Gut Health

Probiotics, prebiotics, and digestive support compounds that nurture the gut microbiome and digestive wellness.

17 items

Articles about Gut Health

performance-recovery

L‑Glutamine for Recovery and Gut Health: Inside the Gut–Muscle Axis

Glutamine sits at the crossroads of muscle, gut, and immune function. Here’s what research says about its role in athletic recovery, gut barrier integrity, immune health in athletes, burn/trauma care, and IBS—with a bridge to the traditional bone broth perspective.

10 min read
Moderate Evidence
gut-immune

Digestive Enzymes and Food Intolerance: What Actually Helps vs. Hype

Targeted digestive enzymes can help specific intolerances—lactase for lactose and alpha-galactosidase for bean-related gas—while broad blends and betaine HCl have limited evidence. Prescription pancreatic enzymes are effective for true pancreatic insufficiency. Traditional aids like ginger, bitters, and CCF tea may complement modern strategies.

10 min read
Moderate Evidence

Supplements for Gut Health

Probiotic

Probiotics

Live beneficial bacteria that support gut microbiome health, digestion, and immune function.

Moderate Evidence

Comparisons

Gastroenterology

Irritable Bowel Syndrome (IBS)

Irritable bowel syndrome (IBS) is a chronic disorder of gut–brain interaction characterized by recurrent abdominal pain and altered bowel habits without structural disease. Under the Rome IV criteria, IBS is defined by abdominal pain, on average, at least one day per week in the last three months, associated with two or more of the following: related to defecation, change in stool frequency, or change in stool form; symptoms start at least six months before diagnosis. Subtypes are based on predominant stool pattern: IBS with diarrhea (IBS-D), IBS with constipation (IBS-C), mixed (IBS-M), or unclassified. Western medicine frames IBS as a multifactorial condition involving disordered gut–brain signaling, visceral hypersensitivity, altered motility, immune activation, psychosocial stressors, and microbiome perturbations. Evidence-based care is individualized and multimodal. Diet is foundational: the low-FODMAP diet—developed and validated by Monash University—has strong evidence for improving global IBS symptoms when delivered in a structured, three-phase format (short-term elimination, personalized reintroduction, and long-term adaptation). Pharmacotherapies target stool form and pain: antispasmodics (e.g., hyoscine, dicyclomine) can reduce cramping; rifaximin is effective for IBS-D; and secretagogues such as linaclotide and plecanatide are effective for IBS-C. Low-dose tricyclic antidepressants (TCAs) and, in selected cases, SSRIs modulate the gut–brain axis to reduce pain and normalize bowel habits. Psychological therapies—especially gut-directed cognitive behavioral therapy (CBT)—have strong support for improving global symptoms and quality of life. Emerging approaches include selective probiotics, postbiotics, and microbiome-directed therapies; evidence is mixed and evolving, and current guidelines are cautious about routine probiotic use for global IBS symptoms due to heterogeneity. Eastern and traditional systems conceptualize IBS through functional patterns.

Moderate Evidence
Gastroenterology

Irritable Bowel Syndrome (IBS)

Irritable bowel syndrome (IBS) is a chronic, relapsing disorder of gut–brain interaction characterized by abdominal pain associated with altered bowel habits, without structural disease that explains the symptoms. Western medicine classifies IBS using the Rome IV criteria: recurrent abdominal pain, on average, at least 1 day per week in the last 3 months, associated with two or more of the following—related to defecation, associated with a change in frequency of stool, and associated with a change in form (appearance) of stool—with symptom onset at least 6 months before diagnosis. Subtypes are defined by predominant stool pattern: diarrhea-predominant (IBS-D), constipation-predominant (IBS-C), mixed (IBS-M), and unclassified. Pathophysiology is multifactorial: visceral hypersensitivity, altered motility, immune activation and barrier dysfunction, dysbiosis, bile acid malabsorption in a subset, and central modulation via the gut–brain axis. Psychosocial stressors and early life adversity can amplify symptoms through bidirectional brain–gut signaling. Evidence-based Western management is multimodal and personalized. First-line lifestyle strategies include regular physical activity, sleep optimization, and diet. The low-FODMAP diet—temporary restriction of fermentable oligo-, di-, monosaccharides and polyols—has strong evidence for reducing global IBS symptoms when delivered in a structured elimination and reintroduction program (best studied by Monash University). Soluble fiber (psyllium) is recommended in IBS-C and some mixed phenotypes, while insoluble fiber may worsen symptoms. Pharmacologic options are matched to subtype and dominant symptoms: antispasmodics (e.g., dicyclomine, hyoscyamine) for cramping; loperamide for urgency/diarrhea control (not for global symptom relief); bile acid sequestrants in suspected bile acid diarrhea; non-absorbed antibiotic rifaximin for IBS-D; secretagogues such as linaclotide and plecanatide for IBS-C; lubiprostone (women with IBS

Moderate Evidence

Topic Relationships

Condition / Condition

IBS & Anxiety

IBS and anxiety frequently travel together through a shared gut–brain axis. IBS is a disorder of gut–brain interaction defined by recurrent abdominal pain with altered bowel habits, while anxiety e...

All topics