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. 2019 Dec 11;9:18817. doi: 10.1038/s41598-019-55473-4

Table 1.

Demographic characteristics, fatigue features, clinical manifestations, comorbid conditions, and laboratory abnormalities of the study population.

Epidemiological characteristics
Patients, n (%) 123
Female/Male 89/34
Duration of illness (months) 72 [36–120]
Age at disease onset (years) 34 [26–41]
   13–19 n (%) 11 (8.9)
   20–29 n (%) 34 (27.6)
   30–39 n (%) 42 (34.1)
   40–49 n (%) 23 (18.7)
   ≥50 n (%) 13 (10.6)
Family history of fatigue 13 (10.6)
Identified disease trigger 87 (70.7)
Infectious triggers 58 (47.2)
Fatigue features
Fatigue severity scale (n = 96) 5.5 [5–6.2]
Fatigue scale (n = 103) 24 [20–27.5]
Modified fatigue impact scale (n = 104)
   Physical subscale 29 [25–32]
   Cognitive subscale 27 [20–32]
   Psychosocial subscale 6 [4–6.5]
Clinical manifestations, n (%)
More severe post-exertional malaise* 62 (50.4)
Difficulty processing information 118 (95.9)
Short-term memory loss 101 (82.1)
Headaches 89 (72.4)
Myalgia 107 (87)
Arthralgia 72 (58.5)
Disturbed sleep patterns 109 (88.6)
Unrefreshed sleep 118 (95.9)
Neurosensory and perceptual disturbances 114 (92.7)
Motor disturbances 112 (91.1)
Flu-like symptoms 92 (74.8)
Recurrent infections 47 (38.2)
Gastrointestinal impairments 105 (85.4)
Urinary impairments 38 (30.9)
Orthostatic intolerance 41 (31.3)
Palpitation 79 (64.2)
Main comorbidities, n (%)
Reactive depression 36 (29.3)
Fibromyalgia 19 (15.5)
Irritable bowel syndrome 50 (40.7)
Main laboratory abnormalities, n (%)
Elevated blood lactate at rest 55 (44.7%)
Serum zinc deficit 39 (31.7)
Serum 25-hydroxyvitamin D deficit§ 61 (49.6)
Low plasma 8 am and/or 8 pm cortisol levels 23 (18.7)

Notes: *Score ≥12 on Centres for Disease Control and Prevention Symptom Inventory auto-questionnaire. One or more blood lactate measurements at rest. Normal range = 0.70–1.25 mg/L, measured by atomic emission spectroscopy/high-frequency induction plasma. §Normal range = 75–250 nmol/L, measured by chemiluminescence technology (CLIA). Normal values = 5–49 µg/L at 8 am, and 30–100 µg/L at 8 pm, measured by Immunoenzymatic chemoluminescznce (12000 ABBOT) method. Cortisol deficit was retained if one or both measurements were reduced. Categorical data were expressed as absolute number and percentage. Continuous data were expressed as median and interquartiles.