Table 1:
Clinical characteristics and budesonide treatment
Case | Age (years) | Sex | GFD Duration (years) | Symptomsa | Symptom Duration following acute gluten reaction | tTG (U/mL)b | Treatment duration and dosage: | Clinical Responsec | Adverse events | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
D | P | N/V | B | C | Extraintestinal manifestations | GI | Non-GI | ||||||||
1 | 28 | F | 12 | D | N/V | Fatigue, rash | 2–3 weeks | Normal | 3 days: 9 mg daily | Substantial | None | ||||
2 | 32 | F | 12 | D | P | N/V | Fatigue, brain fog | 1 weekd | Normal | Substantial | Partial | None | |||
3 | 18 | F | 3 | P | N/V | Fatigue, Headaches | 2 days | < 1 × ULNe | 3 days: 6mg, 6mg, 3mg | Substantial | None | ||||
4 | 64 | F | 2 | D | P | N/V | Headaches, flushing | Few days | Normal | 9 days: 9mg/3d, 6 mg/3d, 3 mg/3d | Substantial | None | |||
5 | 50 | F | 1 | D | P | N/V | Fatigue | 3 weeks | Unknown | 10 days: 9mg daily | Substantial | No response | Headache | ||
6 | 51 | F | 1 | P | B | Brain fog, joint pain, ataxia | 2 weeks | Normal | A few days: 9 mg daily until better | Response | Partial | None | |||
7f | 60 | F | 2 | P | N/V | B | C | Fatigue, brain fog | 2 weeks | Normal | 3 weeks: 6 mg/2w, 3 mg/1w | Substantial | Partial for fatigue | None | |
8 | 41 | F | 11 | D | None | 1 week | <1 × ULNg | 3 weeks: 9 mg/1w, 6 mg/1w, 3 mg/1w | Substantial | NA | None | ||||
9 | 43 | F | 4 | D | P | None | Few weeks | Normal | 3–4 weeks: 9 mg/1–2w, 6 mg/1w, 3 mg/1w | Response | NA | None | |||
10 | 39 | F | 1.6 | D | P | N/V | B | Fatigue, brain fog, joint pain | 3–4 weeks | Normal | Partial | None | |||
11 | 70 | F | 9 | D | None | 4 weeks | Normal | Substantial | NA | Constipation | |||||
12 | 56 | F | 2 | D | P | None | 2 days | Unknown | Response | NA | None | ||||
13 | 35 | F | 2.7 | P | N/V | None | 2 weeks | 2 × ULNg | 4 weeks: 9 mg daily | Partial | NA | None |
F, Female; M, Male; D, Diarrhea; P, Abdominal pain; N/V, nausea and/or vomiting; B, Bloating; C, constipation; ULN, upper limit normal; w, week; d, day;
Symptoms of acute gluten exposure were similar to symptoms at CeD diagnosis, with the exception of case 4 and 9 who were asymptomatic at diagnosis (screened because of family history of CeD or osteoporosis) and after following a GFD, developed symptoms if exposed to gluten;
INOVA anti-human IgA TTG, borderline 20–30, positive >30;
“Substantial” response: patient-reported substantial decrease in symptom severity and duration compared to previous gluten exposures; “partial” response: some degree of improvement in terms of severity, but not duration; “response”: a clinical response was observed, but chart-review was insufficient to properly measure the extent of the response and effect on symptoms duration;
Mostly non-GI symptoms, GI symptoms last about two days;
Patient was exposed several times at the college cafeteria before starting budesonide;
Potential CeD;
Previously not strictly adherent to a GFD, but were on a strict GFD for at least six months at the time of acute symptoms and tTG were trending down.