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the claim
Vitiligo is inherited across generations through genetic factors
the verdict
INSUFFICIENT LEANING
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the weight of evidence
3 sources for · 0 against

Available sources note that genetic make-up is considered a possible factor in vitiligo and report increased prevalence among biological relatives, but do not comprehensively establish intergenerational transmission mechanisms.

Evidence for · 3
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Linkage analysis in a large kindred with autosomal dominant transmission of polyglandular autoimmune disease type II (Schmidt syndrome). Schmidt syndrome (PGA syndrome type II) is a rare condition characterized by polyglandular failure. It is an autosomal dominant trait with variable expressivity that was inherited over four generations in an the Indiana kindred. Association of HLA-B8 has been reported with Schmidt syndrome. Our proband is a 12-year-old boy with Addison disease, insulin dependent diabetes mellitus (IDDM), and vitiligo. Two of his eight sibs had either IDDM (sister) or vitiligo and hyperthyroidism (brother). His mother had hypothyroidism. Seven members of earlier generations apparently were also affected. We obtained peripheral blood for HLA and genetic analysis from 21 relatives in a family with 8 Schmidt syndrome individuals in three generations. HLA studies on 15 affected and unaffected relatives showed only 2 of 7 persons with B8-containing haplotypes. Therefore, no association exists between the B8-containing haplotype and the syndrome. We identified informative marker loci.
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The analysis

rails:sufficiency:partial_only:for=0+3p:against=0+0p | v55:multi_partial_one_side:lean=lean_partial:for:one_sided

More for · 2
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Studies on vitiligo. I. Epidemiological profile in Calcutta, India. An epidemiological profile of vitiligo in Calcutta is presented. Prevalence data were gathered from 15,685 individuals drawn from the general population; pedigree data were collected through 293 vitiligo patients. The overall prevalence of vitiligo is about 5 per 1,000 individuals. There are no significant sex or age differences in prevalence rates. About a 4.5-fold increase in prevalence is observed among close biological relatives of affected individuals. There is, however, no clearcut correspondence between relative risks and kinship coefficients. There are no significant differences in the frequencies of various types of vitiligo between probands with and without positive family history. The overall mean and modal ages of onset are about 22 years and 15 years, respectively. The mean ages among males (24.8 years) and females (19.3 years) are significantly different. Published in Genetic epidemiology (1985)
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function. The causes of vitiligo are not clear, but research suggests several possibilities, including autoimmune reactions, genetic make-up, oxidative stress Human skin color, also known as skin tone, ranges from the darkest brown to the lightest hues. Differences in skin color among individuals is caused by variation in pigmentation, which is largely the result of genetics (inherited from one's biological parents), and in adults in particular, due to exposure to the sun, disorders, or some combination thereof. Differences across populations evolved th Human skin color, also known as skin tone, ranges from the darkest brown to the lightest hues. Differences in skin color among individuals is caused by variation in pigmentation, which is largely the result of genetics (inherited from one's biological parents), and in adults in particular, due to exposure to the sun, disorders, or some combination thereof. Differences across populations evolved through natural selection and sexual selection, because of social norms and differences in environment, as well as regulation of the biochemical effects of ultraviolet radiation penetrating the skin. Human skin color is influenced greatly by the amount of the pigment melanin present. Melanin is produced within the skin in cells called melanocytes; it is the main determinant of the skin color of darker-skin humans. The skin color of people with light skin is determined mainly by the bluish-white connective tissue under the dermis and by the hemoglobin circulating in the veins of the dermis. The red color underlying the skin becomes more visible, especially in the face, when, as a consequence of physical exercise, sexual arousal, or the stimulation of the nervous system (e.g. due to anger or embarrassment), arterioles dilate. Color is not entirely uniform across an individual's skin; for example, the skin of the palm and the soles of the feet is lighter than most other skin; this is more noticeable in darker-skinned people. T Human skin color, also known as skin tone, ranges from the darkest brown to the lightest hues. Differences in skin color among individuals is caused by variation in pigmentation, which is largely the result of genetics (inherited from one's biological parents), and in adults in particular, due to exposure to the sun, disorders, or some combination thereof. Differences across populations evolved through natural selection and sexual selection, because of social norms and differences in environment, as well as regulation of the biochemical effects of ultraviolet radiation penetrating the skin. Human skin color is influenced greatly by the amount of the pigment melanin present. Melanin is produced within the skin in cells called melanocytes; it is the main determinant of the skin color of darker-skin humans. The skin color of people with light skin is determined mainly by the bluish-white connective tissue under the dermis and by the hemoglobin circulating in the veins of the dermis. The red color underlying the skin becomes more visible, especially in the face, when, as a consequence of physical exercise, sexual arousal, or the stimulation of the nervous system (e.g. due to anger or embarrassment), arterioles dilate. Color is not entirely uniform across an individual's skin; for example, the skin of the palm and the soles of the feet is lighter than most other skin; this is more noticeable in darker-skinned people. There is a direct correlation between the geographic distribution of ultraviolet radiation (UVR) and the distribution of indigenous skin pigmentation around the world. Areas that receive higher amounts of UVR, generally located closer to the equator or at higher altitudes, tend to have darker-skinned populations. Areas that are far from the tropics and closer to the poles have lower intensity of UVR, which is reflected in lighter-skinned populations. By the time modern Homo sapiens evolved, all humans were dark-skinned. Some researchers suggest that human populations over the past 50,000 years have changed from dark-skinned to light-skinned and that such major changes in pigmentation may have happened in as little as 100 generations (≈2,500 years) through selective sweeps. Natural skin color can also darken as a result of tanning due to exposure to sunlight. The leading theory is that skin color adapts to intense sunlight irradiation to provide partial protection against the ultraviolet fraction that produces damage and thus mutations in the DNA of the skin cells. The social significance of differences in skin color has varied across cultures and over time, as demonstrated with regard to social status and discrimination. Melanin is produced by cells called melanocytes in a process called melanogenesis. Melanin is made within small membrane–bound packages called melanosomes. As they become full of melanin, they move into the slender arms of melanocytes, from where they are transferred to the keratinocytes. Under normal conditions, melanosomes cover the upper part of the keratinocytes and protect them from genetic damage. One melanocyte supplies melanin to thirty-six keratinocytes according to signals from the keratinocytes. These keratinocytes regulate melanin production and replication of melanocytes. People have different skin colors mainly because their melanocytes produce different amount and kinds of melanin. The genetic mechanism behind human skin color is mainly regulated by the enzyme tyrosinase, which creates the color of the skin, eyes, and hair shades. Vitiligo is a condition that causes depigmentation of sections of skin. It occurs when melanocytes die or are unable to function. The causes of vitiligo are not clear, but research suggests several possibilities, including autoimmune reactions, genetic make-up, oxidative stress, and neural or viral causes. The incidence worldwide is less than 1%. Individuals affected by vitiligo sometimes suffer psychological discomfort because of their appearance.
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This check searched the claim as stated. It did not run a separate search for evidence against it.
  1. PubMed: Linkage analysis in a large kindred with autosomal dominant transmission of polyglandular autoimmune disease type II (Schmidt syndrome).peer-reviewedno side taken
  2. PubMed: Studies on vitiligo. I. Epidemiological profile in Calcutta, India.peer-reviewedno side taken
  3. Human skin colorreferenceno side taken
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