# Association Between Low-Dose Ethambutol Therapy and Optic Neuropathy in Mycobacterium avium Complex Pulmonary Disease: A Retrospective Cohort Study Using Propensity Score Analysis

**Authors:** Yasuhiro Morimoto, Hiroki Matsui, Masaki Ikeda, Norihiko Kubota, Tatsuya Nagai, Ayumu Otsuki, Hiroyuki Ito, Kei Nakashima

PMC · DOI: 10.1093/ofid/ofag127 · Open Forum Infectious Diseases · 2026-03-03

## TL;DR

This study finds that low-dose ethambutol reduces optic neuropathy risk in MAC-PD patients without affecting treatment effectiveness.

## Contribution

The study demonstrates that low-dose ethambutol reduces optic neuropathy risk without compromising treatment outcomes in MAC-PD patients.

## Key findings

- Low-dose ethambutol reduced optic neuropathy risk by 17.1% compared to high-dose.
- Failure of negative culture conversion and macrolide resistance did not differ significantly between groups.
- Low-dose ethambutol offers a safer treatment option without compromising effectiveness.

## Abstract

Current guidelines recommend ethambutol as a first-line agent for treating Mycobacterium avium complex pulmonary disease (MAC-PD) but can induce optic neuropathy. Previous studies suggest that low-dose ethambutol may reduce the incidence of optic neuropathy without compromising its effectiveness, but have not adequately adjusted for risk factors for optic neuropathy. We investigated the association between low-dose ethambutol therapy and optic neuropathy in patients with MAC-PD.

This retrospective cohort study included patients treated for MAC-PD at Kameda Medical Center between April 2003 and July 2024. Patients were categorized into low-dose (<12.5 mg/kg/day) and high-dose (≥12.5 mg/kg/day) ethambutol groups. The primary outcome was the incidence of optic neuropathy. Secondary outcomes included failure of negative culture conversion and macrolide resistance. Propensity score-based overlap weighting was used to adjust for patient characteristics and outcomes were compared using datasets generated through bootstrap resampling.

Of 223 patients, 79 received low-dose (10.7 mg/kg/day) and 144 received high-dose ethambutol (15.4 mg/kg/day). None of the patients in the low-dose group and 4.8% in the high-dose group developed optic neuropathy. After adjustment, the risk of optic neuropathy was significantly lower in the low-dose ethambutol group (risk difference: −17.1%, 95% CI: −32.9% to −5.4%), but the risk difference for failure of negative culture conversion and macrolide resistance did not differ significantly between groups (−20.0%, 95% CI: −45.6% to 2.5%; and −4.9%, 95% CI: −13.5% to 0.0%, respectively).

Low-dose ethambutol therapy may reduce the risk of optic neuropathy without compromising treatment outcomes, offering a safer option for MAC-PD.

Optic neuropathy incidence was significantly lower in the low-dose than the high-dose ethambutol group, whereas incidence of failure of negative culture conversion and macrolide resistance did not differ significantly between groups, demonstrating that low-dose ethambutol reduces toxicity without compromising effectiveness.

## Linked entities

- **Chemicals:** ethambutol (PubChem CID 14052)

## Full-text entities

- **Diseases:** PD (MESH:D010300), optic atrophy (MESH:D009896), toxicity (MESH:D064420), diabetes mellitus (MESH:D003920), COPD (MESH:D029424), bronchiectasis (MESH:D001987), NTM-PD (MESH:D008171), ophthalmic diseases (MESH:C535922), kidney dysfunction (MESH:D007674), nodular bronchiectatic (MESH:D008224), obesity (MESH:D009765), tuberculosis (MESH:D014376), disease (MESH:D004194), Acid (MESH:D011015), NC-NB type disease (MESH:C566924), Infectious Diseases (MESH:D003141), hypertension (MESH:D006973), TB (MESH:D014390), UC (MESH:C562442), ocular toxicity (MESH:D000081028), MAC (MESH:D015270), visual disturbances (MESH:D014786), Optic Neuropathy (MESH:D009901)
- **Chemicals:** Ogawa medium (-), amikacin (MESH:D000583), azithromycin (MESH:D017963), rifampin (MESH:D012293), EMB (MESH:D004977), creatinine (MESH:D003404), macrolide (MESH:D018942), clarithromycin (MESH:D017291), fluoroquinolone (MESH:D024841)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mycobacterium avium (species) [taxon 1764], Mycobacterium avium complex sp. (species) [taxon 37162], Mycobacterium intracellulare (species) [taxon 1767]

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## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12989744/full.md

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Source: https://tomesphere.com/paper/PMC12989744