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Open Access Research article

Effect of statin use on outcome of symptomatic cholelithiasis: a case-control study

Jukka Pulkkinen12*, Matti Eskelinen12, Vesa Kiviniemi3, Tuukka Kotilainen2, Markus Pöyhönen2, Lasse Kilpeläinen2, Pirjo Käkelä12, Helena Kastarinen3 and Hannu Paajanen12

Author Affiliations

1 Department of Surgery, Kuopio University Hospital, P.O. Box 100, FI-70029 KYS Kuopio, Finland

2 School of Medicine, University of Eastern Finland, P.O. Box 1627, FI-70211 Kuopio, Finland

3 Finnish Medicines Agency, P.O. Box 55, FI-00034 FIMEA Kuopio, Finland

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BMC Gastroenterology 2014, 14:119  doi:10.1186/1471-230X-14-119


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-230X/14/119


Received:25 April 2014
Accepted:26 June 2014
Published:3 July 2014

© 2014 Pulkkinen et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Abstract

Background

Statins can modify bile cholesterol and, thus, the formation of gallstones. We examined whether statin use also modifies the severity of symptomatic gallstone disease and its treatment.

Methods

A total of 1,140 consecutive patients with symptomatic gallstone disease were recruited during 2008-2010 at Kuopio university hospital, Finland. Case-control analysis matched the patients using (n = 272) or not using (n = 272) statins by age and sex. The baseline characteristics of the patients, need and type of surgical treatment, duration of operation, perioperative bleeding, postoperative complications and overall mortality rate were compared statistically between the study groups.

Results

Morbidity and subsequent polypharmacy occurred more frequently among the patients with statins compared to the patients without statins. There were no significant differences between the statin users and non-users regarding surgical treatment (open vs. laparoscopic cholecystectomy). The mean operation time for laparoscopic cholecystectomy was 10% shorter for the patients with statin use than for the patients without. In addition, there was a non-significant tendency for statin users to bleed less during laparoscopic operations than the non-users. There were no differences in other procedure-related parameters (e.g., operation urgency, conversions, choledochotomies, complications and mortality) in patients with or without statins.

Conclusions

Compared to no treatment, statin treatment was associated with a shorter operation time for laparoscopy cholecystectomy. Other surgical outcome parameters were similar in patients with or without statins, although statin users had more polypharmacy and circulatory illnesses than non-users.

Keywords:
Cholelithiasis; Statins; Cholecystectomy

Background

Gallstone disease and cholesterol-lowering statin medications are common in Western countries, and they have a high economic impact [1]. Symptomatic gallstones are one of the leading causes of inpatient admissions in general surgery [2]. The prevalence of gallstone disease is increasing because of worldwide epidemics of obesity, insulin resistance and aging. In Western populations, the majority of gallstones formed in the gallbladder consist mainly of cholesterol, as they are formed from cholesterol-supersaturated bile [3]. Cholesterol gallstones account for 80-95% of the gallstones found during cholecystectomy [4,5].

Hypercholesterolemia is an important risk factor for atherosclerosis, which has been the most common cause of death in developed countries. Statins are used to treat dyslipidemia, which prevents cardiovascular or cerebrovascular events. Statins are among the most widely used medications in the Western world [6,7]. As in other Western societies, statin use in Finland has increased exponentially: There has been an 11-fold increase in statin use between 1995 and 2005 [8]. According to the reimbursement register data of the Social Insurance Institute of Finland (population 5.2 million), approximately 660,000 individuals purchased statins in 2012, which is 12% of population.

The relationship between statins and symptomatic gallstone disease is still more or less conflicting, although several studies have reported a significant reduction in the incidence of symptomatic gallstones disease in patients using statin therapy [9]. The most consistent evidence is that bile is desaturated of cholesterol after the long-term administration of statins [10,11]. These observations suggest that statins may reduce the size of cholesterol particles and, subsequently, prohibit gallstone formation and reduce the size of gallstones; therefore, they may also affect the course of symptomatic gallstone disease. The effect of statin therapy on the course and outcome of cholecystectomy is unknown.

We conducted a case control study to assess the influence of statins on complicated gallstone disease. Based on the effect of statins on gallstone formation, we hypothesized that statin use would be associated with less severe acute gallbladder inflammation, fewer stones in the common bile duct and, furthermore, fewer complications.

Methods

A total of 1,140 consecutive patients with symptomatic gallstones were admitted to Kuopio University Hospital, Finland, from 2008-2010. The hospital serves an area of 243,000 inhabitants. A total of 272 of 1,140 patients with symptomatic cholelithiasis underwent statin therapy. The age- and sex-matched controls (n = 272) were randomly selected from the cohort of patients without statin therapy. Patient data were obtained from the hospital records using the following discharge diagnoses (ICD 10): K80 (cholelithiasis), K81 (cholecystitis), K82 (other disease of gallbladder) or K83 (other diseases of biliary tract). The imaging study results (i.e., computed tomography, abdominal ultrasound, magnetic resonance cholangiography) were analyzed. Additional work-ups included a detailed clinical history with records of recent infectious diseases, abdominal traumas, surgery, and endoscopic retrograde cholangiopancreatography (ERCP), as well as data concerning comorbidities and medicine use on arrival. The laboratory data included serum calcium, lipids, liver enzymes and C-reactive protein measurements. The duration of hospital stay, need for intensive care treatment and one-month hospital mortality (2008-2010) were recorded. Data concerning the treatment type (e.g., conservative, laparoscopic, open surgery, conversions, cholecystostomy, and choledochotomies), surgical durations, elective vs. emergency operations, complications, bleeding and number of re-operations were collected from the patients records.

Surgery was performed in both study groups using the same operative principles and by the same group of surgeons. There were no between-group differences in the preoperative or perioperative treatments or procedures. Emergency cholecystectomy was performed if ultrasonography or clinical examination and laboratory parameters revealed signs of cholecystitis in and if the patient was suitable for operation, according to the American Society of Anesthesiologists physical status classification system. If possible, perioperative cholangiography was always performed in acute cholecystitis. Cholecystectomy was primarily performed laparoscopically. In patients with very old age and severe comorbidities, percutaneous cholecystostomy was performed. In patients with long histories of cholecystitis symptoms, the treatment was first conservative, and elective laparoscopy was performed later. According to the Finnish legislation, no ethical assessment or approval is mandatory for a register-based study. As this is a retrospective register study, informed consent from the patients was not needed.

Data were analyzed using IBM SPSS (Statistical Package for the Social Sciences) Statistics 21.0 (IBM Corp. Released 2012. IBM SPSS Statistics for Windows, Version 21.0. Armonk, NY: IBM Corp. USA), and the statistical analyses were performed using independent samples t-tests, Mann-Whitney U-tests and χ2 tests, depending on the distribution of the outcome and distributional assumptions. Adjusted analyses of outcomes were not conducted because of the relatively small number of events in various outcomes of interest. P values less than 0.05 were considered to be statistically significant.

Results

A total of 1140 admissions of the patients with symptomatic cholelithiasis were recorded at our hospital between 2008 and 2010. There were 715 females and 425 males (63% and 37%, respectively). Some 272 patients used statins (24% of the whole study population), 132 females and 140 males (17.6% and 32.9%, respectively), (Table 1). The patients using statin therapy were, on average, older, had a greater incidence of type II diabetes and cardiovascular diseases and were more frequently male than the patients without statin therapy (data not shown).

Table 1. Demographic data of statin users (n = 272) and non-statin users (n = 272) patients with gallstones

Statin users vs. their matched controls

In the case control comparison, hypertension and cardiac diseases were observed more frequently among the statin users compared with the non-users (Table 1). On the contrary, the prevalence of diabetes, neurological, psychiatric, and pulmonary diseases, as well as malignancy, were similar in both study groups. The mean BMI was similar between the groups. In the statin group, simvastatin constituted 73% and atorvastatin 13% of all statins (Table 1).

We also calculated the number of regularly used drugs in both groups. Polypharmacy (>4 medicines) was observed in more than 80% of the patients in the statin group and in 48% of the patients in the no-statin group (p < 0.001). In the non-use group, 28% of the patients were not using any medicines upon admission (data not shown).

We did not observe any statistically significant between-group differences in any of the assessed laboratory parameters, including LDL cholesterol. The mean C-reactive protein concentration was 112 mg/l in the statin group and 113 mg/l in the no-statin group (Table 2).

Table 2. Laboratory data of study groups

Approximately 27% of patients in the statin group and 25% of patients in the non-statin group were treated conservatively (Table 3). Approximately 68% of all operations were elective, and 32% were emergency procedures. Three quarters of the operations were started with laparoscopy. The mean conversion rate to open surgery was 13%. One patient in the non-statin group was re-operated two times: first because of bile leak and again because of abscesses. We found no significant differences between the statin users and non-users regarding the treatment types (elective/emergency, laparoscopic/open) or in the number of conversions or ERCP procedures (Table 3). Furthermore, there were no significant differences in the rate of complications, need for intensive care treatment or hospital mortality. Interestingly, the hospital mortality rates were similar among the statin users and the non-users (Table 3).

Table 3. Treatment and outcome of patients with cholelithiasis

In both study groups, open surgery was more often conducted as an emergency procedure compared with laparoscopic surgery (Table 4).

Table 4. Outcome of cholelithiasis in open and laparoscopic surgery

Interestingly, the mean time for laparoscopic operations was 9.4 minutes shorter in the statin group compared with the control group (p = 0.042). In addition, the time needed for open surgery was shorter in the statin group compared with the non-statin group, although this difference was not statistically significant. Likewise, there was a non-significant trend of increased bleeding among the non-statin group.

Logistic regression analysis was used to adjust for age, gender and outcomes. The results did not differ from the unadjusted results presented in Table 4. Overall, the number of patients having outcomes was too small to conduct more extensive adjusted analyses (i.e., adjusting for co-morbidities). All open and converted patients remained, on average, three days longer in the hospital than the laparoscopic patients (mean 5.8 ± 5.0 and 2.6 ± 9.9, respectively, P < 0.001). There were no between-group differences regarding the hospitalization time (Table 4).

Discussion

The main finding of the present study was that the patients using statins did not have worse outcomes after cholecystectomy than the non-users, although the statin users were older, had polypharmacy and demonstrated more comorbidities than the non-users. Statin therapy was also associated with a shorter laparoscopic operation time. There was also a trend of other benefits from statin use for surgical outcomes, such as less bleeding. These findings are of clinical importance, as one would anticipate that statin users would have more post-surgical complications than non-users. A well-conducted prospective randomized study to show the possible benefits of statins in cholecystectomy is warranted.

The risk of developing symptoms or complications related to gallstones is approximately 1–4% per year [12,13]. The known risk factors for gallstones are female gender, increasing age, obesity, metabolic syndrome, rapid weight loss and gallbladder stasis [14,15]. The most important complications of the gallstone disease are biliary pancreatitis, cholecystitis and cholangitis. Festi et al. showed that during follow-up, approximately 80% of gallstones remain asymptomatic, 10% develop mild symptoms, and 10% develop severe symptoms leading to cholecystectomy [16]. The development of the symptomatic gallstones is associated with obesity and alcohol use, likely because of their effects on serum lipids [17]. It is presently unknown whether statin therapy would transform asymptomatic cholelithiasis to symptomatic.

The use of statins and other lipid-lowering drugs has been greatly increasing in Finland in recent years [8]. This increase has occurred particularly among elderly patients with hypercholesterolemia [18]. Prior to beginning our study, we anticipated that statin users would have less severe acute gallbladder inflammation, fewer stones in the common bile duct and more frequent laparoscopic cholecystectomy than non-users; this hypothesis proved wrong. Statins reduce the bile cholesterol content, which may theoretically reduce the risk of developing micro-gallstones or sludge. In the present study, the 1-year incidence of symptomatic cholelithiasis was approximately 0.22% among statin users and 0.14% among non-statin users (these calculations are based on reimbursement register data, data not shown).

Bodmer et al. performed a case control study using a UK-based database of approximately 5 million patients to investigate statins and the reduced risk of gallstone disease. In this large observational study, a lower incidence of cholecystectomy was noted in patients taking statins [3]. In addition, Tsai et al. performed a large retrospective cohort study among 2479 American women who had histories of gallstones. The authors found that statin use was associated with a reduced risk of cholecystectomy [10]. Smith et al. observed that simvastatin (20 mg/day) decreased plasma and biliary cholesterol levels by reducing cholesterol synthesis after 3 weeks of medication [19]. A long-term study in prairie dogs found that lovastatin alters biliary lipid composition and dissolves gallstones [20]. However, most human studies did not find that statin monotherapy would lead to the complete dissolution of gallstones [11]. In accordance with this finding, the need of surgery of any type or the cholelithiasis outcomes did not differ between the statin and non-statin groups, which contrasted with some previous studies. In a Taiwanese study, the investigators did not find a beneficial association between statin use and gallstone disease [21]. However, in East Asia, there is a lower prevalence of gallstones, and the stones primarily have a brown pigment, which indicates that they are comprised mainly of calcium [1].

Statins were not associated with a lower total serum bilirubin level in our study. In 2011, Ong et al. published a contrasting finding. They investigated whether statins in routine use increase the total bilirubin levels in subjects at high cardiovascular risk; but unexpectedly, the authors found that statin use was associated with lower total bilirubin levels. They suggested that this result could be explained, at least partially, by the effect of statins on glycemia and LDL cholesterol [22].

The clinical outcomes did not differ significantly between the study groups, except for the laparoscopic operation time. A shorter laparoscopic operation time was unexpected, as these patients more often have heart disease or hypertension. Conversely, the patients with cardiac disorders used more medications, thereby affecting the bleeding cascade, which would predispose them to bleeding complications. On average, more bleeding was observed among non-users compared with users during laparoscopic operations, but the difference remained statistically insignificant with a p value of 0.07. However, this finding is in line with the shorter operation time among statin users. Possible mechanisms behind these findings may include smaller size of cholesterol particles and gallstones. More research with larger sample sizes is warranted to confirm these findings. The two-year mortality rate (the study time mortality) was also similar among the statin users and non-users. Four patients died in the hospital. Longer observation time mortality was not studied in this study.

The mechanism by which statins might shorten the operation time or diminish bleeding remains unknown and requires further study. There were no differences in the perioperative procedures between the groups, and the same surgical team was in charge of their treatment. There is evidence that statins might have relevant anti-inflammatory effects independent of their lipid lowering ability [23].

The factors that contribute to supersaturating cholesterol in bile and to the formation of cholesterol gallstones are multifactor. Major sources of cholesterol for biliary secretion are the intestine, liver hepatocytes and circulating lipoproteins. Gallbladder hypomotility, destabilization of bile by kinetic protein factors, abnormal mucins and genetic factors also play roles in cholesterol gallstone disease [24]. Many other factors are associated with cholesterol gallstones formation, such as dietary and life style factors and associated conditions (obesity, estrogen therapy, metabolic syndrome, etc.).

Our study had some limitations. Because this study was a retrospective analysis, we could not determine whether the gallstone formation developed before the statin medication was administered. Gallstone formation occurs over a long time period. Furthermore, we do not have accurate data on the patients’ adherence to statin use nor on the duration of the statin treatment in individual patients. Most gallstones are asymptomatic, and the patient does not require a cholecystectomy or hospital admission [25]. In this study, all patients were hospitalized because they had gallstone-related symptoms or complications. We do not have data from the patients with asymptomatic gallstone disease.

Conclusion

The patients using statins did not have worse outcomes after cholecystectomy than the non-users.

We found that statins might shorten laparoscopic surgery time in patients who have symptomatic cholelithiasis. Statin treatment may also be associated with less bleeding during laparoscopic operations. The beneficial effects of statins were observed, although statin use was associated with more comorbidities and patient polypharmacy. A prospective randomized study is needed to show the protective effects of statins on gallbladder surgery.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

JP revised the data, performed the statistical analysis and drafted the tables and the manuscript. He made substantial contributions to conception and design of study. HK revised manuscript and helped greatly to draft the manuscript. ME, PK revised manuscript. VK revised tables, advised the use of statistics and interpretation of data. TK, MP, LK collected data and drew up a part of the preliminary results. HP conceived of the study and participated in its design and coordination and helped to draft the manuscript and gave final approval of the version to be published. All authors read and approved the final manuscript.

Authors’ information

JP MD and PK MD are surgeons in Kuopio University Hospital. HP and ME are Professors of surgery in Eastern Finland University and surgeons in Kuopio University Hospital. VK PhD statistic and HK MD are experts in Finland Medical Association. TK, MP and LK are medical students in Eastern Finland University.

Acknowledgements

M.Sc. Tuomas Selander, statistic of Kuopio University Hospital, is gratefully acknowledged for valuable statistical advices. There was no external funding for the study.

References

  1. Shaffer EA: Gallstone disease: Epidemiology of gallbladder stone disease.

    Best Pract Res Clin Gastroenterol 2006, 20(6):981-996. OpenURL

  2. Russo MW, Wei JT, Thiny MT, Gangarosa LM, Brown A, Ringel Y, Shaheen NJ, Sandler RS: Digestive and liver diseases statistics, 2004.

    Gastroenterology 2004, 126(5):1448-1453. OpenURL

  3. Bodmer M, Brauchli YB, Krahenbuhl S, Jick SS, Meier CR: Statin use and risk of gallstone disease followed by cholecystectomy.

    JAMA 2009, 302(18):2001-2007. OpenURL

  4. Marschall HU, Einarsson C: Gallstone disease.

    J Intern Med 2007, 261(6):529-542. OpenURL

  5. Schafmayer C, Hartleb J, Tepel J, Albers S, Freitag S, Volzke H, Buch S, Seeger M, Timm B, Kremer B, Folsch UR, Fandrich F, Krawczak M, Schreiber S, Hampe J: Predictors of gallstone composition in 1025 symptomatic gallstones from Northern Germany.

    BMC Gastroenterol 2006, 6:36. OpenURL

  6. Patel J, Abd T, Blumenthal RS, Nasir K, Superko HR: Genetics and Personalized Medicine-a Role in Statin Therapy?

    Curr Atheroscler Rep 2014., 16(1)

    384-013-0384-y

    OpenURL

  7. Squizzato A, Romualdi E, Dentali F, Ageno W: Statins for acute ischemic stroke.

    Cochrane Database Syst Rev 2011, 8(8):CD007551.

    doi(8):CD007551

    OpenURL

  8. Ruokoniemi P, Helin-Salmivaara A, Klaukka T, Neuvonen PJ, Huupponen R: Shift of statin use towards the elderly in 1995-2005: a nation-wide register study in Finland.

    Br J Clin Pharmacol 2008, 66(3):405-410. OpenURL

  9. Cariati A, Piromalli E: Limits and perspective of oral therapy with statins and aspirin for the prevention of symptomatic cholesterol gallstone disease.

    Expert Opin Pharmacother 2012, 13(9):1223-1227. OpenURL

  10. Tsai CJ, Leitzmann MF, Willett WC, Giovannucci EL: Statin use and the risk of cholecystectomy in women.

    Gastroenterology 2009, 136(5):1593-1600. OpenURL

  11. Wang HH, Portincasa P, de Bari O, Liu KJ, Garruti G, Neuschwander-Tetri BA, Wang DQ: Prevention of cholesterol gallstones by inhibiting hepatic biosynthesis and intestinal absorption of cholesterol.

    Eur J Clin Invest 2013, 43(4):413-426. OpenURL

  12. Gurusamy KS, Davidson BR: Surgical treatment of gallstones.

    Gastroenterol Clin North Am 2010, 39(2):229-244.

    viii

    OpenURL

  13. Portincasa P, Moschetta A, Palasciano G: Cholesterol gallstone disease.

    Lancet 2006, 368(9531):230-239. OpenURL

  14. Stinton LM, Myers RP, Shaffer EA: Epidemiology of gallstones.

    Gastroenterol Clin North Am 2010, 39(2):157-169.

    vii

    OpenURL

  15. Tsai CJ, Leitzmann MF, Willett WC, Giovannucci EL: Prospective study of abdominal adiposity and gallstone disease in US men.

    Am J Clin Nutr 2004, 80(1):38-44. OpenURL

  16. Festi D, Reggiani ML, Attili AF, Loria P, Pazzi P, Scaioli E, Capodicasa S, Romano F, Roda E, Colecchia A: Natural history of gallstone disease: Expectant management or active treatment? Results from a population-based cohort study.

    J Gastroenterol Hepatol 2010, 25(4):719-724. OpenURL

  17. Banim PJ, Luben RN, Bulluck H, Sharp SJ, Wareham NJ, Khaw KT, Hart AR: The aetiology of symptomatic gallstones quantification of the effects of obesity, alcohol and serum lipids on risk. Epidemiological and biomarker data from a UK prospective cohort study (EPIC-Norfolk).

    Eur J Gastroenterol Hepatol 2011, 23(8):733-740. OpenURL

  18. Suuronen S, Niskanen L, Paajanen P, Paajanen H: Declining cholecystectomy rate during the era of statin use in Finland: a population-based cohort study between 1995 and 2009.

    Scand J Surg 2013, 102(3):158-163. OpenURL

  19. Smith JL, Roach PD, Wittenberg LN, Riottot M, Pillay SP, Nestel PJ, Nathanson LK: Effects of simvastatin on hepatic cholesterol metabolism, bile lithogenicity and bile acid hydrophobicity in patients with gallstones.

    J Gastroenterol Hepatol 2000, 15(8):871-879. OpenURL

  20. Abedin MZ, Narins SC, Park EH, Smith PR, Kirkwood KS: Lovastatin alters biliary lipid composition and dissolves gallstones: a long-term study in prairie dogs.

    Dig Dis Sci 2002, 47(10):2192-2210. OpenURL

  21. Chiu HF, Chen CC, Kuo HW, Lee IM, Wu TN, Yang CY: Statin use and the risk of gallstone disease: a population-based case-control study.

    Expert Opin Drug Saf 2012, 11(3):369-374. OpenURL

  22. Ong KL, Wu BJ, Cheung BM, Barter PJ, Rye KA: Association of lower total bilirubin level with statin usage: the United States National Health and Nutrition Examination Survey 1999-2008.

    Atherosclerosis 2011, 219(2):728-733. OpenURL

  23. Jain MK, Ridker PM: Anti-inflammatory effects of statins: clinical evidence and basic mechanisms.

    Nat Rev Drug Discov 2005, 4(12):977-987. OpenURL

  24. Chuang SC, Hsi E, Lee KT: Genetics of gallstone disease.

    Adv Clin Chem 2013, 60:143-185. OpenURL

  25. Fujita T: Use of statins and gallstone risk.

    JAMA 2010, 303(12):1146-1147.

    author reply 1147

    OpenURL

Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-230X/14/119/prepub