What are the likely causes of erectile dysfunction (ED) and bilateral partial toe numbness in a patient with chronic kidney disease (CKD) stage 2, borderline 3a, and moderate spondylosis of L5-S1?

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Likely Causes of Erectile Dysfunction and Bilateral Toe Numbness in This Patient

The bilateral toe numbness is most likely caused by peripheral artery disease (PAD) with microvascular ischemia, while the erectile dysfunction is multifactorial—primarily driven by the combination of CKD stage 2-3a and underlying vascular disease, with possible contribution from lumbar spondylosis affecting nerve roots.

Erectile Dysfunction Etiology

Primary Vascular and Renal Causes

  • CKD is a major independent risk factor for ED, with prevalence reaching approximately 80% in CKD patients, and ED severity correlates with declining GFR 1, 2.
  • In patients with CKD stage 2, ED prevalence is significantly elevated, and ED may actually serve as an early clinical marker of CKD progression 3.
  • CKD causes ED through multiple mechanisms: endothelial dysfunction, disturbances in the hypothalamic-pituitary-gonadal axis, autonomic neuropathy, anemia, secondary hyperparathyroidism, and psychological factors 1, 4.
  • ED is a risk marker for systemic cardiovascular disease and shares common pathophysiology with PAD through endothelial dysfunction and atherosclerosis 5.
  • The combination of CKD and vascular disease creates a synergistic effect that substantially amplifies cardiovascular and erectile dysfunction risk 5.

Hormonal Evaluation Required

  • Morning serum total testosterone levels should be measured in all men presenting with ED to identify testosterone deficiency (defined as total testosterone <300 ng/dL with symptoms) 5.
  • Impaired gonadal function is prominent in uremic men, with disturbances in the hypothalamic-pituitary axis contributing to ED 4.

Potential Lumbar Contribution

  • While moderate L5-S1 spondylosis could theoretically affect sacral nerve roots (S2-S4) that control erectile function, this is less likely to be the primary cause given the patient's CKD and vascular risk profile 5.
  • The presence of nocturnal/morning erections would suggest against a purely neurogenic cause from spondylosis 5.

Bilateral Toe Numbness Etiology

Peripheral Artery Disease as Primary Cause

  • The acute onset (1 month ago) of bilateral toe numbness strongly suggests PAD with distal ischemia rather than diabetic neuropathy, which typically develops gradually over years 5.
  • CKD is an established risk factor for PAD, sharing common pathophysiology of inflammation and oxidative stress 5.
  • Patients with CKD, particularly those with end-stage kidney disease, are at markedly elevated risk of amputation due to PAD 5.
  • Microvascular disease (including neuropathy) is associated with increased risk of major adverse limb events in PAD patients 5.

Diagnostic Approach for PAD

  • Ankle-brachial index (ABI) should be measured as the first-line screening test; ABI <0.9 indicates PAD and is inversely related to cardiovascular disease risk 5.
  • Toe-brachial index may provide incremental diagnostic value in CKD patients, though optimal screening strategies remain under investigation 5.
  • Physical examination should assess pedal pulses and perform Semmes-Weinstein monofilament testing to evaluate for loss of protective sensation 5.

Alternative Neurologic Considerations

  • L5-S1 spondylosis typically affects L5 and S1 nerve root distributions, which would cause numbness in specific dermatomal patterns (lateral foot for L5, plantar foot for S1) rather than symmetric involvement of all ten toes 5.
  • The bilateral symmetric distribution affecting all toes is more consistent with vascular insufficiency than radiculopathy from spondylosis 5.

Critical Clinical Actions

Immediate Vascular Assessment

  • Comprehensive foot and vascular examination including visual inspection, monofilament testing, 128-Hz tuning fork for vibratory sensation, and pedal pulse evaluation 5.
  • Consider referral to vascular surgery if ABI is abnormal or if clinical suspicion for PAD remains high despite normal ABI 5.
  • Doppler ultrasound (DUS) is the first-line imaging modality to screen for significant arterial stenosis if PAD is suspected 5.

Cardiovascular Risk Stratification

  • ED serves as a pivotal opportunity to discuss cardiovascular risk, as it is as strong a predictor of future cardiac events as cigarette smoking or family history of myocardial infarction 5.
  • The patient should be counseled that both ED and PAD are risk markers for underlying cardiovascular disease requiring comprehensive evaluation 5.
  • Assessment should include blood pressure measurement, lipid panel, hemoglobin A1c (to exclude diabetes), and consideration of stress testing if cardiac symptoms are present 5.

Laboratory Evaluation

  • Morning serum total testosterone 5
  • Hemoglobin/hematocrit to assess for anemia 1
  • Lipid panel (HDL-cholesterol levels are associated with ED in CKD patients) 6
  • Parathyroid hormone to evaluate for secondary hyperparathyroidism 1
  • Hemoglobin A1c to exclude undiagnosed diabetes 5

Common Pitfalls to Avoid

  • Do not assume the toe numbness is solely due to lumbar spondylosis without vascular evaluation—the bilateral symmetric pattern and acute onset favor PAD 5.
  • Do not attribute ED exclusively to psychological factors in a patient with CKD stage 2-3a, as organic causes predominate in this population 1, 4.
  • Do not overlook that ED may be the earliest clinical manifestation of progressive CKD and cardiovascular disease 3.
  • Failing to screen for PAD in CKD patients can result in missed opportunities for limb-salvage interventions 5.

References

Research

Chronic kidney disease and erectile dysfunction.

World journal of nephrology, 2014

Research

Is erectile dysfunction an early clinical symptom of chronic kidney disease?

The aging male : the official journal of the International Society for the Study of the Aging Male, 2021

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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