Abstract
Background:
Extensive research has explored the potential correlation between thyroid disorders and gallstone disease. The relationship between hypothyroidism and gallstone formation in individuals with different blood types has garnered significant interest, with various hypotheses proposed.Objectives:
This study aims to investigate the association between hypothyroidism and the formation of gallstones in patients with different blood groups. Our goal is to shed light on the potential link between these two conditions and contribute to the existing body of knowledge in this area.Methods:
A retrospective case-control study was conducted in 2023, involving 450 patients. The patients were divided into case and control groups in a 1:2 ratio. Both groups were evaluated for hypothyroidism and blood type. The data were analyzed using statistical tests and a logistic regression model in Statistical Package for the Social Sciences (SPSS) software version 26.Results:
The study included participants with a mean age of 41.42 ± 15.74 years, consisting of 189 males (42.0%) and 56 (12.44%) individuals with hypothyroidism. Analysis revealed a significant correlation between blood type and the occurrence of gallstones (P < 0.001), with the highest frequency of gallstones observed in individuals with blood group B+. Similarly, a significant association was found between blood type and hypothyroidism (P < 0.001), with the highest frequency of hypothyroidism in individuals with blood group O+. Blood type O+ was the most frequent in patients with both disorders (hypothyroidism and gallstones), which was also statistically significant (P = 0.03). Blood type and hypothyroidism together predicted 12% of the changes in gallstone occurrence. Individuals with blood groups A+ and O+ were nearly four times more likely to develop gallstones compared to individuals with other blood groups (OR = 4.06 and OR = 4.16, respectively). Additionally, the presence of hypothyroidism nearly doubled the risk of developing gallstones (OR = 1.93).Conclusions:
The findings of this study suggest that individuals with blood group O+ have a significantly higher susceptibility to hypothyroidism compared to those with other blood types. Furthermore, individuals with hypothyroidism are nearly twice as likely to develop gallstone disease.Keywords
1. Background
Gallstones are a prevalent condition affecting around 10% to 20% of adults and can cause significant economic and social burdens when complications arise (1). While most affected adults do not experience symptoms, the prevalence of gallstones is linked to age, gender, and ethnicity. Women are more prone to gallstones than men, with estrogen thought to play a role in their formation due to its effect on cholesterol (2-4). Gallstones and hypothyroidism are two common medical conditions that can occur due to various factors (5). Hypothyroidism is an endocrine disorder affecting 3.7% of people worldwide, and it is more common in women (4). This condition involves the formation of hard deposits of digestive fluid in the gallbladder, which can cause symptoms such as abdominal pain, nausea, vomiting, and fever. Gallstones can result from various factors, including genetics, obesity, and a high-fat diet (2, 3). Hypothyroidism can be overt (clinical) or subclinical, where the serum level of thyroxine is lower than normal. In cases where serum thyroid hormones are within the normal laboratory range but serum thyroid-stimulating hormone (TSH) levels are slightly elevated, subclinical hypothyroidism (mild thyroid insufficiency) is diagnosed (4). It is essential for individuals experiencing symptoms of gallstones to seek medical attention promptly to prevent complications and ensure proper management of the condition (6).
Studies suggest that approximately 13 - 24% of patients with gallstones have hypothyroidism (4). Recent clinical research indicates a correlation between thyroid activity and gallstone formation (2). The possible reason for this correlation is that movement disorders in the bile duct and sphincter of Oddi, combined with hyperlipidemia, may contribute to gallstone formation in patients with hypothyroidism (5). A study involving 3,749 participants aged 20 to 79 found an independent correlation between the presence of gallstones and elevated serum TSH levels in men, while a positive correlation was observed in women (6). However, another study concluded that there is no apparent correlation between the development of gallstones and hypothyroidism (7). In a study on 746 patients with hypothyroidism, 44.5% of women were found to have gallstones (8). Gallstones are believed to form due to a combination of factors, including cholesterol crystals in the bile. There is a well-established link between thyroid disease and lipid disorders, which can affect the composition and transport of lipoproteins. Hypothyroidism is linked to hypercholesterolemia and increased low-density lipoprotein (LDL) cholesterol levels, while hyperthyroidism leads to lower levels of total cholesterol, LDL, and high-density lipoprotein (HDL) cholesterol. Evidence suggests a possible association between hypothyroidism and cholesterol gallstone disease due to reduced LDL clearance and sphincter of Oddi dysfunction. The absence of thyroxine's pro-relaxing effect on the sphincter of Oddi may cause delayed biliary tract emptying, making individuals more prone to gallstone formation (9). On the other hand, recent studies have discovered a correlation between the ABO blood group system and various types of cancer, as well as several benign and malignant diseases, including some rheumatologic conditions, medullary thyroid cancers among thyroid diseases, and autoimmune diseases. Additionally, a new association between blood groups and autoimmune diseases has emerged. These findings suggest a potential link between the most commonly seen benign thyroid diseases, particularly Hashimoto’s thyroiditis, and blood groups. However, no study has yet shown a direct association between these diseases and blood groups (10).
2. Objectives
Therefore, this study aims to establish a correlation between hypothyroid function and the occurrence of gallstones in patients from different blood groups.
3. Methods
3.1. Study Design and Setting
This is a retrospective case-control study conducted in 2023 on patients with gallstones who were candidates for cholecystectomy in hospitals affiliated with Abadan University of Medical Sciences. Patients with a history of thyroid surgery, those using drugs and substances that cause hypothyroidism (such as amiodarone, lithium, antidepressants, phenytoin, and interferon), as well as drugs that cause gallstones (such as estrogen-like fenofibrate and gemfibrozil) were excluded (11). After applying the inclusion and exclusion criteria, a total of 450 patients were selected for the study, with 150 individuals in the case group (who had been hospitalized for gallstone surgery) and 300 individuals in the control group (who did not suffer from gallstones). Both groups were matched based on age, sex, and place of residence, and were evaluated for blood groups and hypothyroidism.
3.2. Data Collection Tools
Data collection was carried out using a researcher-designed checklist that included information on demographics, blood groups, thyroid test results, duration of infection, and underlying diseases. Interviews and blood tests were conducted to complete the checklist, which was validated through feedback from field experts. Subclinical hypothyroidism was identified in patients through TSH blood tests. The diagnostic criteria for hypothyroidism were set at TSH levels exceeding 5 μIU/mL, alongside normal levels of T4 (12). Venous blood samples were collected from patients to evaluate their TSH and free T4 (FT4) levels. The samples underwent centrifugation and serum separation before being stored at -20°C. A human TSH measurement kit from Pars Azmoun, an Iranian company, was used to determine TSH levels via the ELISA method. The kit, with a sensitivity of 0.05 μIU/mL, had a measurement range of 0.3 to 5 μIU/mL. Additionally, an ELISA kit procured from Pars was used to measure FT4 levels, with a sensitivity of 0.2 ng/dL and a measurement range of 0 - 10 ng/dL. A specialist confirmed the diagnosis of gallstones based on an ultrasound of the gallbladder and bile ducts. Blood groups were determined with a Cinagen blood group detection kit utilizing Cinagen antibodies, and the outcomes were reported accordingly.
3.3. Data Analysis
The normality of the data was assessed using the Kolmogorov-Smirnov test, which indicated a normal distribution. We used central tendency and dispersion measures such as frequency, percentage, and mean ± standard deviation to compare groups. Additionally, the chi-square test and Fisher's exact test were employed. A logistic regression model was applied to determine the impact of variables on the incidence of gallstones. The data were analyzed using the Statistical Package for the Social Sciences (SPSS) version 26, with a significance level set at P < 0.05.
4. Results
The study included a total of 450 patients, with an average age of 41.42 ± 15.74 years. Among them, 189 patients (42.0%) were male. Hypothyroidism was observed in 56 patients (12.44%), and the average duration of the disease was 5.26 ± 1.58 years. When the patients were analyzed in groups, no significant statistical differences were found in terms of age, gender, and duration of the disease (Table 1).
Demographic Variables in the Case and Control Groups a
According to Table 1, the incidence of hypothyroidism was significantly higher in the case group (17.3%) compared to the control group (10.0%). Statistical analysis using Fisher's exact test revealed a significant relationship between gallstones and hypothyroidism (P = 0.03). Additionally, the study analyzed the distribution of blood groups among individuals with gallstones and found that the B+ blood group had the highest frequency (37.3%), while the A- blood group had the lowest frequency (8.7%). The chi-square test results demonstrated a significant association between blood type and gallstones (P < 0.001) (Figure 1).
Gallstone incidence in the blood group of patients in the case group
It was found that the most prevalent blood group among individuals with hypothyroidism was O+ (32.1%). A one-dimensional chi-square test revealed a significant correlation (P < 0.001) between blood group and hypothyroidism, as visually represented in Figure 2.
The incidence of hypothyroidism in the blood group of patients
According to the findings in Table 2, there is a significant statistical correlation between gallstones and hypothyroidism, regardless of blood group, as evaluated through the chi-square test (P = 0.03). Specifically, the highest frequency of patients suffering from both hypothyroidism and gallstones was observed in blood group O+. These results suggest that there may be a relationship between blood group and the occurrence of gallstones in patients with hypothyroidism.
Consensus Table of Blood Group and Gallstones in People with Hypothyroidism a
Variable | Hypothyroidism | P-Value | |
---|---|---|---|
Intervention Group (N = 150) | Control Group (N = 300) | ||
Blood groups | 0.03 b | ||
A+ | 2 (8.0) | 6 (19.4) | |
B+ | 7 (28.0) | 10 (32.3) | |
AB+ | 0 (0.0) | 5 (16.1) | |
O+ | 9 (36.0) | 9 (29.0) | |
O- | 2 (8.0) | 1 (3.2) | |
B- | 5 (20.0) | 0 (0.0) |
Based on the results of the logistic regression test, it was found that an individual's blood group and hypothyroidism status can predict the likelihood of developing gallstones with 12% accuracy. The study revealed that individuals with blood groups A+ and O+ have a significantly higher chance of developing the disease, nearly four times higher than those with other blood groups (13.20 - 1.25 CI: 0.95, OR = 4.06), (12.83 - 1.35 CI: 0.95, OR = 4.16). Additionally, the likelihood of developing gallstone disease nearly doubled for individuals with hypothyroidism, according to the results (3.53 - 1.05 CI: 0.95, OR = 1.93) (Table 3).
Investigating the Effect of Blood Groups and Hypothyroidism on Gallstones by Logistic Regression Model
Variables | Regression Coefficient | Standard Deviation of the Error | Parent Statistics | Degrees of Freedom | Significance Level | Odds Ratio | Odds Ratio CI 95% |
---|---|---|---|---|---|---|---|
Blood groups | - | - | 34.50 | 6 | 0.000 | - | - |
A+ | 1.40 | 0.60 | 5.45 | 1 | 0.019 | 4.06 | 13.20 - 1.25 |
B+ | 0.56 | 0.55 | 1.04 | 1 | 0.307 | 1.76 | 5.20 - 0.59 |
AB+ | -0.20 | 0.59 | 0.12 | 1 | 0.728 | 0.81 | 2.60 - 0.25 |
O+ | 1.42 | 0.57 | 6.15 | 1 | 0.013 | 4.16 | 12.83 - 1.35 |
A- | -0.30 | 0.85 | 0.12 | 1 | 0.723 | 0.73 | 3.95 - 0.14 |
O- | -0.08 | 0.66 | 0.01 | 1 | 0.898 | 0.91 | 3.37 - 0.25 |
Hypothyroidism | 0.65 | 0.31 | 4.58 | 1 | 0.032 | 1.93 | 3.53 - 1.05 |
Constant | -1.23 | 0.73 | 2.81 | 1 | 0.093 | 0.29 | - |
5. Discussion
The objective of this study was to investigate the correlation between hypothyroidism and gallstones in patients' blood groups. Gallstone disease refers to the occurrence of symptoms or complications caused by gallstones, a costly gastrointestinal disorder that often leads to hospital admission (13). Gallstones are classified into two main types based on their anatomical location: Gallbladder stones (also known as cholecystolithiasis) and bile-duct stones. Bile-duct stones can be further categorized into extrahepatic duct stones (mostly common bile duct stones, or EHD stones) and intrahepatic duct stones (also called hepatolithiasis, or IHD stones). Treatment strategies, biomedical components, pathophysiology, and associated factors are thought to be distinct for different gallstone subtypes (14, 15). Gallstones may have different prevalences based on factors such as age, anatomical location, gender, and geographical location. There has been less focus on exploring the potential risk factors associated with different blood groups (16, 17). The ABO blood group system is medically significant for investigating various diseases. Genetic differences in blood groups have led to controversial issues regarding the relationship between the ABO blood group and susceptibility to certain infectious and non-infectious diseases. The presence or absence of antigens in certain blood groups can alter the morphology and function of the blood membrane. Functions associated with the structure of blood groups can actively, and sometimes subtly, contribute to the onset of various diseases (18, 19). Various blood groups may play different roles in various diseases, which require further research. These diseases include infectious diseases, rectal, colon, and stomach cancers, high blood pressure, endocrine diseases, pancreatitis, diabetes, and leukemia. Through analyzing the data collected in this study, we aim to better understand the influence of blood groups compared to previous research (18, 20-22).
The research results indicated that patients with the B+ blood group had the highest prevalence of gallstones. Furthermore, a significant statistical difference was observed between blood type and the occurrence of gallstones. However, previous studies in this field have presented inconsistent findings. For example, Alsisi et al. discovered that 46.1% of the 266 patients with gallstones had the O+ blood group, which was the highest frequency (23). Kratzer et al. reported that AB+ blood type had the highest frequency of 12.1%, but no significant association was identified between gallstones and blood type (24).
In this study, researchers investigated the connection between blood groups and hypothyroidism. They found that individuals with blood group O+ had the highest occurrence of hypothyroidism, which was statistically significant. This finding is consistent with previous studies by Alazmi et al. and Dagdeviren et al. The results of this research can help further understand hypothyroidism and inform future clinical practice (8, 10). Another study by Prakash et al. found that around 45.5% of infected individuals with blood group O+ had hypothyroidism (25). Previous studies have also shown a higher incidence of hypothyroidism in people with blood type O+. Based on the findings of this study, individuals with a history of hypothyroidism are more likely to have blood group O+ and less likely to have blood group AB+ compared to blood group O+. Blood group O+ does not have A and B antigens, while both antigens are present in blood group AB. The abnormal expression of blood group antigens on thyroid cells may lead to tissue damage, ultimately resulting in hypothyroidism in individuals with blood type O+ (17). The results of this study, as well as the Khoshgoeian et al. study, indicate a potential connection between blood group antigens and hypothyroidism, which necessitates further investigation for a comprehensive understanding (26). A study conducted in India also pointed to the role of blood group O+ in the occurrence of hypothyroidism. This study introduces blood groups A and B as a factor in the occurrence of hyperthyroidism (25).
A recent study has found a relationship between hypothyroidism and gallstones, regardless of blood type. The link between gallstone disease and hypothyroidism can be attributed to several factors. Hypothyroidism hinders cholesterol metabolism in the liver and reduces bile secretion. About 90% of hypothyroid patients have high levels of cholesterol and triglycerides in their blood. The elevated levels of serum cholesterol in hypothyroidism can lead to bile saturation with cholesterol. When bile becomes oversaturated with cholesterol, it can result in decreased gallbladder motility, contractility, and impaired filling, which may lead to prolonged retention of bile in the gallbladder. This extended retention provides enough time for sedimentation and growth of gallstones (27). Interestingly, patients with blood type O+ who had both conditions exhibited the highest frequency. This discovery aligns with a previous investigation by Dhoka et al., which found a positive correlation between gallstones and hypothyroidism in 33.7% of the 86 patients examined (28).
Thyroid hormones play a significant role in maintaining physiological homeostasis by influencing both lipid metabolism and the motor function of the biliary system. The modulation of lipid metabolism by thyroid hormones has significant implications for individuals with thyroid disorders, as it can impact cholesterol levels and increase the risk of cardiovascular disease. Moreover, the effects of thyroid hormones on the biliary system can contribute to the development of gallbladder disease, highlighting the importance of further research in this area (28). A study conducted by Issa involving 232 patients diagnosed with gallstones found that only 32 of them were also diagnosed with hypothyroidism. This suggests that there is no significant association between hypothyroidism and the occurrence of gallstones (7). However, it is possible that the observed correlation between hypothyroidism and study outcomes was not statistically significant due to the high levels of alkaline phosphatase discovered in the bile ducts of the 23 hypothyroid patients. This specific enzyme was found to be within normal levels in patients who were either hyperthyroid or euthyroid. It is plausible that secondary thyroid hormones do not affect the receptors responsible for bile movement, which may lead to biliary and sphincter stasis and Oddi dysfunction. These conditions, caused by thyroxine deficiency induced by hypothyroidism, may cause an increase in biliary pressure and elevated levels of alkaline phosphatase (28).
Many studies have explored the link between ABO blood groups and diseases, proposing potential mechanisms. However, conflicting results have made it difficult to reach a definitive conclusion. Despite this, evidence has been gathered to shed light on this association. ABO blood groups may impact the risk of various diseases through both known and unknown mechanisms. It is now understood that ABO blood groups are not the direct cause of diseases, but rather can predispose individuals to certain health problems.
5.1. Limitations
A limitation of this study is its small sample size, especially considering the significance and scope of the research. Additionally, the study was limited to hospitals in specific regions, which may affect the generalizability of the findings.
5.2. Conclusions
The study has demonstrated a significant relationship between hypothyroidism and gallstones in individuals with specific blood groups. Further research on blood group variables is highly recommended to validate the findings of this study and to uncover the underlying pathophysiological mechanisms that may explain the observed correlation.
Acknowledgements
References
-
1.
Pak M, Lindseth G. Risk Factors for Cholelithiasis. Gastroenterol Nurs. 2016;39(4):297-309. [PubMed ID: 27467059]. [PubMed Central ID: PMC8802735]. https://doi.org/10.1097/SGA.0000000000000235.
-
2.
Chen J, Zhou H, Jin H, Liu K. The causal effects of thyroid function and lipids on cholelithiasis: A Mendelian randomization analysis. Front Endocrinol (Lausanne). 2023;14:1166740. [PubMed ID: 37065749]. [PubMed Central ID: PMC10090462]. https://doi.org/10.3389/fendo.2023.1166740.
-
3.
Volzke H, Robinson DM, John U. Association between thyroid function and gallstone disease. World J Gastroenterol. 2005;11(35):5530-4. [PubMed ID: 16222749]. [PubMed Central ID: PMC4320366]. https://doi.org/10.3748/wjg.v11.i35.5530.
-
4.
Ali M, Bayazeed WU, Raza AA, Shahana N, Khan J. Prevalence of hypothyroidism in patients with cholelithiasis: A cross sectional study. Pak J Surg. 2020;36(1):9-14.
-
5.
Ravi PC, Thugu TR, Singh J, Dasireddy RR, Kumar SA, Isaac NV, et al. Gallstone Disease and Its Correlation With Thyroid Disorders: A Narrative Review. Cureus J. 2023;15(9). https://doi.org/10.7759/cureus.45116.
-
6.
Kulkarni V, Ramteke H, Lamture Y, Gharde P. A Review of Synchronous Findings of Hypothyroidism and Cholelithiasis. Cureus J. 2022;14(10). https://doi.org/10.7759/cureus.30316.
-
7.
Issa AH. The prevalence of hypothyroidism in patients with gall stone disease. J Med Sci clinic Res. 2018;6(10). https://doi.org/10.18535/jmscr/v6i10.154.
-
8.
Alazmi NHA, Rasool G, Alanazi AO, Bakr Ali AM, Alotayfi RFS, Alanazie K. ABO & Rh Blood Group as a Risk Factor Of Hypothyroidism. INDO America J Pharmaceutic Sci. 2019;6(4). https://doi.org/10.5281/zenodo.2646261.
-
9.
Wang Y, Yu X, Zhao QZ, Zheng S, Qing WJ, Miao CD, et al. Thyroid dysfunction, either hyper or hypothyroidism, promotes gallstone formation by different mechanisms. J Zhejiang Univ Sci B. 2016;17(7):515-25. [PubMed ID: 27381728]. [PubMed Central ID: PMC4940627]. https://doi.org/10.1631/jzus.B1500210.
-
10.
Dagdeviren M, Ates I, Demir BF, Ergun E, Yildiz C, Altay M. Investigation of blood groups in benign thyroid diseases in Turkey. Endocr J. 2019;66(11):1001-9. [PubMed ID: 31308303]. https://doi.org/10.1507/endocrj.EJ18-0582.
-
11.
Nair K, Siddartha Gowthaman S, Vinoth S, Manickam R. Thyroid function and gallstone disease: is there an association? Int Surg J. 2021;8(5). https://doi.org/10.18203/2349-2902.isj20211856.
-
12.
Ershad E, Ghaderian SB, Rashidi H, Moradi L, Zaman F. [The Prevalence of Overt and Subclinical Hypothyroidism in Patients with Type 2 Diabetes Mellitus Admitted to Imam and Golestan Hospitals, Ahvaz, in 2020-2021]. Iran J Endocrinol Metab. 2021;23(5):311-8. FA.
-
13.
Mallick B, Anand AC. Gallstone Disease in Cirrhosis-Pathogenesis and Management. J Clin Exp Hepatol. 2022;12(2):551-9. [PubMed ID: 35535063]. [PubMed Central ID: PMC9077239]. https://doi.org/10.1016/j.jceh.2021.09.011.
-
14.
Song Y, Ma Y, Xie FC, Jin C, Yang XB, Yang X, et al. Age, gender, geographic and clinical differences for gallstones in China: a nationwide study. Ann Transl Med. 2022;10(13):735. [PubMed ID: 35957733]. [PubMed Central ID: PMC9358507]. https://doi.org/10.21037/atm-21-6186.
-
15.
Shabanzadeh DM, Christensen DW, Ewertsen C, Friis-Andersen H, Helgstrand F, Nannestad Jorgensen L, et al. National clinical practice guidelines for the treatment of symptomatic gallstone disease: 2021 recommendations from the Danish Surgical Society. Scand J Surg. 2022;111(3):11-30. [PubMed ID: 36000716]. https://doi.org/10.1177/14574969221111027.
-
16.
Di Dato F, Ranucci G, Iorio R. Gallstone Disease. Pediatr Hepatol Liver Transplant. 2019. 2019. p. 219-26. https://doi.org/10.1007/978-3-319-96400-3_12.
-
17.
DenİZ MS. Distribution of ABO blood groups and Rh factor in benign and malign thyroid nodules. J Health Sci Med. 2023;6(2):462-6. https://doi.org/10.32322/jhsm.1243805.
-
18.
Abegaz SB. Human ABO Blood Groups and Their Associations with Different Diseases. Biomed Res Int. 2021;2021:6629060. [PubMed ID: 33564677]. [PubMed Central ID: PMC7850852]. https://doi.org/10.1155/2021/6629060.
-
19.
Ewald DR, Sumner SC. Blood type biochemistry and human disease. Wiley Interdiscip Rev Syst Biol Med. 2016;8(6):517-35. [PubMed ID: 27599872]. [PubMed Central ID: PMC5061611]. https://doi.org/10.1002/wsbm.1355.
-
20.
Anstee DJ. The relationship between blood groups and disease. Blood J. 2010;115(23):4635-43. [PubMed ID: 20308598]. https://doi.org/10.1182/blood-2010-01-261859.
-
21.
Wolpin BM, Kraft P, Gross M, Helzlsouer K, Bueno-de-Mesquita HB, Steplowski E, et al. Pancreatic cancer risk and ABO blood group alleles: results from the pancreatic cancer cohort consortium. Cancer Res J. 2010;70(3):1015-23. [PubMed ID: 20103627]. [PubMed Central ID: PMC2943735]. https://doi.org/10.1158/0008-5472.CAN-09-2993.
-
22.
Miao SY, Zhou W, Chen L, Wang S, Liu XA. Influence of ABO blood group and Rhesus factor on breast cancer risk: a meta-analysis of 9665 breast cancer patients and 244,768 controls. Asia Pac J Clin Oncol. 2014;10(2):101-8. [PubMed ID: 23714093]. https://doi.org/10.1111/ajco.12083.
-
23.
Alsisi G, Albouq S, Alaa A, Almutairi A, Mohammed R. Relation Between Abo Blood Groups and Cholelithiasis Among Population In Al-Madina, Saudi Arabia, 2018: Case-Control Study. Indo America J Pharmaceutic Sci. 2019;6(1):2578-83.
-
24.
Kratzer W, de Lazzer K, Wiesneth M, Muche R, Kachele V. [The effect of ABO, Rhesus and Kell blood group antigens on gallstone prevalence. A sonographic study of 1030 blood donors]. Dtsch Med Wochenschr. 1999;124(19):579-83. DE. [PubMed ID: 10365175]. https://doi.org/10.1055/s-2007-1024362.
-
25.
Prakash BG, Babu AR, Mehta P. ABO Blood Group and its Unusual Relationship with Thyroid Disorders. India J Public Health Res Develop. 2020;11(5).
-
26.
Khoshgoeian A, Hosseini-khah Z, Kashi Z, Movahedirad M, Bahar A. Association between ABO Blood Groups and Thyroid Dysfunction. Tabari Biomedical Student Research Journal. Tabari Biomed Stu Res J. 2023;5(3):13-20.
-
27.
Ghimire P, Babugharti B. Association of Gallstone Disease with Hypothyroidism in Western Region of Nepal. Int Organiz Sci Res J Dent Med Sci. 2017;16(8):40-2. https://doi.org/10.9790/0853-1608054042.
-
28.
Dhoka G, Kumar NA, Yatheendranathan GD. Gall stones and hypothyroidism: a double jeopardy. Int Surg J. 2021;8(8). https://doi.org/10.18203/2349-2902.isj20212794.