head, Department of Pathology, Shree Narayan Medical Institute and Hospital, Saharsa, Bihar
Under a Creative Commons license
Open Access
Received
Sept. 18, 2025
Revised
Sept. 30, 2025
Accepted
Oct. 2, 2025
Published
Oct. 9, 2025
Abstract

Background: Medulloblastoma is a the most common malignant tumor of the brain seen in children and is also the most common embryonal tumor of the central nervous system. It has been linked to the ABO-Rh group, however, existing literature data is scarce concerning the same. Aim: The present study was aimed to investigate the potential correlation between ABO-Rh blood types and the occurrence of Medulloblastoma inn Indian subjects and to evaluate the efficacy and use of blood group as a non-modifiable risk factor for medulloblastoma. Methods: The study assessed 174 subjects aged less than 18 years that were diagnosed with medulloblastoma on histopathological assessment at the Institute within the defined study period. Another age and gender matched 200 subjects were included as controls that had no tumor. In both the groups, data were gathered concerning gender, age, Rh factor, and ABO blood group from the records of the Institute. Comparison was done in controls and cases using statistical analysis.   Results: The study results showed that a significant association was noted in A blood group and medulloblastoma. The study results also showed that classical subtype of medulloblastoma was more prevalent in subjects having blood group A, whereas, desmoplastic subtype of medulloblastoma had high association with blood group O as seen in 38.5% study subjects. Conclusion: The present study concludes that a higher risk for development of medulloblastoma is seen in study subjects with blood group A, whereas, least risk was seen in subjects with blood group O. These results suggest that blood group antigen should be taken as a preclinical and non-modifiable risk factor for development of medulloblastoma.

Keywords
INTRODUCTION

Cancer is one of the most vital reasons for the death globally where its treatment is the major cause of concern in affected subjects. Various factors have been assessed for the pathogenesis of the cancer and antigens for ABO blood group as expressed on the red blood cells are one of these factors.1

There have been various studies that confirmed and reported a link between the risk of developing nasopharyngeal, breast, ovarian, pancreatic, and gastric cancer to the distribution of ABO blood group antigens.2

Few studies have been done that reported a correlation in intracranial neoplasm and ABO blood group antigen, however, the results reported have been controversial. Few studies in the literature have reported a high case of glioblastoma in subjects with A blood group, whereas, other studies have reported no significant association in in ABO blood group and CNS (central nervous system) neoplasms.3

Medulloblastoma is the most common malignant central nervous system embryonal neoplasm in child subjects. Existing literature data is scarce concerning the determination of relation between ABO blood group and medulloblastoma in child subjects.4 Hence, the present study was aimed to investigate the potential correlation between ABO-Rh blood types and the occurrence of Medulloblastoma inn Indian subjects and to evaluate the efficacy and use of blood group as a non-modifiable risk factor for medulloblastoma.

MATERIALS AND METHODS

The present cross-control clinical study was aimed to investigate the potential correlation between ABO-Rh blood types and the occurrence of Medulloblastoma inn Indian subjects and to evaluate the efficacy and use of blood group as a non-modifiable risk factor for medulloblastoma. The study subjects were from Department of Pathology, Shree Narayan Medical Institute and Hospital, Saharsa, Bihar. Verbal and written informed consent were taken from all the subjects before study participation.

The study assessed 174 subjects aged less than/equal to 18 years with confirmed diagnosis of medulloblastoma as seen in histopathological assessment at the Institute within the defined study period. Diagnostic criteria used were histopathological assessment following biopsy or surgery from the tissue of the tumor. Rh factor, blood groups, ABO, gender, and age was assessed from all the included subjects from the previous records of the Institute. Another age and gender matched 200 subjects were included as controls that had no tumor. In both the groups, data were gathered concerning gender, age, Rh factor, and ABO blood group from the records of the Institute.

The data gathered underwent statistical analysis using IBM SPSS statistics version 24.0 using chi-square, student t-test, and one-way ANOVA. The data were expressed in number and percentage and mean and standard deviations. The p-value of <0.05 was taken as statistical significance value

RESULTS

The present cross-control clinical study was aimed to investigate the potential correlation between ABO-Rh blood types and the occurrence of Medulloblastoma inn Indian subjects and to evaluate the efficacy and use of blood group as a non-modifiable risk factor for medulloblastoma. The study assessed 174 subjects aged less than 18 years that were diagnosed with medulloblastoma on histopathological assessment at the Institute within the defined study period. Another age and gender matched 200 subjects were included as controls that had no tumor. In both the groups, data were gathered concerning gender, age, Rh factor, and ABO blood group from the records of the Institute. Comparison was done in controls and cases using statistical analysis.  

The study results showed that for demographic data and its correlation with blood group in two groups of study subjects, Rh factor was negative in 3% (n=6) controls and in 3.4% (n=6) cases and was positive in 97% (n=194) controls and 96.6% (n=168) cases. The difference was statistically non-significant with p=0.84. Blood group A, AB, B, and O was seen in 22% (n=44), 8% (n=16), 36% (n=72), and 34% (n=68) subjects from controls and in 41.4% (n=72), 10.3% (n=18), 26.4% (n=46), and 21.8% (n=38) cases. The difference was highly statistically significant with p=0.02. Mean age and gender distribution in two groups was comparable with p=0.324 and 0.97 respectively (Table 1).  

 

S. No

Parameter

Controls (n=200)

Cases (n=174)

p-value

n

%

n

%

1.       

Rh factor

 

 

 

 

 

a)       

Negative

6

3

6

3.4

0.84

b)      

Positive

194

97

168

96.6

2.       

Blood group

 

 

 

 

 

a)       

A

44

22

72

41.4

0.02

b)      

AB

16

8

18

10.3

c)       

B

72

36

46

26.4

d)      

O

68

34

38

21.8

3.       

Mean age (years)

7.95±4.93

7.35±3.74

0.324

4.       

Gender

 

 

 

 

 

a)       

Females

62

31

54

31

0.97

b)      

Males

138

69

120

69

Table 1: Demographic data and its correlation with blood group in two groups of study subjects

 

On assessing the subtypes of medulloblastoma, their characteristics and corelation to ABO blood group, among 38 subjects with O blood groups, classical, desmoplastic, and large cell type was seen in 19.2% (n=28), 38.5% (n=10), and 0 subjects respectively. In 26.4% (n=46) with B blood group, 26% (n=38), 30.8% (n=8), and 0 subjects had classical, desmoplastic, and large cell type. Subjects with AB blood group, classical, desmoplastic, and large cell type was seen in 11% (n=16), 7.7% (n=2), and 0 study subjects respectively. In subjects with A blood group, classical, desmoplastic, and large cell type was seen in 43.8% (n=64), 23.1% (n=6), and 100% (n=2) study subjects. The difference was statistically non-significant with p=0.565 (Table 2).

 

S. No

Blood group n (%)

Classical

Desmoplastic

Large cell

Total

1.       

O

28 (19.2)

10 (38.5)

0

38 (21.8)

2.       

B

38 (26)

8 (30.8)

0

46 (26.4)

3.       

AB

16 (11)

2 (7.7)

0

18 (10.3)

4.       

A

64 (43.8)

6 (23.1)

2 (100)

72 (41.4)

5.       

Total

146 (100)

26 (100)

2 (100)

174 (100)

6.       

p-value

0.565

Table 2: Medulloblastoma subtypes, their characteristics and corelation to ABO blood group

 

It was seen that for prevalence of type of medulloblastoma and its correlation to Rh factor, in 168 Rh-factor positive study subjects, classical, desmoplastic, and large cell type was seen in 95.9% (n=140), 100% (n=26), and 100% (n=2) study subjects respectively. In Rh-factor negative, 6 study subjects, classical type of medulloblastoma was seen in all 6 study subjects. There was total 146, 26, and 2 subjects with classical, desmoplastic, and large cell type medulloblastoma respectively (Table 3).

 

S. No

Rh-factor

Classical

Desmoplastic

Large cell

Total

1.       

Positive

140 (95.9)

26 (100)

2 (100)

168 (96.6)

2.       

Negative

6 (4.1)

0

0

6 (3.4)

3.       

Total

146 (100)

26 (10)

2 (100)

174 (100)

4.       

p-value

0.721

Table 3: Prevalence of type of medulloblastoma and its correlation to Rh factor

DISCUSSION

The study assessed 174 subjects aged less than 18 years that were diagnosed with medulloblastoma on histopathological assessment at the Institute within the defined study period. Another age and gender matched 200 subjects were included as controls that had no tumor. In both the groups, data were gathered concerning gender, age, Rh factor, and ABO blood group from the records of the Institute. Comparison was done in controls and cases using statistical analysis. The design of the present study was similar to the design by the previous studies of Kumarguru BN et al5 in 2017 and Allouh MZ et al6 in 2017 where study design comparable to the present study were also adopted by the authors in their respective studies.

It was seen that for demographic data and its correlation with blood group in two groups of study subjects, Rh factor was negative in 3% (n=6) controls and in 3.4% (n=6) cases and was positive in 97% (n=194) controls and 96.6% (n=168) cases. The difference was statistically non-significant with p=0.84. Blood group A, AB, B, and O was seen in 22% (n=44), 8% (n=16), 36% (n=72), and 34% (n=68) subjects from controls and in 41.4% (n=72), 10.3% (n=18), 26.4% (n=46), and 21.8% (n=38) cases. The difference was highly statistically significant with p=0.02. Mean age and gender distribution in two groups was comparable with p=0.324 and 0.97 respectively. These results were consistent with the findings of Mazumdar et al7 in 2011 and Agrawal A et al8 in 2014 where authors assessed subjects with demographic data and its correlation with blood group in their studies similar to the present study.

The study results showed that on assessing the subtypes of medulloblastoma, their characteristics and corelation to ABO blood group, among 38 subjects with O blood groups, classical, desmoplastic, and large cell type was seen in 19.2% (n=28), 38.5% (n=10), and 0 subjects respectively. In 26.4% (n=46) with B blood group, 26% (n=38), 30.8% (n=8), and 0 subjects had classical, desmoplastic, and large cell type. Subjects with AB blood group, classical, desmoplastic, and large cell type was seen in 11% (n=16), 7.7% (n=2), and 0 study subjects respectively. In subjects with A blood group, classical, desmoplastic, and large cell type was seen in 43.8% (n=64), 23.1% (n=6), and 100% (n=2) study subjects. The difference was statistically non-significant with p=0.565. These findings were in agreement with the results of Hsiao LT et al9 in 2015 and Franchini M et al10 in 2013 where subtypes of medulloblastoma, their characteristics and corelation to ABO blood group comparable to the present study was also reported by the authors in their studies.

On assessing the prevalence of type of medulloblastoma and its correlation to Rh factor, in 168 Rh-factor positive study subjects, classical, desmoplastic, and large cell type was seen in 95.9% (n=140), 100% (n=26), and 100% (n=2) study subjects respectively. In Rh-factor negative, 6 study subjects, classical type of medulloblastoma was seen in all 6 study subjects. There was total 146, 26, and 2 subjects with classical, desmoplastic, and large cell type medulloblastoma respectively. These results were in line with the findings of Franchini M et al11 in 2014 and Jenkins PV et al12 in 2006 where prevalence of type of medulloblastoma and its correlation to Rh factor reported by the authors was comparable to the present study.

CONCLUSION

The present study, considering its limitations, concludes that a higher risk for development of medulloblastoma is seen in study subjects with blood group A, whereas, least risk was seen in subjects with blood group O. These results suggest that blood group antigen should be taken as a preclinical and non-modifiable risk factor for development of medulloblastoma.

REFERENCES
  1. Franchini M, Liumbruno GM, Lippi G. The prognostic value of ABO blood group in cancer patients. Blood Transfus 2015;6:1–7
  2. Liumbruno GM, Franchini M. Hemostasis, cancer, and ABO blood group: the most recent evidence of association. J Thromb Thrombolysis 2014;38:160–166
  3. Liumbruno GM, Franchini M. Beyond immunohaematology: the role of the ABO blood group in human diseases. Blood Transfus 2013;11:491–499
  4. Zhang BL, He N, Huang YB, Song FJ, Chen KX. ABO blood groups and risk of cancer: a systematic review and meta-analysis. Asian Pac J Cancer Prev 2014;15:4643–4650
  5. Kumarguru BN, Pallavi P, Sunila,Manjunath GV, Vasan TS, Rajalakshmi BR. Histopathological study of central nervous system lesions: emphasizing association of neoplasms with ABO blood groups. J Clin Diagn Res 2017;11:EC15–EC20
  6. Allouh MZ, Al Barbarawi MM, Hiasat MY, Al-Qaralleh MA, Ababneh EI. Glioblastoma and ABO blood groups: further evidence of an association between the distribution of blood group antigens and brain tumours. Blood Transfus 2017;15:543–547
  7. Muzumdar D, Deshpande A, Kumar R, et al. Medulloblastoma in childhood-King Edward Memorial hospital surgical experience and review: comparative analysis of the case series of 365 patients. J Pediatr Neurosci 2011;6:S78–S85
  8. Agrawal A, Tiwari AK, Mehta N, et al. ABO and Rh (D) group distribution and gene frequency; the first multicentric study in India. Asian J Transfus Sci 2014;8:121–125
  9. Hsiao LT, Liu NJ, You SL, Hwang LC. ABO blood group and the risk of cancer among middle-aged people in Taiwan. Asia Pac J Clin Oncol 2015;11:e31–e36
  10. Franchini M, Frattini F, Crestani S, Bonfanti C, Lippi G. von Willebrand factor and cancer: a renewed interest. Thromb Res 2013;131:290–292
  11. Franchini M, Crestani S, Frattini F, Sissa C, Bonfanti C. ABO blood group and von Willebrand factor: biological implications. Clin Chem Lab Med 2014;52:1273–1276
  12. Jenkins PV, O’Donnell JS. ABO blood group determines plasma von Willebrand factor levels: a biologic function after all? Transfusion 2006;46:1836–1844.

 

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