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Composition of gallbladder bile in healthy individuals and patients with gallstone disease from north and South India

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Abstract

Background

Gallstones (GS) in south India (SI) are predominantly pure pigment or mixed, while in North India (NI), these are either pure cholesterol or mixed. While cholesterol rich gallbladder (GB) bile predicts cholesterol GS, constituent of bile in primary pigment GS is not known. We compared the composition of GB bile from healthy liver donors and patients with GS from north and south India.

Methods

Gallbladder bile from healthy liver donors from north (10) and south India (8) served as controls. Cases were patients from north (21) and south India (17) who underwent cholecystectomy for GS disease. Gallbladder bile from both cases and controls was analyzed for cholesterol, lecithin (phospholipid), and bile salts. Gallstones were classified as cholesterol, mixed, and pigment based on morphology and biochemical analysis.

Results

The median cholesterol concentration in control bile from north was significantly high compared to south (p<0.001) with no difference in lecithin and bile salts (p NS). Except for one sample each from north and south, the cholesterol solubility of controls was within the critical micellar zone. Mixed GS were most frequent in north India (61.9 %) while pigment GS dominated in south (61.9 %). The median cholesterol concentration in bile samples of cholecystectomy patients from north India was significantly high GS (p < 0.00001) with significant lowering of bile salts and lecithin (p < 0.00001). In south India, patients with mixed GS had high cholesterol content in bile compared to controls and patients with pigment GS; bile in latter had significantly higher concentration of bile salt compared to controls and mixed GS. The ternary plot confirmed the composition of GB bile from north and south India.

Conclusions

Gallbladder bile in controls and patients with GS from north India had significantly high cholesterol concentration. In south India, patients with mixed GS had cholesterol rich bile while pigment GS had higher concentrations of bile salts.

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References

  1. Jayanthi V. Pattern of gallstone disease in Madras City, South India-a hospital based survey. J Assoc Physicians India. 1996;44:461–4.

    CAS  PubMed  Google Scholar 

  2. Ashok M, Nageshwar Reddy D, Jayanthi V, et al. Regional differences in constituents of gall stones. Trop Gastroenterol. 2005;26:73–5.

    CAS  PubMed  Google Scholar 

  3. Ashok M, Krishnan A, Choudhury G, Narayana Kalkura S, Jayanthi V. Regional differences in composition of cholesterol gallstones in India. J Med Sci Res. 2012;3:3–5.

    Google Scholar 

  4. Tandon RK. Pigment gallstone. Indian J Gastroenterol. 1988;7:5–6.

    CAS  PubMed  Google Scholar 

  5. Tandon RK, Thakur US, Basaki AK, Lal K, Jayanthi V, Nijahawan S. Pigment gallstone predominant in South India. Indian J Gastroenterol. 1994;12:A18.

    Google Scholar 

  6. Amin AM, Ananthakrishnan N, Nambinarayanan TK. Composition of gallstone and sequential event in biliary lithognensis—is it different in South India compared to north? J Assoc Physicians India. 2000;48:885–90.

  7. Selvaraju R, Ganapathi Raman R, Thiruppathi G, Valliapan R. Epidemiological study of gallstone in Cuddalore district. Int J Pharm Tech Res. 2010;2:1061–7.

    Google Scholar 

  8. Mohan H, Punia RPS, Dhawan SB, Ahal S, Sekhon MS. Morphological spectrum of gallstone disease in 1100 cholecystecomies in North India. Indian J Surg. 2005;67:140–2.

    Google Scholar 

  9. Sarin SK, Kapur BML, Tandon RK. Cholesterol and pigment gallstones in northern India. A prospective analysis. Dig Dis Sci. 1986;31:1041–5.

    Article  CAS  PubMed  Google Scholar 

  10. Kotwal MR, Rinchen CZ. Gallstone disease in the Himalayas (Sikkim and north Bengal): causation and stone analysis. Indian J Gastroenterol. 1998;17:87–9.

    CAS  PubMed  Google Scholar 

  11. Choudhuri G, Agarwal DK, Negi TS. Polarising microscopy of partially dissolved gallstone powder: a simple technique for gallstone composition. J Gastroenterol Hepatol. 1995;10:241–5.

    Article  CAS  PubMed  Google Scholar 

  12. Jayanthi V, Palanivelu C, Prasanthi R, Mathew S, Srinivasan V. Composition of gallstones in Coimbatore District of Tamil Nadu state. Indian J Gastroenterol. 1998;17:134–5.

    CAS  PubMed  Google Scholar 

  13. Gokulakrishnan S, Murugesan R, Mathew S, et al. Predicting the composition of gallstones by infrared spectroscopy. Trop Gastroenterol. 2001;22:87–9.

    CAS  PubMed  Google Scholar 

  14. Ashok M, Narayana Kalkura S, Kennedy VJ, et al. Trace element analysis of south Indian gallstones by PIXE. Int J PIXE. 2002;12:137–44.

    Article  CAS  Google Scholar 

  15. Ashok M, Rautray TR, Pranaba KN, Vijayan V, Jayanthi V, Kalkura SN. Energy dispersive X-ray fluoroscence analyses of gallstones. J Radioanal Nucl Chem. 2003;257:333–5.

    Article  CAS  Google Scholar 

  16. Rautray TR, Vijayan V, Ashok M, et al. PIXE analysis of gallstones. Int J PIXE. 2005;15:147–52.

  17. Farina A, Dumonceau JM, Lescuyer P. Proteomic analysis of human bile and potential applications for cancer diagnosis. Expert Rev Proteomics. 2009;6:285–301.

    Article  CAS  PubMed  Google Scholar 

  18. Van Erpecum KJ. Pathogenesis of cholesterol and pigment gallstones: an update. Clin Res Hepatol Gastroenterol. 2011;35:281–7.

    Article  CAS  PubMed  Google Scholar 

  19. Thistle JL, Schoenfield LJ. Lithognic bile among young Indian women. Lithogenic potential decreased with chenodeoxycholicacid. In: Diagnosis and Treatment of Prevalent Diseases of North American Indian Populations. Vol, 1. Editor: Melvin Lee. Ardent Media, 1974.

  20. Jüngst D, Lang T, Huber P, Lange V, Paumgartner G. Effect of phospholipids and bile acids on cholesterol nucleationtime and vesicular/micellar cholesterol in gallbladder bile of patients with cholesterol stones. J Lipid Res. 1993;34:1457–64.

    PubMed  Google Scholar 

  21. Trotman BW. Pigment gallstone disease. Gastroenterol Clin N Am. 1991;20:111–26.

    CAS  Google Scholar 

  22. Trotman BW, Bernstein SE, Bove KE, Wirt GD. Studies on the pathogenesis of pigment gallstones in hemolytic anemia. Description and characteristics of a mouse model. J Clin Invest. 1980;65:1301–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Soloway RD, Trotman BW, Maddreuy WC, Nakayam F. Pigment gallstone composition in patients with hemolysis or infection/stasis. Dig Dis Sci. 1986;31:454–60.

    Article  CAS  PubMed  Google Scholar 

  24. Pavithra S, Rao U, Mohan P, Jayanthi V. Bactibilia in pigment gallstone disease. Dig Liver Dis. 2010;42:231–2.

    Article  CAS  PubMed  Google Scholar 

  25. Jayanthi V, Prasanthi R, Mathew S, et al. Epidemiology of gallstone disease—topline findings. Bombay Hosp J. 1999;41:494–502.

    Google Scholar 

  26. Jayanthi V, Anand L, Ashok L, Srinivasan V. Dietary factors in pathogenesis of gall stones disease in southern India—a hospital based case control study. Indian J Gastroenterol. 2005;24:97–9.

    CAS  PubMed  Google Scholar 

  27. Alexander PC, Ramya S, Vijaya S, Srinivas M, Jayanthi V. Risk profile for gallstone disease in south Indian population: is there anything new? Indian J Gastroenterol. 2014;33:254–7.

    Article  Google Scholar 

  28. Sharma R, Soy S, Kumar C, Sachan SG, Sharma SR. Analysis of gallstone composition and structure in Jharkhand region. Indian J Gastroenterol. 2015;34:29–37.

    Article  PubMed  Google Scholar 

  29. Sharma R, Kumar U, Jha NK, Sachan SG, Sharma SR. Consumption of heme iron: a major factor in pigment gallstone formation. Int J Biomed Res. 2014;5:34–7.

    Article  CAS  Google Scholar 

  30. Reinhold JG, Ferguson LK. The reaction of human bile and its relation to gallstone formation. J Exp Med. 1929;49:681–94.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Tera H. Sedimentation of bile constituents. Ann Surg. 1963;157:468–72.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Sutor DJ, Wooley SE. A statistical survey of the composition of gallstones in eight countries. Gut. 1971;12:55–64.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. Parekh AC, Jung DH. Cholesterol determination with ferric acetate-uranium acetate and sulfuric acid-ferrous sulfate reagents. Anal Chem. 1970;42:1423.

    Article  CAS  Google Scholar 

  34. Fiske CH, Subbarrow Y. The colorimetric determination of phosphorus. J Biol Chem. 1925;66:375–400.

    CAS  Google Scholar 

  35. Talalay P. Enzymatic analysis of steroid hormone. Methods Biochem Anal. 1960;8:119–43.

  36. Admirand WH, Small DM. The physicochemical basis of cholesterol gallstone formation in man. J Clin Invest. 1968;47:1043–52.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Fang Y, Weisbrodt N, Moody FG. Essentials of experimental surgery. In: The Biliary Tract. Eds. Gregerson H, Jensen SL, S, Moody F, Hokouh Amin M. The Netherlands Harwood Academic Publishers. 1996; Chap 41: pp 1–10.

  38. Thistle JL, Schoenfield LJ. Induced alteration of bile composition in humand with cholelithiasis. J Lab Clin Med. 1969;74:1020–1.

    Google Scholar 

  39. Small DM, Rapo S. Source of abnormal bile in patients with cholesterol gallstones. N Engl J Med. 1970;283:53–7.

    Article  CAS  PubMed  Google Scholar 

  40. Johnston CG, Ravdin IS, Riegel C, Allison CL. Studies on gallbladder function. IX. The anion-cation content of bile from the normal and infected gallbladder. J Clin Invest. 1933;12:67–75.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  41. Andrews E. Detailed studies of a series of gallbladder cases. Surg Gynec Obst. 1933;57:36.

    Google Scholar 

  42. Andrews E, Schoenheimer R, Hrdina L. Etiology of gallstones. I Chemical factors and the role of the gallbladder. Arch Surg. 1932;25:796.

  43. Riegel C, Ravdin IS, Johnston CG, Morrison PJ. Studies of gall-bladder function. XIII The composition of gall-bladder bile and calculi in gallbladder diseases Surg Gynec Obst. 1936;62:933.

    Google Scholar 

  44. Antsaklis G, Lewin MR, Sutor DJ, Cowie AGA, Clark CG. Gallbladder function, cholesterol stones and bile composition. Gut. 1975;16:937–42.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  45. Heller F, Bouchier IAD. Cholesterol and bile salt studies on the bile of patients with cholesterol gallstones. Gut. 1973;14:83–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Mackay C, Crook JN, Smith DC, McAllister RA. The composition of hepatic and gallbladder bile in patients with gallstones. Gut. 1972;13:759–76.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  47. Simmons F, Ross APJ, Bouchier IAD. Alterations in hepatic bile composition after cholecystectomy. Gastroenterology. 1972;63:466–71.

    CAS  PubMed  Google Scholar 

  48. Vlahcevic ZR, Bell CC Jr, Gregory DH, Buker G, Juttijudata P, Swell L. Relationship of bile acid pool size to the formation of lithogenic bile in female Indians of the southwest. Gastroenterology. 1972;62:73–83.

  49. Vlahcevic ZR, Bell CC Jr, Swell L. Significance of the liver in the production of lithogenic bile in man. Gastroenterology. 1970;59:62–9.

  50. Gustafsson U, Sahlin S, Einarsson C. Biliary lipid composition in patients with cholesterol and pigment gallstones and gallstone free subjects: deoxycholic acid does not contribute to formation of cholesterol gallstones. Eur J Clin Investig. 2000;20:1099–106.

    Article  Google Scholar 

  51. Wang L, Shen W, Wen J, An X, Cao L, Wang B. An animal model of black pigment gallstones caused by nanobacteria. Dig Dis Sci. 2006;51:1126–32.

    Article  PubMed  Google Scholar 

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Correspondence to V . Jayanthi.

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VJ, SS, JV, VV, MS, MSR, VS, GMMR, MR, and SK declare that they have no conflict of interest.

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The authors declare that the study was performed in a manner to conform with the Helsinki declaration of 1975, as revised in 2000 and 2008 concerning human and animal rights, and the authors followed the policy concerning informed consent as shown on Springer.com

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Jayanthi, V..., Sarika, S., Varghese, J. et al. Composition of gallbladder bile in healthy individuals and patients with gallstone disease from north and South India. Indian J Gastroenterol 35, 347–353 (2016). https://doi.org/10.1007/s12664-016-0685-5

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