Breath Tests for the Non-invasive Diagnosis of Small Intestinal Bacterial Overgrowth: A Systematic Review With Meta-analysis

Abstract

Background/Aims

Small intestinal bacterial overgrowth (SIBO) diagnosis is usually based on non-invasive breath tests (BTs), namely lactulose BT (LBT) and glucose BT (GBT). However, divergent opinions and problems of parameter standardization are still controversial aspects. We aim to perform a meta-analysis to analyze diagnostic performance of LBT/GBT for SIBO diagnosis.

Methods

We searched in main literature databases articles in which SIBO diagnosis was achieved by LBT/GBT in comparison to jejunal aspirate culture (reference gold standard). We calculated pooled sensitivity, specificity, positive, and negative likelihood ratios and diagnostic odd ratios. Summary receiver operating characteristic curves were drawn and pooled areas under the curve were calculated.

Results

We selected 14 studies. Pooled sensitivity of LBT and GBT was 42.0% and 54.5%, respectively. Pooled specificity of LBT and GBT was 70.6% and 83.2%, respectively. When delta over baseline cut-off > 20 H₂ parts per million (ppm) was used, GBT sensitivity and specificity were 47.3% and 80.9%; when the cutoff was other than and lower than > 20 ppm, sensitivity and specificity were 61.7% and 86.0%. In patients with abdominal surgery history, pooled GBT sensitivity and specificity gave the impression of having a better performance (81.7% and 78.8%) compared to subjects without any SIBO predisposing condition (sensitivity = 40.6% and specificity = 84.0%).

Conclusions

GBT seems to work better than LBT. A cut-off of delta H2 expired other than and lower than > 20 ppm shows a slightly better result than > 20 ppm. BTs demonstrate the best effectiveness in patients with surgical reconstructions of gastrointestinal tract.

Introduction

Small intestinal bacterial overgrowth (SIBO) is a disease characterized by an increased concentration of bacteria in the small bowel.¹ In healthy subjects, less than 10³ organisms/mL are found in the upper small intestine, and the majority of these are Gram-positive organisms. In addition to the absolute number of organisms, the type of microbial flora seems to play an important role in the appearance of signs and symptoms.² Gram-negative bacteria may produce toxins that damage the intestinal mucosa, inhibiting the absorptive function.³

SIBO develops when the normal mechanisms that control the growth of enteric bacteria are compromised. Several processes predispose to bacterial overgrowth such as anatomical/structural changes of the small intestine (previous gastrointestinal surgery), motility disorders (such as gastroparesis), metabolic disorders (gastric hypochlorhydria and diabetes), organ system dysfunctions (cirrhosis, renal failure, chronic pancreatitis, Crohn’s disease, and celiac disease), medications (prolonged use of proton pump inhibitors and antibiotics), and irritable bowel syndrome (IBS).^4–10 The most common symptoms are diarrhea, abdominal pain and bloating, but weight loss, malnutrition, and deficiency of vitamins (B12, D, A, and E) and minerals (iron and calcium) are possible.¹

The flora of SIBO patients is mainly characterized by the prevalence of coliform bacteria and anaerobes, which cause fermentation of carbohydrates, compete with vitamin and micronutrient absorption and engender microscopic mucosal inflammation, thus leading to the above described symptoms.^1,11,12 Most experts suggest that jejunal aspirate culture (with a bacterial colony count ≥ 10⁵ colony-forming units [CFU]/mL) is the gold standard for the diagnosis of SIBO.^1,13 However, culture has several drawbacks, the most important one being the invasiveness of the procedure. Consequently, other non-invasive tests have been advocated for the diagnosis of SIBO. Hydrogen breath tests (H₂BT) have gained growing consensus for this purpose, and the most commonly employed in clinical practice, as well as in the literature, are the lactulose breath test (LBT) and the glucose breath test (GBT).^1,13

Nevertheless, divergent opinions and problems of parameter standardization still represent controversial aspects. Although the Rome Consensus Conference on Hydrogen Breath Tests endorsed the use of GBT over LBT for SIBO diagnosis,¹⁴ LBT is still used in clinical practice. The main reason for prefer LBT to GBT is based on the presumption that GBT is unable to detect the microbiota in the distal SIBO since glucose is rapidly absorbed in the proximal small bowel.¹⁵ Conversely, lactulose is a non-absorbable sugar, which passes through the entire small bowel, and could be more appropriate for the distal SIBO diagnosis. However, LBT results are often affected by gut motility, especially in patients with diarrhea, thus hampering its widespread use.¹⁶

On these bases, we performed a systematic review with meta-analysis to investigate the diagnostic yield (sensitivity and specificity) of LBT and GBT in comparison to the recognized gold standard, ie, jejunal culture. This was the first meta-analysis on the topic, to the best of our knowledge.

Materials and Methods

Eligibility Criteria and Study Selection

Methods of analysis and inclusion criteria were based on “Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA)” recommendations,¹⁷ and its extension for diagnostic test accuracy (PRISMA-DTA) was taken into account.¹⁸ A PRISMA-DTA checklist is provided in the Supplementary Table 1. We excluded review articles, experimental in vitro studies and single case reports. In cases of studies analyzing overlapping periods from the same registry/database, we considered only the studies that examined the longest period and the largest number of patients.

Data Collection Process

A literature search was performed and updated in January 31st 2019. Relevant publications were identified by a research in PubMed, Web of Science, and Scopus. Only in extenso papers were selected, therefore abstracts or conference proceedings were excluded. The search terms were small intestinal bacterial overgrowth, SIBO, breath test, lactulose, and glucose. We used the following string, using Boolean operators AND/OR: (Small intestinal bacterial overgrowth OR SIBO) AND (culture OR breath test OR lactulose OR glucose). We selected only studies in which a breath test (glucose or lactulose) was compared to jejunal aspirate culture in the same group of patients. Titles and abstracts of papers were screened by 2 reviewers (G.L. and E.I.). Successively, data were extracted from the relevant studies by one reviewer and checked by a second reviewer, and thus inserted into dedicated tables. A third reviewer (F.P.) came to a decision on any disagreements.

Reviewers independently extracted from each paper the following data: (1) publication year; (2) country; (3) single- or multi-center study; (4) study design; (5) number of patients included; (6) patients’ age, sex, and main characteristics/symptoms; (7) cutoffs and protocols used for culture and BT; and (8) number of true positive/negative and false positive/negative results. If the study did not provide sufficient data to extract true positive/negative and false positive/negative outcomes, it was excluded from the final analysis.

Summary Measures and Planned Methods of Analysis

The end-point was to estimate the pooled weighted sensitivity, specificity, likelihood ratio for positive and negative tests (PLR and NLR, respectively), and diagnostic odd ratio (DOR) of GBT and LBT in comparison to culture. Summary receiver operating characteristic (SROC) curves were drawn and pooled areas under the curve (AUC) were calculated. A random effect model was followed in all analyses. Indeed, according to the Cochrane handbook Chapter 9.5.4, the choice between a fixed-effect and a random-effects meta-analysis should never be made on the basis of a statistical test for heterogeneity and one model (most often, the random-effects model) should be chosen a priori for all analyses.³³ We assessed heterogeneity using the χ² test and, if statistically significant, the I² statistic was computed. If necessary, a subgroup analysis was performed. The data were expressed as proportions/percentages, and 95% confidence intervals (CI) were calculated. A P-value < 0.05 was considered statistically significant. All analyses were performed according to the general principles of meta-analysis.³⁴ The Meta-Disc software version 1.4 (University of Madrid, Madrid, Spain) was used.³⁵

Two reviewers (G.L. and G.Le.) independently assessed the quality of the included studies using the Quality Assessment of Diagnostic Accuracy Studies version 2 (QUADAS-2) instrument.³⁶ This tool is designed to assess the quality of primary diagnostic accuracy studies for inclusion in the systematic review. Publication bias was conducted by the Deeks’ funnel plot asymmetry test, with P-value < 0.05 for the slope coefficient indicating significant asymmetry.³⁷

Results

Study Selection and Main Features

Fourteen studies, listed in Table 1^19–32 were selected out of 2123 articles found after the literature search. Further details about the process of article selection are reported in the PRISMA flowchart in Figure 1. The PRISMA-DTA checklist is provided as Supplementary Table 1. In all studies, GBT was used and, in 4 of them, both LBT and GBT were considered.^20,23,24,27 In all studies but one²⁹ an adult population was recruited. A total of 757 subjects were selected across all studies.

Table 1.

Main Characteristics of Studies Included in the Meta-analysis

Study	Nation	Cut off for culture	Cut off for BT	BT protocol	Characteristics of enrolled patients
Berthold et al,19 2009	Germany	> 106 CFU/mL	GBT: -maximal excretion 20 ppm during 2 hr -Δ > 20 ppm -sustained increase from baseline > 12 ppm	50 g of glucose in 300 mL of water	21 patients, 8 F/13 M Age mean 50, range 18–73 -8 cirrhosis -6 diabetes -3 IBD -3 chronic gastritis -3 chronic pancreatitis
Corazza et al,20 1990	Italy	> 106 CFU/mL	GBT: Δ > 10 ppm LBT: Δ > 20 ppm or 2 peaks > 10 ppm	GBT: 75 g of glucose in 375 mL water LBT: 12 g of lactulose in 24 mL water Collection every 10 min for 3 hr	77 consecutive patients -21 gastrointestinal resection -7 PPI or anti-H2 -5 atrophic gastritis -4 Crohn’s disease -3 diabetic neuropathy
Donald et al,21 1992	England	> 105 CFU/mL	GBT: Δ > 20 ppm	50 mg of glucose; collection every 15 min for 2 hr	47 elderly patients with signs suggestive of malnutrition Age median 80, range 70–92
Erdogan et al,22 2015	USA	> 103 CFU/mL	GBT: ΔH2 > 20 ppm or ΔCH4 > 15 ppm	75g of glucose in 250 mL water; collection every 15 min for 2 hr	139 subjects with clinical suspicion of SIBO 33 M/106 F, mean age 47
Ghoshal et al,23 2006	India	> 105 CFU/mL	GBT: Δ > 12 ppm LBT: Δ > 20 ppm	Not described	83 patients with malabsorption; 50 M/33 F, mean age 35 range 14–70 -38 tropical sprue -7 celiac disease -7 immunoglobulin deficiency -1 Crohn’s disease -8 intestinal parasites (Giardia, Strongyloides…)
Ghoshal et al,24 2014	India	> 105 CFU/mL	GBT: Δ > 12 ppm LBT: Δ > 20 ppm or double peak	GBT: 100 g of glucose in 200 mL water; collection every 15 min for 3 hr LBT: 10 g of lactulose in 15 mL water; collection every 15 min for 4 hr	80 patients with irritable bowel syndrome; 65 M/15 F; mean age 34 range 17–67
Kaye et al,25 1995	England	> 105 CFU/mL	GBT: Δ > 20 ppm	50 g of glucose in 200 mL water; collection every 15 min for 2 hr	24 scleroderma patients with malabsorption, but only 20 undergo BT 8 M/16 F; mean age 42.5 range 22–63
Kerlin and Wong,26 1988	Australia	> 105 CFU/mL	GBT: Δ > 12 ppm	50 g of glucose in 250 mL water; collection every 30 min for 4 hr	45 patients with diarrhea, steatorrhea; 17 of them with gastrointestinal resections
King and Toskes,27 1986	USA	> 106 CFU/mL	GBT and LBT; double peak with Δ > 10 ppm or any peak with Δ > 20 ppm	GBT: 80 g of glucose in 300 mL water LBT: 10 g of lactulose in 300 mL water; collection every 5 min in the first 40 min, then every 10–15 min for 3 hr	30 patients with diarrhea, 20 of them with gastrointestinal resections
Mac Mahon et al,28 1996	Ireland	> 105 CFU/mL	GBT: Δ > 10 ppm	50 g of glucose in 250 mL water; collection every 20 min for 2 hr	30 elderly patients, 9 of them with Billroth II resection 19 F/11 M; mean age 79 range 69–90
Pignata et al,29 1990	Italy	> 105 CFU/mL	GBT: Δ > 10 ppm	Water solution of glucose 10% concentration; 2g/Kg	17 children (age range 2–17) with primary immunoglobulin deficiency; only 12 of them undergone culture
Rao et al,30 2018	Germany	> 103 CFU/mL	GBT: ΔH2 > 20 ppm or ΔCH4> 15 ppm or combined Δ> 15 ppm	75 g of glucose in 250 mL water; collection every 15 min for 2 hr	50 colectomy patients (56% partial, 22% subtotal, 22% total); 50 healthy controls 41 F/9 M; mean age 52.3 range 20–85
Stotzer and Kilander,31 2000	Sweden	> 105 CFU/mL	GBT: Δ > 15 ppm	50 g of glucose in 250 mL water; collection every 15 min for 2 hr	46 patients with diarrhea, 16 of them with predisposing conditions -5 partial gastric resection -3 atrophic gastritis -2 small bowel diverticula Mean age 57 range 27–87
Sundin et al,32 2018	USA	> 105 CFU/mL	GBT: ΔH2 > 20 ppm ΔCH4 > 10 ppm	90 g of glucose in 100 mL water; collection every 20 min for 3 hr	18 patients with clinical suspicion of SIBO; 4 M/14 F, age range 26–79

BT, breath test; CFU, colony-forming units; GBT, glucose breath test; LBT, lactulose breath test; F, female; M, male; IBD, inflammatory bowel disease; PPI, proton pump inhibitor; SIBO, small intestinal bacterial overgrowth.

Figure 1.

Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) flow diagram reporting the process of study selection. BT, breath test.

The quality of studies is reported in Supplementary Table 2. All studies achieved a good score, except for the “reference standard” regarding its applicability concern domain. Indeed, it could be expected that a routine jejunal culture cannot be always applied, being an invasive test, even for ethical reasons.

Performance of Glucose Breath Test and Lactulose Breath Test

In all the 14 studies,^19–32 GBT was used in comparison to jejunal culture. In total, 668 patients were considered. The pooled sensitivity was 54.5% (95% CI, 48.20–60.70), and heterogeneity was present (χ² = 61.52, P < 0.001, I² = 78.9%). Pooled specificity was 83.2% (95% CI, 79.10–86.90) and heterogeneity was detected (χ² = 54.76, P < 0.001, I² = 76.3%), as shown in Figure 2A and 2B. In Figure 2C–E pooled PLR, NLR, and DOR are reported. PLR was 2.45 (95% CI, 1.51–3.97), with high heterogeneity (χ² = 38.6, P < 0.001, I² = 66.3%). NLR was 0.60 (95% CI, 0.45–0.80) and heterogeneity was found (χ² = 44.58, P < 0.001, I² = 70.8%). Finally, DOR was 5.17 (95% CI, 2.42–11.05) and heterogeneity was present (χ² = 35.06, P = 0.001, I² = 62.9%). The SROC curve (Fig. 2F) had a pooled AUC = 0.74 ± 0.07.

Figure 2.

Forest plot of pooled sensitivity (A), specificity (B), pooled positive (C) and negative (D) likelihood ratio (LR), diagnostic odd ratio (E), and summary receiver operating characteristic (SROC) curve (F) of glucose breath test for small intestinal bacterial overgrowth diagnosis. AUC, area under the curve.

The Deeks’ funnel plot for this analysis, reported in Supplementary Figure 1, showed a symmetrical distribution of studies, confirmed by a corresponding test for the slope, with P = 0.813. Therefore, no publication bias was detected.

A comparison between LBT and jejunal culture was possible only in 4 studies,^20,23,24,27 enrolling 214 patients overall. The pooled sensitivity was 42.0% (95% CI, 31.6–53.0), with presence of heterogeneity (χ² = 12.34, P = 0.006, I² = 75.7%). Pooled specificity was 70.6% (95% CI, 61.9–78.4) and heterogeneity was detected (χ² = 17.46, P = 0.001, I² = 82.8%), as reported in Figure 3A and 3B. In Figure 3C–E, pooled PLR, NLR, and DOR are shown. PLR was 1.30 (95% CI, 0.77–2.22), and in this case no heterogeneity was found (χ² = 4.22, P = 0.24, I² = 28.9%). NLR was 0.79 (95% CI, 0.57–1.08) and heterogeneity was absent (χ² = 6.772, P = 0.08, I² = 55.4). Finally, DOR was 1.77 (95% CI, 0.72–4.37), and we did not find heterogeneity (χ² = 4.48, P = 0.21, I² = 33%). The SROC curve (Fig. 3F) had a pooled AUC = 0.56 ± 0.09.

Figure 3.

Forest plot of pooled sensitivity (A), specificity (B), pooled positive (C) and negative (D) likelihood ratio (LR), diagnostic odd ratio (E), and summary receiver operating characteristic (SROC) curve (F) of lactulose breath test for small intestinal bacterial overgrowth diagnosis. AUC, area under the curve.

We did not detect publication bias for this analysis, since the test for funnel plot (Supplementary Fig. 2) provided a P-value of 0.250.

Sub-analysis According to Population Sub-categories

A sample size sufficient to perform sub-analysis was possible only for GBT. Indeed, only 4 studies were focused on LBT, so this sub-analysis would have low statistical power with such a small number of articles.

The sub-category of patients who had undergone previous gastrointestinal surgery was considered in 6 studies.^{20,26,28,30,31} The most common surgical procedures were partial gastrectomy and colectomy. We were able to extract sufficient data for sub-group meta-analysis from only 3 studies (93 subjects in total). Pooled sensitivity and specificity were 81.7% and 78.8%, respectively. PLR was 3.23 and NLR was 0.20; overall DOR was 18.58. Finally, AUC was 0.86 ± 0.09. Further details of this sub-analysis are reported in Table 2.

Table 2.

Performance of Glucose Breath Test According to Some Discriminating Factors

Subgroups	Value (95% CI)	Heterogeneity			Publication bias
		χ2	P-value	I2 (%)	P for funnel plot
Patients undergone gastrointestinal surgery					0.781
Sensitivity	81.7% (69.6–90.5)	10.83	0.004	81.6
Specificity	78.8% (61.1–91.0)	2.82	0.242	29.1
PLR	3.23 (1.52–6.89)	2.45	0.291	18.5
NLR	0.20 (0.04–1.00)	11.39	0.003	82.4
DOR	18.58 (2.04–169)	6.41	0.040	68.8
AUC-SROC	0.86 ± 0.09
Patients without predisposing conditions					0.192
Sensitivity	40.6% (31.1–50.5)	28.86	< 0.001	82.7
Specificity	84.0% (78.7–88.4)	39.60	< 0.001	87.4
PLR	1.64 (0.75–3.62)	18.31	0.001	72.7
NLR	0.84 (0.63–1.13)	15.94	0.007	68.6
DOR	2.32 (0.71–7.58)	13.58	0.020	63.2
AUC-SROC	0.59 ± 0.14
Diagnostic cut off for culture > 103 CFU/mL					NE
Sensitivity	40.7% (30.5–51.5)	0.13	0.711	0.0
Specificity	84.0% (75.6–90.4)	0.04	0.843	0.0
PLR	2.54 (1.54–4.19)	0.13	0.720	0.0
NLR	0.71 (0.58–0.86)	0.18	0.670	0.0
DOR	3.59 (1.84–6.99)	0.15	0.700	0.0
AUC-SROC	NE
Diagnostic cut off for culture > 105 CFU/mL					0.722
Sensitivity	55.3% (47.9–62.6)	53.67	< 0.001	83.2
Specificity	83.9% (79.4–87.7)	44.04	< 0.001	79.6
PLR	2.61 (1.47–4.62)	25.23	0.001	69.2
NLR	0.59 (0.42–0.85)	36.00	< 0.001	75.0
DOR	5.88 (2.35–14.91)	25.86	0.002	65.2
AUC-SROC	0.77 ± 0.08
Diagnostic cut off for culture > 106 CFU/mL					0.513
Sensitivity	62.5% (45.8–77.3)	3.55	0.174	43.6
Specificity	77.4% (58.9–90.4)	9.94	0.007	79.9
PLR	2.74 (0.41–18.27)	9.63	0.008	79.2
NLR	0.54 (0.21–1.36)	7.34	0.020	72.8
DOR	5.35 (0.38–74.3)	8.41	0.011	76.2
AUC-SROC	0.37 ± 0.14
Diagnostic cut off for GBT delta > 20 ppm					0.871
Sensitivity	47.3% (38.4–56.3)	27.43	< 0.001	78.1
Specificity	80.9% (74.8–86.0)	15.63	0.020	61.6
PLR	1.95 (0.92–4.11)	17.76	0.007	66.2
NLR	0.66 (0.43–1.02)	27.81	< 0.001	78.4
DOR	3.35 (1.03–10.89)	20.38	0.002	70.6
AUC-SROC	0.70 ± 0.23
Diagnostic cut off for GBT delta > 12 ppm (or other lower than 20)					0.884
Sensitivity	61.7% (52.7–70.2)	28.67	< 0.001	79.1
Specificity	86.0% (80.0–90.7)	37.37	< 0.001	83.9
PLR	3.20 (1.51–6.75)	21.71	0.001	72.4
NLR	0.54 (0.37–0.78)	14.15	0.030	57.6
DOR	8.11 (3.01–21.82)	12.29	0.061	51.2
AUC-SROC	0.79 ± 0.07

PLR, positive likelihood ratio; NLR, negative likelihood ratio; DOR, diagnostic odd ratio; AUC-SROC, area under the curve of summary receiver operating characteristic; CFU, colony-forming units; NE, not estimable for only 2 studies; GBT, glucose breath test.

AUC-SROC data are presented as mean ± SD.

In the group of patients without any predisposing conditions, we included subjects in which factors predisposing to SIBO such as abdominal surgery, celiac disease, connective tissue disorders, and others as listed in.^4–10 In 6 studies the sub-category of patients without any predisposing conditions was considered.^{21,22,24,28,30,32} Three hundred and forty patients were enrolled in this subgroup, which was constituted mainly by healthy controls, elderly patients with diarrhea, and IBS patients. Pooled sensitivity, specificity, PLR, and NLR were 40.6%, 84.0%, 1.64, and 0.84, respectively. Pooled DOR was 2.32 and AUC was 0.59 ± 0.14. If we selected only asymptomatic healthy controls, only 30 subject could be recruited, providing a pooled sensitivity of 9.1%, a specificity of 66.9%, PLR = 0.86, NLR = 1.02, and DOR= 0.01. Further details of these sub-analyses are reported in Table 2.

We did not find publication bias in any of the sub-analyses, since the test for Deeks’ funnel plot was not statistically significant, as reported in Table 2.

Sub-analysis According to Diagnostic Cut-off Values

Culture

Only in 2 studies a value of > 10³ CFU/mL was chosen.^22,30 The pooled sensitivity and specificity were 40.7% and 84.0% respectively. Additionally we found PLR = 2.54, NLR = 0.71, and DOR = 3.59. It was not possible to draw a SROC only for 2 studies.

A cut off > 10⁵ CFU/mL was reported in most of the studies and provided an overall sensitivity of 55.3% and a specificity of 83.9%. PLR, NLR, and DOR were respectively 2.61, 0.59, and 5.88. AUC was 0.77 ± 0.08 (Table 2).

Three studies used a value > 10⁶ CFU/mL.^19,20,27 In this case we found a pooled sensitivity and specificity of 62.5% and 77.4%, respectively. PLR was 2.74, NLR was 0.54, and DOR was 5.35. AUC was 0.37 ± 0.14.

Glucose breath test

A delta value > 20 ppm was used in 7 studies, with 333 patients,^{19,21,22,25,27,30,32} while a value other than and lower than > 20 ppm (> 10, > 12, or > 15) was used in 7 papers (306 patients).^{20,23,24,26,28,29,31}

A cut off > 20 ppm provided a pooled sensitivity of 47.3% and specificity of 80.9%. Overall PLR, NLR, and DOR were 1.95, 0.66, and 3.35, respectively. AUC of SROC was 0.70 ± 0.23.

On the other hand, a cut off other than and lower than > 20 ppm showed a pooled sensitivity and specificity of 61.7% and 86.0%, respectively. Pooled PLR was 3.2, NLR was 0.54, and DOR was 8.11. SROC curve analysis demonstrated an AUC = 0.79 ± 0.07.

Only one study considered the “double peak” as a diagnostic criterion, therefore a sub-analysis was not possible.²⁷ No study considered high basal hydrogen levels as a SIBO diagnostic criterion.

We did not find publication bias in any sub-analysis, since the test for Deeks’ funnel plot was not statistically significant.

Further details about all above mentioned sub-analyses are shown in Table 2.

Discussion

SIBO is a condition characterized by an abnormal colonization of the small bowel by colonic bacteria. The most commonly used diagnostic tools in clinical practice are H₂BTs, however their validation, in comparison to jejunal aspirate culture has shown several pitfalls. Only one systematic review investigated this topic, showing that LBT exhibited a sensitivity ranging from 31% to 68% and a specificity of 44–100%, while GBT showed a range of sensitivity of 20–93% and a specificity of 30–86% across cited studies.³⁸ However, a quantitative examination with a pooled analysis of such data was lacking until now. Therefore, to the best of our knowledge, the present study is the first meta-analysis regarding the performance of H₂BT for SIBO diagnosis.

Our first aim is to ascertain whether GBT and LBT could give similar results in diagnostic accuracy. Indeed, despite the Rome consensus that discouraged the use of LBT,¹⁴ some opinions disagree because LBT could be more effective than GBT in the case of “distal SIBO.” Overall, our results clearly showed that GBT had higher sensitivity and specificity than LBT, and even a better AUC (0.74 versus 0.56). Therefore, our results seem to confirm the statement of the Rome consensus. The poorer performance of LBT may have different explanations. First, the results of LBT are highly influenced by the bowel transit time.³⁹ Therefore, since lactulose is not absorbed in the small bowel, it might rapidly pass into the colon where it could be degraded by colonic bacteria with rapid hydrogen production,⁴⁰ thus leading to false positivity. Additionally, patients with fast transit will display an early peak that may be misinterpreted as SIBO. It is possible that these factors could have affected our finding of low LBT specificity (70.6%) when compared to that of GBT (83.2%). False negative H₂BT results may even be found in non-hydrogen producers: in this case, additional measurement of methane in the breath may improve the diagnosis.⁴¹ However, despite 3 among 14 that estimated methane,^22,30,32 only one study expressed results in a way satisfactory to extract data, therefore a meta-analysis was not possible. We believe that this is a relevant limitation of our analysis, since we were not able to assess the impact of methane detection on BT performance.

Recently, the North American consensus on BT established that a rise of > 20 ppm from baseline should be the optimal cut off for GBT.⁴² In our analysis, 7 studies used this cutoff, providing an overall sensitivity of 47.3% and a specificity of 80.9%, with AUC = 0.70. However, we demonstrated that the performance of GBT was slightly superior, with a sensitivity and specificity of 61.7% and 86.0%, respectively, and AUC = 0.79, when a lower cut off (delta other than and lower than > 20 ppm) was established. Even the DOR was much higher (8.11 versus 3.35) in this case. Therefore, our results suggest that a cut off value other than and lower than > 20 ppm as suggested by the Rome consensus may provide better sensitivity and specificity than the cut off value of > 20 ppm proposed by North American Consensus.

Another strongly debated point is linked to the culture of jejunal aspirate. So far, the gold standard test for SIBO diagnosis has been the culture of jejunal aspirate. It is obtained by means of patient intubation and aspiration at multiple intestinal sites, more rarely during enteroscopy. The amount of liquid, the site of collection (traditionally beyond the ligament of Treitz) and the technical details of the microbiological tests (for both aerobic and anaerobic bacteria), as well as the cut-off value for definition of SIBO are not yet standardized, although many studies use a value of > 10⁵ CFU/mL. Indeed, even if it has been considered so far as the gold standard for SIBO diagnosis, recent evidence and opinions have questioned this statement. First, the cut off value of > 10⁵ CFU/ mL, which was the most widespread in literature, is no longer considered reliable, and the North American consensus has proposed a level of > 10³ CFU/mL. In our systematic review, only 2 studies employed this cut off; as the specificity (84.0%) was high and comparable to other cut-offs, the sensitivity was very low (40.7%), but the scanty number of patients enrolled in this sub-analysis (only 197) is a limit for the discussion of this result. Most of studies used a value of 10⁵ CFU/mL and 3 reports used a value of 10⁶ CFU/ mL. As reported in more detail in Table 2, a value of 10⁵ CFU/ mL provided a slightly higher sensitivity, but lower specificity, while the DOR, PLR, and NLR were comparable. Therefore, it seems that these 2 cut off values could be interchangeable but further studies using the 10³ CFU/mL value are necessary to ascertain the suitability of the North American consensus recommendation. On the other hand, the clinical practice of jejunal culture has several drawbacks. First, it is an invasive procedure that requires a catheter to be placed by endoscopic or fluoroscopic guide. Therefore, patient compliance for this cumbersome procedure aimed to diagnose a hypothetical benign disease is presumably very low. Moreover, it is necessary to use a sterilized catheter and to avoid contact with the oral mucosa, which could cause contamination by oral flora. The limitation of culture for SIBO has been highlighted by Sundin et al,³² who showed that cultures may frequently underestimate the real bacterial load and that the correlation between microbiological results and BT results is weak. Moreover, metagenomic studies have shown that jejunal culture could not detect up to 80.0% of bacterial species, since there are some strains that are not culturable.⁴³

Another interesting finding of our work was that, in patients with surgical reconstruction of the gastrointestinal tract, sensitivity was higher (81.7% versus 40.6%) than in subjects without a predisposing condition. Even the AUC was much better (0.86 versus 0.59), meaning an overall better performance of GBT in this group of patients. A possible explanation is that the prevalence of SIBO may reach the 61.6% in operated patients who are likely to suffer from leakage of anatomical or chemical mechanisms hampering the overgrowth of bacteria in the small bowel.^44,45 For instance, in gastrectomy patients, reduction of acid secretion is a predisposing factor. Additionally, the lack of a “gastric brake” may lead to early stomach emptying, which is the basis of the dumping syndrome as well. Therefore, if the small bowel is rapidly filled up by a hyperosmotic fluid, the excessive sugar content will be degraded by bowel flora, thus leading to bacterial overgrowth. In this perspective, it has been observed that SIBO might be one of the most important causes of post-gastrectomy syndrome associated with intestinal symptoms and late hypoglycemia, and that gas-related symptoms (bloating and abdominal fullness) occur simultaneously with GBT hydrogen peak, suggesting that they could originate from small intestinal bacteria.⁴⁶ Similarly, patients with multiple ileal resections or ileo-cecal valve resection have an increased SIBO risk because of the absence of the ileo-cecal valve, which is a mechanical structure hindering the reflux of colonic bacteria into the small bowel.⁴⁷ Furthermore, we found a quite low BT performance in patients without predisposing conditions. In all the studies we selected, this group of patients was mainly represented by IBS patients. In this regard, despite various meta-analyses showing an increased risk of SIBO in IBS,⁷ recent evidence has shown that BTs have low sensitivity and specificity (around 60.0%) to diagnose SIBO in IBS patients, which is in agreement with our results.^48,49

Some limitations of our study need to be mentioned. For example, the difference in protocols and glucose dose may be an important source of heterogeneity among studies that could not be solved by sub-analysis grouping. Furthermore, sub-analysis often led to grouping of a small number of studies, for instance the analysis of patients with surgical interventions enclosed only 3 studies. Additionally, a head-to-head comparison of GBT and LBT is lacking, and this may be an obstacle to conclude whether GBT is really superior to LBT, despite the results of our analysis. Finally, it is important to be aware that when the number of studies is low, the power of the test for publication bias is low, an event that took place in several subgroup analyses: this underlines the need for additional studies to solve this drawback.

In conclusion, our meta-analysis suggests that GBT has high values of diagnostic yield, more than LBT and, therefore, it should be preferred as suggested by guidelines.^14,42 However, few studies have proposed a head-to-head comparison of these 2 tests,^20,23,24 therefore this direct comparison calls for further investigations and this represents an additional limitation. Additionally, a GBT cut off value with a delta other than > 20 ppm seems to work better, in contrast to that proposed by the North American consensus, and this will be relevant food for thought in future investigations. Finally, the microbiological diagnosis of SIBO is still an unanswered question: a quantitative cut-off is not sufficient, while a qualitative analysis of the microbiota would be preferable, because SIBO is a dynamic syndrome with many differences due to several distinct triggering pathological conditions.^50,51 For such reasons, BT⁵² remain the mainstay for the non-invasive diagnosis of SIBO even if some limitations should be taken into account. Noteworthy, the performance of BT is optimal only when performed in selected populations by using the best available protocol.^53,54