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Lactose intolerance

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Lactose intolerance
Classification and external resources

Lactose (disaccharide of β-D-galactose & β-D-glucose) is normally split by lactase.
ICD-10 E73.
ICD-9 271.3
OMIM 223100 Template:OMIM2
DiseasesDB 7238
MedlinePlus 000276
eMedicine med/3429 ped/1270
MeSH D007787

Lactose intolerance, also called lactase deficiency[1], is the inability to digest and metabolize lactose, a sugar found in milk. It is caused by a lack of the enzyme lactase in the digestive system, required to break down lactose. It results in symptoms including abdominal pain, bloating, flatulence, diarrhea, nausea, and acid reflux.

Most mammals normally become lactose intolerant when they are young; however, some human populations have developed lactase persistence, where lactase production continues into adulthood. It is estimated that 75% of adults worldwide show some decrease in lactase activity during adulthood.[2] The frequency of decreased lactase activity ranges from as little as 5% in northern Europe, up to 71% for Sicily, to more than 90% in some African and Asian countries.[3]

Mechanism

Disaccharides cannot be absorbed through the wall of the small intestine into the bloodstream, so in the absence of lactase, lactose present in ingested dairy products remains uncleaved and passes intact into the colon. The operons of enteric bacteria quickly switch over to lactose metabolism, and the resulting in-vivo fermentation produces copious amounts of gas (a mixture of hydrogen, carbon dioxide, and methane). This, in turn, may cause various abdominal symptoms, including abdominal pain, bloating, flatulence, diarrhea, nausea, and acid reflux. In addition, as with other unabsorbed sugars (such as sorbitol, mannitol, and xylitol), the presence of lactose and its fermentation products raises the osmotic pressure of the colon contents.

Classification

There are three major types of lactose intolerance:[4]

  1. Primary lactose intolerance. Environmentally induced when weaning a child in non–dairy consuming societies.[5] This is found in many Asian and African cultures, where industrialized and commercial dairy products are uncommon.
  2. Secondary lactose intolerance. Environmentally induced, resulting from certain gastrointestinal diseases, including exposure to intestinal parasites such as Giardia lamblia.[6][7] In such cases the production of lactase may be permanently disrupted.[6][7][8] A very common cause of temporary lactose intolerance is gastroenteritis, particularly when the gastroenteritis is caused by rotavirus. Another form of temporary lactose intolerance is lactose overload in infants.[9]
  3. Congenital lactase deficiency. A genetic disorder which prevents enzymatic production of lactase. Present at birth, and diagnosed in early infancy.

Pathological lactose intolerance can be caused by 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 (BMJ Textbook of Gastroenterology, Chapter 11, Celiac Disease, Dr.Jamie Gregor & Dr. Diamond Sherin Alidina).

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.

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 2 hours, depending on other foods and activities.[10] Substantial variability of the clinical response (symptoms of nausea, cramping, bloating, diarrhea, and flatulence) is to be expected, as the extent and severity of lactose intolerance varies among individuals.

When considering the need for confirmation, it is important to distinguish lactose intolerance from a milk allergy, which is an abnormal immune response (usually) to milk proteins. This may be done by giving lactose-free milk to a person displaying a reaction to milk. If the condition is purely lactose intolerance, the sufferer's symptoms will vanish, but if it is a milk allergy, the person will have the same reaction to the lactose-free milk as to normal milk. (An intermediate result might suggest that the person has both conditions.) Since lactose intolerance is the normal state for most adults on a worldwide scale and is not considered a disease condition, a medical diagnosis is not normally required. However, if confirmation is necessary, four tests are available.

Hydrogen breath test

In a hydrogen breath test, after an overnight fast, 50 grams of lactose (in a solution with water) is swallowed. If the lactose cannot be digested, enteric bacteria metabolize it and produce hydrogen. This, along with methane, can be detected in the patient's breath by a clinical gas chromatograph or a compact solid state detector. 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. However, given the need for frequent blood draws, this approach has been largely supplanted by breath testing.

Blood test

In the blood test, after an overnight fast, blood is drawn, and then 50 grams of lactose (in a solution with water) is swallowed. Blood is then drawn again at the 30 minute, 1 hour, 2 hour, and 3 hour mark. If the lactose cannot be digested, blood glucose levels will rise by less than 20 mg/dL.[11]

Stool acidity test

This test can be used to diagnose lactose intolerance in infants, for whom other forms of testing are risky or impractical.[12] The infant is given lactose to drink. If an individual is not intolerant, the lactose is digested and absorbed in the small intestine; if an individual is intolerant, it is not digested and absorbed and it reaches the colon. The bacteria in the colon, mixed with the lactose, cause acidity in stools. The stools passed after the ingestion of the lactose are then tested for levels of acidity. If the stools are acidic, the infant is intolerant to lactose. [13]

Intestinal biopsy

An intestinal biopsy can confirm lactase deficiency following discovery of elevated hydrogen in the hydrogen breath test.[14] Modern techniques have enabled a test to be performed at the patient's bedside identifying the presence/absence of the lactase enzyme in conjunction with upper gastrointestinal endoscopy.[15] However, for research applications such as mRNA measurements a specialist laboratory is required.

History

The ancient Greek physician Hippocrates (460-370 B.C.) first noted gastrointestinal upset and skin problems in some who consumed milk;[16] patients experiencing the former symptom may likely have been suffering from lactose intolerance. However, it was only in the 20th century 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 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. The term Milk drinking syndrome stands for a phenomenon when European experience is extrapolated to the other populations of the world.[17]

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.

Nomenclature

According to Heyman (2006)[4] 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 thisTemplate:By whom 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.

Lactase persistence

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 humans, 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.[18]

However, certain human populations have a mutation on chromosome 2 which eliminates the 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 without difficulty. This appears to be an evolutionarily recent adaptation to dairy consumption, and has occurred independently in both northern Europe and east Africa in populations with a historically pastoral lifestyle.[19] Lactase persistence, allowing lactose digestion to continue into adulthood, is a dominant allele, making lactose intolerance a recessive genetic trait. A noncoding variation in the MCM6 gene has been strongly associated with adult type hypolactasia (lactose intolerance).[5]

Some cultures, such as that of Japan, where dairy consumption has been on the increase compared with traditional dietary patterns, demonstrate a lower prevalence of lactose intolerance in spite of a genetic predisposition.[20]

Lactose intolerance by group

Human group Individuals examined Intolerance (%) Reference Allele frequency
Basques 85 0.3 [21] N/A
Dutch N/A 1 [22] N/A
Danes N/A 4 [23] N/A
Europeans in Australia 160 4 [24] 0.20
Swedes N/A 5-7 [25][26] N/A
British N/A 5–15 [27] 0.184-0.302[28]
Germans 1805 6-23 [29] N/A
Swiss N/A 10 [24] 0.316
European Americans 245 12 [24] 0.346
Tuareg N/A 13 [27] N/A
Finns N/A 14-23 [30] N/A
Eastern Slavs (Russians, Belarusians, Ukrainians) 260 30-50 [31] N/A
Austrians N/A 15–20 [27] N/A
Spaniards (non-Basque) N/A 15 [32] N/A
Northern French N/A 17 [27] N/A
Central Italians 65 19 [33] N/A
Indians N/A 20 [5][34] N/A
African Tutsi N/A 20 [24] 0.447
African Fulani N/A 23 [24] 0.48
Bedouins N/A 25 [27] N/A
Portuguese adults 102 35 [35] N/A
Southern Italians 51 41 [33] N/A
African American Children N/A 45 [5] N/A
Saami (in Russia and Finland) N/A 25–60 [36] N/A
Northern Italians 89 52 [33] N/A
North American Hispanics N/A 53 [27] N/A
Balkans N/A 55 [27] N/A
Mexican American Males N/A 55 [5][34] N/A
Cretans N/A 56 [5] N/A
African Maasai 21 62 [37] N/A
Southern French N/A 65 [27] N/A
Greek Cypriots N/A 66 [5][34] N/A
Jews, Mizrahi (Iraq, Iran, etc.) N/A 85 [38] N/A
Jews, Ashkenazi N/A 68.8 [5][34] N/A
Jews, Sephardic N/A 62 [38] N/A
Jews, Yemenite N/A 44 [38] N/A
Sicilians 100 71 [39][40] N/A
South Americans N/A 65–75 [27] N/A
Rural Mexicans N/A 73.8 [5][34] N/A
African Americans 20 75 [24] 0.87
Kazakhs from northwest Xinjiang 195 76.4 [41]
Lebanese 75 78 [42] N/A
Central Asians N/A 80 [27] N/A
Alaskan Eskimo N/A 80 [5][34] N/A
Australian Aborigines 44 85 [24] 0.922
Inner Mongolians 198 87.9 [41]
African Bantu 59 89 [24] 0.943
Asian Americans N/A 90 [5][34] N/A
Northeastern Han Chinese 248 92.3 [41]
Chinese 71 95 [24] 0.964
Southeast Asians N/A 98 [5][34] N/A
Thais 134 98 [24] 0.99
Native Americans 24 100 [24] 1.00

The statistical significance of these figures vary 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:

Chinese and Japanese populations typically lose between 20 and 30 percent of their ability to digest lactose within three to four years of weaning. Some studies have found that most Japanese can consume 200 ml (8 fl oz) of milk without severe symptoms (Swagerty et al., 2002).[20]

Ashkenazi Jews can keep 20–30 percent of their ability to digest lactose for many years.[22][43][45] 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.[46]

Evolutionary history

The ability to digest lactose into adulthood (lactase persistence) would have only been useful to humans after the invention of animal husbandry and the domestication of animal species that could provide a consistent source of milk. Hunter-gatherer populations before the Neolithic revolution were overwhelmingly lactose intolerant,[47][48] as are modern hunter-gatherers. Genetic studies suggest that the oldest mutations associated with lactase persistence only reached appreciable levels in human populations in the last ten thousand years.[49][50] Therefore lactase persistence is often cited as an example of both recent human evolution[51][52] and, as lactase persistence is a genetic trait but animal husbandry a cultural trait, gene-culture coevolution.[53]

Several genetic markers for lactase persistence have been identified, and these show that the allele has multiple origins in different parts of the world (i.e. it is an example of convergent evolution).[54] The version of the allele most common amongst Europeans is estimated to have risen to significant frequencies about 7,500 years ago in the central Balkans and Central Europe, a place and time approximately corresponding to the archaeological Linearbandkeramik and Starčevo cultures. From there, it most probably spread eastwards as far as India. Likewise, one of the four alleles associated with lactase persistence in African population, is also probably of European origin.[55] Since North Africans also possess this version of the allele it is probable that it actually originated earlier, in the Near East, but that the earliest farmers did not have high levels of lactase persistence and, subsequently, did not consume significant amounts of unprocessed milk.[56] Lactase persistence in Sub-Saharan Africa almost certainly had a separate origin, probably more than one,[57] and it is also likely that there was a separate origin associated with the domestication of the Arabian camel.[58] None of the mutations so far identified have been shown to be causal for the lactase persistence allele, and it is thought that there are several more yet to be discovered.[59]

The evolutionary processes driving the rapid spread of lactase persistence in some populations are not known.[54] In some East African ethnic groups lactase persistence has gone from negligible to near-ubiquitous frequencies in just three thousand years, suggesting a very strong selective pressure.[51][52] But some models for the spread of lactase persistence in Europe attribute it primarily to a form of genetic drift.[60] Competing theories on why the ability to digest lactose might be selected for include nutritional benefits, milk as a water source in times of drought, and increased calcium absorption helping to prevent rickets and osteomalacia in low-light regions.[54]

Roman authors recorded that the people of northern Europe, particularly Britain and Germany, drank unprocessed milk. This corresponds very closely with modern European distributions of lactose intolerance, where the people of Britain, Germany, and Scandinavia have a high tolerance, and those of southern Europe, especially Italy, have a lower tolerance.[61]

In east Asia, historical sources also attest that the Chinese did not consume milk, whereas the nomads who 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 nourishment would be foolish. The nomads also make an alcoholic beverage, called Kumis, from horse milk, although the fermentation process reduces the amount of lactose present.

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[62]).

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 of minimizing the occurrence and severity of symptoms. Berdanier and Hargrove recognise four general principles: avoidance of dietary lactose, substitution to maintain nutrient intake, regulation of calcium intake, and use of enzyme substitute.[14]

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."[1] Label reading is essential, as commercial terminology varies according to language and region.[14]

Lactose is present in two 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. After 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 bovids contains similar lactose percentages (goat milk 4.7%,[63] buffalo 4.86%,[64] yak 4.93%,[65] sheep milk 4.6%)

Butter. The butter-making process separates the majority of milk's water components from the fat components. Lactose, being a water soluble molecule, will still be present in small quantities in the butter unless it is also fermented to produce cultured butter.

Yogurt, Frozen 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. Frozen yogurt, if cultured similarly to its unfrozen counterpart, will contain similarly reduced lactose levels. However, many commercial brands contain milk solids[citation needed], increasing the lactose content.

Cheeses. Traditionally made hard cheese (such as Emmental) 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 Emmental 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.[66] 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.

Sour cream if made in the traditional way, may be tolerable, but most modern brands add milk solids. Consult labels.[67]

Examples of lactose levels in foods. As scientific consensus has not been reached concerning lactose percentage analysis methods [68] (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.[69] These quantities are to be treated as guidelines only.

Dairy product Serving size Lactose content
Milk, regular 250 ml 12 g
Milk, reduced fat 250 ml 13 g
Yogurt, plain, regular 200 g 9 g
Yogurt, plain, low-fat 200 g 12 g
Cheddar cheese 30 g 0.02 g
Cottage cheese 30 g 0.1 g
Butter 1 tsp 0.03 g
Ice cream 50 g 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, flavour and adhesive qualities, and is found in foods such as processed meats[70] (sausages/hot dogs, sliced meats, pâtés), gravy stock powder, margarines,[71] sliced breads,[72][73] breakfast cereals, potato chips,[74] processed foods, medications, pre-prepared meals, meal replacement (powders and bars), protein supplements (powders and bars) and even beers in the milk stout style.

Kosher products labeled pareve or fleishig are 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[70] (although it may also simply indicate that the product was produced on equipment shared with other products containing milk derivatives).

Alternative products

Plant-based milks and derivatives are inherently lactose free: soy milk, rice milk, almond milk, hazelnut milk, oat milk, hemp milk, peanut milk, horchata.

Main article: Milk#Reduction_or_elimination_of_lactose

The dairy industry has created low-lactose or lactose-free products to replace regular dairy.

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.[75][76]

Lactase enzymes similar to 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,[77] 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 can experiment with both timing and dosage to fit their particular needs.

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. 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.[4]

Rehabituation to dairy products

For healthy individuals with secondary lactose intolerance, it may be possible in some cases for the bacteria in the large intestine to adapt to an altered diet and break down small quantities of lactose more effectively[78] by habitually consuming small amounts of dairy products several times a day over a period of time. 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.

Some studies indicate that environmental factors (more specifically, the consumption of lactose) may "play a more important role than genetic factors in the etio-pathogenesis of milk intolerance",[20] but some other publications suggest that lactase production does not seem to be induced by dairy/lactose consumption.[79]

Nutritional concerns

Primary lactose intolerance

Populations where primary lactose intolerance is the norm have demonstrated similar health levels to westerners (outside of malnutrition issues; see the Evolutionary history subsection above), or better health.

Secondary lactose intolerance

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. However, Asian populations for whom dairy is not part of their food culture do not present decreased health and sometimes present above average health, as in Japan.

Plant based milk substitutes are not naturally rich in calcium, potassium, or vitamins A or D (and, like most non-animal products, contain no vitamin B12). However, prominent brands are often voluntarily fortified with many of these nutrients.

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.

Most infants with gastroenteritis due to rotavirus do not develop lactose intolerance,[80] 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.[81] Beyond infancy, individuals with CLD usually have the same nutritional concerns as those affected by secondary lactose intolerance.

See also

References

  1. ↑ 1.0 1.1 National Digestive Diseases Information Clearinghouse (March 2006). "Lactose Intolerance". National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health. http://digestive.niddk.nih.gov/ddiseases/pubs/lactoseintolerance/. 
  2. ↑ "Improved lactose digestion and intolerance among African-American adolescent girls fed a dairy-rich diet.". Journal of the American Dietetic Association. 2000. PMID 10812376. http://www.accessmylibrary.com/coms2/summary_0286-27939567_ITM. Retrieved 2009-02-03. "Approximately 75% of the world's population loses the ability to completely digest a physiological dose of lactose after infancy". 
  3. ↑ Bulhões, A.C.; Goldani, H.A.S.; Oliveira, F.S.; Matte, U.S.; Mazzuca, R.B.; Silveira, T.R. (2007). "Correlation between lactose absorption and the C/T-13910 and G/A-22018 mutations of the lactase-phlorizin hydrolase (LCT) gene in adult-type hypolactasia". Brazilian Journal of Medical and Biological Research 40 (11): 1441–6. doi:10.1590/S0100-879X2007001100004. PMID 17934640. 
  4. ↑ 4.0 4.1 4.2 {{cite journal |author=Heyman MB |title=Lactose intolerance in infants, children, and adolescents |journal=Pediatrics |volum, approximately 70% of the global population cannot tolerate lactose in adulthood. Thus, someTemplate:Who
  5. ↑ 5.00 5.01 5.02 5.03 5.04 5.05 5.06 5.07 5.08 5.09 5.10 5.11 Enattah NS, Sahi T, Savilahti E, Terwilliger JD, Peltonen L, Järvelä I (2002). "Identification of a variant associated with adult-type hypolactasia". Nat. Genet. 30 (2): 233–7. doi:10.1038/ng826. PMID 11788828. 
  6. ↑ 6.0 6.1 Mark Wiser (August 30, 2007). "Intestinal Protozoa". Tulane University. http://www.tulane.edu/~wiser/protozoology/notes/intes.html. Retrieved 2008-01-31. 
  7. ↑ 7.0 7.1 Template:Emedicine Andre Pennardt February 22, 2006
  8. ↑ Swagerty DL, Walling AD, Klein RM (2002). "Lactose intolerance". Am Fam Physician 65 (9): 1845–50. PMID 12018807. http://www.aafp.org/afp/20020501/1845.html. 
  9. ↑ Colic and lactose intolerance
  10. ↑ R. Bowen (December 28, 2006). "Lactose Intolerance (Lactase Non-Persistence)". Pathophysiology of the Digestive System. Colorado State University. http://www.vivo.colostate.edu/hbooks/pathphys/digestion/smallgut/lactose_intol.html. 
  11. ↑ "Lactose tolerance tests". 3-May-2011. http://www.nlm.nih.gov/medlineplus/ency/article/003500.htm. 
  12. ↑ National Digestive Diseases Information Clearinghouse (March 2006). "Lactose Intolerance -- How is lactose intolerance diagnosed?". National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health. http://digestive.niddk.nih.gov/ddiseases/pubs/lactoseintolerance/#diagnosed. 
  13. ↑ "Stool Acidity Test". Jay W. Marks, M.D.. http://www.medicinenet.com/stool_acidity_test/article.htm#stool. Retrieved 20/5/2011. 
  14. ↑ 14.0 14.1 14.2 Hargrove, James L.; Berdanier, Carolyn D. (1993). Nutrition and gene expression. Boca Raton: CRC Press. ISBN 0-8493-6961-4. 
  15. ↑ Kuokkanen et al. (2006). A biopsy-based quick test in the diagnosis of duodenal hypolactasia in upper gastrointestinal endoscopy. Endoscopy; 38 (7): 708-712.
  16. ↑ Wilson J (December 2005). "Milk Intolerance: Lactose Intolerance and Cow's Milk Protein Allergy". Newborn and Infant Nursing Reviews 5 (4): 203–7. doi:10.1053/j.nainr.2005.08.004. 
  17. ↑ Joseph Jordania (2006). Who Asked the First Question? The Origins of Human Choral Singing, Intelligence, Language and Speech. Tbilisi: Logos. ISBN 99940-31-81-3. 
  18. ↑ Soy and Lactose Intolerance Wayback: Soy Nutrition
  19. ↑ Coles Harriet (2007-01-20). "The lactase gene in Africa: Do you take milk?". The Human Genome, Wellcome Trust. http://genome.wellcome.ac.uk/doc_WTX038968.html. Retrieved 2008-07-18. 
  20. ↑ 20.0 20.1 20.2 Yoshida Y, Sasaki G, Goto S, Yanagiya S, Takashina K (1975). "Studies on the etiology of milk intolerance in Japanese adults". Gastroenterol. Jpn. 10 (1): 29–34. PMID 1234085. 
  21. ↑ Enattah, N; Trudeau, A; Pimenoff, V; Maiuri, L; Auricchio, S; Greco, L; Rossi, M; Lentze, M et al. (2007). "Evidence of Still-Ongoing Convergence Evolution of the Lactase Persistence T-13910 Alleles in Humans". The American Journal of Human Genetics 81: 615–25. doi:10.1086/520705. PMID 17701907. 
  22. ↑ 22.0 22.1 Flatz G (1987). "Genetics of lactose digestion in humans". Adv. Hum. Genet. 16: 1–77. PMID 3105269. 
  23. ↑ Timo Sahi (N/A). "Genetics and epidemiology of adult-type hypolactasia with emphasis on the situation in Europe". Scandinavian Journal of Nutrition/Naringsforskning. 
  24. ↑ 24.00 24.01 24.02 24.03 24.04 24.05 24.06 24.07 24.08 24.09 24.10 Kretchmer N (1972). "Lactose and lactase". Sci. Am. 227 (4): 71–8. PMID 4672311. 
  25. ↑ Almon, R; Engfeldt, P; Tysk, C; Sjöström, M; Nilsson, TK (2007). "Prevalence and trends in adult-type hypolactasia in different age cohorts in Central Sweden diagnosed by genotyping for the adult-type hypolactasia-linked LCT -13910C > T mutation". Scandinavian journal of gastroenterology 42 (2): 165–70. doi:10.1080/00365520600825257. PMID 17327935. 
  26. ↑ Torniainen, S.; Hedelin, M.; Autio, V.; Rasinpera, H.; Balter, K. A.; Klint, A.; Bellocco, R.; Wiklund, F. et al. (2007). "Lactase Persistence, Dietary Intake of Milk, and the Risk for Prostate Cancer in Sweden and Finland". Cancer Epidemiology Biomarkers & Prevention 16: 956. doi:10.1158/1055-9965.EPI-06-0985. PMID 17507622. 
  27. ↑ 27.0 27.1 27.2 27.3 27.4 27.5 27.6 27.7 27.8 27.9 de Vrese M, Stegelmann A, Richter B, Fenselau S, Laue C, Schrezenmeir J (2001). "Probiotics--compensation for lactase insufficiency". Am. J. Clin. Nutr. 73 (2 Suppl): 421S–429S. PMID 11157352. http://www.ajcn.org/cgi/content/full/73/2/421S. 
  28. ↑ G.D. Smith et al., Lactase persistence-related genetic variant: population substructure and health outcomes. European Journal of Human Genetics, 2008.
  29. ↑ Flatz, G.; Howell, J.N.; Doench, J.; Flatz, S.D. (1982). "Distribution of physiological adult lactase phenotypes, lactose absorber and malabsorber, in Germany". Human Genetics 62 (2): 152–7. doi:10.1007/BF00282305. PMID 6819221. 
  30. ↑ Heli Rasinperä (April 2006). "ADULT-TYPE HYPOLACTASIA: Genotype-phenotype correlation". https://www.doria.fi/bitstream/handle/10024/1389/adulttyp.pdf?sequence=1. 
  31. ↑ Borinskaia SA, Rebrikov DV, Nefedova VV, Kofiadi IA, Sokolova MV, Kolchina EV, Kulikova EA, Chernyshov VN, Kutsev SI, Polonikov AV, Ivanov VP, Kozlov AI, Iankovskiĭ NK. (2006). "[ Molecular diagnosis and frequencies of primary hypolactasia in populations of RUSSIA and neighboring countries]" (in Russian). Mol Biol (Mosk) 40 (6): 1031-1036. PMID 17209431. 
  32. ↑ http://yannklimentidis.blogspot.com/2007/03/monday-maps-lactase-persistence-in.html
  33. ↑ 33.0 33.1 33.2 Cavalli-Sforza LT, Strata A, Barone A, Cucurachi L (1987). "Primary adult lactose malabsorption in Italy: regional differences in prevalence and relationship to lactose intolerance and milk consumption" (PDF). Am. J. Clin. Nutr. 45 (4): 748–54. PMID 3565303. http://www.ajcn.org/cgi/reprint/45/4/748.pdf. 
  34. ↑ 34.0 34.1 34.2 34.3 34.4 34.5 34.6 34.7 "Lactose Intolerance: The Molecular Explanation". UC Davis Nutritional Genomics. http://nutrigenomics.ucdavis.edu/?page=Information/Concepts_in_Nutrigenomics/Lactose_Intolerance. 
  35. ↑ (Portuguese) Intolerância à lactose Maria do Céu Salgado - Outubro de 2007
  36. ↑ Kozlov A, Lisitsyn D (1997). "Hypolactasia in Saami subpopulations of Russia and Finland". Anthropol Anz 55 (3-4): 281–7. PMID 9468755. 
  37. ↑ Jackson RT, Latham MC (1979). "Lactose malabsorption among Masai children of East Africa". Am. J. Clin. Nutr. 32 (4): 779–82. PMID 581925. 
  38. ↑ 38.0 38.1 38.2 Ernest L. Abel (2001-08). Jewish Genetic Diseases: a Layman's Guide. McFarland & Company, Inc., Publishers. ISBN 9780786409419. http://books.google.com/?id=yUNKaRAVZvMC&pg=PA156&lpg=PA156&dq=lactose+intolerance+among+jews&q=lactose%20intolerance%20among%20jews. 
  39. ↑ Burgio GR, Flatz G, Barbera C, et al. (1984). "Prevalence of primary adult lactose malabsorption and awareness of milk intolerance in Italy" (PDF). Am. J. Clin. Nutr. 39 (1): 100–4. PMID 6691285. http://www.ajcn.org/cgi/reprint/39/1/100.pdf. 
  40. ↑ Vesa TH, Marteau P, Korpela R (2000). "Lactose intolerance". J Am Coll Nutr 19 (2 Suppl): 165S–175S. PMID 10759141. http://www.jacn.org/cgi/content/full/19/suppl_2/165S. 
  41. ↑ 41.0 41.1 41.2 Wang YG, Yan YS, Xu JJ, et al. (1984). "Prevalence of primary adult lactose malabsorption in three populations of northern China". Hum. Genet. 67 (1): 103–6. doi:10.1007/BF00270566. PMID 6235167. 
  42. ↑ Nasrallah SM (1979). "Lactose intolerance in the Lebanese population and in "Mediterranean lymphoma"" (PDF). Am. J. Clin. Nutr. 32 (10): 1994–6. PMID 484518. http://www.ajcn.org/cgi/reprint/32/10/1994.pdf. 
  43. ↑ 43.0 43.1 Sahi T (1994). "Genetics and epidemiology of adult-type hypolactasia". Scand. J. Gastroenterol. Suppl. 202: 7–20. doi:10.3109/00365529409091740. PMID 8042019. 
  44. ↑ Woteki CE, Weser E, Young EA (1976). "Lactose malabsorption in Mexican-American children" (PDF). Am. J. Clin. Nutr. 29 (1): 19–24. PMID 946157. http://www.ajcn.org/cgi/reprint/29/1/19.pdf. 
  45. ↑ Swallow DM (2003). "Genetics of lactase persistence and lactose intolerance". Annu. Rev. Genet. 37: 197–219. doi:10.1146/annurev.genet.37.110801.143820. PMID 14616060. 
  46. ↑ Matthews SB, Waud JP, Roberts AG, Campbell AK (2005). "Systemic lactose intolerance: a new perspective on an old problem". Postgrad Med J 81 (953): 167–73. doi:10.1136/pgmj.2004.025551. PMID 15749792. 
  47. ↑ Swaminathan, N. 2007. Not Milk? Neolithic Europeans Couldn't Stomach the Stuff. Scientific American.
  48. ↑ Malmstrom, H., Linderholm, A., Liden, K., Stora, J., Molnar, P., Holmlund, G., Jakkobson, M., Gotherstrom, A. 2010. High frequency of lactose intolerance in a prehistoric hunter-gatherer population in northern Europe. BMC Evolutionary Biology 10: 89.
  49. ↑ Coelho, M., Luiselli, D., Bertorelle, G., Lopes, A. I., Seixas, S., Destro-Bisol, G. and Rocha, J. 2002. Microsatellite variation and evolution of human lactase persistence. Human Genetics 117(4): 329–339.
  50. ↑ Bersaglieri T., Sabeti P. C., Patterson N., Vanderploeg T., Schaffner S. F., Drake J. A., Rhodes M., Reich D. E. and Hirschhorn J. N. 2004. Genetic signatures of strong recent positive selection at the lactase gene. American Journal of Human Genetics 74(6): 1111–20.
  51. ↑ 51.0 51.1 Wade, N. Study Detects Recent Instance of Human Evolution. The New York Times. December 10, 2006.
  52. ↑ 52.0 52.1 Swaminathan, N. 2006. African Adaptation to Digesting Milk Is "Strongest Signal of Selection Ever". Scientific American.
  53. ↑ Aoki, K. 2001. Theoretical and Empirical Aspects of Gene–Culture Coevolution. Theoretical Population Biology 59(4): 253–261.
  54. ↑ 54.0 54.1 54.2 Swallow, D. M. 2003. Genetics of Lactase Persistence and Lactose Intolerance. Annual Review of Genetics 37: 197–219.
  55. ↑ Itan Y, Powell A, Beaumont MA, Burger J, Thomas MG (2009) The Origins of Lactase Persistence in Europe. PLoS Comput Biol 5(8): e1000491. doi:10.1371/journal.pcbi.1000491
  56. ↑ Myles, S., Bouzekri, N., Haverfield, E., Cherkaoui, M., Dugoujon, J. M. and Ward, R. 2005. Genetic evidence in support of a shared Eurasian-North African dairying origin. Biomedical and Life Sciences 117(1): 34–42.
  57. ↑ Tishkoff, S. A., Reed, F. A., Ranciaro, A., Voight, B. F., Babbitt, C. C., Silverman, J. S., Powell, K., Mortensen, H. M., Hirbo, J. B., Osman, M., Ibrahim, M., Omar, S. A., Lema, G., Nyambo, T. B., Ghori, J., Bumpstead, S., Pritchard, J. K., Wray, G. A. and Deloukas, P. 2006. Convergent adaptation of human lactase persistence in Africa and Europe. Nature Genetics 39: 31–40.
  58. ↑ Enattah, N. S., Jensen, T. G. K., Nielsen, M., Lewinski, R., Kuokkanen, M., Rasinpera, H., El-Shanti, H., Kee Seo, J., Alifrangis, M., Khalil, I. F., Natah, A., Ali, A., Natah, S., Comas, D., Mehdi, S. Q., Groop, L., Vestergaard, E. M., Imtiaz, F., Rashed, M. S., Meyer, B., Troelsen, J., and Peltonen, L. 2008. Independent Introduction of Two Lactase-Persistence Alleles into Human Populations Reflects Different History of Adaptation to Milk Culture. American Journal of Human Genetics 82(1): 57–72.
  59. ↑ Itan, Y., Jones, B. L., Ingram, C. J. E., Swallow, D. M. and Thomas, M. G. 2010. A worldwide correlation of lactase persistence phenotype and genotypes. BMC Evolutionary Biology 10: 36.
  60. ↑ Itan, Y., Powell, A., Beaumont, M. A., Burger, J., Thomas, M. G. 2009. The Origins of Lactase Persistence in Europe. PLoS Computational Biology 5(8): e1000491.
  61. ↑ "Lactose tolerance/intolerance". Gene Expression. January 19, 2004. http://www.gnxp.com/MT2/archives/001681.html. Retrieved 2008-01-31. 
  62. ↑ Template:Emedicine 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.
  63. ↑ Composition of Human, Cow, and Goat Milks - Goat Milk - GOATWORLD.COM
  64. ↑ Peeva (2001). "Composition of buffalo milk. Sources of specific effects on the separate components". Bulg. J. Agric. Sci. 7: 329–35. http://bjas.hit.bg/07/693A.htm. 
  65. ↑ C:\JAG2\Jiang.vp
  66. ↑ http://www.ilovecheese.com/lactose_intolerant_faqs.asp
  67. ↑ Reger, Combs, Coulter and Koch (February 1, 1951). "A Comparison of Dry Sweet Cream Buttermilk and Non-Fat Dry Milk Solids in Breadmaking". Journal of Dairy Science 34 (2): 136–44. doi:10.3168/jds.S0022-0302(51)91682-7. http://jds.fass.org/cgi/content/abstract/34/2/136. 
  68. ↑ Goat Milk Composition
  69. ↑ http://www.gastro.net.au/diets/lactose.html
  70. ↑ 70.0 70.1 "General guidelines for milk allergy". Oregon Health & Science University. http://www.ohsu.edu/xd/health/health-information/topic-by-id.cfm?ContentTypeId=90&ContentId=P01696. 
  71. ↑ "Margarine Regulations". http://www.gov.ns.ca/JUST/REGULATIONS/regs/marge.htm. 
  72. ↑ "Enriched White Bread in Canada". The Canadian Celiac Association. http://www.celiac.ca/Articles/PAB%20Enriching%20GF%20Foods.html. 
  73. ↑ Riggs, Lloyd K; Beaty, Annabel; Johnson, Arnold H (December). "Influence of Nonfat Dry Milk Solids on the Nutritive Value of Bread". Journal of Dairy Science 29 (12): 821–9. doi:10.3168/jds.S0022-0302(46)92546-5. http://jds.fass.org/cgi/content/abstract/29/12/821. 
  74. ↑ "Bartek, food additive company" (PDF). http://www.bartek.ca/pdfs/Applications/SavouryProducts/SavourySnackFoods/Savoury%20Snack%20Foods%20Alphabetical%20List%20of%20Product%20Names.pdf. 
  75. ↑ Montalto M, Curigliano V, Santoro L, et al. (2006). "Management and treatment of lactose malabsorption". World J. Gastroenterol. 12 (2): 187–91. PMID 16482616. http://www.wjgnet.com/1007-9327/12/187.asp. 
  76. ↑ He M, Yang Y, Bian L, Cui H (1999). "[Effect of exogenous lactase on the absorption of lactose and its intolerance symptoms]" (in Chinese). Wei Sheng Yan Jiu 28 (5): 309–11. PMID 12712706. 
  77. ↑ 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. doi:10.1385/ABAB:134:2:179. PMID 16943638. 
  78. ↑ Lactose intolerant? Drink more milk Steve Tally
  79. ↑ Prevalence, Age & Genetics of Lactose Intolerance - foodreactions.org
  80. ↑ Turck D (2007). "[Prevention and treatment of acute diarrhea in infants]" (in French). Arch Pediatr 14 (11): 1375–8. doi:10.1016/j.arcped.2007.06.009. PMID 17629685. 
  81. ↑ Template:Emedicine Guandalini S, Frye R, Rivera-Hernández D, Miller L, Borowitz S


Notes

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