Insights into the Symptom Heterogeneity of Post-Treatment Lyme Disease

Many physicians conceptualize post-treatment Lyme disease as similar to fibromyalgia, with a uniform phenotype and subjective symptoms, many of which overlap with depression. However, individuals with post-treatment Lyme disease are heterogenous, with a wide range of clinical symptoms, many of which can significantly affect quality of life. Previous studies have used validated symptom questionnaires to evaluate this patient population, finding a wide range of symptoms, including musculoskeletal pain, which is relatively common in the general population, is reported with greater frequency and severity in patients with post-treatment Lyme disease.

Results from a study that identified and characterized potentially clinically relevant patient subgroups in post-treatment Lyme disease suggest patients with well-characterized, post-treatment Lyme disease can be categorized into three clinically relevant subgroups: 1) low to moderate level of fatigue and impaired cognitive function, musculoskeletal pain and mood-related symptoms, 2) high levels of musculoskeletal pain and 3) high levels of mood-related symptoms.

Alison W. Rebman, MPH, senior research data analyst at the Johns Hopkins University School of Medicine, Baltimore, and colleagues report these subgroups differ by symptom phenotype, as well as a range of other factors. They published their findings online Jan. 13 in BMJ Open.¹

“It’s not a uniform population,” says John N. Aucott, MD, director of the Johns Hopkins Lyme Disease Clinical Research Center and senior author of the study. He explains that there is a tendency for physicians to believe that all of the symptoms of post-treatment Lyme disease stem from anxiety and depression. However, he and his colleagues found that, although some patients meet this description, many experience a syndrome characterized primarily by musculoskeletal symptoms.

Methods

The researchers enrolled 212 patients (average age 48 years) whose current illness was clearly linked to B. burgdorferi exposure. Participants self-administered a 36-item, post-Lyme questionnaire of symptoms (PLQS) and, for each symptom, indicated its presence and severity over the previous two weeks.

The investigators performed exploratory factor analysis on the data and classified the self-reported symptoms into six groups: fatigue, ocular disequilibrium, infection type, mood related, musculoskeletal pain and neurologic. They used the overall severity of the symptom reporting to identify three patient subgroups: 59.0% of patients reported symptoms in subgroup 1, which was characterized primarily by low to moderate level of fatigue and impaired cognitive function, musculoskeletal pain and mood-related symptoms; 18.9% of patients reported symptoms in subgroup 2, which was characterized by high levels of musculoskeletal pain; and 22.2% of patients reported symptoms in subgroup 3, which was characterized by  the highest levels of mood-related symptoms. Neither the percentage of men vs. women respondents nor the Life Events Checklist total score was statistically significantly different across subgroups.