- Research article
- Open Access
- Open Peer Review
Relation of cholesterol metabolism to pediatric gallstone disease: a retrospective controlled study
BMC Gastroenterologyvolume 15, Article number: 74 (2015)
Cholesterol metabolism may be involved in pediatric gallstone disease. We aimed to reveal cholesterol metabolites and phytosterols and their relation to stone composition of sterols in children having black pigment and cholesterol stones.
We performed retrospective controlled clinical study, in which we examined parameters of cholesterol metabolism and liver function values in serum (n = 28) and gallstones (n = 46) of consecutively cholecystectomized children. Serum values of age-, body mass index- and sex-matched children (n = 82) and adult gallstones (n = 187) served as controls.
Surrogate markers of cholesterol synthesis in serum (squalene/cholesterol, cholestenol/cholesterol and lathosterol/cholesterol) were 26–52 % higher in both stone subclasses compared to controls (p < 0.05 for all). Respectively, cholestanol/cholesterol and plant sterols campesterol/cholesterol and sitosterol/cholesterol (cholesterol absorption markers) had decreasing order in serum: black pigment stone group > controls > cholesterol stone group (p < 0.05 for all). In black pigment stone group, stone cholestanol/cholesterol was associated with serum bile acids (r = 0.620, p = 0.018). In cholesterol stone group, surrogate markers of cholesterol synthesis in serum (e.g., lathosterol/cholesterol) inversely reflected those of absorption (r-range -0.633–-0.706, p-range 0.036–0.015). In cholesterol stone group, serum and stone lathosterol/cholesterol and cholestanol/cholesterol were positively interrelated (r-range 0.727–0.847, p < 0.05 for both).
Gallstone subclasses shared enhanced cholesterol synthesis. Cholesterol stone children were low cholesterol absorbers with intact homeostasis of cholesterol metabolism. Black pigment stone group was characterized by deteriorated cholesterol metabolism, and accumulation of cholestanol, campesterol and sitosterol in serum and stones suggesting their participation in pathogenesis.
Gallstones are quite rare in healthy children, but they more frequently occur in subjects who have a predisposing condition [1, 2]. Recent series document an increasing incidence of pediatric gallstone disease most probably due to increased detection with frequent use of ultrasonography, as well as the growing obesity epidemic . Grading of gallstones into black pigment (BPS), brown pigment (BRPS) and cholesterol stones (CS) can be performed by determining the stone cholesterol content [4–7]. More exact classification methods apply ultrastructural examination with scanning electron microscopy, x-ray diffractometry and infrared spectroscopy .
Numerous conditions have been associated with the pathogenesis of BPS, in which the elevated biliary bilirubin level is the cornerstone phenomenon, and this is frequently a consequence of chronic haemolysis or hepatobiliary disease [2, 6]. In turn, BRPS have been related to parenteral nutrition even more tightly than the BPS . CS, which are more frequent in older children and adults than pigment stones (PS), are formed by several pathophysiologic factors, of which certain properties in cholesterol metabolism play essential roles. These metabolic features include hepatic hypersecretion of biliary lipids, enhanced phase transition of cholesterol, high efficiency of intestinal cholesterol absorption and increased hepatic biosynthesis of cholesterol .
Cholesterol homeostasis is maintained by the interaction between intestinal absorption, de novo synthesis, hepatic output into the bile and fecal secretion of cholesterol . Phytosterols are not synthesized in the human body, but they are normally absorbed to a much lesser extent than cholesterol, and, consequently, their serum levels are only 0.1–0.005 % of total cholesterol concentration . Of phytosterols in serum, campesterol and sitosterol are the most abundant ones, whereas stigmasterol and avenasterol form minor fractions. That ratios to cholesterol of campesterol, sitosterol and cholestanol (a 5-α saturated, enzymatically formed derivative of endogenous cholesterol) in serum are associated with the efficiency of cholesterol absorption among human subjects has been documented in detail [12–17]. Generally in serum, the ratios to cholesterol of squalene, lanosterol and cholesterol demethylated precursor sterols, i.e., cholestenol, desmosterol and lathosterol, positively reflect cholesterol synthesis and inversely cholesterol absorption efficiency and the respective surrogate sterol markers of cholesterol absorption [13–17]. These variables of cholesterol metabolism occur also in bile and gallstones [5, 7]. Additionally, serum level of lathosterol reflects the hepatic HMG-CoA reductase activity [17, 18].
The main focuses of the present study were addressed to the following questions: 1) is the cholesterol metabolism deteriorated in pediatric BPS and CS patients compared to each other or healthy controls and 2) how the serum levels of cholesterol and the surrogate markers of cholesterol metabolism are related to the respective sterol composition of the gallstones. Thus, we analysed variables of cholesterol metabolism in serum samples (n = 28) and gallstones (n = 46) of consecutively cholecystectomized pediatric gallstone patients of a tertiary referral centre, and compared the serum values with age-, BMI- and sex-matched controls (serum) and the gallstone values with respective adult ones.
Gallstones of consecutively cholecystectomized children (<19 years old) from April 2004 – to January 2013, and, respectively, serum samples from January 2009 to January 2013 were retrospectively examined for the purposes of the present study. Preliminary results of solely the analysed gallstones of 18 subjects have been reported earlier .
Gallstones were identified preoperatively with ultrasonography in all patients. In addition, twelve patients underwent MRI cholangiography. Preoperatively bile duct stones were detected in five patients, four of whom had removal of stones by endoscopic sphincterotomy and in one the bile duct stone passed spontaneously into the duodenum. One BPS patient and two CS patients belonged to the cohort with measured composition of sterols in the gallstones. Two BPS patients belonged the cohort with serum measurements.
The term idiopathic gallstone disease was defined as occurrence of gallstones without any associated disease. Other diseases were excluded by clinical examination, abdominal ultrasound and blood samples, which were analysed for haemoglobin, white and red blood cells, platelets, alkaline phosphatase (ALP), alanine and aspartate aminotransferases (ALT and AST, respectively), bile acids, bilirubin, conjugated bilirubin, C-reactive protein, glutamyl transferase (γGT) and sedimentation rate by routine hospital methods. Patient demographic data was obtained including age, gender, height and weight at admission. Past and present medical history was collected including associated medical illnesses and medication. The use of parenteral nutrition was recorded.
The study was performed according to the principles of the 1975 Declaration of Helsinki (6th revision, 2008). The study was approved by the Ethics Committee of the Hospital for Children and Adolescents, University of Helsinki. An informed consent was obtained from parents of each patient included in the study.
Fasting serum samples were drawn at the time of the cholecystectomy. Concentrations of cholesterol, squalene, cholestanol, cholesterol precursor sterols (lanosterol, cholestenol, desmosterol and lathosterol), and plant sterols (campesterol, sitosterol, avenasterol and stigmasterol) in serum were measured from nonsaponifiable material by gas–liquid chromatography (GLC), on a 50-m long SE-30 capillary column (Ultra 1 column, Hewlett-Packard) as described earlier [19, 20]. Serum total, LDL and HDL cholesterol and serum triglycerides were analyzed enzymatically using automated analyzer systems.
During the cholecystectomy, gallstones were collected from the gallbladder for analysis. Gallstone sterols and squalene were determined with GLC as described in detail earlier [5, 7] and shortly reviewed here. The gallstones were washed with distilled water, dried in a desiccator and powdered with mortar. The gallstone pulver (25-100g) was saponified with 2 M KOH in 90 % ethanol for two hours using 5α-cholestane as an internal standard. After saponification, aqua was added to achieve 1:1 (vol/vol) water-ethanol suspension. The nonsaponifiable lipids were extracted with hexane, washed once with 50 % ethanol, dissolved twice with hexan-methanol (2:3 vol/vol), evaporated to dryness and finally silylated to trimethylsilylethers and quantitated by GLC.
Serum levels of bile acids (available in 14 BPS and 10 CS patients), bilirubin, liver enzymes and thromboplastin time were determined by routine hospital methods prior to cholecystectomy.
Classification of the gallstones into CS, BRPS and BPS subclasses was performed as described earlier [5, 7]. Stones containing cholesterol less than 35 % of the stone weight were classified as PS, and greater than 35 % as CS. Based on the cholesterol content, PS were subdivided into BRPS (containing cholesterol 10 to 35 % of the stone weight) and BPS (correspondingly less than 10 %). Practically the BRPS subgroup, characterized by calcium palmitate, included mixed cholesterol gallstones and the BPS included the so-called calcium carbonate stones [8, 21–23].
The results of three patients with BRPS were published in our preliminary report , and, thus, the BRPS group was excluded from the present study. The results of the previously analysed and preliminarily reported  gallstones of 18 children were combined with respective values of 28 subjects, who participated the study from January 2009 onwards, because the composition of gallstone sterols in these two pediatric cohorts were comparable.
To eliminate the effect of varying lipoprotein levels, serum non-cholesterol sterol values were related to serum cholesterol and are expressed in terms of 102 × mmol/mol of cholesterol of the same GLC run (ratios). Ratios of surrogate sterol markers of cholesterol synthesis (e.g., lathosterol) to those of cholesterol absorption (e.g., campesterol) in serum were calculated in order to evaluate differences in cholesterol metabolism.
The serum variables were compared to an age-, sex- and BMI- matched control group of 82 subjects, which consisted of healthy day-case surgery patients (i.e., inguinal hernia, umbilical hernia, undescended testes) without evidence of intestinal disease, diabetes, or dyslipidemia. The Finnish reference values –based body mass index-for-age (ISO-BMI) were used for children over two years old .
The gallstone variables were compared to the respective adult values including 178 cholesterol stones (ACS) and 9 black pigment stones (APS) . In this study, the term “adult controls” refers to gallstone composition of cholesterol and non-cholesterol sterols.
In order to standardize the variations, the stone non-cholesterol sterols were expressed as milligrams by stone weight and in terms of 102 × mmol of non-cholesterol sterol /mol of cholesterol (called proportions or ratios in the text).
The data were analysed for significance and normality with the Number Crunching Statistical Software™ (NCSS™, Statistical Solutions Ltd., 2007, Kaysville, Utah). Logarithmic transforms were calculated for skewed distributions. Comparisons between gallstone subclasses and controls were performed with general linear model analysis of variance using age, ISO-BMIs and gender as covariates. If p-values were below 0.05, comparison between the groups were carried out with two-tailed unpaired t-test. Categorical variables were summarized as count and compared using the chi-squared or Fisher’s exact test where appropriate. Correlations were analysed by calculating Pearson’s correlation test or by Spearman rank correlation test in case of skewed distributions. The sample sizes for the study groups were calculated according to the following hypotheses. Pediatric gallstone sterol compositions differ by several fold between the pediatric BPS and CS patients . Thus, it could be estimated that the difference in serum non-cholesterol sterol ratios (e.g., lathosterol/cholesterol and campesterol/cholesterol) is two-fold or more between BPS and CS patients, and that the differences from the respective control values is 40 % or more. The type I error rate and the power of the study were considered to be 5 % and 80 %, respectively. Consequently, at least 8 patients in a subgroup were required for the study using a two-sided test. A p-value <0.05 was considered significant.
Characteristics of the patients and the gallstones
The whole study group consisted of 46 consecutively cholecystectomized children (median age 13.5 years; range 0.2–18.9; median ISO-BMI 21.5 kg/m2; range 14.4–31.0), of whom 31 were female (Table 1, Fig. 1). All the patients had symptoms related to gallstone disease.
BPS were more abundant in children than in adults (57 % versus 5 %, p < 0.001). The 26 patients with BPS (median age 11.9 years; range 0.2–18.9; median ISO-BMI 19.8 kg/m2; range 14.4–25.5; 15 girls) were on an average 3 years younger than the 20 CS ones (16 girls), and, respectively, the median of their ISO-BMI was 26 % lower (p < 0.05 for both) (Table 1). However, among those children, who participated in serum analysis (n = 28, 17 girls), gender distribution, age and ISO-BMI were equal between the stone subclasses and the controls (Table 1). Analysis of covariance showed that these confounding factors did not change the statistically significant differences in serum and gallstone values between the groups reported here. Two patients were Africans, the other BPS ones were Caucasians.
In the CS-group, most of the gallstones were idiopathic (70 %), whereas in the BPS-group the etiopathogenesis was more heterogeneous, and the most common clinical diagnosis were haemolytic diseases (38 %) and idiopathic (27 %) (Table 2). Only four PS patients had a history of parenteral nutrition. Preoperative serum values of haemoglobin, white and red blood cells, platelets, C-reactive protein and sedimentation rate were within normal limits in both subgroups of patients (not shown). Preoperative serum levels of γGT were elevated by 1.6- - 5-fold in 19 % of the patients with BPS and in 10 % among those with CS (p = 0.33) (Table 3). The median of total bilirubin level in serum was two times higher in BPS than in CS (p = 0.02) (Table 3). Respectively, serum levels of ALP were above the upper limit of normal by 1.1- - 1.3-fold in 8 % (BPS-group) and in 9 % (CS-group) (p = 1.00).
Of the BPS, 23 % were single, 8 % were multiple and 69 % were microlithiasis. Respective percent values for CS were 20 %, 25 % and 55 % (p = 0.267).
Of the five patients with bile duct stones, three had BPS and two had CS. These children had no specific characteristics in their serum sterol levels or in the composition of sterols in the gallstones.
One CS patient was African, one was American Indian, but the other CS ones were Caucasians.
Serum concentrations of enzymatic cholesterol, lipoprotein lipids and bile acids
The mean serum concentrations of lipoprotein lipids and bile acids were equal between the BPS and CS subclasses. The respective concentrations (±SEM) were for enzymatic cholesterol: 3.4 ± 0.3 mmol/l and 4.1 ± 0.3 mmol/l, for LDL-cholesterol 2.0 ± 0.2 mmol/l and 2.6 ± 0.3 mmol/l, for HDL-cholesterol 1.2 ± 0.1 mmol/l and 1.4 ± 0.1 mmol/l, for triglycerides 1.2 ± 0.2 mmol/l and 1.1 ± 0.2 mmol/l and for bile acids 10 ± 8 μmol/l and 21 ± 10 μmol/l.
Serum levels of squalene, cholesterol and non-cholesterol sterols
Compared to the control group, the BPS subclass was characterized by 20–106 % higher ratios to cholesterol of squalene, cholestenol, lathosterol and desmosterol (p < 0.05 for all) (Table 4). Respectively, that of cholestanol was ~11 % higher, but stigmasterol ~41 % lower than control values (p < 0.05 for both).
Compared to the control group, the CS subclass also had high ratios to cholesterol of squalene and cholesterol precursor sterols excluding desmosterol (21–93 %, p < 0.05 for all), but low those of cholestanol and plant sterols (17–41 % below the control values, p < 0.05 for all) (Table 4).
The differences between the subclasses were 18 % lower cholesterol concentration, but 31–34 % higher ratios to cholesterol of cholestanol, campesterol and sitosterol in the BPS group than in the CS one (p < 0.05 for all) (Table 4). The ratio to campesterol of lathosterol in the CS subclass was 3.2-fold (p = 0.010) and 5.5-fold (p < 0.001) higher than in the BPS and the control groups, respectively (Table 4).
Gallstone sterols and squalene
Compared to the adult controls, the gallstones of the BPS-group were characterized by 2.0–3.1 –fold higher lanosterol and desmosterol values (in terms of mmol/mol of cholesterol) (Table 5). Parallel to that, also plant sterols and cholestanol values were 2.6–3.5 –fold above the controls (p < 0.001 for all) (Table 5).
The respective comparison in the CS-group revealed that lanosterol and desmosterol were 2.8–4.0 -fold above the controls (in terms of mmol/mol of cholesterol), and the relative markers of cholesterol absorption, i.e., cholestanol and campesterol, were 1.5–3.4 –fold higher than in controls (p < 0.001 for all) (Table 5).
The comparison of the two stone subclasses with each other showed that the cholesterol content in the BPS stones (mg/100 mg of stone) was, by definition, ~ 2 % of the CS-value (p < 0.001) (Table 5). Compared to the CS, in terms of mmol/mol of cholesterol, the BPS were rich in squalene and lanosterol, but lathosterol was only 46 % of the CS-value (p < 0.001 for both). Respectively, plant sterols sitosterol, stigmasterol and avenasterol, were 3–13 –fold higher in the BPS-subclass (p < 0.001 for all) (Table 5).
The total absolute amount of stone bile acids in BPS was double the controls and 4-times above that of CS (p < 0.05 for both) (Table 5).
The age at the time of the cholecystectomy had practically no relation to the variables studied here. ISO-BMI was inversely related to the stone cholestanol proportion in the CS group only (n = 20, r = −0.586, p = 0.007).
In the patients with BPS, serum cholesterol and non-cholesterol sterols were poorly interrelated. However, squalene, the non-sterol precursor of cholesterol (surrogate marker of cholesterol synthesis), was inversely associated with campesterol and sitosterol in serum (as ratios to cholesterol) (r = −0.575 and r = −0.697, p = 0.025 and 0.004, respectively) (Fig. 2a). Furthermore, the stone cholestanol proportion was positively related to the concentration of serum bile acids (Fig. 2b).
In the patients with CS, the surrogate sterol markers of cholesterol absorption cholestanol, campesterol and sitosterol were almost consistently positively interrelated in serum and gallstones, being most evident between serum cholestanol/cholesterol –ratio and the stone proportions of the three surrogate markers of absorption (r-range: +0.673–+0.727, p < 0.03 for each) (Fig. 2c). Serum cholestanol/cholesterol ratio reflected also those of campesterol and sitosterol in serum. Lathosterol/cholesterol –ratio was inversely related to that of cholestanol in serum (r = −0.633, p = 0.036). Furthermore, ratios to cholesterol of serum and gallstone lathosterol were positively interrelated (r = +0.847, p = 0.001).
The main new results of the present study were that: (I) BPS and CS subgroups had enhanced cholesterol synthesis, (II) in the BPS group, solely serum squalene of the surrogate markers of cholesterol synthesis was logically (inversely) related to those of cholesterol absorption, (III) the children with CS had low absorption of cholesterol, (IV) their homeostatic regulation of cholesterol metabolism was intact and (V), in the CS group, serum non-cholesterol sterols reflected their own proportions in the stone content.
Hepatic hypersecretion of biliary cholesterol with formation of cholesterol crystals from cholesterol supersaturated bile is considered to be the crucial phenomenon in the pathogenesis of the CS . In general, adult gallstone patients (predominantly with CS) have high synthesis of cholesterol parallel to increased biliary output of cholesterol, but relatively low intestinal cholesterol absorption, indicating enhanced whole-body sterol clearance . Opposite to the clinical picture of the CS patients, the subjects with BPS are frequently associated with chronic haemolytic disorders, in which increased biliary excretion of bilirubin may lead to calcium bilirubinate precipitation serving a nucleation core for BPS . Previous data indicate that certain variants of the gene encoding the hepatobiliary sterol hemi-transporter ABCG8 and the Gilbert syndrome-associated UGT1A1 variant are related to increased risk of gallstones suggesting that increased biliary secretions of cholesterol and bilirubin are crucial in the stone pathogenesis [27–29]. The results of the present study showed that the proportions of the serum surrogate markers of cholesterol synthesis were consistently elevated in the children with BPS and CS compared to the control values. These findings are parallel to that reported in a large series of adult gallstone patients, in whom cholesterol synthesis seemed to be equal between CS and BPS groups . Altogether these data indicate that both stone subclasses in children are characterized by enhanced synthesis of cholesterol and, consequently, increased biliary secretion of cholesterol, thus, sharing a common etiopathogenetic factor in the stone formation. The results of the present study also indicate, that CS children with high surrogate markers of cholesterol synthesis have low those of cholesterol absorption, and that these variables are logically inversely related to each other. Furthermore, in the CS group, the higher the ISO-BMI the lower was the serum cholestanol ratio, and, thus, intestinal cholesterol absorption. These findings suggest, first, that cholesterol metabolism in the children with CS resembles that of adult gallstone patients, secondly, homeostasis of cholesterol metabolism is undisturbed among children with CS and, thirdly, overweight together with low intestinal cholesterol absorption are associated with risk of CS in children equally to that described in adults . Interestingly, studies with experimental animals suggest that in most CS-prone humans, the small intestine is flooded continuously with an abundance of liver-secreted cholesterol molecules via bile . Opposite to that found among the CS-subjects, in the BPS group, of the relative cholesterol synthesis marker, solely the early precursor of cholesterol, squalene, inversely reflected those of absorption suggesting that in the BPS group normal cholesterol homeostasis was deteriorated. Comparison between the pediatric BPS and CS groups could be strengthened by expanding the number of patients in these subgroups.
The results of our previous and the present study support the view that solely the history of parenteral nutrition does not explain high proportions of campesterol and sitosterol in BPS . Interestingly, high cholesterol synthesis is associated with increased biliary cholesterol secretion paralleling also increased biliary secretion of sitosterol and campesterol . In the BPS group, the serum proportions of the two most abundant plant sterols – campesterol and sitosterol – were equal to those of controls supporting the view, that, first, intestinal cholesterol absorption was normal in the BPS group, and, secondly, the high proportions of plant sterols in the stones of the BPS group could at least partly be explained by increased biliary secretion of cholesterol.
Plant sterols, especially stigmasterol, have been shown to antagonize nuclear farnesoid receptor X -mediated bile acid homeostasis in hepatocytes and associate with hepatocyte damage [32, 33]. From this point of view, it was interesting to note in the present study that serum stigmasterol/cholesterol was even below that of controls in both stone subclasses making it unobvious that serum stigmasterol interferes with stone pathogenesis. However, stone stigmasterol proportion in the BPS group was high compared to that of CS putatively due to its high biliary secretion. Overall, high proportions of phytosterols (campesterol, sitosterol, avenasterol and stigmasterol) in the stones of the BPS group suggest that, first, the gallstone disease with respect to BPS differs from that of adults, and, secondly, phytosterols may be related to the formation of pediatric BPS.
The present study indicated that the children with BPS were characterized by high serum and stone proportions of cholestanol. Cholestanol is a noncholesterol sterol metabolite of cholesterol that serves as a surrogate marker of cholesterol absorption under normal physiological conditions and reflects sensitively cholestasis in primary biliary cirrhosis and biliary atresia [34, 35]. Paralleling these findings, in BPS patients of the present study, serum bile acid concentration and stone composition of cholestanol (but not plant sterols) were positively interrelated suggesting that high cholestanol proportions in the stones of the BPS group could partly be explained by cholestasis. Cholesterol precursors have been associated with some disorders in human subjects, such as squalene in cardiovascular diseases, desmosterol in steatohepatitis and 7-dehydrocholesterol in Smith-Lemli-Opitz syndrome [36–38]. In addition, subjects affected by autosomally inherited disease phytosterolemia are characterized by very high levels of phytosterols in serum and tissues . So far, serum cholestanol and phytosterols have not been related to the gallstone disease in the absence of parenteral nutrition. In the present study, several subjects in the BPS group had a disease associated with haemolysis, but haemolysis itself had no influence on serum cholestanol or plant sterol proportions. Overall, high stone and serum proportions cholestanol and plant sterols together with deteriorated cholesterol homeostasis (as evaluated by the non-cholesterol sterol surrogate markers) support the views that, first, BPS patients have had at least in their history a high biliary secretion of these sterols, and, secondly, some so far unidentified factors may lie behind accumulation of these non-cholesterol sterols in the stones and serum of the BPS patients. In the pathogenesis of BPS, also several factors in the gallbladder mucosa play crucial roles [40, 41].
In conclusion, the gallstones of the pediatric BPS group are characterized by high proportions of plant sterols and cholestanol, of which solely the latter one reflects cholestasis. This findings support the view that plant sterols may be involved in the pathogenesis of BPS. Further research is needed to evaluate whether screening for high serum cholestanol ratios could be helpful in early detection of gallstones at high risk groups. Cholesterol homeostasis with increased cholesterol synthesis and low cholesterol absorption together with high ISO-BMI in the pediatric CS group resembles those risk factors associated with CS disease described in adults and with the metabolic syndrome. Identification of this clinical connection gives tools to decrease the risk for the pediatric CS disease. High cholesterol synthesis in both stone subclasses support the view of increased biliary cholesterol secretion, which consequently enables cholesterol supersaturation in bile. This phenomenon displays that these two stone subclasses share a similarity with this respect in the pathogenesis of gallstone formation.
Adult cholesterol stones
Adult pigment stones
Black pigment stones
Brown pigment stones
the Finnish reference values –based body mass index-for-age
Palasciano G, Portincasa P, Vinciguerra V, Velardi A, Tardi S, Baldassarre G, et al. Gallstone prevalence and gallbladder volume in children and adolescents: an epidemiological ultrasonographic survey and relationship to body mass index. Am J Gastroenterol. 1989;84:1378–82.
Walker SK, Maki AC, Cannon RM, Foley DS, Wilson KM, Galganski LA, et al. Etiology and incidence of pediatric gallbladder disease. Surgery. 2013;154:927–33.
Fradin K, Racine AD, Belamarich PF. Obesity and symptomatic cholelithiasis in childhood: epidemiologic and case–control evidence for a strong relation. J Pediatr Gastroenterol Nutr. 2014;58(1):102–6.
Soloway RD, Trotman BW, Ostrow JD. Pigment gallstones. Gastroenterology. 1977;72:167–72.
Miettinen TE, Kesäniemi YA, Gylling H, Järvinen H, Silvennoinen E, Miettinen TA. Non-cholesterol sterols in bile and stones of patients with cholesterol and pigment stones. Hepatology. 1996;23:274–80.
Marschall H-U, Einarsson C. Gallstone disease. J Intern Med. 2007;261:529–42.
Koivusalo AI, Pakarinen MP, Sittiwet C, Gylling H, Miettinen TA, Miettinen TE, et al. Cholesterol, non-cholesterol sterols and bile acids in paediatric gallstones. Dig Liver Dis. 2010;42:61–6.
Cariati A. Gallstone classification in western countries. Indian J Surg. 2013. doi:10.1007/s12262-013-0847-y.
Wang HH, Portincasa P, de Bari O, Liu KJ, Garruti G, Neuschwander-Tetri BA, et al. Prevention of cholesterol gallstones by inhibiting hepatic biosynthesis and intestinal absorption of cholesterol. Eur J Clin Invest. 2013;43(4):413–26.
Wang DQ-H. Regulation of intestinal cholesterol absorption. Annu Rev Physiol. 2007;69:221–8.
Ostlund Jr RE. Phytosterols in human nutrition. Annu Rev Nutr. 2002;22:533–49.
Tilvis RS, Miettinen TA. Serum plant sterols and their relation to cholesterol absorption. Am J Clin Nutr. 1986;43:92–7.
Miettinen TA, Tilvis RS, Kesäniemi YA. Serum cholestanol and plant sterol levels in relation to cholesterol metabolism in middle-aged men. Metabolism. 1989;38:136–40.
Miettinen TA, Tilvis RS, Kesäniemi YA. Serum plant sterols and cholesterol precursors reflect cholesterol absorption and synthesis in volunteers of a randomly selected male population. Am J Epidemiol. 1990;131:20–31.
Simonen P, Gylling H, Miettinen TA. The validity of serum squalene and non-cholesterol sterols as surrogate markers of cholesterol synthesis and absorption in type 2 diabetes. Atherosclerosis. 2008;197:883–8.
Nissinen MJ, Gylling H, Miettinen TA. Responses of surrogate markers of cholesterol absorption and synthesis to changes in cholesterol metabolism during various amounts of fat and cholesterol feeding among healthy men. Br J Nutr. 2008;99:370–8.
Björkhem I, Miettinen TA, Reihner E, Ewerth S, Angelin B, Einarsson K. Correlation between serum levels of some cholesterol precursors and activity of HMG-CoA reductase in human liver. J Lipid Res. 1987;28:1137–43.
Kempen HJM, Glatz JFC, Leuven JAG, van der Voort HA, Katan MB. Serum lathosterol concentration is an indicator of whole-body cholesterol synthesis in humans. J Lipid Res. 1988;29:1149–55.
Miettinen TA. Cholesterol metabolism during ketoconazole treatment in man. J Lipid Res. 1988;29:43–51.
Miettinen TA, Koivisto P. Non-cholesterol sterols and bile acid production in hypercholesterolaemic patients with ileal by-pass. In: Paumgartner G, Stiehl A, Gerok W, editors. Bile acids and cholesterol in health and disease. Lancaster: MTP Press; 1983. p. 183–7.
Cetta F. The role of bacteria in pigment gallstone disease. Am J Surg. 1991;213(4):315–26.
Stringer MD, Taylor DR, Soloway RD. Gallstone composition: are children different? J Pediatr. 2003;142:435–40.
Stringer MD, Soloway RD, Taylor DR, Riyad K, Toogood G. Calcium carbonate gallstones in children. J Pediatr Surg. 2007;42:1677–82.
Saari A, Sankilampi U, Hannila M-L, Kiviniemi V, Kesseli K, Dunkel L. New Finnish growth references for children and adolescents aged 0 to 20 years: Length/height-for-age, weight-for-length/height, and body mass index-for-age. Ann Med. 2011;43:235–48.
Krawczyk M, Lütjohann D, Schirin-Sokhan R, Villarroel L, Nervi F, Pimentel F, et al. Phytosterol and cholesterol precursor levels indicate increased cholesterol excretion and biosynthesis in gallstone disease. Hepatology. 2012;55:1507–17.
Van Erpecum KJ. Pathogenesis of cholesterol and pigment gallstones: an update. Clin Res Hepatol Gastroenterol. 2011;35:281–7.
Buch S, Schafmayer C, Völzke H, Becker C, Franke A, von Eller-Eberstein H, et al. A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. Nat Genet. 2007;39(8):995–9.
Buch S, Schafmayer C, Völzke H, Seeger M, Miquel JF, Sookoian SC, et al. Loci from a genome-wide analysis of bilirubin levels are associated with gallstone risk and composition. Gastroenterology. 2010;139:1942–51.
Cariati A, Piromalli E, Morelli N, Bottino G, Andorno E. Indications for laparoscopic cholecystectomy or oral dissolution therapy with ursodeoxycholic acid in symptomatic gallstone disease. Arch Clin Exp Surg. 2014;3:161–5.
Xie M, Kotecha VR, Andrade JDP, Fox JG, Carey MC. Augmented cholesterol absorption and sarcolemmal sterol enrichment slow small intestinal transit in mice, contributing to cholesterol cholelithogenesis. J Physiol. 2012. doi:10.1113/jphysiol.2011.224717.
Sudhop T, Sahin Y, Lindenthal B, Hahn C, Lüers C, Berthold HK, et al. Comparison of the hepatic clearances of campesterol, sitosterol, and cholesterol in healthy subjects suggests that efflux transporters controlling intestinal sterol absorption also regulate biliary secretion. Gut. 2002;51:860–3.
Wang H, Chen J, Hollister K, Sowers LC, Forman BM. Endogenous bile acids are ligands for the nuclear receptor FXR/BAR. Mol Cell. 1999;3:543–353.
Carter BA, Taylor OA, Prendergast DR, Zimmerman TL, Von Furstenberg R, Moore DD, et al. Stigmasterol, a soy lipid-derived phytosterol, is an antagonist of the bile acid nuclear receptor FXR. Pediatr Res. 2007;62:301–6.
Gylling H, Vuoristo M, Färkkilä M, Miettinen TA. The metabolism of cholestanol in primary biliary cirrhosis. J Hepatol. 1996;24:444–51.
Pakarinen MP, Lampela H, Gylling H, Miettinen TA, Koivusalo AI, Nissinen MJ. Surrogate markers of cholesterol metabolism in children with native liver after successful portoenterostomy for biliary atresia. J Pediatr Surg. 2010;45:1659–64.
Rajaratnam RA, Gylling H, Miettinen TA. Independent association of serum squalene and noncholesterol sterols with coronary artery disease in postmenopausal women. J Am Coll Cardiol. 2000;35:1185–91.
Simonen M, Männistö V, Leppänen J, Kaminska D, Kärjä V, Venesmaa S, et al. Desmosterol in human nonalcoholic steatohepatitis. Hepatology. 2013;58:976–82.
Nissinen MJ, Gylling H, Kaski M, Tammisto P, Mieskonen S, Ignatius J, et al. Smith-Lemli-Opitz syndrome and other sterol disorders among Finns with developmental disabilities. J Lab Clin Med. 2000;136:457–67.
Bhattacharyya AK, Connor WE. β-Sitosterolemia and xanthomatosis. A newly described lipid storage disease in two sisters. J Clin Invest. 1974;53:1033–43.
Cariati A, Cetta F. Rokitansky-Aschoff sinuses of the gallbladder are associated with black-pigment gallstone formation: a scanning electron microscopy study. Ultrastruct Pathol. 2003;27(4):265–70.
Cariati A, Piromalli E. Role of parietal (gallbladder mucosa) factors in the formation of black pigment gallstones. Clin Res Hepatol Gastroenterol. 2012;36:e50–1.
The authors declare that they have no competing interests.
AK and MP planned the study, collected the data and participated in writing the manuscript, HG participated in analyzing the data and the content of the manuscript, MJN analyzed most part the data and wrote the manuscript. All authors read and approved the final manuscript.