Background: The sciatic nerve (SN), the largest nerve in the human body, exhibits notable variability in its division and relation to the piriformis muscle. Such variations have profound implications for surgical safety, regional anesthesia, and the diagnosis of deep gluteal pathologies. Objectives: To determine the prevalence, classification, and morphometric parameters of sciatic nerve variations in the gluteal region among adults, and to establish population-specific reference data using imaging correlation. Methods: A prospective observational study was conducted on 300 adults at a tertiary care teaching hospital over 18 months. High-resolution ultrasonography (HRUS) and MRI were performed to assess nerve course, depth, and morphometric relationships with the greater trochanter (GT) and ischial tuberosity (IT). Variations were classified according to the Beaton–Anson system. Intraoperative findings (n = 62) served as reference for validation. Results: Among 288 evaluable cases, 71.9 % exhibited the classical Type I pattern, while 28.1 % showed high-division variants (Types II–VI). The mean ± SD skin-to-nerve depth was 52.6 ± 8.9 mm; SN–GT distance 47.3 ± 6.4 mm; SN–IT distance 40.9 ± 5.8 mm; nerve diameter 9.2 ± 1.4 mm. Males had significantly greater depths (p < 0.001). MRI demonstrated higher diagnostic accuracy (98.1 %) than HRUS (91.2 %). BMI > 25 kg/m² correlated with variant presence (p = 0.041). Conclusion: Nearly one-fourth of individuals possess non-classical sciatic nerve configurations. The morphometric data and imaging validation provide reliable anatomical references for clinical procedures in the gluteal region, enhancing surgical and anesthetic safety.
The sciatic nerve (SN) is the principal continuation of the sacral plexus (L4–S3) and the largest peripheral nerve in the human body, traversing the deep gluteal region before descending into the posterior thigh. It lies between the greater trochanter and the ischial tuberosity, deep to the gluteus maximus, and typically bifurcates at the popliteal fossa into tibial and common peroneal branches ¹.
However, extensive cadaveric and imaging evidence demonstrates that the SN displays considerable variability in its level of division and its relationship to the piriformis muscle ²,³. Beaton and Anson’s (1937) classification remains foundational, describing six patterns ranging from the classical undivided nerve below the piriformis (Type I) to multiple high-division and piercing variants (Types II–VI) ⁴. Such deviations, though often asymptomatic, carry direct clinical relevance. During posterior hip arthroplasty or acetabular fixation, an unrecognized variant may increase the risk of iatrogenic nerve injury ⁵. Similarly, in regional anesthesia, early bifurcation of the SN may cause incomplete sciatic nerve blocks ⁶.
The depth of the nerve from the skin and its distance to bony landmarks are critical parameters guiding safe needle trajectories and surgical dissections ⁷. Population-specific morphometric data are especially necessary in South Asian cohorts, where pelvic dimensions and gluteal muscle bulk differ from Western norms. Despite abundant cadaveric literature, in-vivo studies integrating HRUS, MRI, and intraoperative correlation remain limited ⁸,⁹.
Therefore, the present prospective anatomical study aimed to quantify the prevalence and morphometric characteristics of sciatic nerve variations in the gluteal region, classify them using standard criteria, and establish normative data through imaging validation. By linking anatomical observation with radiological precision, the study bridges traditional morphology and modern clinical application, providing surgeons, anesthesiologists, and anatomists with a population-relevant anatomical reference.
A prospective observational study was conducted over 18 months at a tertiary-care teaching hospital in collaboration between the Departments of Anatomy, Radiology, and Orthopaedics/Anaesthesiology.
Participants:
Three hundred adults (≥ 18 years) undergoing posterior hip procedures, gluteal pain evaluation, or sciatic nerve blocks were recruited after informed consent. Exclusion criteria included prior gluteal surgery or trauma, neuromuscular disorders, and MRI contraindications.
Imaging protocol:
Sample size:
Calculated for an expected 20 % prevalence, α = 0.05, precision ± 5 %, yielding n = 273; rounded to 300.
Data analysis:
Continuous variables expressed as mean ± SD; categorical as percentages. Chi-square and t-tests assessed group differences; logistic regression determined correlates of variant presence. Inter-observer reliability used intraclass correlation coefficient (ICC) and Cohen’s κ. Significance p < 0.05.
Ethics:
Institutional Ethics Committee approval obtained. Study posed minimal risk; confidentiality maintained.
Table 1. Demographic profile of study participants (n = 300)
Parameter |
Mean ± SD |
Range |
Males (n = 165) |
Females (n = 135) |
p-value |
Age (years) |
46.2 ± 13.4 |
18–82 |
45.7 ± 12.8 |
47.3 ± 13.9 |
0.42 (NS) |
Height (cm) |
165.5 ± 9.8 |
142–188 |
170.3 ± 7.5 |
159.4 ± 8.2 |
< 0.001* |
Weight (kg) |
68.9 ± 10.3 |
48–98 |
72.1 ± 9.4 |
64.9 ± 8.7 |
< 0.001* |
BMI (kg/m²) |
25.3 ± 3.1 |
19.4–31.8 |
24.9 ± 2.9 |
25.8 ± 3.4 |
0.09 (NS) |
*Significant at p < 0.05; NS = not significant.
Table 2. Distribution of sciatic-nerve variations according to Beaton & Anson classification (n = 288)
Type |
Description |
Frequency (n) |
Percentage (%) |
I |
Undivided nerve below piriformis |
207 |
71.9 |
II |
Common peroneal piercing piriformis; tibial below |
45 |
15.6 |
III |
Common peroneal above; tibial below piriformis |
20 |
6.9 |
IV |
Undivided nerve piercing piriformis |
7 |
2.4 |
V |
Both divisions piercing piriformis |
5 |
1.7 |
VI |
Undivided nerve above piriformis |
4 |
1.4 |
Total variants (II–VI) |
81 |
28.1 % |
Table 3. Side-wise distribution and bilaterality of sciatic-nerve variations
Side examined |
Variants observed (n) |
Percentage (%) |
Bilateral symmetry (%) |
Right |
85 |
29.5 |
84.7 |
Left |
78 |
27.0 |
84.7 |
Bilateral variants |
42 |
— |
— |
Variants occurred slightly more often on the right side; ~85 % of subjects displayed bilateral symmetry.
Table 4. Morphometric parameters of the sciatic nerve in the gluteal region (HRUS-based)
Parameter (mm) |
Mean ± SD |
Range |
Males |
Females |
p-value |
Skin-to-nerve depth |
52.6 ± 8.9 |
35–72 |
56.4 ± 7.8 |
48.1 ± 8.4 |
< 0.001* |
Distance from GT |
47.3 ± 6.4 |
32–61 |
49.8 ± 5.9 |
44.1 ± 6.1 |
0.002* |
Distance from IT |
40.9 ± 5.8 |
28–55 |
41.7 ± 5.6 |
39.8 ± 5.9 |
0.046* |
SN diameter |
9.2 ± 1.4 |
6.5–12.3 |
9.5 ± 1.2 |
8.9 ± 1.5 |
0.037* |
*Significant at p < 0.05. GT = greater trochanter; IT = ischial tuberosity.
Table 5. Comparative diagnostic performance of imaging modalities (n = 62 intra-operative confirmations)
Modality |
Sensitivity (%) |
Specificity (%) |
Accuracy (%) |
κ agreement |
High-resolution ultrasound (HRUS) |
91.2 |
95.0 |
93.4 |
0.89 |
Magnetic resonance imaging (MRI) |
98.1 |
97.6 |
97.8 |
0.94 |
MRI demonstrated slightly higher diagnostic accuracy, though HRUS remained highly reliable.
Table 6. Association between demographic variables and presence of sciatic-nerve variant (binary logistic regression)
Variable |
β coefficient |
Odds Ratio (OR) |
95 % CI |
p-value |
Male sex |
0.31 |
1.36 |
0.84–2.21 |
0.217 |
BMI > 25 kg/m² |
0.55 |
1.74 |
1.02–2.98 |
0.041 * |
Age > 50 years |
–0.12 |
0.89 |
0.53–1.46 |
0.621 |
Right side |
0.44 |
1.55 |
0.94–2.55 |
0.083 |
*Significant at p < 0.05.
Table 7. Inter-observer reliability for imaging measurements (n = 60)
Parameter |
ICC (95 % CI) |
Interpretation |
Skin-to-nerve depth |
0.912 (0.887–0.938) |
Excellent |
SN–GT distance |
0.874 (0.835–0.912) |
Good |
SN–IT distance |
0.852 (0.802–0.898) |
Good |
Variant classification (κ) |
0.91 |
Excellent |
The present study demonstrates that nearly one-quarter of the population exhibits high-division or variant courses of the sciatic nerve. This prevalence (28.1 %) agrees with previous Indian cadaveric reports (20–30 %) ¹⁰ and Mediterranean data ¹¹, but exceeds the 10–20 % rates in East Asian and Western cohorts ¹². Such variability likely reflects ethnic and morphometric influences on pelvic development.
The measured mean skin-to-nerve depth (≈ 5 cm) corroborates Rajasekaran et al. (2016) and has direct procedural relevance. Increased depth in males aligns with greater gluteal muscle mass, whereas higher BMI correlated with variant presence—potentially due to altered pelvic tilt and muscle orientation. These findings reinforce the need for individualized needle length and insertion angle during posterior approaches.
The study also validates imaging as a reliable anatomical tool. MRI achieved near-perfect sensitivity and specificity, while HRUS provided real-time guidance suitable for anesthesia practice. High inter-observer ICC (> 0.85) confirms reproducibility, strengthening its pedagogical and clinical utility. Importantly, the integration of imaging and intraoperative data bridges the gap between cadaveric anatomy and living-body variation.
Anatomically, high-division variants alter the topographic relationships of the nerve with the piriformis, gemelli, and obturator internus, predisposing to entrapment syndromes and procedural complications. Surgeons must anticipate such variants during posterior hip exposure, while anesthesiologists should employ ultrasound mapping to ensure complete nerve blockade.
Approximately one in four individuals demonstrates non-classical sciatic nerve anatomy in the gluteal region. MRI and HRUS reliably delineate these variations, enabling safer surgical corridors and more effective nerve blocks. The morphometric reference values established herein provide a region-specific anatomical framework for clinicians and educators alike.