D-lactic acidosis is characterized by brain fogginess (BF) and elevated D-lactate and occurs in short bowel syndrome. Whether it occurs in patients with an intact gut and unexplained gas and bloating is unknown. We aimed to determine if BF, gas and bloating is associated with D-lactic acidosis and small intestinal bacterial overgrowth (SIBO).
Patients with gas, bloating, BF, intact gut, and negative endoscopic and radiological tests, and those without BF were evaluated. SIBO was assessed with glucose breath test (GBT) and duodenal aspiration/culture. Metabolic assessments included urinary D-lactic acid and blood L-lactic acid, and ammonia levels. Bowel symptoms, and gastrointestinal transit were assessed.
Thirty patients with BF and 8 without BF were evaluated. Abdominal bloating, pain, distension and gas were the most severe symptoms and their prevalence was similar between groups. In BF group, all consumed probiotics. SIBO was more prevalent in BF than non-BF group (68 vs. 28%, p = 0.05). D-lactic acidosis was more prevalent in BF compared to non-BF group (77 vs. 25%, p = 0.006). BF was reproduced in 20/30 (66%) patients. Gastrointestinal transit was slow in 10/30 (33%) patients with BF and 2/8 (25%) without. Other metabolic tests were unremarkable. After discontinuation of probiotics and a course of antibiotics, BF resolved and gastrointestinal symptoms improved significantly (p = 0.005) in 23/30 (77%).
We describe a syndrome of BF, gas and bloating, possibly related to probiotic use, SIBO, and D-lactic acidosis in a cohort without short bowel. Patients with BF exhibited higher prevalence of SIBO and D-lactic acidosis. Symptoms improved with antibiotics and stopping probiotics. Clinicians should recognize and treat this condition.
Abdominal bloating, gas and distension are common gastrointestinal symptoms that are caused by many conditions including carbohydrate intolerance and small intestinal bacterial overgrowth (SIBO)1. Brain Fogginess (BF) describes a constellation of symptoms comprised of mental confusion, impaired judgment, poor short-term memory, and difficulty with concentration, which is often transient and disabling. Previously, similar symptoms, along with slurred speech and gait disturbances have been described in patients with short bowel syndrome2,3. These patients were found to have metabolic acidosis with elevated levels of D-lactic acid in the serum. Others have described brain fogginess in association with other chronic disorders including postural orthostatic tachycardia syndrome4,5. Recently, probiotic use has been implicated in the production of D-lactic acidosis, both in short bowel syndrome patients and in the first 2 weeks of life in infants who were fed probiotic-containing formula6,7. Typically, D-lactic acidosis is caused by the fermentation of ingested carbohydrate by D-lactic producing bacteria such as lactobacillus and bifidobacterium in the bowel2,3.
In a preliminary report, we described seven patients who presented with both unexplained abdominal bloating and BF and who were consuming probiotics8. Whether there is a link between abdominal bloating, distention, gas, D-lactic acidosis, and small intestinal bacterial overgrowth (SIBO), and probiotic usage is not known. We examined whether small intestinal bacterial overgrowth (SIBO), particularly with D-lactic acid producing bacteria may cause a syndrome of BF, gas, bloating, and neurocognitive symptoms.
Our aim was to evaluate a consecutive series of patients with unexplained BF, abdominal bloating and gas, for SIBO, using both duodenal aspirate and cultures, and a glucose breath test (GBT), and simultaneously assess for metabolic acidosis.
We conducted a prospective observational study of consecutive adult patients referred to our tertiary care center over 3 years. Patients presenting with unexplained abdominal gas, bloating and distension, and BF were included. BF was defined as presence of two or more of the following symptoms for more than 3 months during their initial clinic visit: mental confusion, cloudiness, impaired judgment, poor short-term memory, and difficulty with concentration. Given the multiple constellation of abdominal symptoms, our patients could not be definitively categorized into any one of the Rome III classification of functional gastrointestinal disorders, and hence they were categorized as unexplained symptoms. Additionally only subjects with normal upper endoscopy and duodenal biopsy, normal colonoscopy and biopsy, and normal abdominal CT imaging, and normal hematological and biochemical profiles were enrolled. Patients with a history of small bowel or colonic surgery, those with known intestinal dysmotility (scleroderma or pseudo-obstruction), and those with a history of recent antibiotic use (in the previous 6 weeks), or history of known neurological or neuropsychiatric problems or celiac disease or Helicobacter Pylori infection or renal or liver failure were excluded from the study. We also evaluated a cohort of patients with similar symptom profiles and who met the inclusion and exclusion criteria, but without brain fogginess (Non-BF). The institutional review board approved this study, number 611925–2.
All patients filled out a validated questionnaire9 that assessed 9 symptoms; abdominal pain, belching, bloating, fullness, indigestion, nausea, diarrhea, vomiting and gas. The frequency, intensity and duration of each symptom was rated on a 0–3 point Likert scale8,9,10. A mean total score was calculated, and symptoms were assessed at baseline and after treatment. A score ≥5 was considered severe. All patients were followed up for 6 months. Additionally, we inquired about probiotic use, a history of food fads, yogurt consumption, and use of over the counter medications and recent antibiotic use. Patients were asked to discontinue the use of laxatives and drugs that affect intestinal motility (opioids, anticholinergics, and anti-diarrheals) at least one week prior to the study, but were allowed to continue with other maintenance medications.
Patients had duodenal aspirate and cultures and glucose breath test within one week10,11,12. No new medications were allowed during testing. Blood samples were collected for bun, electrolytes, creatinine and liver biochemistry. Metabolic testing included assessment of blood glucose, insulin, ammonia and L-lactate levels and urinary D-lactic acid levels after a carbohydrate challenge. Assessment of gastrointestinal transit consisted of the wireless motility capsule test (SmartPill ®, Medtronic Corporation, Minneapolis, MN) where a subject ingested a capsule containing pressure, pH, and temperature sensors, and wore a recorder for 5 days to assess regional and whole gut transit13,14. Alternatively, they had a gastric emptying test with radioactive technetium meal and a colonic transit test where the subject ingested a capsule with 24 radio-opaque markers and had a plain abdomen X-ray at 120 h13,14.
After an overnight fast, an upper endoscope was passed into the distal duodenum with minimal air insufflation. Using aseptic technique, a 2 mm nasobiliary catheter (Liguory ®, COOK Medical, Bloomington, IN, US) was advanced through the endoscope into the distal duodenum, and 3–5 ml of fluid was aspirated and sent to the microbiology laboratory for standard aerobic, anaerobic and fungal cultures. The duodenal culture results were considered as positive for SIBO if one or more organisms (aerobic or anaerobic) were cultured with a colony count of ≥103 CFU/ml10,11.
After an overnight fast, 75 g of glucose dissolved in 250 ml water was administered orally. Breath samples were obtained at baseline and at 15 min intervals for 2 h, and analyzed for both hydrogen and methane using gas chromatography (QuinTron Micro Analyzer ®, QuinTron Instrument Company Inc. Milwaukee, WI)10,11,12. Throughout the study, the patients scored the presence and severity of symptoms on a likert scale7. GBT was considered positive for SIBO if there was ≥20 p.p.m. increase above baseline for H2 or for combined H2 and CH411,15,16,17,18. In 3 subjects with diabetes, fructose breath test was performed using previously described methods19.
In order to assess lactic acidosis we used a novel method of assessing blood and urine lactic acid levels after an oral carbohydrate challenge (Glucose) i.e., simultaneously alongside the glucose breath test. Blood samples were collected at baseline, 1/2, 1, 2, and 3 h after administration of glucose, and sent for serum L-lactic acid, and ammonia levels. L-Lactic acid levels ≥2.2 mmo/L were considered positive and indicative of acidosis. Urine samples for D-lactic acid were collected at baseline, 1 h, and 3 h during and after the GBT and analyzed in specialist lab (Mayo Clinic Laboratories, Rochester, MN). D-Lactic acid levels ≥0.22 mmol/L were considered abnormal and indicative of acidosis. Urinary as opposed to blood D-lactic acid assessment was chosen due to its stability at room temperature and for remote processing as recommended by the specialist lab.
Symptoms and global satisfaction data were compared before and after treatment using Chesapeake Test. CHI square test was used to compare data between the BF and non-BF groups with regards to the prevalence of D-lactic acidosis, and SIBO and symptoms.
We evaluated a total of 42 patients, of whom 34 had BF and 8 had no BF (non-BF) (Fig. 1). Four patients in the BF group were excluded because of recent antibiotic use (1), inability to complete all tests or technical problems with collection/transport of samples (2), and new diagnosis of Parkinson’s disease (1). Thirty patients, f/m = 19/11, mean age 52 years were included (Table 1A). Six patients were on gluten-restricted, 3 on FODMAP-restricted, and 1 on Paleo diets. All 8 patients (f/m = 5/3, mean age 49 years) in the non-BF group met inclusion criteria (Table 1B). Two patients were on FODMAP restricted diet.
SIBO small intestinal bacterial overgrowth
The most common symptoms in the BF group were abdominal pain (96.7%), bloating (93.3%), distention (90%), fullness (90%), gas (90%), cramping (80%), diarrhea (76.7%), and belching (90). Severe bloating with significant and rapid increase in abdominal size from normal to full distension within few minutes was described by 6/30 (20%) patients in BF group only. In the non-BF group, the most common symptoms were abdominal pain (75%), bloating (100%), distention (88%), fullness (88%), gas (100%), belching (88%), diarrhea (50%), and cramping (75%). Severe symptoms (≥5), were pain, bloating, distention, and gas in both groups.
Neurocognitive symptoms including BF or mental confusion or impaired judgment, poor short-term memory, and difficulty with concentration were described by all of the patients in the BF group. These symptoms lasted between 30 min to several hours, often post-prandial, and intermittently during the course of the day. Also 28/30 (94%) patients reported post-prandial fatigue and weakness, and 2/30 reported persistent daily fatigue unrelated to meal intake. BF was so severe that 4/30 (13.3%) had quit their jobs. One patient had recurrent near syncopal episodes after carbohydrate-rich meals. One patient had symptoms of bloating and BF with a blistering rash on the palms. Another patient’s symptoms caused her to be bed-ridden for up to a week after consuming a large carbohydrate-rich meal.
All patients in the BF group were taking probiotics (range 3 months to 3 years), some were taking 2–3 different varieties containing lactobacillus species, and/or bifidobacterium species or streptococcus thermophillusand others. Additionally 11 (36.7%) were using cultured yogurt daily, and 2 (6.7%) large amounts (20 oz.) of homemade cultured yogurt daily. Opioid use was found in 7/30 (23.3%), and PPI use and multivitamins in 13/30 (43.3%). Fish Oil and Biotin supplementation in 4/30 patients and 1/30 (3.3%) were taking ubiquinone, dessicated thyroid, simethicone, melatonin, curcumin, saw palmetto, samento extract, and artemisinin extract. One patient (12%) in the non-BF group took probiotics (Lactobacillus rhamnosus), 3/8 (37%) were using PPI, 3/8 (37%) multivitamin and fish oil supplements, and one opioids.
In the BF group, breath testing was positive for SIBO in 11/30 (36.6%) patients (Table 1, Fig. 1). The patient’s typical BF symptom(s) experienced at home was reproduced during the breath test in 20/30 (66%) and all of them had evidence of SIBO either with the breath test or with culture. In the non-BF group, breath test was positive in 1 (14%) and negative in 7 (16%); D-lactic acidosis was seen in 2/7 (28%) patients with negative breath test.
In the BF group, cultures for SIBO were positive in 14 (46.7%) patients and negative in 14 patients (46.7%) (Fig. 2); 2 patients did not have duodenal aspiration. Aerobic strains were grown in 22 (64.7%), and anaerobic bacteria in 9 (26.5%) patients. The predominant aerobic organisms were Streptococcus species, Staphylococcus species, Neisseria species, and Hemophilus species, and the predominant anaerobic organisms were gram negative rods, and cocci, gram positive rods – lactobacillus species, and prevotella species. The disposition of D and/or L-lactic acidosis is summarized in Fig. 2. In the non-BF group, 2/8 (25%) had positive culture for SIBO and one subject grew streptococcus species, and neisseria, and second subject grew rothia species and pseudomonas, and 1/8 (14%) grew candida species.
groups
In the BF group, D-lactic acidosis was seen in 23 (76.7%) patients along with concurrent L-lactic acidosis in 9 (30%) patients (Table 1A). The mean BUN level was 13.5 mg/dl (normal <23), mean creatinine level was 0.74 mg/dl (normal <1.6), and mean ALT level was 27.8 U/l (normal <49). The mean baseline ammonia level was 23.4 umol/l (normal <35) with normal liver chemistries, but 9/30 (30%) had mild elevations (39–51 umol/l) of ammonia during the breath test. In the non-BF group, 2 (28%) patients had D-lactic acidosis and one of them also had l-lactic acidosis (Table 1B). The BUN and liver chemistry was normal and mean baseline ammonia level was 18.1 umol/l, and 2/8 (38–54 umol/l) had mild elevations during the breath test. The prevalence of D-lactic acidosis was significantly higher in the BF group when compared to the non-BF group (76.7 vs. 25%, p < 0.006). Also 10/13 (78%) PPI users and 4/7 opioid users had D-lactic acidosis.
In the BF group, 17 patients had wireless motility capsule test (WMC), 13 had gastric emptying scintigraphy, and 7 had colonic transit study with radioopaque markers12,13. Overall 10/30 patients (33%) had abnormal gastrointestinal transit and evidence of dysmotiltiy. Gastroparesis was diagnosed in 5/30 (16.7%) patients, 1 of whom had concurrent prolonged small bowel transit time, and another concurrent slow colonic transit. Rapid gastric emptying was seen in 1 patient with normal small bowel or colonic transit, and the rest had normal gastric emptying. Slow transit constipation was found in 6/24 (25%) patients who had colonic transit studies, 1 of whom had gastroparesis, and another had slow small bowel transit. All 10 patients with dysmotility had evidence of SIBO and evidence for lactic acidosis. In the non-BF group (based on WMC), 2 patients (25%) had gastroparesis, and 3 patients (37%) had slow colonic transit; one of whom had concurrent upper dysmotility. There was no difference (p ≥ 0.2) in prevalence of abnormal transit between groups.
In the BF group, metabolic testing for D-lactic acid/L-lactic acid production was positive in 24/30 (80%) patients, duodenal aspirate/culture was positive in 14 (46.7%), and glucose BT in 11 (36.6%). Based on either a positive GBT and/or duodenal aspirate/culture, 19 (63.3%) patients were diagnosed with SIBO and all of them had d-lactic acidosis. The prevalence of SIBO was significantly higher in the BF group when compared to the non-BF group (63.3 vs. 25%, p = 0.05).
In the BF group, all patients with evidence of lactic acidosis and/or SIBO were treated with various antibiotics (amoxicillin, amoxicillin-clavulanic acid, cotrimoxazole, rifaximin, metronidazole, tinidazole, and ciprofloxacin) based on the individual allergy profile and culture/sensitivity results, and were asked to discontinue probiotics (N = 23). The remaining patients without evidence of SIBO were asked to discontinue probiotics and yogurt use (N = 7). 24/30 (80%) attended follow-up clinic visits at 6 weeks and 3 months and rest were assessed by phone inquiry. GI symptoms were inquired through a validated questionnaire9, including global improvement using a 0–10 visual analog scale. We also inquired about the presence or absence of BF. After treatment, 70% of patients reported significant improvement in their symptoms with a significant change in the mean global VAS score (P = 0.005), (Fig. 3). 85% of patients reported complete resolution of BF. There were also significant (p < 0.05) improvements in the individual mean symptom scores (before vs. after) for abdominal pain (6.17 vs. 4.17), cramping (3.17 vs. 2.17), bloating (6.5 vs. 4.08), fullness (5.58 vs. 3.5), and distention (5.75 vs. 3.75); but not for other symptoms. Likewise, in the non-BF group, all 4 patients with SIBO/D-lactic acidosis received antibiotics and reported significant improvement in symptoms at 3-month follow-up; abdominal pain (7.2 vs 2.2), cramping (4.1 vs 2), bloating (7.8 vs 3.1), fullness (4.9 vs 2.4), and distension (6.1 vs 3.2). There was no difference in symptom(s) improvement between the two groups. (p > 0.2). Mean global satisfaction (VAS) score also improved (2.0 ± 1.3 vs. 7.4 ± 2.1, p < 0.05).
fogginess
We describe a cohort of patients with an intact gut who reported brain fogginess associated with unexplained abdominal bloating, pain, gas and distension, and in whom there was evidence of probiotic use, D-lactic acidosis and SIBO. The prevalence of both D-lactic acidosis and SIBO was significantly higher in patients with BF compared to those without BF.
The unique feature of this cohort was the presence of BF, which was described as variable in severity and intensity, often post-prandial, and forced some patients to quit their jobs. Also they reported significant bloating, abdominal pain, distention, and fullness. Additional symptoms included extreme fatigue, restlessness, weakness, and disorientation. These symptoms occurred at variable times and could last 30 min to a few hours. Few described excessive belching, diarrhea, abdominal cramping and headache. During the breath test, brain fogginess was reproduced in 66% of patients. This suggests that the carbohydrate meal provoked brain fogginess and reproduced their typical symptom experienced at home. Furthermore, 63% of patients had SIBO (as evidenced by duodenal aspirate/culture or breath test), and 80% had D-lactic acid/L-lactic acidosis. In contrast, SIBO and D-lactic acidosis was seen in a significantly lower proportion (28%) of patients with similar gastrointestinal symptoms, but without BF. These data provide compelling evidence for possible link between brain fogginess, SIBO and d-lactic acidosis. Unlike previous reports, our cohort developed d-lactic acidosis and BF without impaired renal or hepatic function and/or short bowel syndrome3.
D-lactic acidosis was first described by Oh et al in 1979 in a patient with short bowel syndrome who presented with unexplained anion gap metabolic acidosis and episodes of severe neuropsychological symptoms2. The L-isomer of lactic acid is the main form of lactic acid in the human body and is produced by the enzymatic (L-lactate dehydrogenase) reduction of pyruvate. D-lactate is produced in much smaller quantities by the enzyme D-2-hydroxyl acid dehydrogenase that also metabolizes D-lactate in the human liver3. Unlike L-lactate that is efficiently metabolized, the breakdown of D-lactate via the methylglyoxal pathway is slow and limited and can be confounded by comorbid conditions causing significant accumulation and acidosis3,20. In short bowel syndrome, if the colon is colonized by D-lactate producing bacteria, the delivery of large amounts of unabsorbed carbohydrate causes rapid fermentation, gaseous distension, and production of large amounts of d-lactic acid overwhelming hepatic clearance20, and causing D-lactic acidosis and encephalopathy.
Here, the BF was likely induced by the production of toxic metabolites such as D-lactic acid in the small intestine from bacterial fermentation of carbohydrate substrates. The use of prolonged or excessive probiotics and/or cultured yogurt further contributed to the small intestinal colonization by lactobacilli and other bacteria. These bacteria are generally resistant to usual antibiotics3, further explaining the refractory nature of symptoms.
Probiotics are considered to be safe and beneficial including improvement in gut barrier function and gut transit21. Although a meta-analysis of 57 studies indicated that probiotics are safe22, caution against its use has been recommended in subjects who are immunosuppressed, pregnant, and with structural heart lesions, acute abdomen, neutropenia, chemotherapy and radiotherapy22,23. However, studies have not been well designed, and safety outcomes have been inconsistently reported. The Agency for Healthcare Research and Quality concluded that there is inadequate literature on the safety of probiotics, especially given their widespread and OTC use24. There are reports of fungemia, bacteremia and gut ischemia in at risk, critically ill populations, many using Saccharomyces species or Lactobacillus23,24,25,26,27.
Lactobacillus species and bifidobacterium are the most common bacteria in probiotic formulations21,28, and are felt to be useful in the treatment of irritable bowel syndrome, inflammatory bowel disease, and other intestinal problems29. Both bacteria produce D-lactic acid. D-lactic acidosis has been described with Salmonella enteritidis and with probiotics30. Probiotics are designed to deliver bacteria to the colon but whether this is achieved has not been reliably shown21,22,23,27,28,31. In contrast, they may colonize the small bowel, especially in the presence of dysmotility or low acid conditions that favor bacterial overgrowth. We found a variety of aerobic and anaerobic species of bacteria in the proximal small bowel and three patients had Lactobacilli and/or Prevotella species. Also these bacteria are resistant to routine antibiotics. Interestingly, some Lactobacillus species such as Lactobacillus GG only produce L-lactate30,32. Hence, both D-lactate and L-lactate should be measured when assessing this condition, and the most practical way for its diagnosis is to administer a carbohydrate meal and assess D-lactate in urine and L-lactate in blood, over the next 3 h along with breath samples for hydrogen and methane.
We treated all patients with evidence of SIBO with antibiotics and discontinuation of probiotics, and the rest with dietary advice and stopping probiotics. These measures led to significant improvement of symptoms in 70% of our patients and complete resolution of brain fogginess in 85% of patients, reaffirming that the symptoms were related to D-lactic acidosis and SIBO. Likewise, the group of patients without BF, but with either SIBO or D-lactic acidosis also showed similar degree of improvement in symptoms after antibiotics.
One possible reason for bacterial colonization is intestinal dysmotility10Similarly dumping or rapid upper gut transit may cause colonic fermentation similar to short bowel. We measured regional and whole gut transit time using validated techniques14. In the BF group, except one patient, none showed evidence for dumping. About 1/3rd of our subjects had gastrointestinal dysmotility including gastroparesis, delayed small bowel and colonic transit that may have contributed to SIBO10,11,13,14, but rest had normal transit. Likewise in the non-BF group, 25% had gastroparesis and 37% had slow transit constipation that may have contributed to SIBO, but there was no difference between the two groups suggesting that dysmotility by itself may not contribute to brain fogginess. Additionally, opioids and PPI use may have predisposed patients to SIBO as 78% of PPI users had D-lactic acidosis10.
Our study has several limitations including the observational nature, although we examined a consecutive series of patients. Also, we did not culture fluid from the distal small bowel where most of the colonization may have occurred from probiotics because of the practical limitation of reaching this portion of the gut using standard endoscopy. This may have limited our ability to accurately link the probiotic use with SIBO. We did not retest these subjects to check if SIBO had resolved. There is no medical definition or criteria for BF, and therefore we relied on patient’s description of symptoms, and used the presence of ≥2/5 symptoms suggestive of BF. Also, whether the BF group had SIBO prior to using probiotics is unclear.
In conclusion, we describe a syndrome of a constellation of symptoms that comprises of post-prandial abdominal bloating, distension, gas and BF that were associated with the use of probiotics, and possibly caused by SIBO and D-lactic acidosis. The prevalence of SIBO and D-lactic acidosis was significantly higher in patients with BF than those without BF. We advise caution against excessive and indiscriminate use of probiotics especially without a well-defined medical indication, and particularly in patients with gastrointestinal dysmotility, and/or those using long term PPI and opioids.
D-lactic acidosis is rarely encountered in routine GI practice, but occasionally seen in patients with short bowel syndrome.
Recently, we have encountered several patients with unexplained brain fogginess, associated with significant gas, bloating and abdominal pain. Whether these symptoms are due to D-lactic acidosis and are associated with small intestinal bacterial overgrowth (SIBO) is not known.
We found that over 2/3rd of patients with brain fogginess demonstrated D-lactic acidosis,along with significantly higher prevalence of SIBO when compared to those without brain fogginess.
Discontinuation of probiotics along with the use of antibiotics led to resolution of symptoms. Clinicians should recognize, diagnose and treat this unique syndrome.
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We thank Ms. Collier Badger for assistance with breath and metabolic tests and Ms. H. Smith for superb secretarial assistance and Dr. J. Bhagatwala and Dr. X. Xiang with additional data and statistical analysis. Portions of this work were presented as a poster at Digestive Diseases Week; May 2014; Chicago, IL. (Gastroenterology. May 2014. Volume 146, Issue 5, Supplement 1, S-850–S-851).
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