| Literature DB >> 35832690 |
Simona Ascanelli, Cristina Bombardini, Laura Chimisso, Paolo Carcoforo1, Silvia Turroni2, Federica D'Amico3, Maria Luisa Caniati, Eleonora Baldi, Valeria Tugnoli4, Chiara Morotti, Giorgia Valpiani5, Gabriele Bazzocchi6.
Abstract
Background: Constipation and faecal incontinence are not so uncommon in patients with multiple sclerosis, impairing quality of life. The gut microbiota is altered in multiple sclerosis patients and likely contributes to disease pathogenesis. Trans-anal irrigation has been proven to allow treatment of neurogenic bowel dysfunction and may affect gut microbiota.Entities:
Keywords: Bowel dysfunction; constipation; faecal incontinence; gut microbiota; gut–brain axis; multiple sclerosis; quality of life; trans-anal irrigation
Year: 2022 PMID: 35832690 PMCID: PMC9272186 DOI: 10.1177/20552173221109771
Source DB: PubMed Journal: Mult Scler J Exp Transl Clin ISSN: 2055-2173
Figure 1.Summary of the study protocol.
Figure 2.Flow diagram summarizing the phases of patient enrolment according to STROBE statement.
Demographic (a) and questionnaire (b) baseline characteristics of the study population (*for statistical significance).
| Included (constipation group) PAC-QoL≥32 (n = 37) | Excluded (non-constipation group) PAC-QoL<32 (n = 43) | Total (n = 80) | |||
|---|---|---|---|---|---|
|
| 49.51 ± 11.34 | 41.92 ± 10.89 | 45.57 ± 11.67 | 0.004* | |
|
|
| 4 (10.8) | 13 (30.2) | 17 (21.2) | 0.038* |
|
|
| 33 (89.2) | 30 (69.8) | 63 (78.8) | |
|
|
| 23 (62.2) | 41 (95.4) | 64 (80) | <0.001* |
|
|
| 10 (27) | 2 (4.6) | 12 (15) | 0.003* |
|
|
| 4 (10.8) | 0 (0) | 4 (5) | 0.049* |
|
| 15 [9–21] | 8.5 [5–14.5] | 12 [6–18] | 0.012* | |
|
| 4 [2–6.5] | 2 [1–3.5] | 3 [1.5–5] | <0.001* | |
| Included PAC-QoL≥32 (n = 37) | |||||
|
| 47 [42–57] | ||||
|
| 4 [0–6] | ||||
|
| 6 [3–11] | ||||
|
| 10 [9–15] | ||||
|
| 9 [6–13] | ||||
|
| 0 [0–4] | ||||
|
| 76.8 [51.6–104.4] | ||||
A-W, Agachan-Wexner constipation score; EDSS, Expanded Disability Status Scale; F, female; FI-CCI, Fecal Incontinence Cleveland Clinic Index; M, male; MS, multiple sclerosis; NBD, neurogenic bowel dysfunction; ODS, obstructed defecation syndrome (or Altomare Questionnaire); PAC-QoL, Patient Assessment of Constipation Quality of Life; PP, primarily progressive; RR, relapsing-remitting; SP, secondary progressive; TT, intestinal transit time.
Differences between pre and post-trans-anal irrigation (TAI) adoption in the 12 patients who completed the study.
| Variables | Pre-TAI (n = 12) | Post-TAI (n = 12) | |
|---|---|---|---|
|
| 44 [41.5–65] | 27 [12–44.5] | 0.0022* |
|
| 3.5 [1–5] | 11.5 [7–12] | 0.0024* |
|
| 6.5 [3.5–15.5] | 1 [1–3.5] | 0.0024* |
|
| 11 [9.5–15] | 4 [3.5–6.5] | 0.0021* |
|
| 9 [7–14.5] | 1 [1–3] | 0.0022* |
|
| 0 [0–5.5] | 0 [0–2.5] | 0.0466* |
|
| 76.8 [51.6–104.4] | 56.4 [37.2–90.2] | 0.3877 |
A-W, Agachan-Wexner constipation score; FI-CCI, Fecal Incontinence Cleveland Clinic Index; NBD, neurogenic bowel dysfunction; ODS, obstructed defecation syndrome (or Altomare Questionnaire); PAC-QoL, Patient Assessment of Constipation Quality of Life; TT, intestinal transit time.
Figure 3.The gut microbiota of multiple sclerosis (MS) patients compared to healthy controls. (a) Alpha diversity estimated according to the inverse Simpson index for MS patients at baseline (T0) and age- and sex-matched healthy controls from the same geographical area. A trend towards greater diversity was observed for MS patients (p = 0.08; Wilcoxon test). (b) Principal Coordinates Analysis (PCoA) based on Bray–Curtis dissimilarity between the genus-level profiles of MS patients and healthy controls. Significant separation between groups was found (p = 0.001; permutation test with pseudo-F ratio). Ellipses include a 95% confidence area based on the standard error of the weighted average of sample coordinates. (c) Boxplots showing the relative abundance distribution of genera differentially represented between study groups (p < 0.05; Wilcoxon test).
Figure 4.The gut microbiota dynamics in multiple sclerosis (MS) patients undergoing trans-anal irrigation (TAI). (a) Alpha diversity estimated according to the number of observed Operational Taxonomic Units (OTUs) and the Chao1 index. A significant increase was observed over time with both metrics (*, p < 0.05; Wilcoxon test). (b) Bar plots showing the phylum (left) and family (right)-level composition of the gut microbiota (GM) of MS patients during TAI adoption. Only taxa with relative abundance >0.1% in at least 1 sample are shown. (c) Boxplots showing the relative abundance distribution of genera differentially represented over time (*, p < 0.05; #, 0.05
Figure 5.Beta diversity of the gut microbiota of multiple sclerosis (MS) patients during trans-anal irrigation (TAI) adoption. Principal Coordinates Analysis (PCoA) based on unweighted (left) and weighted (right) UniFrac distances between faecal samples from MS patients during TAI adoption. No significant separation was found over time (p = 1; permutation test with pseudo-F ratio). Ellipses include a 95% confidence area based on the standard error of the weighted average of sample coordinates. T0, baseline; T1–T4, samples collected once a week during TAI adoption for up to 1 month.
Figure 6.Associations between genus-level relative abundances and ms-related bowel dysfunction variables before and after the adoption of trans-anal irrigation (TAI). Statistically significant correlations (p < 0.05) or trends (p < 0.1) with an absolute Kendall rank correlation coefficient >0.4 are shown. Black dots, T0 (baseline); blue dots, T4 (after 1 month of TAI adoption).