Table 1.
Basic characteristics of studies included in the review
| Study, year, country, type | Ptsa on MTFb Sex, age | Weight, diabetes, PCOSc | Hurley stage | Monotherapy, dose | Control group | Txd duration | Follow-up duration | Tx outcome | Adverse events |
|---|---|---|---|---|---|---|---|---|---|
| Arun and Loffeld (2009) [3], UK, case report | 1 (fe) 50 | 146 kg Type II diabetes No PCOS |
NRf | Yes 500 mg odg for 3 months, then 1 g od |
No | NR (>4 months) | 4 months | Less frequent and shorter flares at 3 months, no leaking of previously persistent left-axilla fistula and reduced pain at 4 months | None |
|
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| Verdolini et al. (2013) [2], UK, prospective | 25 (22 f) 31.5 (17–49) |
22 f pts were “moderately overweight, had impaired glucose tolerance and PCOS” (no diabetics) | NR | Yes 500 mg od for a week, 500 mg bdh after a week, and then 500 mg tdsi after a week |
No | “Most patients continued on the treatment well past the trial” | 24 weeks | SSj mean±SDk dropped from 30.1 ±9.2 to 18.4±7.2 (p < 0.0001). DLQI'sl mean±SD dropped from 13.6±4.2 to 6.3±5.5 (p < 0.000001) Lost work-days dropped from 1.5 per month to 0.4 |
Mild Glm disturbance at the beginning of treatment |
|
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| Sanz Bueno et al. (2017) [8], NFn | 11 (5 f) NF |
NF | NF | Yes Doses ranging from 450 to 2,550 mg daily |
No | NF | 24 weeks | SS ≥30% reduction in 2 pts Glucose tolerance normalization in 5 pts DLQI improvement in 4 pts (median reduction 5.5 points) DLQI increase in 4 pts (median increase 4.2 points) 2 pts discontinued tx because of more severe flares |
Mild Gl discomfort (number of pts NR) |
|
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| Jennings et al. (2019) [1], Ireland, retrospective | 53 (45 f) 37 (19–62) |
mean weight 102 kg (67–160 kg) 4 diabetes 5 PCOS |
I 4% II 72% III 24% |
Yes 500 mg od and then bd after 2 weeks (further increases applicable) – mean daily dose 1.5 g/day |
No | 11.3 months (mean) (1–36 months) | At least 3 months | 19% complete response (no active HS) – only HIIp 58% of HII and 55% of HIIIq significant partial response 68% subjective clinical improvement Non-significant CRPr reduction 25% stopped due to non-response 21% needed 2nd agent |
Gl complaints (6 patients) (3 stopped tx) |
|
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| Moussa et al. (2020) [6], USA, retrospective | 16 peds pts NF NF |
NF | I 69% II 31% |
No | No | NF | NF | 5 pts improved (decreased flare frequency) 5 pts did not improve 6 pts were lost to f/ut 1 pt stopped tx due to lack of improvement |
Gl distress and mood changes (2, stopped tx) |
|
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| Segura Palacios et al. (2021) [7], Spain, retrospective | 27 (18 f) 32.1 |
70.4% overweight or obese NR NR |
I 51.8% II 48.2% |
Yes between 1.7 and 2.55 g per day | No | At least 12 weeks | 24 weeks | DLQI reduction (median: 13 to 9), p = 0.001 No significant PGAu reduction | Gl complaints (3 pts stopped tx because of them) |
Pts: patients.
MTF: metformin.
PCOS: polycystic ovarian syndrome.
Tx: treatment.
f:female.
NR: not reported.
od: once daily.
bd: twice daily.
tds: three times daily.
SS: Sartorius score.
SD: Standard deviation.
DLQI: Dermatology life quality index.
GI: Gastrointestinal.
NF: Not found.
EADV: European Academy of Dermatology and Venereology.
HII: Hurley stage II.
HIII: Hurley stage III.
CRP: C-reactive protein.
ped: pediatric.
:f/u: follow-up.
PGA: Physician Global Assessment.