T118M Variant of PMP22 Gene Presents with Painful Peripheral Neuropathy and Varying Charcot-Marie-Tooth Features: A Case Series and Review of the Literature

Ho, Kwo Wei David; Jerath, Nivedita U.

doi:https://doi.org/10.1155/2018/2618071

Case Reports in Genetics

On this page

Abstract Introduction Methods Literature Review Discussion Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Case Report | Open Access

Volume 2018 | Article ID 2618071 | https://doi.org/10.1155/2018/2618071

T118M Variant of PMP22 Gene Presents with Painful Peripheral Neuropathy and Varying Charcot-Marie-Tooth Features: A Case Series and Review of the Literature

Kwo Wei David Ho¹and Nivedita U. Jerath¹

Academic Editor: Balraj Mittal

Received29 Aug 2018

Revised07 Nov 2018

Accepted09 Dec 2018

Published25 Dec 2018

Abstract

The clinical effect of T118M variant of the PMP22 gene has been controversial. Several studies have suggested that it may be autosomal recessive, partial loss of function, or a benign variant. Here we report three cases in further support that the T118M variant of the PMP22 gene is a partial loss of function variant. These three unrelated cases were heterozygotes with the T118M variant of the PMP22 gene. All three cases presented with painful peripheral neuropathy and varying degrees of Charcot-Marie-Tooth exam features. Electrophysiological studies revealed polyneuropathy with axonal and demyelinating features in one case, but there were minimal electrophysiological changes in the other two cases. We propose that the T118M variant can cause painful peripheral neuropathy, which may be an underrecognized feature of this variant.

1. Introduction

PMP22 is a myelin membrane protein expressed in Schwann cells. Missense mutations in PMP22 cause a variety of neuropathies, including Charcot-Marie-Tooth disease (CMT)[1] and hereditary neuropathy with liability to pressure palsies (HNPP). The majority of these mutations act in autosomal dominant pattern [2–5], and a few mutations are autosomal recessive in nature [2, 6, 7]. A missense mutation at codon 118 (T118M) in PMP22 has been reported in several reports in the context of familial neuropathy. However, the clinical relevance of the T118M variant of the PMP22 gene has been controversial. Several studies have suggested that it may be autosomal recessive [2], partial loss of function [8–10], or a benign variant [11]. In this study, we report three cases in support that the T118M variant of the PMP22 gene is a partial loss of function mutation rather than a benign variant. We propose that the T118M variant can cause painful peripheral neuropathy and varying degrees of Charcot-Marie-Tooth features.

2. Methods

2.1. Genetic Testing

All subjects received care at the neurology clinic at the University of Florida. Genetic testing was performed by Invitae Co. (San Francisco, CA). Genomic DNA obtained from the submitted sample is enriched for targeted regions using a hybridization-based protocol and sequenced using Illumina technology. Unless otherwise indicated, all targeted regions are sequenced with ≥50x depth or are supplemented with additional analysis. Reads are aligned to a reference sequence (GRCh37), and sequence changes are identified and interpreted in the context of a single clinically relevant transcript, indicated below. Enrichment and analysis focus on the coding sequence of the indicated transcripts, 10bp of flanking intronic sequence (20bp for BRCA1/2), and other specific genomic regions demonstrated to be causative of disease at the time of assay design. Promoters, untranslated regions, and other noncoding regions are not otherwise interrogated. Exonic deletions and duplications are called using an in-house algorithm that determines copy number at each target by comparing the read depth for each target in the proband sequence with both mean read-depth and read-depth distribution, obtained from a set of clinical samples. All clinically significant observations are confirmed by orthogonal technologies, except individually validated variants and variants previously confirmed in a first-degree relative. Confirmation technologies include any of the following: Sanger sequencing, Pacific Biosciences SMRT sequencing, MLPA, MLPA-seq, or Array CGH.

The following transcripts were used in this analysis: AARS (NM_001605.2), AIFM1 (NM_004208.3), ATL1 (NM_015915.4), ATL3 (NM_015459.4), ATP7A (NM_000052.6), BICD2 (NM_001003800.1), BSCL2 (NM_032667.6), CHCHD10 (NM_213720.2), DCTN1 (NM_004082.4), DNAJB2 (NM_001039550.1), DNM2 (NM_001005360.2), DNMT1 (NM_001130823.1), DST (NM_001723.5), DYNC1H1 (NM_001376.4), EGR2 (NM_000399.3), FAM134B (NM_001034850.2), FBXO38 (NM_030793.4), FGD4 (NM_139241.3), FIG4 (NM_014845.5), GAN (NM_022041.3), GARS (NM_002047.2), GDAP1 (NM_018972.2), GJB1 (NM_000166.5), GNB4 (NM_021629.3), HARS (NM_002109.5), HINT1 (NM_005340.6), HSPB1 (NM_001540.3), HSPB8 (NM_014365.2), IGHMBP2 (NM_002180.2), IKBKAP (NM_003640.3), INF2 (NM_022489.3), KIF1A (NM_004321.6), LITAF (NM_004862.3), LMNA (NM_170707.3), LRSAM1 (NM_138361.5), MED25 (NM_030973.3), MFN2 (NM_014874.3), MORC2 (NM_014941.2), MPZ (NM_000530.6), MTMR2 (NM_016156.5), NDRG1 (NM_006096.3), NEFL (NM_006158.4), NGF (NM_002506.2), NTRK1 (NM_001012331.1), PDK3 (NM_001142386.2), PLEKHG5 (NM_020631.4), PMP22 (NM_000304.3), PRPS1 (NM_002764.3), PRX (NM_181882.2), RAB7A (NM_004637.5), REEP1 (NM_022912.2), SBF2 (NM_030962.3), SCN11A (NM_014139.2), SCN9A (NM_002977.3), SH3TC2 (NM_024577.3), SIGMAR1 (NM_005866.3), SLC25A46 (NM_138773.2), SLC52A2 (NM_024531.4), SLC52A3 (NM_033409.3), SLC5A7 (NM_021815.2), SPG11 (NM_025137.3), SPTLC1 (NM_006415.3), SPTLC2 (NM_004863.3), TFG (NM_006070.5), TRIM2 (NM_001130067.1), TRPV4 (NM_021625.4), TTR (NM_000371.3), UBA1 (NM_003334.3), VAPB (NM_004738.4), VRK1 (NM_003384.2), WNK1 (NM_018979.3), YARS (NM_003680.3).

2.2. Literature Review

We performed a literature review on the published clinical studies on T118M variant in the PMP22 gene. The following terms were used to search in Pubmed and Google Scholar: “T118M” and “PMP22”. We restricted our review to published full articles since 1950 in the English language. We excluded basic science research articles that did not present new patients with the variant.

3. Clinical Report

3.1. Case 1

The first patient was a 64-year-old male presenting with painful burning pain at the bottom of his feet for six months. The pain extended from his feet up to his legs, hips, and back in a sharp shooting manner. It was constant and it was so severe that it limited his activities. As a child, he started walking later than his peers and he was always the slowest runner. He used leg braces because his knees were “together” and he had a surgery for it at age 15. He had occasional muscle cramps and fasciculations as a child. His mother was always clumsy in her feet as well. He had no siblings or children. He had a CMT examination score of 8 out of 28. On exam, there was pes cavus bilaterally and tight Achilles tendons. His feet could not be easily brought into a neutral position. There was atrophy of the hands and feet, length-dependent pinprick and vibratory sense loss, and absent reflexes. MRI of the lumbar spine was unremarkable. Electrophysiological studies revealed moderate chronic sensorimotor, axonal polyneuropathy (Table 1). There were absent sensory responses in the bilateral sural and superficial peroneal nerves. Motor studies showed reduced amplitude in the left tibial nerve and reduced conduction velocities ranging from 32-36 m/s in the bilateral peroneal nerves and left tibial nerve. F wave in the bilateral peroneal nerve showed prolonged latency. F wave in the bilateral tibial nerve was absent. Sequencing of 72 neuropathy genes [15] showed one copy of a pathogenic variant, T118M in the PMP22 gene.

3.2. Case 2

The second patient was a 73-year-old man from Cuba presenting with leg pain which he described as a constant burning pain in his feet and aching pain in his legs. He was never a fast runner as a child and he was not athletic. His sister had similar symptoms of flat and painful feet. Exam revealed flat feet (Figure 1(a)), absent reflexes, and absent vibratory sense at the toes and reduced at the ankles. Electrophysiological study was unremarkable except for a mildly reduced peroneal nerve conduction velocity at the fibular head (Table 1). CMT examination score was 6 out of 28. Genetic testing revealed heterozygous T118M variant of the PMP22 gene and heterozygous R275L variant of the SLC52A2 gene. The sister was unable to undergo genetic testing.

(a)

(b)

3.3. Case 3

The third patient was a 56-year-old male with past medical history of Sjögren’s syndrome and rheumatoid arthritis who presented with chronic severe burning pain in the hands and feet necessitating the chronic use of narcotics to allow him to continue his profession. As a child he did have some difficulties with coordination and playing basketball. He had a daughter who also had flat feet and not athletic. He did not have other siblings. Exam showed decreased vibratory sense in the toes and flat feet with low arches (Figure 1(b)). Reflexes were present. CMT examination score was 2 out of 28. Electrophysiological study was unremarkable except for a mildly reduced tibial motor conduction velocity at the popliteal fossa (Table 1). Skin biopsy of the right distal leg and proximal thigh revealed normal epidermal small fiber densities. Sjögren’s syndrome profile showed positive salivary protein IgA antibodies, parotid specific protein IgG, IgA, IgM antibodies, positive rheumatoid factor, and anticyclic citrullinated peptide antibody. ANA, double stranded DNA antibody, TSH, and free T4 were negative. Genetic testing showed heterozygous T118M variant of the PMP22 gene and heterozygous Y22C variant of the TFG gene (c.98 A> G). The daughter declined genetic testing.

4. Literature Review

The result of the literature review is presented in Table 2. Eight studies have been published on the clinical impact of T118M variant in the PMP22 gene. There was one retrospective case-control study, six family case series, and one case report. Three small family case series introduced the notion that the T118M variant is either a benign polymorphism or an autosomal recessive mutation [2, 10, 12]. However, other studies presented data in support of it being a deleterious variant. The largest study is a case-control study with 1018 healthy subjects, 104 unrelated patients with hereditary neuropathy with liability to pressure palsies (HNPP), and 187 patients with Charcot-Marie-Tooth disease type 1 (CMT1) [11]. It found T118M to be associated with CMT1A without the 1.5-Mb duplication (P=0.0429), but not associated with HNPP or CMT1 with the 1.5Mb duplication. The allele frequency of T118M was much higher in CMT1 without duplication (AF=0.05) compared to the general population (AF=0.007). One case series [8] and one case report [14] gave further support to the notion that the T118M is rather a loss of function variant to cause varying degrees of neuropathies. Shy et al. [8] reported the first homozygous case presenting with severe axonal neuropathy, while the heterozygotes in the same study presented with milder form of neuropathy similar to HNPP.

5. Discussion

In this case series, we demonstrated that patients with the T118M variant of the PMP22 gene can present with peripheral neuropathic pain and varying features of CMT. None of the cases presented here harbor the typical 1.5-Mb deletion in 17p11.2 seen in HNPP, or the typical duplication of the same locus in CMT1. This study supports the notion that the T118M variant of the PMP22 gene can be a partial loss of function variant to possibly lead to a disease state marked by painful peripheral neuropathy and certain CMT features.

The T118M variant, or rs104894619, is a rare variant having a minor allele frequency of 0.0008 in the 1000 genome project [16]. Several previous studies have suggested that the T118M variant can be a benign polymorphism (Table 1). However, Shy et al. refuted such a notion with a patient homozygous for this variant, and this patient presented with severe axonal neuropathy [8]. This study also found varying degrees of clinical and electrophysiological features of a neuropathy similar to HNPP in heterozygous patients and they concluded that the T118M variant is a loss of function mutation. The largest case control study [11] also suggests that this variant is associated with CMT1 in the absence of the typical PMP22 duplication. Our report adds to the literature by proposing that painful peripheral neuropathy can be a feature of this variant as well.

The T118M variant has been shown to cause cellular disruptions in several in vitro studies. When PMP22 with the T118M allele was expressed in the absence of wild-type PMP22, the apoptotic-like phenotype of the NIH-3T3 cells was reduced. Coexpression of the T118M-PMP22 with the wild-type PMP22 restored the apoptotic phenotype [17]. In another study, the T118M allele has altered intracellular trafficking compared to the wild type [18]. It is therefore not surprising that the T118M variant can produce an abnormal phenotype.

Despite the common T118M variant among the three cases, electrophysiological findings were quite varied. Case 1 presented with severe sensorimotor polyneuropathy with both axonal and demyelinating features, while cases 2 and 3 presented with mild reduction in conduction velocities. It is unclear why case 2 had decreased vibratory sense loss, absent reflexes but only mildly abnormal electrophysiological study. It has been reported that electrographically recorded deep tendon reflex can be present even in the absence of clinical deep tendon reflex [19]. The varied EMG findings are consistent with previous findings that patients carrying this variant can have electrophysiological findings ranging from mildly prolonged latency to severe axonal neuropathy [8]. This study is in further support of such varied presentation.

Genetic factors are known to impact pain perception and formation. Common genetic polymorphisms have been shown to affect the development and perception of pain [20, 21]. Rare, single-gene variants causing painful phenotype are less common [22–24]. Painful peripheral neuropathy is a common feature in both CMT [1] and HNPP [25]. However, peripheral neuropathic pain is often overlooked due to other predominant features in CMT and HNPP. In patients presenting with an isolated painful neuropathy without many CMT or HNPP features, genetic testing is rarely performed. Given the findings in this case series, the T118M variant of the PMP22 gene can be a possible cause of painful neuropathy even without significant nerve conduction abnormalities. With genetic testing becoming more readily available, genetic variants such as T118M in PMP22 should be considered in patients presenting with idiopathic painful peripheral neuropathy.

The skin biopsy of case 3 showed normal epidermal small fiber densities. The significance of this finding is unclear. The most likely explanation is that the biopsied sites (leg and thigh) were unaffected by the disease process, given that the symptomatic sites were hands and feet. An alternative explanation may be that the variant does not affect epidermal nerve fiber density in mild cases. In addition to the normal skin biopsy, case 3 also had Sjögren’s syndrome and rheumatoid arthritis. Both Sjögren’s syndrome and rheumatoid arthritis are known to cause peripheral neuropathy [26, 27]. It is unclear if these rheumatological factors contributed to this patient’s painful polyneuropathy.

Two of the three cases presented here were tested positive for genetic variants other than T118M in PMP22. One of them was heterozygous for R275L variant of the SLC52A2 gene and one of them was heterozygous for Y22C variant of the TFG gene. Both individuals had minimal electrophysiological changes. Variants in SLC52A2 gene have been found to be associated with autosomal recessive Brown-Vialetto-Van Laere syndrome, which is characterized by infancy onset sensorineural deafness and pontobulbar palsy. The R275L variant has not been reported to be associated with this particular disease and the patient presented here did not exhibit any symptoms characteristic of Brown-Vialetto-Van Laere syndrome. A variant in TFG (p.Gly269Val) has been associated with CMT2 phenotype. However, Y22C has not been reported to cause any CMT2 phenotype and its significance is currently unknown.

In summary, we demonstrated that the T118M variant of the PMP22 gene can present with peripheral neuropathic pain and features of CMT. This case series supports the argument that the T118M variant of the PMP22 gene can be a partial loss of function mutation to possibly lead to a disease state marked by painful peripheral neuropathy.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

Dr. Ho conceptualized and drafted the manuscript. Dr. Jerath conceptualized and critically reviewed the article and provided revisions for intellectual content.

Acknowledgments

The authors would like to acknowledge Invitae Genetics and Alnylam in providing the ability to genetically test these subjects.

References

N. Y. Jeong, Y. H. Shin, and J. Jung, “Neuropathic pain in hereditary peripheral neuropathy,” Journal of Exercise Rehabilitation, vol. 9, no. 4, pp. 397–399, 2013.
View at: Publisher Site | Google Scholar
B. B. Roa, C. A. Garcia, L. Pentao et al., “Evidence for a recessive PMP22 point mutation in Charcot Marie Tooth disease type 1A,” Nature Genetics, vol. 5, no. 2, pp. 189–194, 1993.
View at: Publisher Site | Google Scholar
W. Marques Jr., P. K. Thomas, M. G. Sweeney, L. Carr, and N. W. Wood, “Dejerine-Sottas neuropathy and PMP22 point mutations: A new base pair substitution and a possible 'hot spot' on Ser72,” Annals of Neurology, vol. 43, no. 5, pp. 680–683, 1998.
View at: Publisher Site | Google Scholar
V. V. Ionasescu, R. Ionasescu, C. Searby, and R. Neahring, “Dejerine-sottas disease with de novo dominant point mutation of the pmp22 gene,” Neurology, vol. 45, no. 9, pp. 1766-1767, 1995.
View at: Publisher Site | Google Scholar
B. B. Roa, C. A. Garcia, U. Suter et al., “Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene,” The New England Journal of Medicine, vol. 329, no. 2, pp. 96–101, 1993.
View at: Publisher Site | Google Scholar
Y. Parman, V. Planté-Bordeneuve, A. Guiochon-Mantel, M. Eraksoy, and G. Said, “Recessive inheritance of a new point mutation of the PMP22 gene in Dejerine-Sottas disease,” Annals of Neurology, vol. 45, no. 4, pp. 518–522, 1999.
View at: Publisher Site | Google Scholar
C. Numakura, C. Lin, N. Oka, I. Akiguchi, and K. Hayasaka, “Hemizygous mutation of the peripheral myelin protein 22 gene associated with Charcot-Marie-Tooth disease type 1,” Annals of Neurology, vol. 47, no. 1, pp. 101–103, 2000.
View at: Publisher Site | Google Scholar
M. E. Shy, M. T. Scavina, and A. Clark, “T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy,” Annals of Neurology, vol. 59, no. 2, pp. 358–364, 2006.
View at: Publisher Site | Google Scholar
W. Marques Jr., M. G. Sweeney, and N. W. Wood, “Thr(118)Met amino acid substitution in the peripheral myelin protein 22 does not influence the clinical phenotype of Charcot-Marie-Tooth disease type 1A due to the 17p11.2-p12 duplication,” Brazilian Journal of Medical and Biological Research, vol. 36, no. 10, pp. 1403–1407, 2003.
View at: Publisher Site | Google Scholar
P. Seeman, R. Mazanec, T. Marikova, and B. Rautenstrauss, “Charcot-Marie-Tooth 1A: Heterozygous T118M mutation over a CMT1A duplication has no influence on the phenotype,” Annals of the New York Academy of Sciences, vol. 883, pp. 485–489, 1999.
View at: Publisher Site | Google Scholar
P. Young, F. Stögbauer, B. Eller et al., “PMP22 Thr118Met is not a clinically relevant CMT1 marker,” Journal of Neurology, vol. 247, no. 9, pp. 696–700, 2000.
View at: Publisher Site | Google Scholar
E. Nelis, B. Holmberg, R. Adolfsson, G. Holmgren, and C. van Broeckhoven, “PMP22 Thr(118)Met: recessive CMT1 mutation or polymorphism?” Nature Genetics, vol. 15, no. 1, pp. 13-14, 1997.
View at: Publisher Site | Google Scholar
I. V. Mersiyanova, S. M. Ismailov, A. V. Polyakov et al., “Screening for mutations the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients,” Human Mutation, vol. 15, no. 4, pp. 340–347, 2000.
View at: Publisher Site | Google Scholar
N. U. Jerath, J. Kamholz, T. Grider, A. Harper, A. Swenson, and M. E. Shy, “Coexistence of a T118M PMP22 missense mutation and chromosome 17 (17p11.2-p12) deletion,” Muscle & Nerve, vol. 52, no. 5, pp. 905–908, 2015.
View at: Publisher Site | Google Scholar
Invitae Comprehensive Neuropathies Panel, test code 03200.
“Database of Single Nucleotide Polymorphisms (dbSNP). Bethesda (MD): National Center for Biotechnology Information, National Library of Medicine. dbSNP accession: rs104894619 , (dbSNP Build ID: 151),” http://www.ncbi.nlm.nih.gov/SNP/.
View at: Google Scholar
E. Fabbretti, P. Edomi, C. Brancolini, and C. Schneider, “Apoptotic phenotype induced by overexpression of wild-type gas3/PMP22: Its relation to the demyelinating peripheral neuropathy CMT1A,” Genes & Development, vol. 9, no. 15, pp. 1846–1856, 1995.
View at: Publisher Site | Google Scholar
R. Naef and U. Suter, “Impaired intracellular trafficking is a common disease mechanism of PMP22 point mutations in peripheral neuropathies,” Neurobiology of Disease, vol. 6, no. 1, pp. 1–14, 1999.
View at: Publisher Site | Google Scholar
K. R. Sharma, D. Saadia, A. G. Facca, S. Resnick, and D. R. Ayyar, “Clinical and electromyographic deep tendon reflexes in polyneuropathy: Diagnostic value and prevalence,” Acta Neurologica Scandinavica, vol. 119, no. 4, pp. 224–232, 2009.
View at: Publisher Site | Google Scholar
K. W. David Ho, M. R. Wallace, K. T. Sibille et al., “Single nucleotide polymorphism in the COL11A2 gene associated with lowered heat pain sensitivity in knee osteoarthritis,” Molecular Pain, vol. 13, 2017.
View at: Google Scholar
R. B. Fillingim, M. R. Wallace, D. M. Herbstman, M. Ribeiro-Dasilva, and R. Staud, “Genetic contributions to pain: a review of findings in humans,” Oral Diseases, vol. 14, no. 8, pp. 673–682, 2008.
View at: Publisher Site | Google Scholar
D. M. Kullmann and S. G. Waxman, “Neurological channelopathies: new insights into disease mechanisms and ion channel function,” The Journal of Physiology, vol. 588, no. 11, pp. 1823–1827, 2010.
View at: Publisher Site | Google Scholar
C. F. Barrett, A. M. J. M. van den Maagdenberg, R. R. Frants, and M. D. Ferrari, “Familial Hemiplegic Migraine,” Advances in Genetics, vol. 63, pp. 57–83, 2008.
View at: Publisher Site | Google Scholar
K. W. Ho and N. U. Jerath, “V144D Mutation of SPTLC1 Can Present with Both Painful and Painless Phenotypes in Hereditary Sensory and Autonomic Neuropathies Type I,” Case Reports in Genetics, vol. 2018, Article ID 1898151, 3 pages, 2018.
View at: Publisher Site | Google Scholar
U. Yilmaz, T. T. Bird, G. T. Carter, L. H. Wang, and M. D. Weiss, “Pain in hereditary neuropathy with liability to pressure palsy: An association with fibromyalgia syndrome?” Muscle & Nerve, vol. 51, no. 3, pp. 385–390, 2015.
View at: Publisher Site | Google Scholar
F. Gemignani, A. Marbini, G. Pavesi et al., “Peripheral neuropathy associated with primary Sjögren's syndrome,” Journal of Neurology, Neurosurgery & Psychiatry, vol. 57, no. 8, pp. 983–986, 1994.
View at: Publisher Site | Google Scholar
V. Agarwal, R. Singh, Wiclaf et al., “A clinical, electrophysiological, and pathological study of neuropathy in rheumatoid arthritis,” Clinical Rheumatology, vol. 27, no. 7, pp. 841–844, 2008.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2018 Kwo Wei David Ho and Nivedita U. Jerath. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

2222

Downloads

1383

Citations