Malabsorption of dietary lactose in the small intestine results in gastrointestinal symptoms such as abdominal pain, bloating, passage of loose, watery stools, and excessive flatus. Lactose intolerance is generally a lifelong inherited condition but can be a temporary result of an infection or other insult to the jejunal mucosa. Recognition of this prevalent condition is important, as it is easily managed by simple dietary adjustments. Accurate diagnosis of lactose intolerance can significantly relieve patient anxiety and avoid inappropriate investigation and treatment.
The lactase enzyme is located in the brush border (microvilli) of the small intestine enterocyte. The enzyme splits and hydrolyzes dietary lactose into glucose and galactose for transport across the cell membrane. The enzyme activity and the transit time of lactose through the jejunum mucosa are important for proper absorption. If lactase enzymes are absent or deficient (hypolactasia), unabsorbed sugars osmotically attract fluid into the bowel lumen. The fluid influx into the bowel is approximately triple the predicted amount based on the osmolality of the sugar content alone, because the intestine cannot maintain a high electrochemical gradient between contents and blood.1
In addition to increasing the volume and fluidity of the gastrointestinal contents, unabsorbed lactose entering the colon is affected by bacteria. Fermentation produces gas and results in the cleavage of lactose into monosaccharides. These monosaccharides cannot be absorbed by the colonic mucosa, thus increasing osmotic pressure and drawing more fluid into the bowel. In lactase-deficient patients, some of the carbohydrates reaching the colon can be metabolized by bacteria into short-chain fatty acids and absorbed, but the net result of ingestion of lactose is a substantial rise in fluid and gas in the bowel.
Epidemiology and Etiology
Lactose malabsorption is a normal physiologic pattern.2 The condition occurs in three main types: primary, secondary, and congenital lactase deficiency. The most common form of lactase deficiency is primary adult hypolactasia. [ corrected] Secondary or acquired hypolactasia can follow any gastrointestinal illness that damages the brush border or significantly decreases transit time in the jejunum mucosa (Table 1).3 Lifelong complete absence of lactase (congenital alactasia) is rare.
|Sprue (celiac and tropical)|
|Whipple's disease (intestinal lipodystrophy)|
|Colchicine-induced in patients with familial Mediterranean fever|
All land mammals have a dramatic decrease in lactase after weaning. Worldwide, humans lose 90 to 95 percent of birth lactase levels by early childhood, and there is a continuous decline in lactase during the course of a lifetime. However, the prevalence of hypolactasia varies widely among ethnic backgrounds (Table 2).1 Estimates range from 2 percent in persons from Northern Europe to nearly 100 percent in adult Asians and American Indians. Blacks and Ashkenazi Jews have prevalences of 60 to 80 percent, and Latinos have a prevalence of 50 to 80 percent.
The wide variation in prevalence has caused speculation that lactase deficiency is the “normal” or “natural” state, and the persistence of significant lactase activity into adult life in northern European populations is an “abnormal” mutation that provides a selective advantage to groups using diary products.1 It is unknown whether the continued use of dairy products after weaning leads to the retention of lactase activity or if the persistence of lactase enables the incorporation of dairy products into the diet.
Hypolactasia results in up to 75 percent of dietary lactose passing unaltered through the small intestine into the colon, where it is rapidly metabolized by colonic bacteria, producing excessive fluid and gas in the bowel.4 The symptoms patients experience vary, however, according to the quantity of lactose ingested and patients' ability to digest lactose.
In patients with common adult-type hypolactasia, the amount of ingested lactose required to produce symptoms varies but is reported to be about 12 to 18 g, or 8 to 12 oz of milk. Several factors affect the severity of symptoms after lactose ingestion, including the patient's ethnic origin and age; older patients are more susceptible.1 Ingestion of small to moderate amounts of lactose usually produces bloating, cramps, and flatulence but not diarrhea. Ingestion of larger amounts of lactose, a faster gastric emptying time, and faster intestinal transit time all contribute to more severe symptoms. Conversely, increased lactase activity in the small intestine reduces symptoms. Other foods and the presence of suitable microflora in the colon can cause patients to be more symptomatic.
Symptoms are directly related to the osmotic pressure of substrate in the colon and occur about two hours after ingestion of lactose. Patients have usually learned to avoid milk products and often have a strong family history of similar problems. Admixtures of dairy products may offer improved tolerance so that some patients may be able to ingest chocolate milk, skim milk, and ice cream. In particular, yogurts with live cultures are usually well-tolerated because they contain bacterial-derived lactases.5
Consideration of differential diagnoses is important in patients with primary hypolactasia (Table 3).3 Acquired lactase deficiency or secondary lactose intolerance are present in a variety of gastrointestinal diseases with histologic evidence of mucosal damage. Irritable bowel syndrome (IBS) is a benign gastrointestinal disorder with complex multifactor pathology.6 Lactose intolerance and IBS have similar symptom complexes and incidences. The difficulty of making a positive diagnosis of either of these conditions has led to misdiagnosis of lactose intolerance in some patients. Establishing a positive diagnosis for either condition is difficult because patients with IBS frequently report intolerance of food, particularly dairy products.7 Compounding the diagnostic problem is the fact that at least 25 percent of patients with IBS also have lactose malabsorption.8 Because lactose intolerance is organic rather than functional in nature, it is fundamentally different from IBS. Lactose restriction may result in improvement of symptoms in both groups of patients.
|Irritable bowel syndrome|
|Bowel neoplasm or polyp|
|Iatrogenic: inadvertent ingestion of laxative in nonprescription or alternative medicine, or ingestion of bran|
|Mechanical bowel compromise from previous endometriosis, adhesions, or gynecologic mass|
|Viral and bacterial infections|
|Parasitic disease, such as giardiasis|
Diagnosis of lactose intolerance can usually be made on the basis of the history, supported by dietary manipulation. Diagnostic tests range from changes in breath hydrogen levels or serum glucose levels after ingestion of standard doses of lactose to biopsy of the small bowel.
Two formal tests are commonly used in patients suspected of having lactose intolerance. The lactose tolerance test consists of administering an oral dose of approximately 1 to 1.5 g of lactose per kg of body weight and obtaining serial blood samples for measurement of blood glucose levels. The test is positive if intestinal symptoms occur and the blood glucose level increases less than 20 mg per dL (1.1 mmol per L) above the fasting level. However, false-positive and false-negative test results occur in 20 percent of normal subjects because of the influence of variable gastric emptying and glucose metabolism.
The measurement of breath hydrogen after ingestion of 25 to 50 g of lactose is more sensitive and specific than the lactose tolerance test. The breath hydrogen test has become widely available and is often used rather than the lactose tolerance test. The breath hydrogen test is based on the principle that carbohydrate in the colon is detectable in pulmonary excretion of hydrogen and other gases.9 A rise in breath hydrogen concentration greater than 20 ppm over baseline after lactose ingestion suggests hypolactasia.
The lactose breath hydrogen test is positive in 90 percent of patients with lactose malabsorption. The amount of lactose used for the breath hydrogen test is not physiologic.10 Many physicians reduce the dose to a physiologic or dietary range, such as the 12 g of lactose present in an 8-oz glass of cow's milk. False-negative results occur in cases of absence of bacterial flora, recent use of oral antibiotics, or recent high colonic enema. Sleep, exercise, previous use of aspirin, and smoking may increase breath hydrogen secretion unrelated to lactose.
Adult Dietary Management
Patients should be informed that having lactose malabsorption does not mean they are allergic to milk, dairy products, or dairy foods. A milk allergy is related to the proteins in milk rather than the lactose. The degree of lactose malabsorption varies widely among patients, but most patients do not require a totally lactose-free or severely restricted diet.11,12 Dairy products should not be totally eliminated because they provide key nutrients such as calcium, vitamins A and D, riboflavin, and phosphorus.12
Diary products provide approximately 75 percent of the calcium available in the U.S. food supply.13 Adult patients with lactose intolerance should maintain a calcium intake of 1,200 to 1,500 mg per day, including actual dairy products up to their individual threshold for symptoms. Milk intake commonly has to be limited to less than 250 to 375 mL (8 to 12 oz) per day. Patients should consider drinking lactose-reduced milk or taking calcium supplements. Patients should also be advised to avoid medications that contain lactose as filler and certain food products that may contain unrecognized lactose (Table 4). Patient education is usually highly useful in patients with lactose intolerance (see patient information handout).
Patients with mild lactose malabsorption may benefit from using lactase enzyme supplements, such as Dairy Ease. The incubation of milk with lactase enzymes may also be helpful. However, patients should be warned that the lactase enzymes might not completely relieve the symptoms because the digestion of lactose is incomplete or because it is difficult to determine the effective dose of lactase enzyme. Therefore, enzyme supplementation should be an adjunct to, not a substitute for, dietary restriction. Nondairy synthetic drinks, such as Coffee-Mate, are a useful substitute for milk. Soy milk and rice milk are also well-tolerated.
|Although milk and foods made from milk are the only natural sources, lactose is often added to prepared foods. People with very low tolerance for lactose should know about the many food products that may contain even small amounts of lactose, including the following:|
|Bread and other baked goods|
|Processed breakfast cereals|
|Mixes for pancakes, biscuits, and cookies|
|Instant potatoes, soups, and breakfast drinks|
|Nonkosher luncheon meats|
|Candies and other snacks|
Recent evidence2,14–16 suggests that patients with medically confirmed lactose malabsorption can ingest the number of servings of milk and dairy products recommended by the American Dietetic Association without experiencing gastrointestinal discomfort. Some patients increase their tolerance to lactose with repeated intake.2,17
Patients with secondary lactose intolerance require further investigation to identify the primary problem. Effective treatment of the underlying condition, such as administration of metronidazole (Flagyl) for treatment of giardiasis or a gluten-free diet for management of celiac disease, may not only ameliorate symptoms but also improve lactose intolerance. Patients with bacterial overgrowth may benefit from antibiotics such as tetracycline, metronidazole, or ciprofloxacin (Cipro).