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Lactose intolerance

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**Lactose intolerance**
*Classification & external resources*

Lactose, a disaccharide of β-D-galactose & β-D-glucose, that is normally split by lactase.
ICD-10	E73.
ICD-9	271.3
OMIM	223100 150220
DiseasesDB	7238
MedlinePlus	000276
eMedicine	med/3429 ped/1270

Lactose intolerance (or hypolactasia) is the term used to describe a decline in the level of lactase, an enzyme needed for proper metabolization of lactose (a sugar that is a constituent of milk and other dairy products), in human beings. An estimated 70%^[1] of adult humans are considered lactose intolerant and therefore, from a world view, lactose intolerance can be regarded as "normal" for adult humans whereas lactose tolerance may be considered a form of neoteny.

There are three major types of lactose intolerance^[2]:

Primary lactose intolerance. Environmentally induced when weaning a child in non dairy consuming societies^[3]. This includes many Asian and African cultures, where industrialized and commercial dairy is uncommon.
Secondary lactose intolerance. Environmentally induced, resulting from certain gastrointestinal diseases, including exposure to intestinal parasites such as giardia^[4]^[5]. In such cases the production of lactase may be permanently disrupted.[7] + (Wiser 2000, Pennardt 2006). A very common cause of temporary lactose intolerance is gastroenteritis, particularly when the gastroenteritis is caused by rotavirus.
Congenital lactase deficiency. A genetic disorder which prevents enzymatic production of lactase. Present at birth, and diagnosed in early infancy.

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Overview

Without lactase, the lactose disaccharide in many dairy products remains uncleaved and cannot be absorbed through the intestinal wall into the bloodstream, so remains in the intestines. Enteral bacteria adapt to the relative abundance of this undigested sugar and their operons quickly switch over to lactose metabolism, which produces copious amounts of gas by fermentation.

This also causes a range of unpleasant abdominal symptoms, including stomach cramps, bloating, flatulence and diarrhea. As with other unabsorbed sugars (mannitol), the lactose raises the osmotic pressure of the colon contents, preventing the colon from reabsorbing water and hence causing a laxative effect to add to the excessive gas production.

Lactase biology

The enzyme lactase, also called beta-D-galactosidase, is synthesized if at least one of the two genes for it are present. Only when both gene expressions are affected is lactase enzyme synthesis reduced, which in turn reduces lactose digestion.^[6]. Lactase persistence, allowing lactose digestion to proceed, is the dominant allele. Physiological lactose intolerance, therefore, is an autosomal recessive trait.

However, cultures such as that of Japan, where dairy consumption has been on the increase, demonstrate a lower prevalence of lactose intolerance in spite of a genetic predisposition^[7].

The normal mammalian condition is for the young of a species to experience reduced lactase production at the end of the weaning period (a species-specific length of time). In non dairy consuming societies, lactase production usually drops about 90% during the first four years of life, although the exact drop over time varies widely. However, certain human populations have a mutation on chromosome 2 which results in a bypass of the common shutdown in lactase production, making it possible for members of these populations to continue consumption of fresh milk and other dairy products throughout their lives.

Pathological lactose intolerance can occur due to Coeliac disease, which damages the villi in the small intestine that produce lactase. This lactose intolerance is temporary. Lactose intolerance associated with coeliac disease ceases after the patient has been on a gluten-free diet long enough for the villi to recover^{[citation needed]}.

Certain people who report problems with consuming lactose are not actually lactose intolerant. In a study of 323 Sicilian adults, Carroccio et al. (1998) found only 4% were both lactose intolerant and lactose maldigesters, while 32.2% were lactose maldigesters but did not test as lactose intolerant. However, Burgio et al. (1984) found that 72% of 100 Sicilians were lactose intolerant in their study and 106 of 208 northern Italians (i.e., 51%) were lactose intolerant.

Lactose intolerance by group

Human groups	Individuals Examined	Percent Intolerant	Allele frequency
Dutch	N/A	1%^[8]	N/A
Swedes	N/A	2%^[9]	0.14
Europeans in Australia	160	4%^[9]	0.20
White people of Northern European and Scandinavian descent	N/A	5%^[3]^[10]	N/A
Danes	N/A	5%^[11]	N/A
British	N/A	5–15%^[12]	N/A
Swiss	N/A	10%^[9]	0.316
White Americans	245	12%^[9]	0.346
Tuareg	N/A	13%^[12]	N/A
Germans	N/A	15%^[12]	N/A
Austrians	N/A	15–20%^[12]	N/A
Eastern Slavs (Russians, Belarusians, Ukrainians)	N/A	15%^[13]	N/A
Northern French	N/A	17%^[12]	N/A
Finns	134	18%^[9]	0.424
Central Italians	65	19%^[14]	N/A
Indian Children	N/A	20%^[3]^[10]	N/A
African Tutsi	N/A	20%^[9]	0.447
African Fulani	N/A	23%^[9]	0.48
Bedouins	N/A	25%^[12]	N/A
Northern Indians	N/A	27%^[15]	N/A
African American Children	N/A	45%^[3]	N/A
Indian Adults	150	50%^[3]^[10]^[16]	N/A
Southern Italians	51	41%^[14]	N/A
Saami (in Russia and Finland)	N/A	25–60%^[17]	N/A
Northern Italians	89	52%^[14]	N/A
North American Hispanics	N/A	53%^[12]	N/A
Balkans	N/A	55%^[12]	N/A
Mexican American Males	N/A	55%^[3]^[10]	N/A
Cretans	N/A	56%^[3]	N/A
African Maasai	21	62%^[18]	N/A
Southern French	N/A	65%^[12]	N/A
Greek Cypriots	N/A	66%^[3]^[10]	N/A
North American Jews	N/A	68.8%^[3]^[10]	N/A
Southern Indians	N/A	70%^[15]	N/A
Sicilians	100	71%^[19]^[20]	N/A
South Americans	N/A	65–75%^[12]	N/A
Rural Mexicans	N/A	73.8%^[3]^[10]	N/A
African Americans	20	75%^[9]	0.87
Kazakhs from northwest Xinjiang	195	76.4% ^[21]
Lebanese	75	78%^[22]	N/A
Central Asians	N/A	80%^[12]	N/A
Alaskan Eskimo	N/A	80%^[3]^[10]	N/A
Australian Aborigines	44	85%^[9]	0.922
Inner Mongolians	198	87.9%^[21]
African Bantu	59	89%^[9]	0.943
Asian Americans	N/A	90%^[3]^[10]	N/A
Northeastern Han Chinese	248	92.3%^[21]
Chinese	71	93%^[9]	0.964
Southeast Asians	N/A	98%^[3]^[10]	N/A
Thais	134	98%^[9]	0.99
Native Americans	24	100%^[9]	1.00

The statistical significance varies greatly depending on number of people sampled.

Lactose intolerance levels also increase with age. At ages 2 - 3 yrs., 6 yrs., and 9 - 10 yrs., the amount of lactose intolerance is, respectively:

6% to 15% in white Americans and northern Europeans
18%, 30%, and 47% in Mexican Americans
25%, 45%, and 60% in black South Africans
approximately 30%, 80%, and 85% in Chinese and Japanese
30–55%, 90%, and >90% in Mestizos of Peru^[23]^[24]

Chinese and Japanese populations typically lose between 80 and 90 percent of their ability to digest lactose within three to four years of weaning. Most Japanese can consume 200 ml (8 fl oz) of milk without severe symptoms (McGee 2004; Swagerty et al, 2002).^[7]

Ashkenazi Jews can keep 20 - 30 percent of their ability to digest lactose for many years.^[23]^[25] Of the 10% of the Northern European population that develops lactose intolerance, the development of lactose intolerance is a gradual process spread out over as many as 20 years.^[26]

Diagnosis

To assess lactose intolerance, the intestinal function is challenged by ingesting more dairy than can be readily digested. Clinical symptoms typically appear within 30 minutes but may take up to 1-2 hours depending on other foods and activities^[27]. Substantial variability of the clinical response (symptoms of nausea, cramping, bloating, diarrhea, and flatulence) are to be expected as the extent and severity of lactose intolerance varies between individuals.

When considering the need for confirmation, it is important to distinguish lactose intolerance from milk allergy, which is an abnormal immune response (usually) to milk proteins. Since lactose intolerance is the normal state for most adults on a worldwide scale, and not considered a disease condition, a medical diagnosis is not normally required. However, if confirmation is necessary, three tests are available:

Hydrogen breath test

In a hydrogen breath test, after an overnight fast, 50 grams of lactose (in a solution with water) are swallowed. If the lactose cannot be digested, enteric bacteria metabolize it and produce hydrogen. This can be detected in the air the patient exhales. The test takes about 2 to 3 hours. A medical condition with similar symptoms is fructose malabsorption.

In conjunction, measuring the blood glucose level every 10 - 15 minutes after ingestion will show a "flat curve" in individuals with lactose malabsorption, while the lactase persistent will have a significant "top", with an elevation of typically 50 to 100% within 1 - 2 hours.

Stool acidity

Required for a clinical diagnosis.^[28]

Intestinal biopsy

An intestinal biopsy can confirm lactose intolerance following discovery of elevated hydrogen in the hydrogen breath test^[29].

History of diagnosis

The ancient Greek physician Hippocrates (460-370 B.C.) first noted gastrointestinal upset and skin problems in some who consumed milk;^[30] patients experiencing the former symptom may likely have been suffering from lactose intolerance. However, it was only in the last few decades that the syndrome was more widely described by modern medical science.

The condition was first recognized in the 1950s and 1960s when various organizations like the United Nations began to engage in systematic famine-relief efforts in countries outside Europe for the first time. Holzel et al (1959) and Durand (1959) produced two of the earliest studies of lactose intolerance. As anecdotes of embarrassing dairy-induced discomfort increased, the First World donor countries could no longer ascribe the reports to spoilage in transit or inappropriate food preparation by the Third World recipients.

Because the first nations to industrialize and develop modern scientific medicine were dominated by people of Western and Northern European descent, adult dairy consumption was long taken for granted. Westerners for some time did not recognize that the majority of the human ethno-genetic groups could not consume dairy products during adulthood. Although there had been regular contact between Europeans and non-Europeans throughout history, the notion that large-scale medical studies should be representative of the ethnic diversity of the human populations (as well as all genders and ages) did not become well-established until after the American Civil Rights Movement.

Since then, the relationship between lactase and lactose has been thoroughly investigated in food science due to the growing market for dairy products among non-Europeans.

Originally it was hypothesised that gut bacteria such as E. coli produced the lactase enzyme needed to cleave lactose into its constituent monosaccharides and thus become metabolisable and digestible by humans. Some form of human-bacteria symbiosis was proposed as a means of producing lactase in the human digestive tract. Genetics and protein analysis techniques by the early 1970s revealed this to be untrue; humans produce their own lactase enzyme natively in intestine cells.

According to Heyman (2006), approximately 70% of the global population cannot tolerate lactose in adulthood. Thus, some argue that the terminology should be reversed — lactose intolerance should be seen as the norm, and the minority groups should be labeled as having lactase persistence. A counter argument to this is that the cultures that don't generally consume unmodified milk products have little need to discuss their intolerance to it, leaving the cultures for which lactose intolerance is a significant dietary issue to define its terminology.

History of genetic prevalence

Lactose intolerance has been studied as an aid in understanding ancient diets and population movement in prehistoric societies. Milking an animal vastly increases the efficiency of raising it in regards to the calories that can be extracted compared to consumption of its meat alone. It is not surprising then, that consuming milk products became an important part of the agricultural way of life in the Neolithic. Given that at that time the majority of the population of all areas was lactose intolerant^{[citation needed]} , it is believed that most of the milk was used to make mature cheeses which are mostly lactose free.

Roman authors recorded that the people of northern Europe, particularly Britain and Germany drank unprocessed milk (as opposed to the Romans who made cheese).^{[citation needed]} This corresponds very closely with modern European distributions of lactose intolerance, where the people of Britain, Germany and Scandinavia have a good tolerance, and those of southern Europe, especially Italy, have a poorer tolerance.[8]

In east Asia, historical sources also attest that the Chinese did not consume milk, whereas the nomads that lived on the borders did. Again, this reflects modern distributions of intolerance. China is particularly notable as a place of poor tolerance, whereas in Mongolia and the Asian steppes horse milk is drunk regularly. This tolerance is thought to be advantageous as the nomads do not settle down long enough to process mature cheese. Given that their prime source of income is generated through horses, to ignore their milk as a source of calories would be greatly detrimental. The nomads also make an alcoholic beverage, called Kumis, from horse milk, although the fermentation process reduces the amount of lactose present.

The African Fulani have a nomadic origin and their culture once completely revolved around cow, goat, and sheep herding. Dairy products were once a large source of nutrition for them. As might be expected if lactase persistence evolved in response to dairy product consumption, they are particularly tolerant to lactose (about 77% of the population). Many Fulani live in Guinea-Conakry, Burkina Faso, Mali, Nigeria, Niger, Cameroon, and Chad.

There is some debate on exactly where and when genetic mutation(s) occurred. Some argue for separate mutation events in Sweden (which has one of the lowest levels of lactose intolerance in the world) and the Arabian Peninsula around 4000 BC. However, others argue for a single mutation event in the Middle East at about 4500 BC which then subsequently radiated. Some sources suggest a third and more recent mutation in the East African Tutsi. Whatever the precise origin in time and place, most modern Western Europeans and people of European ancestry show the effects of this mutation (that is, they are able to safely consume milk products all their lives) while most modern East Asians, sub-Saharan Africans and native peoples of the Americas and Pacific Islands do not (making them lactose intolerant as adults)[9].

The Maasai ability to consume dairy without exhibiting symptoms may be due to a different genetic mutation than Westeners.^[31]"

A thorough scientific overview of genetic polymorphisms of intestinal lactase activity in adult hypolactasia, is in chapter 76 of OMMBID.^[32] A noncoding variation in the MCM6 gene has been strongly associated with adult type hypolactasia.^[33]

Managing lactose intolerance

For persons living in societies where the diet contains relatively little dairy, lactose intolerance is not considered a condition that requires treatment. However, those living among societies that are largely lactose-tolerant may find lactose intolerance troublesome. Although there are still no methodologies to reinstate lactase production, some individuals have reported their intolerance to vary over time (depending on health status and pregnancy^[34]). Lactose intolerance is not usually an all-or-nothing condition: the reduction in lactase production, and hence, the amount of lactose that can be tolerated varies from person to person. Since lactose intolerance poses no further threat to a person's health, managing the condition consists in minimizing the occurrence and severity of symptoms. Berdanier and Hargrove recognise 4 general principles: 1)avoidance of dietary lactose, 2)substitution to maintain nutrient intake, 3)regulation of calcium intake, 4)use of enzyme substitute.

Avoiding lactose-containing products

Since each individual's tolerance to lactose varies, according to the US National Institute of Health, "Dietary control of lactose intolerance depends on people learning through trial and error how much lactose they can handle."[10]. Label reading is essential as commercial terminology varies according to language and region^[29].

Lactose is present in 2 large food categories: Conventional dairy products, and as a food additive (in dairy and non dairy products).

Dairy products

Lactose is a water soluble molecule. Therefore fat percentage and the curdling process have an impact on which foods may be tolerated. In the curdling process lactose is found in the water portion along with whey and casein, but is not found in the fat portion. Dairy products which are "fat reduced" or "fat free" generally have a slightly higher lactose percentage. Additionally, low fat dairy foods also often have various dairy derivatives such as milk solids added to them to enhance sweetness, increasing the lactose content.

Milk. Human milk has the highest lactose percentage at around 9%. Unprocessed cow milk has 4.7% lactose. Unprocessed milk from other mammals contains similar lactose percentages (goat milk 4.1%^[35], buffalo 4.86%^[36], yak 4.93%^[37], sheep milk 4.6% ^[38]).

Butter. The butter making process by definition separates milk's water components from the fat components. Lactose, being a water soluble molecule, will not be present in the butter unless milk solids are added to the ingredients.

Yogurt and kefir. People can be more tolerant of traditionally made yogurt than milk because it contains lactase enzyme produced by the bacterial cultures used to make the yogurt. However, many commercial brands contain milk solids, increasing the lactose content.

Cheeses. Traditionally made hard cheese (such as Swiss cheese) and soft ripened cheeses may create less reaction than the equivalent amount of milk because of the processes involved. Fermentation and higher fat content contribute to lesser amounts of lactose. Traditionally made Swiss or Cheddar might contain 10% of the lactose found in whole milk. In addition, the traditional aging methods of cheese (over 2 years) reduces their lactose content to practically nothing[11]. Commercial cheese brands, however, are generally manufactured by modern processes that do not have the same lactose reducing properties, and as no regulations mandate what qualifies as an "aged" cheese, this description does not provide any indication of whether the process used significantly reduced lactose.

Buttermilk, sour cream and ice cream, like yogurt, if made the traditional way, will generally be quite tolerable, but most modern brands add milk solids. ^[39] Consult labels ^[40].

Examples of lactose levels in foods. As scientific consensus has not been reached concerning lactose percentage analysis methods ^[41] (non-hydrated form or the mono-hydrated form), and considering that dairy content varies greatly according to labeling practices, geography and manufacturing processes, lactose numbers may not be very reliable. The following are examples of lactose levels in foods which commonly set off symptoms [12]. These quantities are to be treated as guidelines only.

Dairy product	Lactose Content
Yogurt, plain, low-fat, 240 mL	5 g
Milk, reduced fat, 240 mL	11 g
Swiss cheese, 28 g	1 g
Ice cream, 120 mL	6 g
Cottage cheese, 120 mL	2–3 g

Lactose in non-dairy products

Lactose (also present when labels state lactoserum, whey, milk solids, modified milk ingredients, etc) is a commercial food additive used for its texture, flavor and adhesive qualities, and is found in foods such as processed meats^[42] (sausages/hot dogs, sliced meats, Pâtés), margarines^[43], sliced breads^[44]^[45], breakfast cereals^[42], dried fruit, processed foods, medications, preprepared meals, meal replacement (powders and bars), protein supplements (powders and bars).

Kosher products labeled pareve are mostly free of milk. However, if a "D" (for "Dairy) is present next to the circled "K," "U," or other hechsher, the food likely contains milk solids^[42] (although it may also simply indicate that the product was produced on equipment shared with other products containing milk derivatives).

Alternative products

Milk. The dairy industry has created quality low-lactose or lactose-free products to replace regular dairy. Lactose-free milk can be produced by passing milk over lactase enzyme bound to an inert carrier: once the molecule is cleaved, there are no lactose ill-effects. A form is available with reduced amounts of lactose (typically 30% of normal), and alternatively with almost 0%. Finland has had "HYLA" (acronym for hydrolysed lactose) products available for many years, even though the number of lactose intolerant people there is relatively small. These low-lactose level cow's milk products, ranging from ice cream to cheese, use a Valio patented chromatographic separation method to remove lactose. The ultra-pasteurization process, combined with aseptic packaging ensures a long shelf-life. Recently, the range of low-lactose products available in Finland has been augmented with milk and other dairy products (such as ice cream, butter, and buttermilk) that contain no lactose at all. The remaining about 20% of lactose in HYLA products is taken care of enzymatically. These typically cost 2 - 4 times more than equivalent products containing lactose. Valio also markets these products in Sweden.

Alternatively, a bacterium such as L. acidophilus may be added, which affects the lactose in milk the same way it affects the lactose in yogurt (see above).

Plant based milks and derivatives are the only ones to be 100% lactose free (soy milk, almond milk, oat milk, rice milk, hemp milk, peanut milk) ^[46].

Lactase supplementation

When lactose avoidance is not possible, or on occasions when a person chooses to consume such items, then enzymatic lactase supplements may be used.^[47]^[48]

Lactase enzymes similar to the those produced in the small intestines of humans are produced industrially by fungi of the genus aspergillus. The enzyme, β-galactosidase, is available in tablet form in a variety of doses, in many countries without a prescription. It functions well only in high-acid environments, such as that found in the human gut due to the addition of gastric juices from the stomach. Unfortunately, too much acid can denature it,^[49] and it therefore should not be taken on an empty stomach. Also, the enzyme is ineffective if it does not reach the small intestine by the time the problematic food does. Lactose-sensitive individuals should experiment with both timing and dosage to fit their particular need. But supplements such as these may not be able to provide the accurate amount of lactase needed^{[citation needed]} to adequately digest the lactose contained in dairy products, which may lead to symptoms similar to the existing lactose intolerance.

While essentially the same process as normal intestinal lactose digestion, direct treatment of milk employs a different variety of industrially produced lactase. This enzyme, produced by yeast from the genus kluyveromyces, takes much longer to act, must be thoroughly mixed throughout the product, and is destroyed by even mildly acidic environments. It therefore has been much less popular as a consumer product^{[citation needed]} (sold, where available, as a liquid) than the aspergillus-produced tablets, despite its predictable effectiveness. Its main use is in producing the lactose-free or lactose-reduced dairy products sold in supermarkets.

Enzymatic lactase supplementation may have an advantage over avoiding dairy products, in that alternative provision does not need to be made to provide sufficient calcium intake, especially in children.^[50]

Rehabituation to dairy products

Wiktionary has an entry for rehabituation.

For healthy individuals with Secondary lactose intolerance, it may be possible to train bacteria in the large intestine to break down lactose more effectively[13] by consuming small quantities of dairy products several times a day over a couple of weeks. Reintroducing dairy in this way to people who have an underlying or chronic illness, however, is not recommended, as certain illnesses damage the intestinal tract in a way which prevents the lactase enzyme from being expressed.
However, other studies have shown that lactase production does not seem to be induced by dairy/lactose consumption.[14]

Nutritional concerns

Primary lactose intolerance

Populations where primary lactose intolerance is the norm have demonstrated similar health levels to westeners (outside of malnutrition issues; see the History of genetic prevalence subsection above) or better health (Japan).

Secondary lactose intolerance

While secondary lactose intolerance does not inherently affect an individual's nutritional needs, according to mainstream media and "accepted" doctrines in western European and North American countries, dairy is an essential part of a healthy diet. Dairy products are relatively good and accessible sources of calcium and potassium and many countries mandate that milk be fortified with vitamin A and vitamin D. Consequently, in dairy consuming societies, dairy is often a main source of these nutrients; and, for lacto-vegetarians, a main source of vitamin B12. Individuals who reduce or eliminate consumption of dairy must obtain these nutrients elsewhere. Asian populations for whom dairy is not part of their food culture do not present decreased health and sometimes present above average health, like Japan.

Plant based milk substitutes are not naturally rich in calcium, potassium, or vitamins A or D (and, like all non-animal products, contain no vitamin B12). However, prominent brands are often voluntarily fortified with many of these nutrients; one should read the label to be certain.

An increasing number of calcium-fortified breakfast foods, such as orange juice, bread, and dry cereal, have been appearing on supermarket shelves. Many fruits and vegetables are rich in potassium and vitamin A; animal products like meat and eggs are rich in vitamin B12, and the human body itself produces some vitamin D from exposure to direct sunlight. Finally, a dietitian or physician may recommend a vitamin or mineral supplement to make up for any remaining nutritional shortfall.

Lactose reduced dairy products have the same nutritional content as their full-lactose counterparts, but their taste and appearance may differ slightly.

Most infants with gastroenteritis due to rotavirus do not develop lactose intolerance,^[51] so these infants do not benefit from being put on a lactose-free diet unless symptoms of lactose intolerance are severe and persistent.

Congenital lactase deficiency

Congenital lactase deficiency, or CLD, is an autosomal recessive disorder which prevents the expression of lactase[15]. Before the 20th century, infants with this disease rarely survived. As substitute and lactose-free infant formulas later became availabe, nursing infants affected with CLD could now have their normal nutritional needs met. Beyond infancy, individuals with CLD usually have the same nutritional concerns as those affected by secondary lactose intolerance.

References

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^ "Intestinal Protozoa" Mark Wiser 2000
^ "Giardiasis" Andre Pennardt February 22, 2006
^ [1] Soy Nutrition
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^ ^a ^b Lactose intolerance in North and South Indians, Tandon RK, Joshi YK, Singh DS, Narendranathan M, Balakrishnan V, Lal K., Am J Clin Nutr 1981;35:943–6, 1981.
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^ Lactose malabsorption among Masai children of East Africa, RT Jackson, MC Latham, Am J Clin Nutr. 1979 Apr;32(4):779–82.
^ Prevalence of primary adult lactose malabsorption and awareness of milk intolerance in Italy, G Roberto Burgio, Gebhard Flatz, Cristiana Barbera, Rosario Patan, Attilio Boner, Cinzia Cajozzo, and Sibylle D Flaiz, The American Journal of Clinical Nutrition 39: pp 100–104, January 1984.
^ Lactose Intolerance, Tuula H. Vesa, Philippe Marteau, and Riitta Korpela, Journal of the American College of Nutrition, Vol. 19, No. 90002, 165S-175S (2000)
^ ^a ^b ^c Prevalence of primary adult lactose malabsorption in three populations of northern China, Wang YG, Yan YS, Xu JJ, Du RF, Flatz SD, Kühnau W, Flatz G., Hum Genet. 1984;67(1):103-6.
^ Lactose intolerance in the Lebanese population and in “Mediterranean lymphoma”, Salah M. Nasrallah, The American Journal of Clinical Nutrition 32 , pp. 1994–1996, October, 1979.
^ ^a ^b Genetics and epidemiology of adult-type hypolactasia, Sahi T., Scand J Gastroenterol Suppl ;29:202:7–20, 1994
^ Lactose malabsorption in Mexican-American children, Woteki CE, Weser E, Young EA, Am J Clin Nutr;29:19–24, 1976
^ Genetics of lactase persistence and lactose intolerance, Swallow DM., Annu Rev Genet ;37:197 - 219, 2003.
^ Systemic lactose intolerance: a new perspective on an old problem, S B Matthews, J P Waud, A G Roberts and A K Campbell, Postgraduate Medical Journal;81:167 - 173, 2005.
^ http://www.vivo.colostate.edu/hbooks/pathphys/digestion/smallgut/lactose_intol.html Colorado State University - Hypertexts for biomedical science - Digestive System
^ http://digestive.niddk.nih.gov/ddiseases/pubs/lactoseintolerance/#diagnosed
^ ^a ^b Berdanier, Hargrove, Nutrition and Gene Expression. CRC Press. 1993. ISBN 0849369614
^ Milk Intolerance: Lactose Intolerance and Cow's Milk Protein Allergy, J. Wilson, Newborn and Infant Nursing Reviews, Volume 5, Issue 4, Pages 203-207, Dec. 2005
^ Swaminathan, Nikhil. Adaptation to Digesting Milk Is "Strongest Signal of Selection EverDecember 11, 2006, Scientific American.com.
^ Charles Scriver, Beaudet, A.L., Valle, D., Sly, W.S., Vogelstein, B., Childs, B., Kinzler, K.W. (Accessed 2007). The Online Metabolic and Molecular Bases of Inherited Disease. New York: McGraw-Hill. - Summaries of 255 chapters, full text through many universities. There is also the OMMBID blog.
^ Enattah N, Sahi T, Savilahti E, Terwilliger J, Peltonen L, Järvelä I (2002). "Identification of a variant associated with adult-type hypolactasia". Nat Genet 30 (2): 233-7. PMID 11788828.
^ Lactose Intolerance. Roy, Barakat, Nwakakwa, Shojamanesh, Khurana, July 5, 2006 About 44% of lactose intolerant women regain the ability to digest lactose during pregnancy. This might be caused by slow intestinal transit and intestinal flora changes during pregnancy.
^ http://www.goatworld.com/articles/goatmilk/colostrum.shtml
^ [http://bjas.hit.bg/07/693A.htm| Peeva. Composition of buffalo milk. Sources of specific effects on the separate components. 2001. Bulg. J. Agric. Sci., 7: 329-335
^ http://jag.igr.poznan.pl/2004-Volume-45/2/pdf/2004_Volume_45_2-215-224.pdf
^ http://en.wikipedia.org/wiki/Goat_milk
^ [2] University of Guelph, Dept. of Food Science, Dairy Science and Technology
^ [3] Reger, Combs, Coulter and Koch. A Comparison of Dry Sweet Cream Buttermilk and Non-Fat Dry Milk Solids in Breadmaking. Journal of Dairy Science Vol. 34 No. 2 136-144
^ Goat Milk Composition
^ ^a ^b ^c [4] General guidelines for milk allergy, Oregon Health & Science University
^ http://www.gov.ns.ca/JUST/REGULATIONS/regs/marge.htm Margarine Regulations
^ [5] Enriched White Bread in Canada The Canadian Celiac Association
^ [6] Influence of Nonfat Dry Milk Solids on the Nutritive Value of Bread. Journal of Dairy Science Vol. 29 No. 12 821-829
^ http://en.wikipedia.org/wiki/Plant_milk
^ Montalto M, Curigliano V, Santoro L, Vastola M, Cammarota G, Manna R, Gasbarrini A, Gasbarrini G (2006). "Management and treatment of lactose malabsorption.". World J Gastroenterol 12 (2): 187-91. PMID 16482616.
^ He M, Yang Y, Bian L, Cui H (1999). "[Effect of exogenous lactase on the absorption of lactose and its intolerance symptoms]". Wei Sheng Yan Jiu 28 (5): 309-11. PMID 12712706.
^ O'Connell S, Walsh G (2006). "Physicochemical characteristics of commercial lactases relevant to their application in the alleviation of lactose intolerance.". Appl Biochem Biotechnol 134 (2): 179-91. PMID 16943638.
^ Heyman M (2006). "Lactose intolerance in infants, children, and adolescents.". Pediatrics 118 (3): 1279–86. PMID 16951027 doi:10.1542/peds.2006-1721.
^ PubMed

Durand, P. "Lactosurie et saccharosurie", In: BibI. Paediat. IV. Carbohydrate Metabolism in Children, edited by E. Rossi, E. Gautier, and J. W. Weber. Basel: S. Karger, 1959, pp. 496–502.
Holzel, A., V. Schwarz and K. W. Sutcliffe, "Defective lactose absorption causing malnutrition in infancy", The Lancet 1: 1126, 1959.
Carroccio, Montalto, Cavera, Notarbatolo (1998). "Lactose Intolerance and Self-Reported Milk Intolerance: Relationship with Lactose Maldigestion and Nutrient Intake". Journal of the American College of Nutrition 17: 631–636.
McGee, Harold (2004). "Milk after infancy: dealing with lactose", On Food and Cooking (Revised Edition). Scribner, pp 14–15. ISBN 0-684-80001-2.
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v • d • e Digestive system - Gastroenterology (primarily K20-K93, 530-579)
Esophagus	Esophagitis - GERD - Achalasia - Boerhaave syndrome - Nutcracker esophagus - Zenker's diverticulum - Mallory-Weiss syndrome - Barrett's esophagus
Stomach/ duodenum	Peptic (gastric/duodenal) ulcer - Gastritis - Gastroenteritis - Duodenitis - Dyspepsia - Pyloric stenosis - Achlorhydria - Gastroparesis - Gastroptosis - Portal hypertensive gastropathy
Hernia	Inguinal (Indirect, Direct) - Femoral - Umbilical - Incisional - Diaphragmatic - Hiatus
Noninfective enteritis and colitis	IBD (Crohn's, Ulcerative colitis) - noninfective gastroenteritis
Other intestinal	vascular (Abdominal angina, Mesenteric ischemia, Ischemic colitis, Angiodysplasia) - Ileus/Bowel obstruction (Intussusception, Volvulus) - Diverticulitis/Diverticulosis - IBS other functional intestinal disorders (Constipation, Diarrhea, Megacolon/Toxic megacolon, Proctalgia fugax) - Anal fissure/Anal fistula - Anal abscess - Rectal prolapse - Proctitis (Radiation proctitis)
Liver/hepatitis	Alcoholic liver disease - Liver failure (Acute liver failure) - Cirrhosis - PBC - NASH - Fatty liver - Peliosis hepatis - Portal hypertension - Hepatorenal syndrome
Accessory digestive	Gallbladder (Gallstones, Choledocholithiasis, Cholecystitis, Cholesterolosis, Rokitansky-Aschoff sinuses) Biliary tree (Cholangitis, Cholestasis/Mirizzi's syndrome, PSC, Biliary fistula, Ascending cholangitis) Pancreas (Acute pancreatitis, Chronic pancreatitis, Pancreatic pseudocyst, Hereditary pancreatitis)
Other/general	Appendicitis - Peritonitis (Spontaneous bacterial peritonitis) Malabsorption (celiac, Tropical sprue, Blind loop syndrome, Whipple's) postprocedural: Gastric dumping syndrome - Postcholecystectomy syndrome bleeding: Hematemesis - Melena - Gastrointestinal bleeding (Upper, Lower)
See also congenital

v • d • e Metabolic pathology / Inborn error of metabolism (E70-90, 270-279)
Amino acid	Aromatic (Phenylketonuria, Alkaptonuria, Ochronosis, Tyrosinemia, Albinism, Histidinemia) - Organic acidemias (Maple syrup urine disease, Propionic acidemia, Methylmalonic acidemia, Isovaleric acidemia, 3-Methylcrotonyl-CoA carboxylase deficiency) - Transport (Cystinuria, Cystinosis, Hartnup disease, Fanconi syndrome, Oculocerebrorenal syndrome) - Sulfur (Homocystinuria, Cystathioninuria) - Urea cycle disorder (N-Acetylglutamate synthase deficiency, Carbamoyl phosphate synthetase I deficiency, Ornithine transcarbamylase deficiency, Citrullinemia, Argininosuccinic aciduria, Hyperammonemia) - Glutaric acidemia type 1 - Hyperprolinemia - Sarcosinemia
Carbohydrate	Lactose intolerance - Glycogen storage disease (type I, type II, type III, type IV, type V, type VI, type VII) - fructose metabolism (Fructose intolerance, Fructose bisphosphatase deficiency, Essential fructosuria) - galactose metabolism (Galactosemia, Galactose-1-phosphate uridylyltransferase galactosemia, Galactokinase deficiency) - other intestinal carbohydrate absorption (Glucose-galactose malabsorption, Sucrose intolerance) - pyruvate metabolism and gluconeogenesis (PCD, PDHA) - Pentosuria - Renal glycosuria
Lipid storage	Sphingolipidoses/Gangliosidoses: GM2 gangliosidoses (Sandhoff disease, Tay-Sachs disease) - GM1 gangliosidoses - Mucolipidosis type IV - Gaucher's disease - Niemann-Pick disease - Farber disease - Fabry's disease - Metachromatic leukodystrophy - Krabbe disease Neuronal ceroid lipofuscinosis (Batten disease) - Cerebrotendineous xanthomatosis - Cholesteryl ester storage disease (Wolman disease)
Fatty acid metabolism	Lipoprotein/lipidemias: Hyperlipidemia - Hypercholesterolemia - Familial hypercholesterolemia - Xanthoma - Combined hyperlipidemia - Lecithin cholesterol acyltransferase deficiency - Tangier disease - Abetalipoproteinemia Fatty acid: Adrenoleukodystrophy - Acyl-coA dehydrogenase (Short-chain, Medium-chain, Long-chain 3-hydroxy, Very long-chain) - Carnitine (Primary, I, II)
Mineral	Cu Wilson's disease/Menkes disease - Fe Haemochromatosis - Zn Acrodermatitis enteropathica - PO₄^3�' Hypophosphatemia/Hypophosphatasia - Mg²⁺ Hypermagnesemia/Hypomagnesemia - Ca²⁺ Hypercalcaemia/Hypocalcaemia/Disorders of calcium metabolism
Fluid, electrolyte and acid-base balance	Electrolyte disturbance - Na⁺ Hypernatremia/Hyponatremia - Acidosis (Metabolic, Respiratory, Lactic) - Alkalosis (Metabolic, Respiratory) - Mixed disorder of acid-base balance - H₂O Dehydration/Hypervolemia - K⁺ Hypokalemia/Hyperkalemia - Cl^�' Hyperchloremia/Hypochloremia
Purine and pyrimidine	Hyperuricemia - Lesch-Nyhan syndrome - Xanthinuria
Porphyrin	Acute intermittent, Gunther's, Cutanea tarda, Erythropoietic, Hepatoerythropoietic, Hereditary copro-, Variegate
Bilirubin	Unconjugated (Lucey-Driscoll syndrome, Gilbert's syndrome, Crigler-Najjar syndrome) - Conjugated (Dubin-Johnson syndrome, Rotor syndrome)
Glycosaminoglycan	Mucopolysaccharidosis - 1:Hurler/Hunter - 3:Sanfilippo - 4:Morquio - 6:Maroteaux-Lamy - 7:Sly
Glycoprotein	Mucolipidosis - I-cell disease - Pseudo-Hurler polydystrophy - Aspartylglucosaminuria - Fucosidosis - Alpha-mannosidosis - Sialidosis
Other	Alpha 1-antitrypsin deficiency - Cystic fibrosis - Amyloidosis (Familial Mediterranean fever) - Acatalasia

Categories: Metabolic disorders | Conditions diagnosed by stool test

This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Lactose_intolerance". A list of authors is available in Wikipedia.