- Short report
- Open Access
Compound heterozygosity in sodium channel Nav1.7 in a family with hereditary erythermalgia
Molecular Painvolume 4, Article number: 21 (2008)
Hereditary erythermalgia is a painful and debilitating genetic disorder associated with mutations in voltage-gated sodium channel Nav1.7. We have previously reported a Canadian family segregating erythermalgia consistently with a dominant genetic etiology. Molecular analysis of the proband from the family detected two different missense mutations in Nav1.7. In the present study we have performed a long-term follow-up clinical study of disease progression in three affected family members. A more extensive molecular study has also been completed, analyzing the segregation of the two missense variants in the family. The two variants (P610T, L858F) segregate independently with respect to clinical presentation. Detailed genotype/phenotype correlation suggests that one of the two variants (L858F) is causal for erythermalgia. The second variant (P610T) may modify the phenotype in the proband. This is the second reported study of potential compound heterozygosity for coding polymorphisms in Nav1.7, the first being in a patient with paroxysmal extreme pain disorder.
A Canadian family segregating erythermalgia as an apparent dominant genetic trait was originally ascertained and reported in 1979. At the time, the female proband was 14 years old. She was reported to have two affected brothers, however only the proband's condition was described. She had already suffered double leg amputations at age 13, with regular severe episodes of pain and redness in the extremities. A brief report of the family in 1987 noted that the proband had suffered a near-fatal case of hypothermia due to excessive use of a cooling apparatus to relieve painful symptoms. One brother had suffered two leg amputations at age 20. The family was subsequently included in a cohort of families used to map a locus for erythermalgia to chromosome 2q31-32, and eventually molecular analysis of the proband identified two missense variants in voltage-gated sodium channel Nav1.7, amino acids P610T and L858F. Segregation of these two variants in the remaining affected and unaffected family members was not feasible at that time.
We have now revisited the affected family members in a long-term clinical follow-up (see Fig. 1).
Proband (III/3): The proband is a female now 43-years-old. She has continued to suffer extremely debilitating episodes of pain. On a scale of 1–10, with 10 the most extreme, she reports her pain as 10 in the absence of mitigating treatments. She has had no further amputations since the original ones at age 14. She reports burning, redness and pain in hands, arms and legs (above the amputations) as well as eartips, but not her nosetip. She does not suffer diarrhea. Symptoms are provoked by exercise or warm temperatures or use of bed sheets, and are more common during summertime. She is unable to wear shoes, and unable to work. Symptoms are incompletely alleviated by application of cold water or ice, air conditioning, elevation of the painful extremity, or by treatment with some medications.
Brother (III/1): The oldest brother is now age 49. He reports having symptoms from birth, with burning and reddened hands and ears. Both legs were partially amputated at age 20, he continues to experience symptoms in the legs in the vicinity of the stumps. Symptoms are provoked by heat or use of bed sheets and are alleviated by application of ice or use of a ventilator. He does not wear shoes and symptoms interfere with his ability to work or leave the home. He does not use pain medication.
Brother (III/2): The second brother is now age 48. He reports having symptoms from birth, with reddened and burning painful hands, feet, and ears. He reports warm and reddened but not painful nosetip. On a scale of 1–10 he reports pain at 8–9. He has suffered no amputations but has discolored and ulcerated skin in the affected regions. Symptoms are provoked by heat, exercise or use of bed sheets, and increase during summertime. He employs a ventilator but not ice or ice water for alleviation of symptoms. He does not wear shoes. He has worked sporadically and has experienced difficulties with adapting to inflexible work and school environments. Alcohol use exacerbates symptoms.
Overall, although it is difficult to assess given the subjective nature of painful sensation, the proband appears to experience significantly greater pain and discomfort than her two siblings. This is based on the patients reports according to a numeric rating scale, the need for stronger medication and the requirement for amputations at a young age. The development of a near fatal case of hypothermia resulting from attempts to cool the extremities in a search for relief is also suggestive of more severe pain.
Mother (II/1): The proband reports her mother was affected with symptoms from childhood, but the mother was unavailable for direct clinical examination.
In the original molecular study of this family the entire coding region of Nav1.7 was sequenced in DNA from the proband. Two missense mutations were reported, at nucleotides C1828A and C2572T, corresponding to amino acid changes P610T and L858F respectively. We have now performed mutation analysis for these two variants in all available family members, including the affected mother, three affected and two unaffected siblings (see Figure 1). The figure shows the segregation of the two amino acid variants, as well as the microsatellite haplotypes determined as part of the original fine mapping of the locus.
All three affected siblings and the affected mother carry the L858F variant. Somewhat surprisingly however, the second variant, P610T, is shared by the proband and the unaffected but not the affected siblings. Microsatellite haplotypes support the inference that the two variants are in trans in the proband. Presumably the P610T variant was transmitted from the unsampled father.
The L858F variant was independently reported in a Chinese patient with erythermalgia. L858 is located within the DII/S4–S5 linker which is conserved among all mammalian sodium channels, indicating a critical role in controlling biophysical properties of these channels. Interestingly, a different mutation at the same residue, L858H, was found in a different Chinese family with erythermalgia. Electrophysiological studies document that the L858F mutation affects the normal physiological function of the channel and leads to increased hyperexitability, as the mutant channel produces larger response to only small stimuli. The mutant channel also recovers more quickly from inactivation. In addition, cooling decreases the current density, slows deactivation and increases ramp currents. This brings the function of the channel within the range of the wild type protein.
Our findings are intriguing with respect to genotype/phenotype correlations of missense variants in Nav1.7. To a first approximation, the disease in the family appears to be caused by inheritance of the L858F mutation. This is consistent with other genetic and functional studies of the gene. Of itself P610T has no obviously demonstrable phenotype in carriers in our pedigree. P610 is located within the cytosolic linker joining transmembrane segment S6 of domain I and transmembrane segment S1 of domain II and appears to be located within a conserved region of SCN9a. However residues 609–611, though partly conserved, are not invariant among vertebrate species (see Table 1). Moreover, we found P610T in 10 out of 210 control Caucasian chromosomes. This further suggests that P610T is not a highly penetrant pathogenic mutation. The question remains whether P610T is able to modulate e.g. exacerbate the phenotype of the proband carrying the main causal variant, or to subtly influence sensitivity to pain independently. This could arise through either of two possibilities. First, P610T may be a very weak gain of function (gof) allele of Nav1.7. Second, P610T may be a loss of function (lof) allele. Human patients carrying loss of function alleles of Nav1.7 suffer a rare genetic hypoalgesia disorder called congenital indifference to pain (CIP) [8–10]. However CIP is recessive, so that affected patients are either homozygous or compound heterozygous for two, normally nonsense, mutations in the gene. Heterozygous carriers of Nav1.7 lof alleles have normal pain thresholds, suggesting the absence of a strong dose-sensitivity for Nav1.7. In the presence of a presumptive hyperalgesic gof allele (such as L858F), the occurrence of an lof allele in trans could potentially exacerbate the phenotype, due to the reduction in wild type functional gene product. Our suggestion of functional consequences of P610T is necessarily preliminary. A direct test through in vitro electrophysiology is beyond the scope of the present study. Such a test, complemented by population based association tests of differential pain sensitivity, would be required to explore our hypotheses directly.
The genetics of Nav1.7 provides substantial complexities. Broadly, mutations in the gene lead to one of three different phenotypes[11, 12]. As noted, lof alleles lead to recessive hypoalgesia. A class of aberrant, or gof mutations, confirmed in many cases by electrophysiological studies, cause erythermalgia[4–7, 13–24]. A third class of alleles cause another hyperalgesia condition, known originally as familial rectal pain and now as paroxysmal extreme pain disorder (PEPD) [25–27]. PEPD alleles of Nav1.7 are likewise missense variants, suggesting that they also have aberrant function (gof). They cause spontaneous rectal, ocular or submandibular pain with reddening. The reasons for the different tissue distribution of the symptoms of erythermalgia and PEPD remain to be determined. The causal alleles for each condition are distributed across various regions of the gene (see Figure 1 of Drenth and Waxman), although most mutant PEPD alleles are further C-terminal than most erythermalgia alleles. Expression and further electrophysiological studies have partly clarified this issue, with subtle differences in in vitro biophysical effects of PEPD versus erythermalgia mutant alleles. One likely case of compound heterozygosity for two missense Nav1.7 alleles was reported in a PEPD patient, making this the second report of a potential compound heterozygote for two mutant alleles in this gene.
A challenge with interpretation of the case literature on treatment of these diseases is the occurrence of non-genetic disorders with very similar presentation (i.e. phenocopies). Particularly in the case of erythermalgia, there is an extensive literature on other causes of the condition, although in most cases a potential genetic etiology was probably not explored or even discussed. So far, genetic analyses of familial and sporadic cases have been mostly restricted to cases with known childhood onset, on the presumption that adult onset is more likely to be caused by other non-genetic factors. This remains an assumption however, and will require further molecular genetic study. There are clearly many additional questions to answer about the role of Nav1.7 in sporadic and provoked pain sensation.
Approval for this project was obtained from the research ethics board of the Queen Elizabeth II hospital at Dalhousie University. Written informed consent was obtained from the patients for the work and for this publication.
Thompson GH, Hahn G, Rang M: Erythromelalgia. Clin Orthop Relat Res 1979, 249–254.
Kirby RL: Erythromelalgia – not so benign. Arch Phys Med Rehabil 1987, 68: 389.
Drenth JP, Finley WH, Breedveld GJ, Testers L, Michiels JJ, Guillet G, Taieb A, Kirby RL, Heutink P: The primary erythermalgia-susceptibility gene is located on chromosome 2q31–32. Am J Hum Genet 2001, 68: 1277–1282. 10.1086/320107
Drenth JP, te Morsche RH, Guillet G, Taieb A, Kirby RL, Jansen JB: SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels. J Invest Dermatol 2005, 124: 1333–1338. 10.1111/j.0022-202X.2005.23737.x
Han C, Rush AM, Dib-Hajj SD, Li S, Xu Z, Wang Y, Tyrrell L, Wang X, Yang Y, Waxman SG: Sporadic onset of erythermalgia: a gain-of-function mutation in Nav1.7. Ann Neurol 2006, 59: 553–558. 10.1002/ana.20776
Yang Y, Wang Y, Li S, Xu Z, Li H, Ma L, Fan J, Bu D, Liu B, Fan Z, et al.: Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia. J Med Genet 2004, 41: 171–174. 10.1136/jmg.2003.012153
Han C, Lampert A, Rush AM, Dib-Hajj SD, Wang X, Yang Y, Waxman SG: Temperature dependence of erythromelalgia mutation L858F in sodium channel Nav1.7. Mol Pain 2007, 3: 3. 10.1186/1744-8069-3-3
Ahmad S, Dahllund L, Eriksson AB, Hellgren D, Karlsson U, Lund PE, Meijer IA, Meury L, Mills T, Moody A, et al.: A stop codon mutation in SCN9A causes lack of pain sensation. Hum Mol Genet 2007, 16: 2114–2121. 10.1093/hmg/ddm160
Cox JJ, Reimann F, Nicholas AK, Thornton G, Roberts E, Springell K, Karbani G, Jafri H, Mannan J, Raashid Y, et al.: An SCN9A channelopathy causes congenital inability to experience pain. Nature 2006, 444: 894–898. 10.1038/nature05413
Goldberg YP, MacFarlane J, MacDonald ML, Thompson J, Dube MP, Mattice M, Fraser R, Young C, Hossain S, Pape T, et al.: Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations. Clin Genet 2007, 71: 311–319. 10.1111/j.1399-0004.2007.00790.x
Waxman SG: Nav1.7, its mutations, and the syndromes that they cause. Neurology 2007, 69: 505–507. 10.1212/01.wnl.0000268068.02343.37
Drenth JP, Waxman SG: Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders. J Clin Invest 2007, 117: 3603–3609. 10.1172/JCI33297
Choi JS, Dib-Hajj SD, Waxman SG: Inherited erythermalgia: limb pain from an S4 charge-neutral Na channelopathy. Neurology 2006, 67: 1563–1567. 10.1212/01.wnl.0000231514.33603.1e
Cohen IJ, Samorodin CS: Familial erythromelalgia. Arch Dermatol 1982, 118: 953–954. 10.1001/archderm.118.11.953
Cummins TR, Dib-Hajj SD, Waxman SG: Electrophysiological properties of mutant Nav1.7 sodium channels in a painful inherited neuropathy. J Neurosci 2004, 24: 8232–8236. 10.1523/JNEUROSCI.2695-04.2004
Dib-Hajj SD, Rush AM, Cummins TR, Hisama FM, Novella S, Tyrrell L, Marshall L, Waxman SG: Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons. Brain 2005, 128: 1847–1854. 10.1093/brain/awh514
Drenth JP, te Morsche RH, Michiels JJ: [From gene to disease; primary erythermalgia – a neuropathic disease as a consequence of mutations in a sodium pump gene]. Ned Tijdschr Geneeskd 2006, 150: 194–196.
Harty TP, Dib-Hajj SD, Tyrrell L, Blackman R, Hisama FM, Rose JB, Waxman SG: Na(V)1.7 mutant A863P in erythromelalgia: effects of altered activation and steady-state inactivation on excitability of nociceptive dorsal root ganglion neurons. J Neurosci 2006, 26: 12566–12575. 10.1523/JNEUROSCI.3424-06.2006
Lampert A, Dib-Hajj SD, Tyrrell L, Waxman SG: Size matters: Erythromelalgia mutation S241T in Nav1.7 alters channel gating. J Biol Chem 2006, 281: 36029–36035. 10.1074/jbc.M607637200
Lee MJ, Yu HS, Hsieh ST, Stephenson DA, Lu CJ, Yang CC: Characterization of a familial case with primary erythromelalgia from Taiwan. J Neurol 2007, 254: 210–214. 10.1007/s00415-006-0328-3
Michiels JJ, te Morsche RH, Jansen JB, Drenth JP: Autosomal dominant erythermalgia associated with a novel mutation in the voltage-gated sodium channel alpha subunit Nav1.7. Arch Neurol 2005, 62: 1587–1590. 10.1001/archneur.62.10.1587
Novella SP, Hisama FM, Dib-Hajj SD, Waxman SG: A case of inherited erythromelalgia. Nat Clin Pract Neurol 2007, 3: 229–234. 10.1038/ncpneuro0425
Waxman SG, Dib-Hajj S: Erythermalgia: molecular basis for an inherited pain syndrome. Trends Mol Med 2005, 11: 555–562. 10.1016/j.molmed.2005.10.004
Zhang LL, Lin ZM, Ma ZH, Xu Z, Yang YL, Yang Y: Mutation hotspots of SCN9A in primary erythermalgia. Br J Dermatol 2007, 156: 767–769. 10.1111/j.1365-2133.2006.07727.x
Fertleman CR, Baker MD, Parker KA, Moffatt S, Elmslie FV, Abrahamsen B, Ostman J, Klugbauer N, Wood JN, Gardiner RM, Rees M: SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes. Neuron 2006, 52: 767–774. 10.1016/j.neuron.2006.10.006
Fertleman CR, Ferrie CD: What's in a name – familial rectal pain syndrome becomes paroxysmal extreme pain disorder. J Neurol Neurosurg Psychiatry 2006, 77: 1294–1295. 10.1136/jnnp.2006.089664
Fertleman CR, Ferrie CD, Aicardi J, Bednarek NA, Eeg-Olofsson O, Elmslie FV, Griesemer DA, Goutieres F, Kirkpatrick M, Malmros IN, et al.: Paroxysmal extreme pain disorder (previously familial rectal pain syndrome). Neurology 2007, 69: 586–595. 10.1212/01.wnl.0000268065.16865.5f
Buttaci CJ: Erythromelalgia: a case report and literature review. Pain Med 2006, 7: 534–538. 10.1111/j.1526-4637.2006.00240.x
We thank Hanka Venselaar, Centre for Molecular and Biomolecular Informatics, Nijmegen Centre for Molecular Life Sciences, Nijmegen, The Netherlands, for fruitful discussions. MES was supported by Dalhousie University, the University of Montreal, the Centre de Recherche du CHUM, Genome Atlantic, and Genome Canada. JPD is a recipient of a Netherlands Organization for health Research and development VIDI award research grant. ML is supported by the Department of Anesthesia of Dalhousie University.
We gratefully acknowledge the participation of the family.
The authors declare that they have no competing interests.
Dr. S coordinated the study and drafted the manuscript, Dr. D supervised molecular genetic experiments, RtM performed molecular genetic experiments, Dr. L performed clinical studies of the patients. All authors have read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.