Prior studies indicate a possible association between depression and cholecystectomy, but no study has compared the risk of post-operative depressive disorders (DD) after cholecystectomy. This retrospective follow-up study aimed to examine the relationship between cholecystectomy and the risk of DD in patients with gallstones in a population-based database.
Using ambulatory care data from the Longitudinal Health Insurance Database 2000, 6755 patients who received a first-time principal diagnosis of gallstones at the emergency room (ER) were identified. Among them, 1197 underwent cholecystectomy. Each patient was then individually followed-up for two years to identify those who were later diagnosed with DD. Cox proportional hazards regressions were performed to estimate the risk of developing DD between patients with gallstone who did and those who did not undergo cholecystectomy.
Of 6755 patients with gallstones, 173 (2.56%) were diagnosed with DD during the two-year follow-up. Among patients who did and those who did not undergo cholecystectomy, 3.51% and 2.36% later developed depressive disorder, respectively. After adjusting for the patient’s sex, age and geographic location, the hazard ratio (HR) of DD within two years of gallstone diagnosis was 1.43 (95% CI, 1.02–2.04) for patients who underwent cholecystectomy compared to those who did not. Females, but not males, had a higher the adjusted HR of DD (1.61; 95% CI, 1.08–2.41) for patients who underwent cholecystectomy compared to those who did not.
Citation: Tsai M-C, Chen C-H, Lee H-C, Lin H-C, Lee C-Z (2015) Increased Risk of Depressive Disorder following Cholecystectomy for Gallstones. PLoS ONE 10(6): e0129962. doi:10.1371/journal.pone.0129962
Academic Editor: Daimei Sasayama, National Center of Neurology and Psychiatry, JAPAN
Received: January 27, 2015; Accepted: May 13, 2015; Published: June 8, 2015
Copyright: © 2015 Tsai et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: Data (LHID2000) was obtained from the National Health Research Institute (http://nhird.nhri.org.tw/date_01.html) and is available upon request to qualified researchers in Taiwan by contacting firstname.lastname@example.org.
Funding: The authors received no specific funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Gallstones, or cholelithiasis, are a common condition worldwide [1,2]. Its prevalence rate ranges from 10% to 15% in the United States and 3% to 10% for Asian countries [3,4]. Cholecystectomy is considered the curative intervention [5–7]. However, previous follow-up studies report that some residual gastrointestinal problems may continue to bother patients who had undergone cholecystectomy .
Studies reveal that after cholecystectomy, about 7–47% of patients are dissatisfied with the procedure, most of which are related to post-cholecystectomy syndrome (PCS) [8–13]. Previous studies report that PCS has a strong relationship with functional gastrointestinal disorders (FGIDs) [13–18]. Patients with FGIDs are reported to have a high prevalence of psychosocial disturbance [17–21]. Furthermore, persistent PCS have been correlated the feeling of depression [18,22–24]. Two small cohort studies report that the prevalence and incidence rates of depression following cholecystectomy are 2.7% and 3%, respectively [25,26]. A multi-center cohort study reports that 0.9% of patients have feelings of severe anxiety or depression and that 15% have mild depression one year after laparoscopic cholecystectomy . One recent study also observes that 8% of patients with PCS caused by dysfunction of Oddi reportedly have depression an average of four years after cholecystectomy .
However, although prior studies indicate a possible association between depression and cholecystectomy, such studies have all relied on regional samples or on data from selected hospitals or sub-populations of patients. As such, these do not permit unequivocal conclusions. Furthermore, previous studies have focused on the relationship between cholecystectomy and the presentation of depressive symptoms, rather than on the diagnosis of depressive disorder (DD). To date, no study has attempted to compare the risk of post-operative depressive disorders following cholecystectomy. Therefore, this retrospective follow-up study aimed to examine the relationship between cholecystectomy and the subsequent risk of DD among patients with gallstone, using a population-based database.
Materials and Methods
This retrospective cohort study utilized data retrieved from the Longitudinal Health Insurance Database (LHID2000). The LHID2000 was derived from the Taiwan National Health Insurance (NHI) program and included the medical claims for 1,000,000 enrollees randomly selected from all the enrollees (n = 23.72 million) listed in the 2000 Registry of Beneficiaries under the Taiwan National Health Insurance (NHI) program. Three domains were linked by the patient’s individual identity.
The LHID2000 consists of de-identified secondary data released to the public for research purposes by the National Health Research Institute. The LHID2000, which was open to the researchers in Taiwan, was available from the National Health Research Institute (http://nhird.nhri.org.tw/date_01.html). The LHID2000 has been utilized by numerous researchers, which have reported the high validity of data from the NHI program [28–30]. This study was approved by institutional review board (IRB) of Taipei Medical University's IRB (TMU-JIRB 201412008).
There were 7213 patients who received a first-time principal diagnosis of gallstones (International Classification of Diseases, 9th edition, Clinical Modification (ICD-9-CM) code 574.0–574.4, 574.6–574.9) in emergency departments between January 1, 2001 and December 31, 2010. Among them, 1324 subsequently underwent cholecystectomy. The date of cholecystectomy was designated as the index date for patients who underwent a cholecystectomy. For those who did not undergo cholecystectomy (n = 5889), the date of the first gallstone diagnosis in the emergency department was defined as the index date. Patients who already had a diagnosed of DD (ICD-9-CM codes 296.2, 296.3, 300.4, and 311) prior to their index date were further excluded (n = 458). Ultimately, 6755 patients with gallstones were included.
Each patient was then individually followed-up for two years, beginning from the index date, to identify those who were diagnosed with DD within the follow-up period.
All statistical analyses were performed using the SAS statistical software (version 9.1 for Windows; SAS Institute, Inc., Cary, NC, USA). Statistical significance was set at p<0.05. The potential confounders were considered and included based upon both literature and statistical modeling. In previous studies on the issues of depression and cholecystectomy, these reported confounders may consist of characteristics of sex [31–34], age [31–34], and residential areas [32, 35]. Then, differences in sex, age group, monthly income (NT$ 0–15,840; NT$ 15,841–25,000, and NT$ >25,001), geographical location (Northern, Central, Eastern, and Southern Taiwan), and urbanization level of the patient’s residence (5 levels, 1 being the most urbanized and 5 being the least) between gallstone patients who did and those who did not undergo cholecystectomy were compared by Pearson Chi-square tests. Log-rank analysis was used to compare the difference in two-year DD-free survival rates between these two cohorts. We checked possible influential observations and assured that none deletion from the dataset would noticeably change the results presented.
In addition, Cox proportional hazards regressions were conducted to estimate the risk of developing DD during the two-year follow-up period between gallstone patients who underwent and those who did not undergo cholecystectomy, with cases censored if individuals were lost to follow-up during that time. Of all 334 censored cases during the follow-up period, 62 were from gallstone patients who underwent cholecystectomy and 272 were from gallstone patients who did not undergo cholecystectomy. Interaction terms were added to the Cox regression models to examine potential modifying effects of demographic characteristics. As the association between the risk of developing DD between gallstone patients who underwent and those who did not undergo cholecystectomy was different in males and in females, further analysis were performed stratified by sex. Hazard ratios (HR) and their corresponding 95% confidence intervals (95% CI) were used to report the risk of DD.
Finally, we checked the proportionality assumptions for Cox models. In the graphs with the survival function versus survival time, the shapes of the curves of the predictor (gallstone patients with and without undergoing cholecystectomy) were basically the same and the separation between the curves remained proportional over time. We further generated the time dependent covariates by creating interactions of the predictors and a function of survival time and included in the model. None of the time dependent covariates were significant. We examined for each covariate as well as globally to ensure the conformance with the proportionality assumption. In addition, the assumption of uninformative censoring was considered. We found no statistical significance in examining baseline characteristics of those who censored and retained.
The patients had a mean age of 52.0±16.9 years, 53.9±15.5 and 51.6±17.1 years for patients who underwent and those who did not undergo cholecystectomy, respectively (p<0.001, Table 1). There were no significant differences in monthly income (p = 0.180) and urbanization level of the patients’ residence (p = 0.351) between patients who underwent and those who did not undergo cholecystectomy. However, patients who underwent cholecystectomy had a significantly greater tendency to reside in northern part of Taiwan (p<0.001) than those who did not undergo cholecystectomy.
In terms of the incidence of DD within the two-year period following the index date (Table 2), 173 out of 6755 (2.56%) gallstone patients were diagnosed with DD within the two-year follow-up period. In total, 3.51% and 2.36% of patients who did and did not undergo cholecystectomy subsequently diagnosis of DD, respectively. Log-rank test revealed a statistically significant difference in two-year DD-free accumulated survival rate between the two groups (Chi-square value = 5.216, p = 0.022).
The crude and adjusted HRs for DD during the two-year follow-up period were also shown in Table 2. Cox proportional analysis indicated that patients who underwent cholecystectomy had higher risk of developing DD compared to patients who did not undergo cholecystectomy (HR 1.51; 95% CI, 1.07–2.14). After adjusting for the patients’ geographical location and censoring those were lost to follow-up, the HR of DD within the two-year follow-up period was 1.43 (95% CI, 1.02–2.04) for patients who underwent cholecystectomy compared to those who did not.
The HR of the two groups as stratified according to sex revealed that for females, the adjusted HR of DD for patients who underwent cholecystectomy was 1.61 (95% CI = 1.08–2.41) compared to patients who did not undergo cholecystectomy (Table 3). There were no similar findings for males (adjusted HR, 0.95; 95% CI, 0.44–2.06).
This retrospective cohort study shows that 3.51% of patients with gallstones who undergo cholecystectomy received a diagnosis of DD within two years from the diagnosis of gallstones. Among patients with gallstones, those who undergo cholecystectomy also have a significantly higher risk of DD than those who do not (adjusted HR, 1.43).
The current findings parallel those of prior studies, all of which reported that 0.9% to 3.0% of patients develop depression following cholecystectomy [25–27]. The high prevalence of depression among post-cholecystectomy patients may be explained by post-cholecystectomy syndrome (PCS), which may be a factor leading to depression. As the name implies, PCS involves abdominal symptoms that range from mild, ill-defined digestive symptoms to severe attacks of abdominal pain and jaundice that recur or persist after cholecystectomy [8,36–38]. According to different methods of evaluation and variable recorded symptoms, PCS occurs in up to 50% of patients, with 10–15% as the most reasonable range [8,12,37–39]. Reports also show that about 50% of PCS are affected by psychosomatic or extra-intestinal disease [39,40]. Previous studies report that PCS are significantly associated with a long history of complaints (e.g., biliary pain, symptoms, and attacks) [12,15,22]. Thus, PCS may be a possible explanation for the increasing risk of DD following cholecystectomy. The present study further analyzed the data but failed to establish a relationship between PCS and the subsequent risk of DD within the two-year follow-up period (adjusted HR = 0.71, 95% CI = 0.08–4.36).
Another mechanism may be the increased risk of metabolic syndrome and non-alcoholic fatty liver disease (NAFLD) after cholecystectomy [41,42]. Previous studies suggest that resistance to insulin effects on central neurons play a role in depression [43,44]. In addition, according to the DSM-IV criteria, DD is significantly related to insulin resistance as indexed by the homeostasis model assessment method . The correlation between insulin resistance and depression has also been established by one intervention study, wherein insulin sensitivity is improved by treating depression . Thus, cholecystectomy itself may be a risk factor and pathogenic link between insulin resistance and DD.
The present study has found an increasing risk of DD after cholecystectomy only in females, but not in males. One prior study suggests that female sex is significantly negatively associated with post-cholecystectomy health-related quality of life (HRQOL), as evaluated by the GIQLI and short Form-36 after a six-month follow-up . Previous studies consistently report that PCS occurs frequently in women, while middle-aged women also have a high prevalence of DD [1,2,8].
This study has several strengths. First, a nationwide population-based dataset with ample sample size is used to clarify the relationship between cholecystectomy and the subsequent risk of DD. Second, DD based on established clinical diagnostic criteria is used rather than the presentation of depressive symptoms reported by survey. The diagnosis of DD has a very high validity since mental illness is still culturally taboo in Taiwan. A physician will not make a diagnosis of DD unless there is relative certainty.
Nonetheless, there are two limitations in the present study. First, there are no records of concomitant functional dyspepsia, which may contribute to the increased incidence of DD in post-cholecystectomy patients. Second, the LHID2000 does not provide information on operative time, gallbladder specimen histology, and the patient’s employment, marital status, educational level and body mass index (BMI). All of these may influence the outcome of cholecystectomy [6,7,37]. Since patients undergoing cholecystectomy are more likely to have frequent out-patient consults, which may lead to an early detection of DD, there may be a possible surveillance bias.
Despite the aforementioned limitations, this study demonstrates an association between cholecystectomy and subsequent risk of DD. Clinicians must be alert to the increased prevalence of clinical depressive symptoms in patients who underwent cholecystectomy.
Conceived and designed the experiments: MCT CZL. Analyzed the data: H. Lin. Wrote the paper: MCT CZL CHC H. Lin H. Lee. CHC Literature review: MCT CHC CZL H. Lee.
- 1. Lowenfels AB, Velema JP. Estimating gallstone incidence from prevalence data. Scand J Gastroenterol. 1992; 27: 984–986. pmid:1295496
- 2. Rahman GA. Cholelithiasis and cholecystitis: Changing prevalence in an African community. J Natl Med Assoc. 2005; 97: 1534–1538. pmid:16334500
- 3. Stinton LM, Shaffer EA. Epidemiology of gallbladder disease: cholelithiasis and cancer. Gut Liver. 2012; 6: 172–187. doi: 10.5009/gnl.2012.6.2.172. pmid:22570746
- 4. Huang J, Chang CH, Wang JL, Kuo HK, Lin JW, Shau WY, et al. Nationwide epidemiological study of severe gallstone disease in Taiwan. BMC Gastroenterol. 2009; 9: 63. doi: 10.1186/1471-230X-9-63. pmid:19698126
- 5. Lien HH, Huang CC, Wang PC, Huang CS, Chen YH, Lin TL, et al. Changes in quality-of-life following laparoscopic cholecystectomy in adult patients with cholelithiasis. J Gastrointest Surg. 2010; 14: 126–130. doi: 10.1007/s11605-009-1062-9. pmid:19830502
- 6. Shi HY, Lee KT, Lee HH, Uen YH, Tsai JT, Chiu CC. Post-cholecystectomy quality of life: A prospective multicenter cohort study of its associations with preoperative functional status and patient demographics. J Gastrointest Surg. 2009; 13: 1651–1658. doi: 10.1007/s11605-009-0962-z. pmid:19582516
- 7. Hsueh LN, Shi HY, Wang TF, Chang CY, Lee KT. Health-related quality of life in patients undergoing cholecystectomy. Kaohsiung J Med Sci. 2011; 27: 280–288. doi: 10.1016/j.kjms.2011.03.002. pmid:21757146
- 8. Ros E. Zambon D. Post-cholecystectomy symptoms: a prospective study of gallstone patients before and two years after surgery. Gut. 1987; 28: 1500–1504. pmid:3428678
- 9. Scriven MW, Burgess NA, Edwards EA, Morgan AR, Bundred NJ, Lewis MH. Cholecystectomy: a study of patient satisfaction. J R Coll Surg Edinb. 1993; 38: 79–81. pmid:8478838
- 10. Jørgensen T, Teglbjerg JS, Wille-Jørgensen P, Bille T, Thorvaldsen P. Persisting pain after cholecystectomy: a prospective investigation. Scand J Gastroenterol. 1991; 26: 124–128. pmid:2006393
- 11. Vander Velpen CJC, Shimi SM, Cuschiere A. Outcome after cholecystectomy for symptomatic gall stone disease and effect of surgical access: laparoscopic v open approach. Gut. 1993; 34: 1448–1451. pmid:8244119
- 12. Weinert CR, Arnett D, Jacobs D Jr, Kane RL. Relationship between persistence of abdominal symptoms and successful outcome after cholecystectomy. Arch Intern Med. 2000; 160(7): 989–995. pmid:10761964
- 13. Lorusso D, Porcelli P, Pezzolla F, Lantone G, Zivoli G, Guerra V, et al. Persistent dyspepsia after laparoscopic cholecystectomy. The influence of psychological factors. Scand J Gastroenterol. 2003; 38: 653–658. pmid:12825875
- 14. Schoenemann J, Zeider J. Sequelae of cholecystectomy. Z Gastroenterol. 1997; 35: 139–145. pmid:9163227
- 15. Mertens MC, De Vries J, Scholtes VP, Jansen P, Roukema JA. Prospective 6 weeks follow-up post-cholecystectomy: the predictive value of preoperative symptoms. J Gastrointest Surg. 2009; 13: 304–311. doi: 10.1007/s11605-008-0718-1. pmid:18923876
- 16. Brawman-Mintzer O, Durkalski V, Wu Q, Romagnuolo J, Fogel E, Tarnasky P, et al. Psychosocial characteristics and pain burden of patients with suspected sphincter of Oddi dysfunction in the EPISOD multi-center trial. Am J Gastroenterol. 2014; 109: 436–442. doi: 10.1038/ajg.2013.467. pmid:24445573
- 17. Levy RL, Olden KW, Naliboff BD, Bradley LA, Francisconi C, Drossman DA, et al. Psychosocial aspects of functional gastrointestinal disorders. Gastroenterology. 2006; 130: 1447–1458. pmid:16678558
- 18. Shmidt M, Sondenaa K, Dumot JA, Rosenblatt S, Hausken T, Ramnefjell M, et al. Post-cholecystectomy symptoms were caused by persistence of a functional gastrointestinal disorder. World J Gastroenterol. 2012; 18: 1365–1372. doi: 10.3748/wjg.v18.i12.1365. pmid:22493550
- 19. Drossman DA, Camillerri M, Mayer EA, Whitehead WE. AGA technical review on irritable bowel syndrome. Gastroenterology. 2002; 123: 2108–2131. pmid:12454866
- 20. Mertz HR. Irritable bowel syndrome. N Engl J Med. 2003; 349(22): 2136–2146. pmid:14645642
- 21. Stefaniak T, Vingerhoets A, Babinska D, Trus M, Glowacki J, Dymecki D, et al. Scand J Gastroenterol. 2004; 39(2): 127–132. pmid:15000273
- 22. McMahon AJ, Ross S, Baxter JN, Russell IT, Anderson JR, Morran CG, et al. Symptomatic outcome 1 year after laparoscopic and mini-laparotomy cholecystectomy: a randomized trial. Br J Surg. 1995; 82: 1378–1382. pmid:7489171
- 23. Kahokehr A, Broadbent E, Wheeler BR, Sammour T, Hill AG. The effect of peri-operative psychological intervention on fatigue after laparoscopic cholecystectomy: a randomized controlled trial. Surg Endosc. 2012; 26: 1730–1736 doi: 10.1007/s00464-011-2101-7. pmid:22258294
- 24. Parkman HP, Yates K, Hasler WL, Nguyen L, Pasricha PJ, Snape WJ, et al. Cholecystectomy and clinical presentation of gastroparesis. Dig Dis Sci. 2013; 58: 1062–1073. doi: 10.1007/s10620-013-2596-y. pmid:23456496
- 25. Barker MG. Psychiatric illness after hysterectomy. Br Med J. 1968; 2: 91–95. pmid:5646099
- 26. Sehlo MG, Ramadani H. Depression following hysterectomy. Curr Psychiatry. 2010; 17: 1–6.
- 27. Nilsson E, Ros A, Rahmqvist M, Bäckman K, Carlsson P. Cholecystectomy: costs and health-related quality of life: a comparison of two techniques. Int J Qual Health Care. 2004; 16: 473–482. pmid:15557357
- 28. Chen YC, Yeh HY, Wu JC, Haschler I, Chen TJ, Wetter T. Taiwan’s National Health Insurance Research Database: administrative health care database as study object in bibliometrics. Scientometrics. 2011; 86: 365–380.
- 29. Kang JH, Chen YH, Lin HC. Co-morbidity profiles among patients with ankylosing spondylitis: a nationwide population-based study. Ann Rheum Dis. 2010; 69: 1165–1168. doi: 10.1136/ard.2009.116178. pmid:20375121
- 30. Cheng CL, Kao YH, Lin SJ, Lee CH, Lai ML. Validation of the National Health Insurance Research Database with ischemic stroke cases in Taiwan. Pharmacoepidemiol Drug Saf. 2011; 20: 236–242. doi: 10.1002/pds.2087. pmid:21351304
- 31. Weissman MM, Bland RC, Canino GJ, Faravelli C, Greenwald S, Hwu HG, et al. Cross-national epidemiology of major depression and bipolar disorder. JAMA. 1996; 276(4):293–9. pmid:8656541
- 32. Liao SC, Chen WJ, Lee MB, Lung FW, Lai TJ, Liu CY, et al. Low prevalence of major depressive disorder in Taiwanese adults: possible explanations and implications. Psychol Med. 2012; 42(6):1227–37. doi: 10.1017/S0033291711002364. pmid:22051196
- 33. Pålsson SH, Sandblom G. Influence of gender and socioeconomic background on the decision to perform gallstone surgery: a population-based register study. Scand J Gastroenterol. 2015; 50(2):211–6. doi: 10.3109/00365521.2014.978818. pmid:25413566
- 34. Huang J, Chang CH, Wang JL, Kuo HK, Lin JW, Shau WY, Lee PH. Nationwide epidemiological study of severe gallstone disease in Taiwan. BMC Gastroenterol. 2009 22; 9:63.
- 35. Kemp JA, Zuckerman RS, Finlayson SR. Trends in adoption of laparoscopic cholecystectomy in rural versus urban hospitals. J Am Coll Surg. 2008; 206(1):28–32. pmid:18155565
- 36. Womack NA, Crider RL. The persistence of symptoms following cholecystectomy. Ann Surg. 1947; 126(1): 31–55. pmid:17858976
- 37. Luman W, Adams WH, Nixon SN, Mcintyre IM, Hamer-Hodges D, Wilson G, et al. Incidence of persistent symptoms after laparoscopic cholecystectomy: A prospective study. Gut 1996; 39: 863–866. pmid:9038671
- 38. Jaunoo SS, Mohandas S, Almond LM. Post-cholecystectomy syndrome (PCS) Int J Surg. 2010; 8: 15–17. doi: 10.1016/j.ijsu.2009.10.008. pmid:19857610
- 39. Girometti R, Brondani G, Cereser L, Como G, Del Pin M, Bazzocchi M, et al. Post-cholecystectomy syndrome: spectrum of biliary findings at magnetic resonance cholangio-pancreatography. Br J Radiol. 2010; 83: 351–361. doi: 10.1259/bjr/99865290. pmid:20335441
- 40. Schofer JM. Biliary cause of post-cholecystectomy syndrome. J Emerg Med. 2010; 39: 406–410. doi: 10.1016/j.jemermed.2007.11.090. pmid:18722735
- 41. Ruhi CE, Everhart JE. Relationship of non-alcoholic fatty liver disease with cholecsytectomy in the US population. Am J Gastroenterol. 2013; 108: 952–958. doi: 10.1038/ajg.2013.70. pmid:23545713
- 42. Shen C, Wu X, Xu C, Yu C, Chen P, Li Y. Association of cholecystectomy with metabolic syndrome in a Chinese population. PLoS One. 2014; 9: e88189. doi: 10.1371/journal.pone.0088189. pmid:24505425
- 43. McCarty MF. Enhancing central and peripheral insulin activity as a strategy for the treatment of endogenous depression—an adjuvant role for chromium picolinate? Med Hypotheses. 1994; 43: 247–252. pmid:7838010
- 44. Ramasubbu R. Insulin resistance: a metabolic link between depressive disorder and atherosclerotic vascular disease. Med Hypotheses. 2002; 59: 537–551. pmid:12376076
- 45. Pearson S, Schmidt M, Patton G, Dwyer T, Blizzard L, Otahal P, et al. Depression and Insulin Resistance: Cross-sectional associations in young adults. Diabetes Care. 2010; 33(5): 1128–1133. doi: 10.2337/dc09-1940. pmid:20185745
- 46. Asghar S, Magnusson A, Hussain A, Diep LM, Bhowmik B, Thorsby PM. Depression and insulin resistance in non-diabetic subjects: An intervention study with insulin clamp technique. Int J Clin Med. 2012; 3: 575–581.