Abstract
Background
Posterior femoral cutaneous nerve (posterior cutaneous nerve of the thigh) is a sensory nerve arises from the sacral plexus. Its terminal part supplies the skin of the posterior surface of the thigh and popliteal fossa, and it extends for a variable length below the popliteal fossa till the mid-calf region. The aim was to assess the posterior femoral cutaneous nerve antidromic sensory conduction technique and estimate its different sensory nerve action potential parameters’ reference values in a sample of apparently healthy Egyptian participants. One hundred and twenty lower limbs of 60 apparently healthy Egyptian volunteers were included. Clinical evaluation and sensory conduction study for the posterior femoral cutaneous nerve were done.
Results
Posterior femoral cutaneous nerve sensory nerve action potential was elicited in 98 lower limbs (81.6%) of 52 individuals (86.7%). The obtained results of different parameters of posterior femoral cutaneous nerve sensory nerve action potential were as the following: onset latency (2.04 ± 0.21 ms), peak latency (2.86 ± 0.25 ms), conduction velocity (59.45 ± 6.36 m/s) and amplitude (6.16 ± 2.29 μV). No significant differences between the two genders were found regarding different parameters of posterior femoral cutaneous nerve sensory nerve action potential except for amplitude which was significantly larger among male participants (P = 0.030). No significant differences between the right and left lower limbs were found regarding different parameters of sensory nerve action potential. There was a statistical significant negative correlation between age and posterior femoral cutaneous nerve conduction velocity (P = 0.008). There was a statistical significant positive correlation between height and peak latency (P ≤ 0.0001), as well as, a statistical significant negative correlation between height and conduction velocity (P ≤ 0.0001). There was a statistical significant negative correlation between body mass index and posterior femoral cutaneous nerve peak latency (P = 0.008).
Conclusions
The research provides a reliable electrophysiological antidromic sensory conduction study for the posterior femoral cutaneous nerve and normal cut-off reference values for posterior femoral cutaneous nerve sensory nerve action potential parameters. This is essential for the evaluation of suspected posterior femoral cutaneous nerve lesions.
Similar content being viewed by others
Background
Posterior femoral cutaneous nerve (PFCN) is a sensory nerve arises from the sacral plexus. It is known as posterior cutaneous nerve of the thigh as well as lesser sciatic nerve [1,2,3]. Its nerve roots are the first, second and third sacral (S) nerve roots and the S2 nerve root is the main one [4,5,6]. To enter the gluteal region, it travels through the greater sciatic foramen. Within the foramen, PFCN is inferior to the piriformis muscle and immediately posteromedial to the sciatic nerve. In the gluteal region, it descends downward deep to the gluteus maximus muscle [2]. It lies superficial to the hamstring muscles within the muscular groove present between the medial and lateral hamstring muscles. The hamstring muscles separate it from the sciatic nerve [4,5,6]. In the subgluteal region, it gives two cutaneous branches; the gluteal branch and the perineal branch. The gluteal branch (known as inferior cluneal nerve) (S1 and S2 nerve roots) innervates the skin over the gluteal fold of the buttock region [7]. The perineal branch (known as long pudendal nerve or inferior pudendal nerve) (S2 and S3 nerve roots) passes medially to innervate the skin of the lateral aspect of the perineum and proximal aspect of the medial surface of the thigh [2, 3, 8]. The terminal part of the PFCN supplies the skin of the posterior surface of the thigh and popliteal fossa, and it extends for a variable length below the popliteal fossa till the mid-calf region (Figs. 1 and 2) [4,5,6, 8].
The electrophysiological study of the PFCN is clinically essential. It improves the physicians’ awareness regarding PFCN lesions and its role in the evaluation of patients with many neurological problems in the lower limbs. It assesses the functional integrity of the PFCN in a variety of clinical conditions [1, 9,10,11,12,13,14,15]. These include clinical situations associated with PFCN neuropathy, as well as, the localization and determination of the extent of neurological lesions [1, 8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28]. It helps in the differentiation between sacral radiculopathy (preganglionic lesion) and sacral plexopathy (post-ganglionic lesion) [16]. Isolated PFCN neuropathy could be due to many etiologies [1, 8, 9, 11, 17,18,19,20,21,22,23,24,25,26,27]. Lesions affecting the PFCN could involve the sciatic nerve due to the close anatomical relationship between PFCN and sciatic nerve in the gluteal and back of the thigh regions [13]. In addition, the electrophysiological study of the PFCN is important in the assessment of the peripheral nervous system of the lower limbs in case of difficulty in assessing the distal routinely assessed nerves [1, 8, 16, 17].
There were few previous studies in the literature that assessed the antidromic sensory nerve conduction of PFCN [1, 29, 30]. The aim was to assess the PFCN antidromic sensory conduction technique and estimate its different sensory nerve action potential (SNAP) parameters’ reference values in a sample of apparently healthy Egyptian participants.
Methods
One hundred and twenty lower limbs of 60 apparently healthy Egyptian volunteers were included. The volunteers did not have risk factors for neuropathy as diabetes mellitus, rheumatologic disorders and metabolic disorders. They did not have neurological symptoms. They had normal clinical neurological examination of both lower limbs. The examiner explained the purpose to the participants. An informed consent was obtained from each volunteer. Research Ethics Committee warranted the proposal.
Demographic data in the form of age and gender were collected. Body mass index (BMI) was calculated [31]. Complete clinical examination for the lower limbs was done.
The PFCN antidromic sensory conduction study was performed as the following technique. The active recording surface electrode was placed in the midline of the posterior surface of the thigh at 6 cm proximal to the mid-popliteal region [1, 32]. The reference surface electrode was placed 3 cm distal to the active recording surface electrode in the midline of the posterior surface of the thigh. The electrical stimulation was done by placing the bipolar stimulator 12 cm proximal to the active recording surface electrode on an imaginary line connecting the active recording surface electrode with the ischial tuberosity. The stimulator was placed in the intermuscular groove between the medial and lateral hamstring muscles. This groove was detected manually by palpating the posterior aspect of the thigh, while the volunteer flexed the knee slightly while lying in a prone position [1, 32]. The ground electrode was placed between the active recording surface electrode distally and the stimulation site proximally. During stimulation of the PFCN, the patient should be completely relaxed [1]. Details and illustration of the performed PFCN antidromic sensory conduction study are demonstrated in Fig. 3 [1, 32,33,34,35,36].
Statistical package for the social sciences (version 17) software was used for analyzing data. Analytic tests included Student’s t-test, paired t-test, Chi-square test and Pearson correlation test. Significance was assigned for any P value less than 0.05. Cutoff values were estimated by rounding the mean ± two standard deviations (SD).
Results
One hundred and twenty lower limbs of 60 apparently healthy Egyptian volunteers [31 men (51.7%) and 29 women (48.3%)] were engaged in the research. Their age was 37.86 ± 13.42 years (ranged from 18 to 75 years). Their characteristics are illustrated in Table 1. No statistical significant differences were shown between men and women regarding different assessed characteristics (Table 1).
Bilateral study of the PFCN was performed to all participants. The PFCN SNAP was easily elicited bilaterally in the majority of the participated volunteers (Table 2). It was elicited in 98 lower limbs (81.6%) of 52 individuals (86.7%) (Table 2). All of them tolerated the PFCN conduction study. Table 3 demonstrates the cutoff values for different PFCN SNAP parameters. PFCN SNAPs are illustrated in Figs. 4 and 5.
No significant differences between the two genders were appeared regarding different parameters of PFCN SNAP except for SNAP amplitude which was significantly larger among male participants (Table 4).
No significant differences between the right and left lower limbs were found regarding different parameters of PFCN SNAP (Table 5). The intra-subject side-to-side differences of different parameters of PFCN SNAP are tabulated in Table 6.
Correlations between volunteers’ age and different anthropometric measures with different parameters of PFCN SNAP are tabulated in Table 7. Significant negative correlation was found between volunteers’ age and PFCN conduction velocity (CV); between height and PFCN CV; and between BMI and PFCN peak latency (PL). A significant positive correlation was found between height and PFCN PL (Table 7).
Discussion
In spite of that there are many available neurophysiological techniques for evaluating different sensory and motor nerves of the lower limbs, there is not any well-assessed and standardized neurophysiological study for the evaluation of PFCN [1, 16, 37, 38]. The study aimed to assess the PFCN antidromic sensory conduction technique and to estimate its different SNAP parameters’ reference values in a sample of apparently healthy Egyptian participants.
The PFCN SNAP was elicited in only 86.7% of the participants. It was recorded unilaterally in 10% of the participants. This was not similar to previous studies.They recorded the PFCN SNAP in all their participants [1, 29, 30]. The difference between this research and these studies could be explained by the following: (A) the difference in the gender distribution of the participants between different studies. (B) The difference in the race of the included volunteers in different studies [39]. (C) The presence of a volume-conducted motor potential from the hamstring muscles which could be large enough to interfere with the recording of the PFCN SNAP and obscuring it [33, 34]. (D) The presence of anomalous innervation in which there could be agenesis and absence of the PFCN and its replacement by cutaneous branches that could arise from the sciatic nerve in the back of the thigh or any other nearby adjacent cutaneous nerve that innervate part or all of the sensory territory of the PFCN similar to other anomalous innervation that could take place in the peripheral nervous system [40,41,42]. Meng et al. reported the absence of the PFCN (i.e. PFCN agenesis) in one lower limb (3.8%) of their assessed lower limbs obtained from cadavers [40]. It was reported that the origin of the PFCN is variable and that its perineal branch was absent in 15% of the assessed lower limbs [43, 44].
Sensory nerve conduction study of the PFCN should be done with caution. A volume-conducted motor potential usually appeared following the PFCN SNAP. It could be large enough to mask the PFCN SNAP wave. This was due to the coincidental co-stimulation of the motor fibers within the sciatic nerve in the thigh with orthodromic spread of excitation impulses, consequently depolarization of the hamstring muscles took place. This appeared with the use of an excessively high electrical stimulus intensity, in spite of that PFCN is separated from the sciatic nerve by the bulk of the medial and lateral hamstring muscles [1]. Rarely, there could be an anomalous innervation in the form of a muscular branch arising from the PFCN and suppling the hamstring muscles. This could contribute to the occurrence of the volume-conducted motor potential from the hamstring muscles [3]. In this circumstances, to minimize the appearance of this volume-conducted motor potential, the operator should increase the stimulus intensity slowly, so that supramaximal stimulation of the PFCN could take place with an electrical stimulus insufficient to stimulate the sciatic nerve motor fibers. Subsequently, this could avoid the appearance of the volume-conducted motor potential [1, 16, 33, 34]. The PFCN sensory conduction study is a meticulous study. The relaxation of the thigh muscles during the performance of the technique was essential to easily obtain the PFCN potential. Therefore, proper instruction to the individual to completely relax the thigh was critical for obtaining the PFCN SANP [1]. Sometimes, a local stimulus-induced hamstring muscle contraction could take place in association with higher stimulus intensity [1]. However, Dumitru et al. mentioned that the antidromic sensory conduction technique for PFCN was not associated with volume-conducted motor potential, because the sciatic nerve is deep enough in the thigh [1]. The difference between the present study and Dumitru et al.’s study could be due to differences in the anthropometric characteristics of the studied population and differences in the maneuvering used to obtain the SNAP [1].
No significant differences were obtained between both genders regarding different parameters of the PFCN SNAP except for the SNAP amplitude. It was significantly larger among male volunteers. This was coincided with earlier studies in which gender had no effect on SNAP PL and CV [1, 29, 30, 33, 34, 45,46,47]. However, it was not coincided with other studies in the literature regarding the effect of gender on the SANP amplitude [1, 33, 34, 47]. This could be due to differences in the age, anthropometric characteristics and racial factors of the included volunteers in the current study in comparison to previous studies [1, 33, 34, 39, 47]. In spite of the effect of gender on nerve conduction study, it was unnecessary to apply individual corrections in the assessed SNAP parameters regarding gender [48].
The study was in line with earlier researches regarding the lack of differences of PFCN SNAP parameters between the right and left sides [1, 33, 34, 46, 49].
There was a significant negative correlation between age and CV. This was in harmony with literature [1, 16, 50,51,52]. This could be secondary to the normal process of sensory neuron loss that could take place with aging. It could be more apparent among geriatric individuals (i.e., individuals aged 65 years or more) [16].
The height had a significant positive correlation with PL and a significant negative correlation with CV. This was like literature [16, 39, 48, 49, 52,53,54,55,56]. This could be due to the following. With increasing individual height, more tapering of the sensory nerve trunk takes place distally with more thinning of the nerve, as well as, lower limbs are cooler distally. It is known that cool temperature slows the nerve CV [16]. These two issues subsequently prolong SNAP PL and slow SNAP CV with increased height [16].
There was a significant negative correlation between BMI and PL. This coincided with literature [52, 57]. This could be due to the inclusion of height in the equation of BMI calculation, in which the height had a significant positive correlation with PL [31].
The intra-subject side-to-side differences was not mentioned previously regarding the PFCN SNAP. Regarding the inter-side amplitude ratio, its reference lower limit was 0.4. Subsequently, PFCN involvement should be suspected when the SNAP amplitude decreased to be less than 40% of the contralateral limb. This result was of the same opinion as literature [16, 33, 34].
The results of the study were in line with the results obtained from previous work assessed the PFCN neurophysiological technique (Table 8) [1, 29, 30].
Study boundary was the inclusion of Egyptians from Alexandria governorate and the nearby governorates only. Multi-center study is recommended with the inclusion of volunteers from different Egyptian governorates aiming to represent all Egyptians in the study.
The PFCN is similar to other not routinely assessed nerves as the ulnar palmar cutaneous nerve, dorsal ulnar cutaneous nerve, superficial radial nerve, posterior antebrachial cutaneous nerve and medial calcaneal nerve in which their lesions and their electrophysiological assessment techniques are ignored and not mentioned in many textbooks of clinical neurophysiology [16, 33, 34, 37, 58,59,60]. This makes the physicians and clinical neurophysiologists unaware of the lesions of the PFCN. Subsequently, PFCN lesions remain undiagnosed. PFCN was only mentioned in the literature as case reports and research articles [11,12,13, 15, 24]. As a fact, it was reported that PFCN neuropathy is uncommon and rare [9,10,11,12,13,14,15, 19, 24]. However, there were many cases supposed to be missed in the clinical practice due to physicians’ lack of knowledge and awareness regarding the presence and existence of PFCN focal neuropathy.
The presence of a valid and well-studied electrophysiological technique for the assessment of the integrity of the PFCN makes the physicians able to detect and diagnose suspicion cases of PFCN lesions [1]. This will help in proper diagnosis and subsequently, proper management of these cases [13]. This assessed and validated technique could increase the clinical awareness of the clinical neurophysiologists for PFCN lesions and make the detection of PFCN mononeuropathy to be reachable.
Conclusions
The research provides a reliable electrophysiological PFCN antidromic sensory conduction study and normal cut-off reference values for PFCN SNAP parameters. This is essential for the evaluation of suspected PFCN lesions.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Abbreviations
- BMI:
-
Body mass index
- CV:
-
Conduction velocity
- PFCN:
-
Posterior femoral cutaneous nerve
- PL:
-
Peak latency
- S:
-
Sacral
- SD:
-
Standard deviations
- SNAP:
-
Sensory nerve action potential
References
Dumitru D, Nelson MR. Posterior femoral cutaneous nerve conduction. Arch Phys Med Rehabil. 1990;71:979–82.
Tunali S, Cankara N, Albay S. A rare case of communicating branch between the posterior femoral cutaneous and the sciatic nerve. Rom J Morphol Embryol. 2011;52(1):203–5.
Garg S, Srivastava SK, Singla V, Singla A. Muscular branches of the posterior femoral cutaneous nerve. J Community Health Manag. 2016;3(2):64–6.
Sinnatamby CS. Last’s anatomy. 12th ed. Philadelphia: Churchill Livingstone (Elsevier); 2011.
Drake RL, Vogl AW, Mitchell AWM. Gray’s basic anatomy. International. Philadelphia: Churchill Livingstone (Elsevier); 2012.
Agur AMR, Dalley AF. Grant’s atlas of anatomy. 14th ed. Philadelphia: Wolters Kluwer; 2017.
Prunskis TD. Inferior cluneal nerve entrapment: low back. In: Trescot AM, editor. Peripheral nerve entrapments: clinical diagnosis and management. Cham: Springer; 2016. p. 565–70.
Murinova N, Krashin D, Trescot AM. Posterior femoral cutaneous nerve entrapment: low back. In: Trescot AM, editor. Peripheral nerve entrapments: clinical diagnosis and management. Cham: Springer; 2016. p. 605–13.
Arnoldussen W, Korten J. Pressure neuropathy of the posterior femoral cutaneous nerve. Clin Neurol Neurosurg. 1980;82(1):57–60.
Obach J, Aragones JM, Ruano D. The infrapiriformis foramen syndrome resulting from intragluteal injection. J Neurol Sci. 1983;58(1):135–42.
Chutkow JG. Posterior femoral cutaneous neuralgia. Muscle Nerve. 1988;11:1146–8.
Iyer VG, Shields CB. Isolated injection injury to the posterior femoral cutaneous nerve. Neurosurg. 1989;25(5):835–8.
Kim JE, Kang JH, Choi JC, Lee JS, Kang SY. Isolated posterior femoral cutaneous neuropathy following intragluteal injection. Muscle Nerve. 2009;40(5):864–6.
Tong HC, Haig A. Posterior femoral cutaneous nerve mononeuropathy: a case report. Arch Phys Med Rehabil. 2000;81(8):1117–8.
Mobbs R, Szkandera B, Blum P. Posterior femoral cutaneous nerve entrapment neuropathy: operative exposure and technique. Br J Neurosurg. 2002;16(3):309–11.
Preston D, Shapiro B. Electromyography and neuromuscular disorders: clinical-electrophysiologic correlations. 3rd ed. Pennsylvania: Elsevier Saunders; 2013.
Murinova N, Krashin D, Trescot AM. Posterior femoral cutaneous nerve entrapment: pelvic. In: Trescot AM, editor. Peripheral nerve entrapments: clinical diagnosis and management. Cham: Springer; 2016. p. 491–8.
McKain CW, Urban DJ. Pain and cluneal neuropathy following intragluteal injection. Anesth Analg. 1978;57(1):138–41.
Dellon AL. Pain with sitting related to injury of the posterior femoral cutaneous nerve. Microsurgery. 2015;35:463–8.
Johnson CS, Johnson RL, Niesen AD, Stoike DE, Pawlina W. Ultrasound-guided posterior femoral cutaneous nerve block: a cadaveric study. J Ultrasound Med. 2018;37:897–903.
Chang KV, Mezian K, Nanka O, Wu WT, Lou YM, Wang JC, et al. Ultrasound imaging for the cutaneous nerves of the extremities and relevant entrapment syndromes: from anatomy to clinical implications. J Clin Med. 2018;7:457. https://doi.org/10.3390/jcm7110457.
Ploteau S, Salaud C, Hamel A, Robert R. Entrapment of the posterior femoral cutaneous nerve and its inferior cluneal branches: anatomical basis of surgery for inferior cluneal neuralgia. Surg Radiol Anat. 2017;39:859–63.
Williams SE, Swetenburg JT, Zachary AB, Asa RC, Black AC Jr. Posterior femoral cutaneous neuropathy in piriformis syndrome: a vascular hypothesis. Med Hypotheses. 2020;144:109924. https://doi.org/10.1016/j.mehy.2020.109924.
Gomceli YB, Kapukiran A, Kutlu G, Baysal AI. A case report of an uncommon neuropathy: posterior femoral cutaneous neuropathy. Acta Neurol Belg. 2005;105:43–5.
Dumitru D, Marquis S. Posterior femoral cutaneous nerve neuropathy and somatosensory evoked potentials. Arch Phys Med Rehabil. 1988;69(1):44–5.
Windhofer C, Brenner E, Moriggl B, Papp C. Relationship between the descending branch of the inferior gluteal artery and the posterior femoral cutaneous nerve applicable to flap surgery. Surg Radiol Anat. 2002;24:253–7.
Godbout E, Farmer L, Bortoluzzi P, Laberge CL. Donor-site morbidity of the inferior gluteal artery perforator flap for breast reconstruction in teenagers. Can J Plast Surg. 2013;21:19–22.
Zenn MR, Millard JA. Free inferior gluteal flap harvest with sparing of the posterior femoral cutaneous nerve. J Reconstr Microsurg. 2006;22(7):509–12.
Brooks JBB, Silva C, Kai MR, Leal GXP. Electrophysiological study of the posterior cutaneous femoral nerve: normative data. J Neurol Neurophysiol. 2011;2:119. https://doi.org/10.4172/2155-9562.1000119.
Park JM, Jang KE, Sook H, Kim HK, Jeong KK, Park DS. Medial femoral cutaneous nerve and posterior femoral cutaneous nerve conduction study in Korean. J Korean Acad Rehab Med. 1998;22(1):142–6.
Agu AU, Esom EE, Anyaeji PS, Nzekwe KC, Chime SC, Ikele II, et al. Obesity indices and academic performance of medical students of Igbo extraction at College of Medicine, University of Nigeria. World J Med Sci. 2019;16(4):191–5.
Delisa JA, Lee HJ, Baran EM, Lai KS, Spielholz N. Manual of nerve conduction velocity and clinical neurophysiology. 3rd ed. New York: Raven Press; 1994.
Saba EKA. Electrophysiological study of the ulnar palmar cutaneous nerve in normal individuals. Egypt Rheumatol Rehabil. 2016;43:184–9. https://doi.org/10.4103/1110-161X.192258.
Saba EKA. Electrophysiological study of posterior antebrachial cutaneous nerve in a sample of normal subjects. Egypt Rheumatol Rehabil. 2020;47:21. https://doi.org/10.1186/s43166-020-00007-4.
Saba EKA. Association between carpal tunnel syndrome and trigger finger: a clinical and electrophysiological study. Egypt Rheumatol Rehabil. 2021;48:33. https://doi.org/10.1186/s43166-021-00080-3.
Saba EK, Sultan HA. Subclinical pronator syndrome in patients with carpal tunnel syndrome: an electrophysiological study. Egypt Rheumatol. 2015;37:197–202. https://doi.org/10.1016/j.ejr.2014.12.005.
Robinson LP. Entrapment neuropathies and other focal neuropathies (including carpal tunnel syndrome). In: Pease WS, Lew HL, Johnson EW, editors. Practical electromyography. 4th ed. Philadelphia: Lippincott Williams and Wilkins; 2007. p. 259–95.
Lew HL, Tsai S. Pictorial guide to nerve conduction techniques. In: Pease WS, Lew HL, Johnson EW, editors. Practical electromyography. 4th ed. Philadelphia: Lippincott Williams & Wilkins; 2007. p. 213–55.
Fong SY, Goh KJ, Shahrizaila N, Wong KT, Tan CT. Effects of demographic and physical factors on nerve conduction study values of healthy subjects in a multi-ethnic Asian population. Muscle Nerve. 2016;54:244–8.
Meng S, Lieba-Samal D, Reissig LF, Gruber GM, Brugger PC, Platzgummer H, Bodner G. High-resolution ultrasound of the posterior femoral cutaneous nerve: visualization and initial experience with patients. Skelet Radiol. 2015;44:1421–6.
Saba EKA. Electrophysiological study of Martin-Gruber anastomosis in a sample of Egyptians. Egypt Rheumatol Rehabil. 2017;44:153–8. https://doi.org/10.4103/err.err_12_17.
Saba EKA. Electrophysiological study of accessory deep peroneal nerve in a sample of Egyptian subjects. Egypt Rheumatol Rehabil. 2019;46:251–6. https://doi.org/10.4103/err.err_19_19.
Tubbs RS, Miller J, Loukas M, Shoja MM, Shokouhi G, Cohen-Gadol AA. Surgical and anatomical landmarks for the perineal branch of the posterior femoral cutaneous nerve: implications in perineal pain syndromes. Laboratory investigation. J Neurosurg. 2009;111(2):332–5.
Nakanishi T, Kanno Y, Kaneshige. Comparative morphological remarks on the origin of the posterior femoral cutaneous nerve. Anat Anz. 1976;139(1–2):8–23.
Izzo KL, Aravabhumi S, Jafri A, Sobel E, Demopoulos JT. Medial and lateral antebrachial cutaneous nerves: standardization of technique, reliability and age effect on healthy subjects. Arch Phys Med Rehabil. 1985;66:592–7.
Sajadi S, Mansoori K, Raissi GR, Razavi SZE, Ghajarzadeh M. Normal values of posterior antebrachial cutaneous nerve conduction study related to age, gender, height, and body mass index. J Clin Neurophysiol. 2014;31:523–8.
Fujimaki Y, Kuwabara S, Sato Y, Isose S, Shibuya K, Sekiguchi Y, et al. The effects of age, gender, and body mass index on amplitude of sensory nerve action potentials: multivariate analyses. Clin Neurophysiol. 2009;120:1683–6.
Weber RJ, Turk M. Basic nerve conduction techniques. In: Pease WS, Lew HL, Johnson EW, editors. Johnson’s practical electromyography. 4th ed. Philadelphia: Lippincott Williams and Wilkins; 2007. p. 29–64.
Shehab D, Moussa MAA. Normal values of lower limb nerve conduction in Kuwait. Med Princ Pract. 1999;8:134–7.
Palve SS, Palve SB. Impact of aging on nerve conduction velocities and late responses in healthy individuals. J Neurosci Rural Pract. 2018;9(1):112–6. https://doi.org/10.4103/jnrp.jnrp_323_17.
Huang CR, Chang WN, Chang HW, Tsai NW, Lu CH. Effects of age, gender, height, and weight on late responses and nerve conduction study parameters. Acta Neurol Taiwan. 2009;18:242–9.
Elmagzoub MS, Noury AO. Normal neurophysiologic parameters of the sural nerve among adult healthy Sudanese population. J Neurol Stroke. 2021;11(1):12–5. https://doi.org/10.15406/jnsk.2021.11.00446.
Soudmand R, Ward LC, Swift TR. Effect of height on nerve conduction velocity. Neurology. 1982;32(4):407–10. https://doi.org/10.1212/wnl.32.4.407.
Campbell WW, Ward LC, Swift TR. Nerve conduction velocity varies inversely with height. Muscle Nerve. 1981;4(6):520–3. https://doi.org/10.1002/mus.880040609.
Bennal AS, Pattar MY, Taklikar RH. Effect of height and BMI on nerve conduction velocity. Indian J Clin Anat Physiol. 2015;2(4):231–4.
Al-Salmi K, Wali FS, Nadeem ASM, Al-Salti A. Does gender have a significant effect on normal nerve conduction studies values? J Neurol Stroke. 2019;9(6):306–11.
Thakur D, Paudel BH, Jha CB. Nerve conduction study in healthy individuals a preliminary age based study. Kathmandu Univ Med J. 2010;8(31):311–6.
Saba EK, El-Tawab SS. Ulnar nerve changes associated with carpal tunnel syndrome not affecting median versus ulnar comparative studies. World J Med Sci. 2014;11(4):600–8. https://doi.org/10.5829/idosi.wjms.2014.11.4.91113.
Saba EKA. Superficial radial neuropathy: an unobserved etiology of chronic dorsoradial wrist pain. Egypt Rheumatol Rehabil. 2021;48:29. https://doi.org/10.1186/s43166-021-00077-y.
Saba EKA, El-Tawab SS, Sultan HA. Medial calcaneal neuropathy: a missed etiology of chronic plantar heel pain. Egypt Rheumatol Rehabil. 2017;44:147–52. https://doi.org/10.4103/err.err_16_17.
Acknowledgements
The author is grateful to Mariam Kamal Aziz Saba for her assistance in the statistical analysis. The author is grateful to Maria Kamal Aziz Saba for her assistance in the preparation of the figures.
Funding
The author received no specific funding for this work.
The author declares that no financial or material support was provided by any parties and that there are no equity interests, patent rights or corporate affiliations for this work. This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
There were no sponsors or funders (other than the named author) played any role in study design, data collection and analysis, decision to publish and preparation of the manuscript.
All research facilities are available in our department with no restrictions.
Author information
Authors and Affiliations
Contributions
The author (EKAS) contributed in the concepts, design, definition of intellectual content, literature search, clinical studies, data acquisition and analysis, manuscript preparation, editing and revision. The author read and approved the final manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
The local Ethics Committee of Faculty of Medicine, Alexandria University, Egypt (IRB NO:00012098-FWA NO:00018699) approved the study. Date of approval: 17/12/2020; Serial number: 0304951. A written informed consent was given by each participant.
Consent for publication
Consent for publication was given by each participant.
Competing interests
The author declares that he has no competing interests.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Saba, E.K.A. Posterior femoral cutaneous nerve sensory conduction study in a sample of apparently healthy Egyptian volunteers. Egypt J Neurol Psychiatry Neurosurg 58, 162 (2022). https://doi.org/10.1186/s41983-022-00581-8
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s41983-022-00581-8