Neonatal Cholestasis Over Time: Changes in Epidemiology and Outcome in a Cohort of 154 Patients From a Portuguese Tertiary Center

Introduction: In the last two decades there have been advances in the diagnosis and management of neonatal cholestasis, which may have changed its epidemiology, diagnostic accuracy, outcomes, and survival. Our goal was to characterize these changes over time in our setting.

Methods: Retrospective cohort study in a tertiary center, enrolling patients born between January 1985 and October 2019. The cohort was divided into two periods, before (A; n = 67) and after (B; n = 87) the year 2000; and in two groups, according to patient's outcome (favorable, unfavorable). Overall survival and survival with and without orthotopic liver transplant (OLT) were evaluated in the two periods (A and B) and in different subgroups of underlying entities.

Results: We found that the age of cholestasis recognition decreased significantly from period A to period B [median 43 days and 22 days, respectively, (p < 0.001)]; the changes in epidemiology were relevant, with a significant decrease in alpha-1-antitrypsin deficiency (p < 0.001) and an increase in transient cholestasis (p = 0.004). A next-generation sequencing (NGS) panel available since mid-2017 was applied to 13 patients with contributory results in 7, but, so far, only in 2 patients led to conclusive diagnosis of underlying entities. The number of cases of idiopathic cholestasis did not vary significantly. Over time there was no significant change in the outcome (p = 0.116). Overall survival and survival without OLT had no significant improvement during the period of observation (in periods A and B, 86 vs. 88%, and 85 vs. 87%, respectively). However, in period B, with OLT we achieved the goal of 100% of survival rate.

Conclusions: Our data suggest that transient cholestasis became a very important subset of neonatal cholestasis, requiring specific guidance. The NGS panels can provide important inputs on disease diagnosis but, if applied without strict criteria and expertise, they can open a Pandora's box due to misinterpretation. Despite all the advances in accurate diagnosis and timely management—including early recognition of cholestasis—the improvement in patient outcomes and survival were still not significant.

Introduction

In the twenty-first century, neonatal cholestasis (NC) remains a major clinical challenge for several reasons. Recognition of NC among jaundiced neonates is delayed in a significant number of cases, often due to the lack awareness of healthcare professionals (1–3). Furthermore, the diagnosis is difficult due to the great diversity of underlying entities, some of them with specific treatment that should be offered in a timely manner to improve prognosis. Finally, morbidity and mortality are still high and many patients survive at the expense of orthotopic liver transplantation (OLT) (4).

Nevertheless, in the last two decades, diagnosis and management has improved, which may have had a significant impact in epidemiology and outcome of NC (5–7). New underlying entities have been added to the long list of etiological causes of NC (3) requiring specialized diagnostic tools and clinical expertise (8). Next-generation sequencing (NGS) technology is a new and appealing diagnostic tool in this field, yet to be incorporated in clinical practice (9). Additionally, the recent advances in understanding the pathophysiology of NC has not yet fully translated into new treatments or prevention strategies (10).

A few studies (11–14) have focused on NC epidemiology and how outcomes have changed over time. A systematic review of 17 studies including a total of 1,692 patients recruited ascertained from 12 countries and 5 continents from 1963 to 2011, focused only in the etiology of NC and was flawed by the inconsistency of diagnostic approach (15).

Moreover, the variations in the terminology used over time and in different centers make it even more difficult to analyse the underlying etiologies. For example, sometimes the term “neonatal hepatitis” is used regardless of existence of a known underlying entity; similar patients may be classified as “transient cholestasis” or as “total parenteral nutrition (TPN) associated cholestasis;” and finally, there is barely no consensus on which cases should be under the broad label of “idiopathic cholestasis.” In addition, the selected studies do not allow us to draw conclusions about the epidemiological trends over time. Outcomes and survival were not systematically assessed.

The aim of this study—the first one in Portugal—was to characterize NC evolution over time, epidemiology, diagnostic accuracy, outcomes, and survival.

Patients and Methods

Patients and Study Design

Retrospective cohort study of NC patients diagnosed and treated at the hepatology clinic of a single tertiary hospital, from 1 January 1985 to 31 October 2019. The study was based on the analysis of clinical charts and institutional database records. Patients with incomplete clinical records were excluded.

This study was compliant with the ethical standards of the participating healthcare institution committee [Studies N/REF.ª 2016. 081 (069-DEFI/066-CES) and N/REF.ª 2016. 084 (072-DEFI/069-CES)], and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Patients were referred from institutional departments of Emergency, Neonatology and Pediatrics as well as external institutions (primary and secondary healthcare providers).

We analyzed the cohort according to the period of diagnosis using the year 2000 as a symbolic landmark: period (A) from 1985 to 1999, and period (B) from 2000 to 2019. The cohort was also analyzed according to the outcome (I), unfavorable [death, OLT, advanced chronic liver disease], or (II) favorable (mild chronic liver disease, cure of liver disease). Furthermore, we studied the 7 subgroups of underlying entities of our cohort [biliary diseases, alpha-1-antitrypsin deficiency (A1ATD), infectious diseases, metabolic diseases, transient cholestasis, other diseases, idiopathic cholestasis].

Clinical Data, Diagnostic Approach and Treatment

Patients Were Managed by the Same Nuclear Team Throughout the Years

NC was defined as jaundice with conjugated bilirubin ≥1 mg/dl (and > 20% of total bilirubin, if total bilirubin >5.0 mg/dl), detected in a newborn or infant younger than 4 months old, according to the Guideline of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition (NASPGHAN) and European Society for Pediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) (16). For the retrospective analysis, transient cholestasis was defined as the presence of cholestatic jaundice, with known risk factors, in the same age group, and complete and spontaneous normalization of liver function tests within the first 6 months of life (17, 18).

The risk factors for NC included those described by Champion et al. (19), as well as sepsis and asphyxia, among others (20, 21). Signs and symptoms of sepsis were moaning, lethargy, hypotonia, fever, and/or hypothermia. Signs and symptoms of liver failure were coagulopathy not correctable by vitamin K administration, ascites, and hypoglycaemia, in accordance to the Pediatric Acute Liver Failure Study Group (22).

Diagnostic approaches evolved over the years reflecting the evolution of international guidelines and accumulated personal experience (8, 16). Diagnosis of underlying entities was based on biochemical, imaging, histological, and enzymatic tests; molecular studies were also performed when appropriate and available. Diagnosis of biliary atresia was confirmed by per-operatory cholangiography (with simultaneous liver biopsy). Diagnosis of liver disease for A1ATD was based on the serum level of the protein and its phenotype, and on liver histology.

Since 2005 the national newborn screening program (performed between the 3rd and 6th day of life) includes the screening of 24 treatable disorders, namely hypothyroidism, tyrosinemia, argininemia, citrullinemia type II, some organic acidurias and beta-oxidation fatty acids disorders, and cystic fibrosis (23).

In the mid-2017 a customized NGS panel targeting inborn errors of metabolism and genetic cholestatic disorders became available—initially comprised of 54 genes, and currently 95 genes (Table 1). This panel was offered to some patients fulfilling the following criteria: no known underlying entity (liver failure survivors, and/or with evolving chronic liver disease), suspicion of a second underlying entity, and cholestasis evolving transiently without risk factors.

TABLE 1

Table 1. List of genes included in the next generation sequence (NGS) panel.

Patients with biliary atresia were submitted to Kasai porto-enterostomy (PE), performed by a stable and skilled surgical team after January 2000 (24). Patients with A1ATD born after 1994 were treated by ursodeoxycholic acid (UDCA), 15–20 mg/kg/day, bid (25). Metabolic diseases were treated with special diets and specific drugs, according to the state of art, which included OLT in some patients (26, 27). Pediatric OLT was available in our country since January 1994 (one center); before was only available through foreign centers. All patients with chronic cholestasis were managed with supportive therapy in accordance to international guidelines (28).

Statistical Analysis

Clinical, biochemical, and genetic data were compared by using the following tests, as appropriate: chi-square, Fisher's and Mann-Whitney. Overall survival and survival without OLT were compared between groups using the Kaplan-Meier method and the Log Rank. The significance level used was P < 0.05. Statistical analysis was performed using the software Statistical Package for the Social Sciences v. 24.0.

Results

We analyzed 154 clinical charts of NC patients (6 were excluded due to insufficient data). The descriptive analysis of the cohort is available on Table 2.

TABLE 2

Table 2. Descriptive analysis of the cohort and comparisons between periods A (before year 2000) and B (after year 2000).

The male gender showed a higher prevalence (n = 92; 60%). Parental consanguinity was present in 9 patients (6%) and 11 (7%) had siblings affected by related clinical conditions.

A comparison between period A (before year 2000) and period B (after year 2000) is also available in Table 2. We analyzed 67 patients in period A and 87 patients in period B. The median follow-up was, as expectable, significantly longer in period A (p < 0.001].

Cholestasis Recognition Over Time

The median age of onset of jaundice, cholestasis recognition, and admission to the tertiary center, before and after year 2000 are described and compared in Table 2.

We verified that the age of cholestasis recognition decreased significantly after the year 2000 [median = 43 days (IQ: 21–72) vs. 22 days (IQ: 6–42), p < 0.001], while the time interval between the cholestasis recognition and admission to the tertiary center increased significantly [median 6 days (IQ: 0–14) vs. 12 days (IQ: 1–49), p = 0.017]; however, the age of admission to the tertiary center decreased in period B, but non significantly.

Role of Risk Factors

Risk factors for developing neonatal cholestasis were present in 45% (n = 69/85) of the cohort. Gestational age (p < 0.001) and birth weight (p = 0.002) were both significantly lower in period B.

All patients from the subgroup of transient cholestasis had at least one risk factor, and the same was observed in 35% (n = 45/85) of all other patients (p < 0.001) (Table 3).

TABLE 3

Table 3. Risk factors for neonatal cholestasis: comparison between transient cholestasis and other patients.

The presence of one or more risk factors was significantly less frequent in patients with biliary atresia in comparison to other patients, even when patients with transient cholestasis were excluded from analysis (p = 0.008), which is in contrast to what was observed with A1ATD patients (p = 0.541).

Diagnosis of Underlying Entities Over Time

A1ATD (n = 34, 22%) and biliary atresia (n = 24, 16%) were the most prevalent underlying entities. Transient cholestasis was one of the major sub-groups of patients (n = 24, 16%). Over the years, epidemiological trends underwent significant changes in our cohort (Figure 1).

FIGURE 1

Figure 1. Underlying entities in the cohort of patients with neonatal cholestasis (N = 154). Comparison between periods of time A and B.

Biliary Atresia and A1ATD—The Old Players

While the frequency of biliary atresia remained stable, A1ATD has significantly lost prominence over the years [period A: n = 25 (37%); period B: n = 9 (10%), p < 0.001]. The A1AT phenotypes were ZZ (n = 29), SZ (n = 3), M1Z (n = 1), and FZ (n = 1). One of the SZ patients had concomitantly biliary atresia.

Transient Cholestasis—The New Kid on the Block

From 33 patients referred with transient cholestasis, only 24 remained with this diagnosis after investigation; in 9 of these patients we identified post-natal Cytomegalovirus (CMV) infection, A1ATD, choledochal cyst, and chromosomal disorders. Transient cholestasis emerged as the major subgroup of patients in period B [n = 4 (6%) vs. n = 20 (23%), p = 0.004].

Idiopathic Neonatal Cholestasis—What's Been Left in the Bag

Idiopathic neonatal cholestasis accounted for 8% (n = 12) of all patients, and the difference over time was not significant.

Contribution of Molecular Studies

Molecular studies were more commonly used in period B (n = 21; 24%) than in period A (n = 6; 9%) (p = 0.014). Time lag between admission and etiological diagnosis was significantly longer than in patients who did not undergo genetic testing [23 days (IQ: 3–91) vs. 6 days (IQ: 4–11), p = 0.011].

In period A, molecular studies were performed in three patients with galactosemia, one with argininemia (29), and one with MacCune-Albright syndrome (30), previously reported. In period B, molecular studies were performed in patients with Alagille syndrome and some metabolic diseases (27).

Additionally, since the NGS panel became available, we applied it, so far, to 13 patients of this series (see details in Table 4) (31–36). We highlight a pair of siblings (brother and sister), diagnosed with neonatal sclerosing cholangitis in period A, based on clinical, biochemical, imaging, and histological criteria (26). NGS panel in the sister (the brother declined testing) allowed us to identify the genetic basis of their disease (case 1).

TABLE 4

Table 4. Results from NGS panel in 13 patients.

Treatment

Kasai's surgery was performed at a significantly younger age over time (p = 0.002) (Table 2), but the success of this surgery did not increase significantly after the year 2000 (22 vs. 60%), p = 0.072).

Treatment with UDCA, administered to patients with A1ATD was not associated with a significantly better outcome (55 vs. 83%, p = 0.111). Four out of the 23 treated patients had unfavorable outcome, in comparison with 5 out of 11 untreated patients; no side effects were observed.

OLTs were significantly more frequent in period A (p = 0.014). Differences in relation to the median age at which they were performed were not significant. In both periods, OLT performance varied significantly according to the underlying entity. In period A, OLT was performed in 6 out of 9 patients with biliary atresia, 6 out of 25 with A1ATD, 2 out of 2 with neonatal sclerosing cholangitis, 2 out of 2 with tyrosinemia, 1 out of 1 with argininemia, and 1 out of 3 with Alagille syndrome (p = 0.035). In period B, OLT was performed in 8 out of 15 patients with biliary atresia, and in 2 out of 9 with A1ATD (p = 0,020).

Outcome, Morbidity, and Mortality

Outcome was unfavorable in 47 patients (31%), without significative difference over time. Co-morbidities were identified in 26% (n = 40) and death occurred in 12% (n = 18), both not significantly different over time (Table 5). Early death rate (<12 months-old) occurred in 7% (n = 10; 55% of all mortality), from which 7 patients had metabolic or infectious diseases or idiopathic cholestasis—the fast killers. Mortality was not significantly different between genders.

TABLE 5

Table 5. Outcome, morbidity and mortality: comparison between periods A and B.

Mortality details were as follows: 9 patients died in period A (biliary atresia n = 3, Caroli disease n = 1, A1ATD n = 1, Alagille syndrome n = 1, Herpes infection n = 1, idiopathic cholestasis n = 2); from those, 5 deaths were potentially avoidable: 3 died while waiting for OLT (2 with biliary atresia and 1 with neonatal idiopathic hepatitis), 1 with Caroli disease died from sepsis, and one with A1ATD died from CMV infection; additionally, 2 died after OLT complications. The same number of patients died in period B (mitochondrial disorders n = 3, Zellweger syndrome n = 1, Menkes disease n = 1, Short-bowel syndrome n = 1, idiopathic cholestasis n = 2), but these were unavoidable deaths and none died after OLT.

Overall survival and survival without OLT had no significant improvement during the period of observation (in periods A and B, 86 vs. 88%, and 85 vs. 87%, respectively). However, in period B, with OLT we achieved the goal of 100% of survival rate. Survival rates of patients with and without OLT are disclosed in Figure 2.

FIGURE 2

Figure 2. Overall survival and survival without OLT of patients with neonatal cholestasis, before (A) and after (B) the year 2000.

Survival rates were different according to subgroups of underlying entities. The idiopathic cholestasis subgroup exhibited significantly lower overall survival rates than other patients (63 vs. 89%) as well as the metabolic diseases subgroup (72 vs. 89%) (Figure 3). The survival rate in patients with biliary atresia, with and without OLT, was not significantly different (93 vs. 75%); the same happened with patients with A1ATD (100 vs. 96%).

FIGURE 3

Figure 3. Survival curves for patients with idiopathic cholestasis vs. other patients, and metabolic diseases vs. other patients.

Discussion

NC is the form of expression of many types of liver injury with a myriad of underlying entities (15). Geographic variability is explained by genetic and environmental factors, and also depends on the expertise of the healthcare services and their technical resources. Over time, advances in diagnostic tools has changed the epidemiological landscape of this entity.

Biliary atresia is the most common cause of NC (15). A1ATD was the first genetic disease to be reported presenting with NC and progressing to liver cirrhosis (37) and played an important role in some European populations, namely in England (38) and Sweden (39). However, this may no longer be the case in England taking into account the different results obtained by Humphrey et al. (13) vs. Mieli-Vergani et al. (38). In our series, A1ATD was overall more frequent than biliary atresia, with a slightly higher rate than what had been observed in English and Swedish studies, and much higher than the rate of 4% described in the systematic review (15). The prominence of this specific condition in our cohort may be explained by the high prevalence of the disease in Northern Portugal (40), a region known for its Celtic genetic heritage. Noteworthy, we have seen a prevalence decrease over the past two decades. Several reasons can explain the lower number of cases: decrease in birth rate, greater diagnostic capacity in secondary healthcare facilities, better outcome due to early diagnosis and better supportive treatment, and our availability for external consultancy, all together avoiding the referral. In parallel with the loss of predominance of A1ATD after the year 2000, we observed the arrival and rise of the “new kid on the block”—the transient cholestasis—surpassing the “old players.”

After the year 2000, several studies reported an emergent subset of patients, denominated as “transient,” “prematurity-associated,” “TPN-associated,” or “sepsis-associated” (15). This new subset of patients shares a higher level of exposure to risk factors (19, 41). Their role as determinants or co-factors of NC is far from being totally clear. In our study, one third of the other patients also had risk factors. Interestingly, the biliary atresia patients had significantly less risk factors. This is in contrast with the A1ATD patients in which the pathophysiology of the liver disease (42), may be affected by the risk factors, and so the prevention or treatment of those may also be contributing to the downtrend in prevalence. On the other hand, the increase in transient cholestasis may be explained by the increased rate of prematurity and survival of premature and sick newborns, and an increase in referrals of these to tertiary centers. Previous studies (17, 18) did not address underlying entities as possible determinants or cofactors of cholestasis in patients with transient cholestasis, but in our study we have verified that in out of 9 patients referred with this diagnosis we could identify both sporadic (e.g., CMV infection, choledochal cyst) and genetic etiologies (e.g., A1ATD). Finally, identification of etiological diagnosis might have been limited due to insufficient diagnostic tools. The assumption of the diagnosis of transient cholestasis is one of exclusion and the current guidelines for diagnostic approach do not fully address this problem (8). In clinical practice the current main question is: “how far should we investigate these patients for underlying entities?”

The prevalence of idiopathic cases has decreased significantly according to a recent European study (11). In our center, the prevalence rate has not decreased over time—as a matter of fact, we obtained similar figures to the ones reported by Hoerning et al. Improved detection rate is likely to be attained with the availability of new molecular technologies. Recently, Nicastro et al. (43) developed a prospective study that included 125 patients, of which 50 subjects underwent a through diagnostic protocol that included genetic testing—and they obtained a detection rate of 60% which is much higher than reported in previous studies (44). Our preliminary data supports the perspective that patients that remain undiagnosed despite standard of care diagnostic tools may benefit from NGS panels for further clarification. Neonatal sclerosing cholangitis is the poster child of this paradigm as it allowed to establish a genetic basis and point to the possible pathophysiology—a novel liver-based non-motile ciliopathy, sometimes associated to nephronophthisis (45, 46); which our study also supports since we describe a novel variant. Still, despite the advances that new molecular technologies brought to this field, a word of caution is warranted as genetic studies can be misleading (e.g., case 8, Alagille syndrome, later unconfirmed), of difficult interpretation (e.g., case 5, co-existence of 3 variants in heterozygosity) or raise more questions instead of simply giving us answers (e.g., when parental testing is required for re-classification of variants which comes at increased costs). We did not offer NGS panel testing to patients with transient cholestasis but we did offer it to patients with transiently evolving cholestasis without risk factors, mainly searching for some treatable diseases such as Niemman-Pick type C (47) or citrin deficiency (48), and we had some surprising results requiring further clarification.

According to Feldman and Sokol (7), genetic evaluation will necessarily change the diagnostic paradigm and give rise to current and emerging diagnosis algorithms that will certainly include this tool. From our experience, NGS panel should be used with caution and in selected cohorts. As we recently stated elsewhere (27), we believe that this tool must not be used as first-line, and should definitely not be used in the absence of skilled clinical guidance. Therefore, it does not make sense to talk about a paradigm shift, since any decision algorithm must always have clinical and biochemical markers. Additional work is needed to formally assess the cost-effectiveness of these studies and to understand what is their ideal place in the algorithm tree. In Portugal, we still need to improve on NGS panel availability and turn-around times that allow for diagnosis in a timely manner. We propose its use as previously described by Moreira da Silva et al. (27). In clinical practice we do not recommend transient cholestasis patients to be offered NGS panels. However, including these patients in research studies will be useful as they might contribute to a better understanding of the pathophysiology of NC. We highlight the fact that no positive genetic test will ever subside one of our greatest sources of anxiety—the exclusion of biliary atresia—since it can coexist with other entities.

Despite all the advances, NC remains globally associated with high mortality and morbidity (14). Our data is in line with this observation, as one third of the patients had an unfavorable outcome. In addition, a significant number of patients with “favorable outcome” presented mild chronic liver disease and their long-term outcome (adulthood) is uncertain. Mortality and morbidity rates are difficult to compare, due to the different follow-up periods in each study. However, the comparison of our findings with the study by Hoerning et al. (11) showed a similar mortality rate, but, contrary to this study, which found a higher mortality rate in biliary atresia (before and after OLT), in our study, metabolic diseases and idiopathic cases were the main responsible for mortality.

As far as we know, there are no publications with long-term survival studies, except in the subgroup of biliary atresia that has been well-studied. In biliary atresia, first the Kasai surgery (49, 50), then OLT (51, 52), and, more recently, in some countries the centralization of diagnosis and treatment (5, 6), and in others, universal newborn screening programs (53), produced advances with impact on overall survival and survival with native liver (5, 54). Our study presents the survival curves of a cohort of 154 patients with NC for a period of nearly 35 years, namely overall survival and survival without OLT, as well as the comparison of these curves before and after the year 2000. We concluded that outcomes and survival did not improve significantly over time, and the number of patients who survived due to the benefits of OLT was not significant. Outcomes and survival varied with the underlying entities. In our study, patients with biliary atresia had long-term overall survival similar to other patients, and survival rates without OLT were not significantly lower. Metabolic diseases and idiopathic cholestasis showed significantly shorter survival curves than those of other patients.

Early recognition of cholestasis is fundamental to attain a better outcome (55). In our cohort, early recognition of cholestasis improved significantly over time. This was due to a continuous investment in the postgraduate training of pediatricians and pediatric nurses—in a pilot study developed locally that entailed a survey and photographs of normal and pale stools, these healthcare professionals obtained the best results (3). However, there is still room for improvement, especially at the level of primary healthcare services. Taking in to account the high morbidity and mortality, a universal screening program for neonatal cholestasis would be very useful; however, there are numerous underlying entities expressing at variable timings, which makes screening a very complex task. So far, only one screening method has been developed successfully: the stool color card that screens for biliary atresia. This screening tool as not been adopted in our country yet—but could easily be integrated into our Health Surveillance program of the Child and Adolescent. There are some promising studies using serum levels of conjugated bilirubin in the first days of life (56, 57) as a screening tool; these studies, if validated in larger populations, could point toward a screening method for other underlying entities in addition to biliary atresia. In our country, this parameter can also be easily added to the existing endocrine-metabolic screening program (23).

Other factors may interfere with the outcome of patients, such as the accuracy in the diagnosis of the underlying entities and the availability of specific medical and surgical treatments (10). In our center, patients had access to modern diagnostic techniques, as well as medical and surgical therapies according to international guidelines and to our institutional resources over time. After the year 2000, patients benefited from a qualified and stable surgical team, but the improvement in the success rate of Kasai surgery was not significant. Given the low number of cases/year, and according to data from other countries (6), since April 2019, the patients managed in our center were referred to perform Kasai surgery at the only pediatric liver transplant center in Portugal.

In summary, our data suggest that transient cholestasis became a very important etiology of NC, it can hide underlying entities, and requires specific guidance. The challenge on to what extent pursuing an etiological diagnosis still remains. The role played by risk factors in NC is far from clear. NGS panels can provide important inputs on disease diagnosis, but if applied without strict criteria and expertise they can open a Pandora's box due to misinterpretation. Despite all the advances in accurate diagnosis and timely management—including early recognition of cholestasis—the improvement in patient outcomes and survival were still not significant.

Data Availability Statement

The data analyzed in this study is subject to the following licenses/restrictions: The data are recorded in the patients' clinical files and in the hospital databases. In order to have access, it is necessary to ask for authorization from the Ethics Committee and the Board of Directors of the hospital. This authorization was requested and obtained to carry out this study. Requests to access these datasets should be directed to Ethics Committee, secretariado.etica@chporto.min-saude.pt, and Departement of Education, Training and Research (DEFI), secretariado.cg.defi@chporto.min-saude.pt.

Ethics Statement

This study, involving human participants, was analyzed and approved by the Ethics Committee (Comissão de Ética para a Saúde, CES) and by the Research Coordinating Office of the Department of Education, Training, and Research (Gabinete Coordenador da Investigação do Departamento de Educação, Formação, e Investigação, DEFI) and afterwards reviewed and approved by the board of administration (Conselho de Administração) of our hospital (Centro Hospitalar e Universitário do Porto, Portugal).

Author Contributions

ES diagnosed and followed patients, designed the study, collected and analyzed data, and elaborated the draft of the manuscript. AA and SF diagnosed and followed patients, created databases, and collected and analyzed data. EM diagnosed and followed patients and collected data. MV analyzed data and critically reviewed the manuscript. AS-S and AL critically reviewed the manuscript. All authors contributed to the article and approved the submitted version.

Funding

This work was supported by Applied Molecular Biosciences Unit (UCIBIO), which was financed by national funds from FCT/MCTES (UID/MULTI/04378/2019).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

Many thanks to Doctor Isabel Alonso (IBMC, I3S) for her collaboration in the execution and interpretation of the NGS panel.

References

1. Bakshi B, Sutcliffe A, Akindolie M, Vadamalayan B, John S, Arkley C, et al. How reliably can paediatric professionals identify pale stool from cholestatic newborns? Arch Dis Child Faetal Neonatal. (2012) 97:385–7. doi: 10.1136/fetalneonatal-2010-209700

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Palermo JJ, Joerger S, Turmelle Y, Putnam P, Garbutt J. Neonatal cholestasis: opportunities to increase early detection of neonatal cholestasis. Acad Pediatr. (2012) 12:283–7. doi: 10.1016/j.acap.2012.03.021

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Santos Silva E, Moreira Silva H, Azevedo Lijnzaat L, Melo C, Costa E, Martins E, et al. Clinical practices among healthcare professionals concerning neonatal jaundice and pale stools. Eur J Pediatr. (2017) 176:361–9. doi: 10.1007/s00431-016-2847-y

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Kelly D. Diseases of the Liver and Biliary System in Children. 4th ed. (2017). Chichester, UK: Wiley-Blackwell.

Google Scholar

5. Serinet MO, Wildhaber BE, Broue P, Lachaux A, Sarles J, Jacquemin E, et al. Impact of age at kasai operation on its results in late childhood and adolescence: a rational basis for biliary atresia screening. Pediatrics. (2009) 123:1280–6. doi: 10.1542/peds.2008-1949

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Davenport M, Ong E, Sharif K, Alizai N, McClean P, Hadzic N, et al. Biliary atresia in England and Wales: results of centralization and new benchmark. J Pediatr Surg. (2011) 46:1689–94. doi: 10.1016/j.jpedsurg.2011.04.013

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Feldman A, Sokol, RJ. Neonatal cholestasis: emerging molecular diagnostics and potential novel therapeutics. Nat Rev Gastroenterol Hepatol. (2019) 16:346–60. doi: 10.1038/s41575-019-0132-z

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Fawaz R, Baumann U, Ekong U, Fischler B, Hadzic N, Mack CL, et al. Guideline for the evaluation of cholestatic jaundice in infants: joint recommendations of the north American society for pediatric gastroenterology, hepatology, and nutrition and the european society for pediatric gastroenterology, hepatology, and nutrition. J Pediatr Gastroenterol Nutr. (2017) 64:154–68. doi: 10.1097/MPG.0000000000001334

CrossRef Full Text | Google Scholar

9. Nicastro E, D'Antiga L. Next generation sequencing in pediatric hepatology and liver transplantation. Liver Transpl. (2018) 24:282–93. doi: 10.1002/lt.24964

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Bezerra JA, Wells R, Mack CL, Karpen SJ, Hoofnagle JH, Doo E, et al. Biliary atresia: clinical and research challenges for the 21st century. Hepatology. (2018) 68:1163–73. doi: 10.1002/hep.29905

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Hoerning A, Raub S, Dechene A, Brosch MN, Kathemann S, Hoyer PF, et al. Diversity of disorders causing neonatal cholestasis - the experience of a tertiary pediatric center in Germany. Front Pediatr. (2014) 2:65. doi: 10.3389/fped.2014.00065

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Lee WS, Chai PF, Boey CM, Looi LM. Aetiology and outcome of neonatal cholestasis in Malaysi. Singapore Med J. (2010) 51:434–9.

PubMed Abstract | Google Scholar

13. Humphrey TM, Stringer MD. Biliary atresia: US diagnosis. Radiology. (2007) 244:845–51. doi: 10.1148/radiol.2443061051

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Aanpreung P, Laohapansang M, Ruangtrakool R, Kimhan J. Neonatal cholestasis in thai infants. J Med Assoc Thai. (2005) 88:S9–15.

PubMed Abstract | Google Scholar

15. Gottesman LE, Del Vecchio MT, Aronoff SC. Etiologies of conjugated hyperbilirubinemia in infancy: a systematic review of 1692 subjects. BMC Pediatrics. (2015) 15:192. doi: 10.1186/s12887-015-0506-5

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Moyer V, Freese DK, Whitington PF, Olson AD, Brewer F, Colletti RB, et al. Guideline for the evaluation of cholestatic jaundice in infants: recommendations of the North American society for pediatric gastroenterology, hepatology and nutrition. J Pediatr Gastroenterol Nutr. (2004) 39:115–28. doi: 10.1097/00005176-200408000-00001

CrossRef Full Text | Google Scholar

17. Jacquemin E, Lykavieris P, Chaoui N, Hadchouel M, Bernard O. Transient neonatal cholestasis: origin and outcome. J Pediatr. (1998) 133:563–7. doi: 10.1016/S0022-3476(98)70070-8

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Ciocca M, Alvarez F. Transient neonatal cholestasis. Arch Argent Pediatr. (2011) 109:163–6. doi: 10.1590/S0325-00752011000200017

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Champion V, Carbajal R, Lozar J, Girard I, Mitanchez D. Risk factors for developing transient neonatal cholestasis. J Pediatr Gastroenterol Nutr. (2012) 55:592–8. doi: 10.1097/MPG.0b013e3182616916

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Satrom K, Gourley G. Cholestasis in preterm infants. Clin Perinatol. (2016) 43:355–73. doi: 10.1016/j.clp.2016.01.012

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Herzog D, Chessex P, Martin S, Alvarez F. Transient cholestasis in newborn infants with perinatal asphyxia. Can J Gastroenterol. (2003) 17:179–82. doi: 10.1155/2003/108473

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Squires RH, Shneider BL, Bucuvalas J Alonso E, Sokol RJ, Narkewicz MR, et al. Acute liver failure in children: the first 348 patients in the pediatric acute liver failure study group. J Pediatr. (2006) 148:652–8. doi: 10.1016/j.jpeds.2005.12.051

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Vilarinho L, Rocha H, Sousa C, Marcao A, Fonseca H, Bogas M, et al. Four years of expanded newborn screening in Portugal with tandem mass spectrometry. J Inherit Metab Dis. (2010) 33(Suppl. 3):S133–8. doi: 10.1007/s10545-010-9048-z

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Santos Silva E, Medina M, Rocha P, Bonet B, Ferreira de Sousa JA, Enes C. Atrésia das vias biliares extrahepáticas: estudo clínico retrospectivo. Nascer Crescer. (2011) 20:9–15. Available online at: http://www.scielo.mec.pt/scielo.php?script=sci_arttext&pid=S0872-07542011000100002&lng=pt

Google Scholar

25. Santos Silva E, Moreira Silva H, Melo C, Rocha H, Medina M, Martins E. Alpha-1- antitrypsin deficiency presenting as neonatal cholestasis: predictors of outcome and effect of ursodeoxycholic acid. J Liver. (2015) 4:185. doi: 10.4172/2167-0889.1000185

CrossRef Full Text | Google Scholar

26. Santos Silva E, Cardoso ML, Vilarinho L, Medina M, Barbot C, Martins E. Liver transplantation prevents progressive neurological impairment in argininemia. JIMD Rep. (2013) 11:25–30. doi: 10.1007/8904_2013_218

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Moreira Silva H, Maio I, Bandeira A, Gomes Martins E, Santos Silva E. Metabolic liver diseases presenting with neonatal cholestasis: at the crossroad between old and new paradigms. Eur J Pediatr. (2019) 178:515–23. doi: 10.1007/s00431-019-03328-5

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Baker A, Stevenson R, Dhawan A, Goncalves I, Socha P, Sokal E. Guidelines for nutritional care for infants with cholestatic liver disease before liver transplantation. Pediatr Transplant. (2007) 11:825–34. doi: 10.1111/j.1399-3046.2007.00792.x

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Santos Silva E, Martins E, Cardoso ML, Barbot C, Vilarinho L, Medina M. Liver transplantation in a case of argininaemia. J Inherit Metab Dis. (2001) 24:885–7. doi: 10.1023/A:1013960712516

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Santos Silva E, Lumbroso S, Medina M, Gillerot Y, Sultan C, Sokal EM. Demonstration of McCune-Albright mutations in the liver of children with high gammaGT progressive cholestasis. J Hepatol. (2000) 32:154–8. doi: 10.1016/S0168-8278(00)80202-0

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Cardoso ML, Martins E, Vasconcelos R, Vilarinho L, Rocha J. Identification of a novel R21X mutation in the liver-type arginase gene (ARG1) in four Portuguese patients with argininemia. Hum Mutat. (1999) 14:355–6. doi: 10.1002/(SICI)1098-1004(199910)14:4<355::AID-HUMU20>3.0.CO;2-I

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Jacquemin E, Malan V, Rio M, Davit-Spraul A, Cohen J, Landrieu P, et al. Heterozygous FIC1 deficiency: a new genetic predisposition to transient neonatal cholestasis. J Pediatr Gastroenterol Nutr. (2010) 50:447–9. doi: 10.1097/MPG.0b013e3181cd2725

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Goto K, Sugiyama K, Sugiura T, Ando T, Mizutani F, Terabe K, et al. Bile salt export pump gene mutations in two japanese patients with progressive familial intrahepatic cholestasis. J Pediatr Gastroenterol Nutr. (2003) 36:647–50. doi: 10.1097/00005176-200305000-00012

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Nukiwa T, Brantly M, Garver R, Paul L, Courtney M, LeCocq JP, et al. Evaluation of “at risk” alpha 1-antitrypsin genotype SZ with synthetic oligonucleotide gene probes. J Clin Invest. (1986) 77:528–37. doi: 10.1172/JCI112333

PubMed Abstract | CrossRef Full Text | Google Scholar

35. LaDuca H, Farwell KD, Vuong H, Hsiao-Mei L, Wenbo M, Shahmirzadi L, et al. Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels. PLoS ONE. (2017) 12:e0170843. doi: 10.1371/journal.pone.0170843

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Fanen P, Ghanem N, Vidaud M, Besmond C, Martin J, Costes B, et al. Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctions. Genomics. (1992) 13:770–6. doi: 10.1016/0888-7543(92)90152-I

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Sharp HL, Bridges RA, Krivit W, Freier EF. Cirrhosis associated with alpha-1-antitrypsin deficiency. J Lab Clin Med. (1969) 73:934–9.

PubMed Abstract | Google Scholar

38. Mieli-Vergani G, Howard ER, Mowat AP. Liver disease in infancy: a 20 year perspective. Gut. (1991) 32:S123–8. doi: 10.1136/gut.32.Suppl.S123

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Fischler B, Papadogiannakis N, Nemeth A. Aetiological factors in neonatal cholestasis. Acta Paediatr. (2001) 90:88–92. doi: 10.1111/j.1651-2227.2001.tb00261.x

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Meira L, Boaventura R, Seixas S, Sucena M. Alpha-1 antitrypsin deficiency detection in a portuguese population. COPD. (2018) 15:4–9. doi: 10.1080/15412555.2017.1414779

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Tufano M, Nicastro E, Giliberti P, Vegnente A, Raimondi F, Iorio R. Cholestasis in neonatal intensive care unit: incidence, aetiology and management. Acta Paediatr. (2009) 98:1756–61. doi: 10.1111/j.1651-2227.2009.01464.x

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Teckman JH, Mangalat N. Alpha-1 antitrypsin and liver disease: mechanisms of injury and novel interventions. Expert Rev Gastroenterol Hepatol. (2015) 9:261–8. doi: 10.1586/17474124.2014.943187

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Nicastro E, Di Giorgio A, Marchetti D, Barboni C, Cereda A, Iascone M, et al. Diagnostic yield of an algorithm for neonatal and infantile cholestasis integrating next generation sequencing. J Pediatr. (2019) 211:54–62.e4. doi: 10.1016/j.jpeds.2019.04.016

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Togawa T, Sugiura T, Ito K, Endo T, Aoyama K, Ohashi K, et al. Molecular genetic dissection and neonatal/infantile intrahepatic cholestasis using targeted next-generation sequencing. J Pediatr. (2016) 171:171–7.e1–4. doi: 10.1016/j.jpeds.2016.01.006

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Grammatikopoulos T, Sambrotta M, Strautnieks S, Foskett P, Knisely AS, Wagner B, et al. Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis. J Hepatol. (2016) 65:1179–87. doi: 10.1016/j.jhep.2016.07.017

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Girard M, Bizet AA, Lachaux A, Gonzales E, Filhol E, Collardeau-Franchon S, et al. DCDC2 mutations cause neonatal sclerosing cholangitis. Hum Mutat. (2016) 37:1025–9. doi: 10.1002/humu.23031

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Gumus E, Haliloglu G, Karhan AN, Demir H, Gurakan F, Topcu M, et al. Niemann-Pick disease type C in the newborn period: a single-center experience. Eur J Pediatr. (2017) 176:1669–76. doi: 10.1007/s00431-017-3020-y

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Hutchin T, Preece MA, Hendriksz C, Chakrapani A, McClelland V, Okumura F, et al. Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) as a cause of liver disease in infants in the UK. J Inherit Metab Dis. (2009) 32:S151–S5. doi: 10.1007/s10545-009-1116-x

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Kasai M, Suzuki M. A new operation for non-correctable biliary atresia: hepatic portoenterostomy. Shujutsu. (1959) 13:733–9.

Google Scholar

50. Altman RP. The portoenterostomy procedure for biliary atresia: a five year experience. Ann Surg. (1978) 188:351–62. doi: 10.1097/00000658-197809000-00010

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Iwatsuki S, Shaw BW Jr, Starzl TE. Liver transplantation for biliary atresia. World J Surg. (1984) 8:51–6. doi: 10.1007/BF01658363

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Barshes NR, Lee TC, Balkrishnan R, Karpen SJ, Carter BA, Goss JA. Orthotopic liver transplantation for biliary atresia: the U.S. experience. Liver Transpl. (2005) 11:1193–200. doi: 10.1002/lt.20509

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Hsiao CH, Chang MH, Chen HL, Lee HC, Wu TC, Lin CC, et al. Universal screening for biliary atresia using an infant stool color card in Taiwan. Hepatology. (2008) 47:1233–40. doi: 10.1002/hep.22182

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Nio M. Japanese biliary atresia registry. Pediatr Surg Int. (2017) 33:1319–25. doi: 10.1007/s00383-017-4160-x

PubMed Abstract | CrossRef Full Text | Google Scholar

55. Benchimol EI, Walsh CM, Ling SC. Early diagnosis of neonatal cholestatic jaundice: test at 2 weeks. Can Fam Physician. (2009) 55:1184–92.

PubMed Abstract | Google Scholar

56. Harpavat S, Finegold MJ, Karpen SJ. Patients with biliary atresia have elevated direct/conjugated bilirubin levels shortly after birth. Pediatrics. (2011) 128:e1428–33. doi: 10.1542/peds.2011-1869

PubMed Abstract | CrossRef Full Text | Google Scholar

57. Harpavat S, Garcia-Prats JA, Shneider BL. Newborn bilirubin screening for biliary atresia. New Engl J Med. (2016) 375:605–6. doi: 10.1056/NEJMc1601230

PubMed Abstract | CrossRef Full Text | Google Scholar