Hereditary Renal Cystic Diseases: Autosomal Recessive Polycystic Kidney Disease
Does this patient have autosomal recessive polycystic kidney disease (ARPKD)?
- What tests to perform?
How should patients with ARPKD be managed?
What happens to patients with ARPKD?
How to utilize team care?
- Are there clinical practice guidelines to inform decision making?
What is the evidence?
Does this patient have autosomal recessive polycystic kidney disease (ARPKD)?
Autosomal recessive polycystic kidney disease (ARPKD) is a rare autosomal recessive kidney disease (
Pedigree of a family affected with autosomal recessive kidney disease.
Many severely affected fetuses with impaired renal function, reduced fetal urinary output, and a history of oligohydramnios also have pulmonary dysplasia. Most of these infants, an estimated 30%-50%, die from pulmonary complications shortly after birth. Less severe forms of ARPKD may not be diagnosed until adolescence.
Approximately 83% of ARPKD patients develop congenital hepatic fibrosis (CHF). CHF results from a malformation of the ductal plate, secondary biliary structures, and periportal fibrosis, which results in the development of portal hypertension. Patients who are affected with CHF are at an increased risk for developing ascending cholangitis and benign and malignant liver tumors, especially cholangiocarcinoma. The presence of cholangitis may influence the status of the CHF and the prognosis of the disease.
On ultrasonographic imaging, kidneys will appear enlarged, but retain a normal reniform shape. Cross-sections of the kidneys will reveal radially arranged cysts, more consistent with dilatations, extending from the cortex to the medulla. In neonates and young children, the kidneys are usually enlarged, but with age, will regress in size and lead to progressive renal insufficiency. Abnormal prenatal ultrasound findings include enlarged, hyperechogenic kidneys with or without oligohydramnios. Ultrasound appearances of ARPKD in children can often be indistinguishable from ADPKD.
A clinical diagnosis can typically be made when a child presents with clinical and ultrasonographic findings and also, when both parents have a negative ultrasound after 30 years of age, thus excluding the presence of ADPKD. If diagnostic clarification is still needed, then a histological examination of a kidney or liver biopsy can usually distinguish between ADPKD and ARPKD. Other symptomatic indications of ARPKD include: severe and early hypertension requiring multidrug therapy to control; urinary tract infections; decreased glomerular filtration rate (GFR) which is rare in ADPKD children; palpable abdominal masses; and growth retardation associated with renal insufficiency.
Definitive diagnostic criteria for ARPKD have yet to be established. However, the criteria listed below are typically used by pediatric nephrologists:
Ultrasonographic features of enlarged, echogenic kidneys, with poor corticomedullary differentiation;and
One or more of the following:
absence of renal cysts by sonography in both parents, particularly if they are>30 years of age
clinical, laboratory, or radiographic evidence of hepatic fibrosis
hepatic pathology demonstrating characteristic ductal plate abnormalities
previous affected sibling with pathologically confirmed disease
parental consanguinity suggestive of autosomal recessive inheritance
What tests to perform?
Management of ARPKD includes ordering CBC diff platelets and comprehensive chemistry panels with phosphorus. For those with advanced renal insufficiency (CKD Stage 3 or 4) PTH, Vit D 25 and Vit D 1,25 would also be included. All patients with underlying renal disease will need a lipid panel since they are at higher risk for cardiovascular disease. Children with underlying renal disease should also have growth hormone levels checked regularly.
During the prenatal and neonatal periods, fetal ultrasonographic imaging is the primary modality for the evaluation of ARPKD. Ultrasound images of CHF typically show increased echogenicity of the liver, cysts in the hepatic parenchyma, and an enlarged spleen due to the presence of portal hypertension.
In older children, computed tomography (CT) and magnetic resonance imaging (MRI) can be used to evaluate the liver for the presence of congenital hepatic fibrosis. Contrast-enhanced CT imaging may also be used. Given the need for contrast materials and radiation exposure, this method is less desirable to use in infants. There is also a relatively new, noninvasive method using MRI called rapid acquisition with relaxation enhancement (RARE-MR). This method can provide an image of the whole urinary tract system within seconds and does not involve the use of contrast materials or radiation. MRI may be used to characterize the findings of ARPKD in utero.
ARPKD is an autosomal recessive disorder with a birth incidence of 1 case per 10,000-40,000 population. This is a monogenetic disorder resulting from mutations in the PKHD1 gene on chromosome 6p21.1-p12. The protein product of the PKHD gene is called polyductin or fibrocystin. The mutation frequency in this gene is estimated to be at 1 case per 70 in the general population. Since ARPKD is a recessive disease, both parents are carriers and carry one mutated copy of the ARPKD gene. Each pregnancy carries a 25% risk of inheriting the disease, while unaffected siblings have a 50% chance of being a carrier.
Newborns who present with clinical manifestations of severe ARPKD often die shortly after birth. In these individuals, two truncating mutations are typically identified. These types of mutations occur in a minority of ARPKD individuals who often have at least one missense mutation. Additionally, molecular diagnostic testing using direct sequential analysis is also available and can establish an ARPKD diagnosis between 77%-85% certainty.
Prenatal testing is possible using DNA extracted from fetal cells obtained by amniocentesis usually performed at approximately 15 to 18 weeks' gestation or chorionic villus sampling (CVS) at approximately ten to 12 weeks' gestation. Another form of genetic testing is pre-implantation genetic diagnosis (PGD). PGD is used to analyze the genetic make-up of embryos created through in- vitro fertilization (IVF) and can determine whether or not an embryo is free of disease.
Overall interpretation of test results
Infants who survive the first year of life have a relatively good prognosis, with a probability of 80% beyond 15 years. Generally, the renal and hepatic diseases are inversely proportional to each other in individual patients. Children with severe kidney disease often have mild CHF and vice versa. With milder renal disease, the degree of renal functional impairment is less severe and perinatal respiratory compromise is not typical. These infants tend to present at slightly older ages with renal impairment. Infants with very little renal disease may have no renal functional impairment. In these patients, CHF leads to the development of portal hypertension. It is thought that the milder forms of renal disease in ARPKD enable the patients to survive longer and to undergo the inevitable progression of CHF.
Controversies in genetic testing
Genetic testing for ARPKD is difficult for confirmation of a positive diagnosis. The complexity of the gene, the variability in mutation detection efficiency, and the high frequency of missense mutations requiring confirmation in parents or other affected sibs have complicated diagnostic testing capabilities and the interpretation of detected sequence variants.
Another issue with genetic testing is the presence of single-nucleotide polymorphisms (SNPs). While both SNPs and missense mutations can alter the severity or progression of the disease, mutations occur within a gene's coding or regulatory regions and affect the function of the protein encoded by the gene. Unlike mutations, SNPs do not always affect the way a protein functions.
In order to provide accurate genetic based diagnoses, it has been recommended that haplotype analysis be used in conjunction with PKHD1 genetic testing. There is evidence that missense changes are more frequently observed among patients with a milder clinical course, while chain-terminating mutations are more commonly associated with a severe phenotype. Currently, there is no information available on the sensitivity and specificity of genetic testing for ARPKD.
How should patients with ARPKD be managed?
Patients with ARPKD should be evaluated using an imaging modality as needed once a diagnosis has been confirmed. Renal and liver complications drive the need for repeat imaging. Complications of ARPKD include, hypertension, urinary tract infections, and decreased GFR. Hypertension is typically severe and may be a presenting feature of ARPKD.
Angiotensin converting enzyme inhibitors and angiotensin receptor blocking agents are recommended for the first line therapy for the treatment of hypertension in this disorder. Cardiac hypertrophy, congestive heart failure, can also occur, with evidence of portal hypertension with our without evidence of congenital hepatic fibrosis.
Urinary tract infections should be treated quickly with agents that are appropriately dosed for the level of kidney function avoiding nephrotoxic agents with a long duration of therapy to assure sterilization of the urinary space. Evidence has also shown recombinant human growth hormone (rhGH) may benefit prepubertal children with growth failure. In addition, children with ARPKD may develop anemia and require intermittent injections of erythropoietin, which stimulates the production of red blood cells.
What happens to patients with ARPKD?
The diagnosis of ARPKD usually relies on a combination of imaging data, a complete family history, and genetic and clinical findings. Information from multiple ARPKD-affected children from the same family indicates that disease severity tends to be similar within families. This should be taken into account when counseling families.
Impaired renal function is present in 70-80% of infants, and discrete renal cysts in children may be an incidental finding. More than 50% of affected individuals progress to end-stage renal disease (ESRD), usually in the first decade of life. Hypertension is found in approximately 70% of ARPKD children, is relatively severe, and usually requires multi-drug therapy at a median age of 6 months. Both liver and renal disease gets progressively worse with age at variable rates.
Renal transplantation is the recommended renal replacement therapy in ARPKD-affected children. Affected kidneys typically terminate in ESRD, while liver synthetic function can remain normal, despite the presence of portal hypertension. Complications of portal hypertension are common as ARPKD children transition to adulthood and can be controlled with sclerotherapy or shunt surgery.
Ascending cholangitis is the most common life-threatening complication in young adult ARPKD patients. Liver transplantation may be needed for patients suffering from the effects of severe portal hypertension. Combined liver-kidney transplantation is an option for ARPKD patients suffering from severe portal hypertension and ESRD.
How to utilize team care?
Specialty consultations: A genetic counselor is needed to evaluate families considering DNA analysisfor their own carrier status and for potential future ARPKD screenings.Families of ARPKD patients should receive patient education on the risk for inheritance of the disease and potential progression of renal and hepatic disease for the individual if possible
Pediatric nephrologists for the diagnosis, treatment, and management of ARPKD
Pediatric hepatologists for the management of CHF in affected children
Vascular surgeons for vascular access for hemodialysis
General surgeons for peritoneal dialysis access and hepatic shunting procedures
Transplant surgeons for kidney or liver transplantation in affected patients
Transplant nephrologists and/or hepatologists for organ procurement and allocation, HLA techniques, immunosuppressive medications, management of the renal or liver transplant recipient and their complications, ultrasound evaluation of the kidney o rliver allograft and kidney or liver biopsy and interpretation
After adolescence, the transition between pediatric practitioners to adult practitioners should be seamless, so as to not disrupt treatment of the patient. Special care should be given to these situations:
Nurses administer blood pressure checks and oral or IV medications; collect urine for urinalysis. Nurses must also educate pediatric patients about adequate water intake and appropriate sodium supplementation.
Pharmacists dispense blood pressure and other necessary medications.
Dietitians assist in the institution and maintenance of a renal diet, which reduces the amount of phosphate, protein, sodium and acid intake. Aggressive nutritional support that is high in calories is often required to optimize weight gain and growth. Due to compression of the stomach by enlarged kidneys or liver, feedings via nasogastric or gastrostomy tubes may be utilized as a supplement.
A therapist may be necessary for children who are struggling educationally, socially, or emotionally.
Are there clinical practice guidelines to inform decision making?
Since ARPKD can resemble other cystic kidney diseases (ADPKD, glomerulocystic kidney disease, medullary sponge kidney), it is important for clinicians to be aware of the diagnostic criteria for ARPKD. It is critical for clinicians to be aware of the recessive nature and heritability of the disease, in order to inform future diagnoses of it.
MIMs code: #263200 (Polycystic Kidney Disease and Hepatic Disease, Autosomal Recessive; ARPKD)
Emory University Genetics Laboratory
What is the evidence?
Guay-Woodford, LM, Muecher, G, Hopkins, SD, Avner, ED, Germino, GG, Guillot, AP, Herrin, J, Holleman, R, Irons, DA, Primack, W, Thomson, PD, Waldo, FB, Lunt, PW, Zerres, K. "The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1-p12: implications for genetic counseling". Am J Hum Genet. vol. 56. 1995. pp. 1101-1107.(This early publication identified the ARPKD gene, later re-named PKHD1.)
Beaunoyer, M, Snehal, M, Li, L, Concepcion, W, Salvatierra, O, Sarwal, M. "Optimizing outcomes for neonatal ARPKD". Pediatr Transplant. vol. 11. 2007. pp. 267-271.(A retrospective analysis of 10 cases of neonatal ARPKD: the results demonstrate that pre-emptive bilateral nephrectomy, supportive PD and early aggressive nutrition minimized affected infant mortality and prepared the infants well for transplantation.)
Guay-Woodford, LM, Galliani, CA, Musulman-Mroczek, E, Spear, GS, Guillot, AP, Bernstein, J. "Diffuse renal cystic disease in children: morphologic and genetic correlations". Pediatr Nephrol. vol. 12. 1998. pp. 173-182.(A histopathological study on childhood renal cystic diseases and related hepatic dysgenesis that revealed the difficulties in distinguishing the etiology in childhood renal cystic diseases.)
Kaplan, BS, Fay, J, Shah, V, Dillon, MJ, Barratt, TM. "Autosomal recessive polycystic kidney disease". Pediatr Nephrol. vol. 3. 1989. pp. 43-49.(An earlier British study on improved prognosis for ARPKD, a condition then thought to be fatal.)
Capisonda, R, Phan, V, Traubuci, J, Daneman, A, Balfe, JW, Guay-Woodford, LM. "Autosomal recessive polycystic kidney disease: outcomes from a single-center experience". Pediatr Nephrol. vol. 18. 2003. pp. 119-126.(A ten year retrospective study on a multi-ethnic ARPKD cohort; most of the clinical data are comparable to previous published data collected from European-origin patients.)
Wisser, J, Hebisch, G, Froster, U, Zerres, K, Stallmach, T, Leumann, E, Schinzel, A, Huch, A. "Prenatal sonographic diagnosis of autosomal recessive polycystic kidney disease (ARPKD) during the early second trimester". Prenat Diagn. vol. 15. 1995. pp. 868-871.(A case report on early sonographic diagnosis with additional information from analysis of parental blood, blood of an affected sibling, and microsatellite DNA analysis, may provide relatively accurate diagnosis on ARPKD fetus.)
Ecder, T, Godelam, FM, Schrier, RW, Schrier, RW. "Polycystic kidney disease". Diseases of the kidney & urinary tract. 2007. pp. 502-540.(A textbook chapter that covers polycystic kidney diseases.)
Zerres, K, Hansmann, M, Mallmann, R, Gembruch, U. "Autosomal recessive polycystic kidney disease. Problems of prenatal diagnosis". Prenat Diagn. vol. 8. 1988. pp. 215-229.(An earlier publication on ARPKD emphasizing the importance of prenatal diagnosis.)
Kern, S, Zimmerhackl, LB, Hildebrandt, F, Ermisch-Omran, B, Uhl, M. "Appearance of autosomal recessive polycystic kidney disease in magnetic resonance imaging and RARE-MR-urography". Pediatr Radiol. vol. 30. 2000. pp. 156-160.(Authors suggest RARE-MR-uropraphy is a supportive diagnosis method to confirm ARPKD diagnosis.)
Zerres, K, Rudnik-Schoneborn, S, Deget, F, Holtkamp, U, Brodehl, J, Geisert, J, Scharer, K. "Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender". Arbeitsgemeinschaft fur Padiatrische, Nephrologie Acta Paediatr. vol. 85. 1996. pp. 437-445.(An earlier observational cohort on ARPKD; authors pointed out a statistically significant difference indicating that the disease progressed more severely in girls than in boys.)
Adeva, M, El-Youssef, M, Rossetti, S, Kamath, PS, Kubly, V, Consugar, MB, Milliner, DM, King, BF, Torres, VE, Harris, PC. "Clinical and molecular characterization defines a broadened spectrum of autosomal recessive polycystic kidney disease (ARPKD)". Medicine (Baltimore),. vol. 85. 2006. pp. 1-21.(Mayo retrospective study on ARPKD records between 1961-2004, which concluded a broadened spectrum for the ARPKD phenotype presented in affected infants and adults.)
Bergmann, C, Senderek, J, Kupper, F, Schneider, F, Dornia, C, Windelen, E, Eggermann, T, Rudnik-Schoneborn, S, Kirfel, J, Furu, L, Onuchic, LF, Rossetti, S, Harris, PC, Somlo, S, Guay-Woodford, L, Germino, GG, Moser, M, Buttner, R, Zerres, K. "PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD)". Hum Mutat. vol. 23. 2004. pp. 453-463.(A comprehensive review on all known PKHD1 mutations and polymorphisms/sequence variants.)
Fonck, C, Chauveau, D, Gagnadoux, MF, Pirson, Y, Grunfeld, JP. "Autosomal recessive polycystic kidney disease in adulthood". Nephrol Dial Transplant. vol. 16. 2001. pp. 1648-1652.(A study of the outcomes in terms of renal and liver function in ARPKD adults (>18yrs) who survived the neonatal period, often associated with high mortality rate.)
Avni, F, Guissard, G, Hall, M, Janssen, F, DeMaertelaer, V, Rypens, F. "Hereditary polycystic kidney diseases in children: changing sonographic patterns through childhood". Pediatr Radiol. vol. 32. 2002. pp. 169-174.(A sonographic study in children with ADPKD (n=13) and ARPKD (n=16), where the authors concluded a strong association between the development of diffuse hyperechoic foci and the onset of renal failure.)
Bergmann, C, Senderek, J, Schneider, F, Dornia, C, Kupper, F, Eggermann, T, Rudnik-Schoneborn, S, Kirfel, J, Moser, M, Buttner, R, Zerres, K. "PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD)". Hum Mutat. vol. 23. 2004. pp. 487-495.(An earlier prenatal diagnostic study employing PKHD1 mutation screening by DHPLC after the identification of PKHD1 gene. The PKHD1 mutation analysis has proven to be efficient for clinical diagnosis.)
Bergmann, C, Senderek, J, Windelen, E, Kupper, F, Middeldorf, I, Schneider, F, Dornia, C, Rudnik-Schoneborn, S, Konrad, M, Schmitt, CP, Seeman, T, Neuhaus, TJ, Vester, U, Kirfel, J, Buttner, R, Zerre, K. "Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)". Kidney Int. vol. 67. 2005. pp. 829-848.(The first study that reported the long-term outcome of ARPKD patients with defined PKHD1 mutations.)
Zerres, K, Mucher, G, Becker, J, Steinkamm, C, Rudnik-Schoneborn, S, Heikkila, P, Rapola, J, Salonen, R, Germino, GG, Onuchic, L, Somlo, S, Avner, ED, Harman, LA, Stockwin, JM, Guay-Woodford, LM. "Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology". Am J Med Genet. vol. 76. 1998. pp. 137-144.(An attempt at prenatal diagnosis by employing PCR amplification and haplotype-based analysis), done the years PKHD1 was mapped in 1994 on chromosome 6p and finally identified in 2004.)
Lonergan, GJ, Rice, RR, Suarez, ES. "Autosomal recessive polycystic kidney disease: radiologic-pathologic correlation". Radiographics. vol. 20. 2000. pp. 837-855.(A study on the correlation between pathologic and radiologic demonstrations of kidney and liver in ARPKD.)
Blyth, H, Ockenden, BG. "Polycystic disease of kidney and liver presenting in childhood". J Med Genet. vol. 8. 1971. pp. 257-284.(An early (1970s) publication on childhood polycystic disease in kidney and liver.)
Sharp, AM, Messiaen, LM, Page, G, Antignac, C, Gubler, MC, Onuchic, LF, Somlo, S, Germino, GG, Guay-Woodford, LM. "Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts". J Med Genet. vol. 42. 2005. pp. 336-349.(A refined mutation detection strategy was tested on ARPKD families, the best mutation detection rate then reported in any study.)
Lilova, M, Kaplan, BS, Meyers, KE. "Recombinant human growth hormone therapy in autosomal recessive polycystic kidney disease". Pediatr Nephrol. vol. 18. 2003. pp. 57-61.(A study focusing on using recombinant human growth hormone for growth retardation in children with ARPKD. Authors concluded that rhGH therapy in ARPKD is safe, effective and improves patients’ overall well being.)
Seikaly, MG, Salhab, N, Warady, BA, Stablein, D. "Use of rhGH in children with chronic kidney disease: lessons from NAPRTCS". Pediatr Nephrol. vol. 22. 2007. pp. 1195-1204.(A report on current usage of rhGH in children with CKD; data were acquired from NAPRTCS. Authors concluded that the use of rhGH appears to be most effective in prepubertal children with chronic renal insufficiency.)
Sweeney, WE, Avner, ED. "Diagnosis and management in childhood polycystic kidney disease". Pediatr Nephrol. vol. 26. 2011. pp. 675-692.(A review of ADPKD and ARPKD diagnosis and developing therapies in childhood polycystic kidney disease care.)
Guay-Woodford, LM, Desmond, RA. "Autosomal recessive polycystic kidney disease: the clinical experience in North America". Pediatrics. vol. 111. 2003. pp. 1072-1080.(Authors created a large longitudinal clinical database for ARPKD and reported new clinical insights by initial data analysis.)
Roy, S, Dillon, MJ, Trompeter, RS, Barratt, TM. "Autosomal recessive polycystic kidney disease: long-term outcome of neonatal survivors". Pediatr Nephrol. vol. 11. 1997. pp. 302-306.(An earlier publication documenting a British ARPKD cohort and the long term clinical outcomes.)
Zerres, K, Rudnik-Schoneborn, S, Steinkamm, C, Becker, J, Mucher, G. "Autosomal recessive polycystic kidney disease". J Mol Med (Berl). vol. 76. 1998. pp. 303-309.(A full review on the disease and genetic linkage analysis prior to the discovery of the PKHD1 gene.)
Jamil, B, McMahon, LP, Savige, JA, Wang, YY, Walker, RG. "A study of long-term morbidity associated with autosomal recessive polycystic kidney disease". Nephrol Dial Transplant. vol. 14. 1999. pp. 205-209.(Authors presented multiple ARPKD cases and attempted genetic linkage study in three families.)
Dell, KMR, Sweeney, WE, Avner, E, Avner, E, Harmon, W, Niadet, P, Yoshikawa, N. "Polycystic kidney disease". Pediatr Nephrol. Springer-Verlag. 2009. pp. 849-888.(A chapter on polycystic kidney diseases in pediatric health care.)
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