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        "titulo" => "Perspetivas de biologia evolutiva da predisposi&#231;&#227;o gen&#233;tica para hipertens&#227;o arterial essencial&#44; estudada com base em polimorfismos gen&#233;ticos nas atuais popula&#231;&#245;es humanas globais"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">The article by Sousa et al&#46; in this issue of the <span class="elsevierStyleItalic">Journal</span><a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">1</span></a> raises several interesting questions related to the association of the C825T polymorphism of the <span class="elsevierStyleItalic">GNB3</span> gene&#44; which codes for the beta 3 subunit of G proteins &#40;responsible for the transduction of messages resulting from activation of G protein-coupled receptors&#41;&#44; with hypertension and cardiovascular risk&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">The first question concerns differences in susceptibility to essential hypertension in modern human populations that result from the natural selection of genes over the last 30<span class="elsevierStyleHsp" style=""></span>000 years associated with environmental factors during the global expansion of humanity after ancestral populations left Africa&#44; as described in an important article by Young et al&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">2</span></a> The factors acting at that time were temperature and humidity&#44; inversely related to latitude in Africa&#44; which activated compensatory adaptive hypertensive mechanisms secondary to decreased volume-dependent blood pressure associated with severe loss of sodium chloride by sweating&#46; Young et al&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">2</span></a> identified several polymorphic variants of five genes encoding proteins involved in these compensatory mechanisms of volume change and vascular reactivity secondary to salt loss&#46; The genetic variant most strongly associated with current global variation in susceptibility to hypertension is the C825T polymorphism of the <span class="elsevierStyleItalic">GNB3</span> gene&#46; The frequency distribution of genetic variants associated with adaptive mechanisms&#44; especially the one analyzed by Sousa et al&#46;&#44; is independent of the continent where they occur&#44; as shown by the similarity of their distribution in Native Americans of the equatorial zones to that of modern African populations&#46; We performed a study<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">3</span></a> of the Hp1 polymorphic variant &#40;only found in humans&#41; of haptoglobin&#44; an acute phase protein that for more than 30 years has been associated with higher blood pressure sensitivity to sodium&#46; In this work we found very similar allelic frequencies of the <span class="elsevierStyleItalic">HP</span> gene in Honduras &#40;Central America&#41; and in Mozambique &#40;Africa&#41;&#46; These countries are at similar latitudes&#44; although in the case of Native American populations the adaptations occurred over the course of less than 20<span class="elsevierStyleHsp" style=""></span>000 years&#46; This is the result of movements in Eurasia&#44; in the opposite direction &#40;north to south&#41; to the initial movement subsequent to the departure from Africa of the original populations in which these gene variants were initially fixed&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">With regard to the same Hp allele&#44; we published a paper in the <span class="elsevierStyleItalic">Journal</span> in 2000&#44;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">4</span></a> the results of which showed a different nocturnal blood pressure response in salt-sensitive hypertensive individuals&#44; compared to normotensive and non-sensitive individuals&#44; after a change of diet from low to high sodium&#46; The Hp1-1 allele was found in 100&#37; of both normotensive and hypertensive salt-sensitive subjects&#46; In this study we also showed that in urban settings in modern African populations&#44; these individuals have increased cardiovascular risk&#44; even compared to those in the current African diaspora&#44; which confirms the epidemiological transition of these populations with respect to the original ones 50 years ago&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">As further evidence of the effect of these ancestral gene variants&#44; the work by Sousa et al&#46; shows that the risk for obesity conferred by the 825T allele of the <span class="elsevierStyleItalic">GNB3</span> gene in Madeira&#44; also demonstrated in other populations&#44; is associated with a higher risk of essential hypertension&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">5</span></a> The frequency of this morbid allele is higher in hypertensive patients than in controls in the population of the Madeira archipelago&#44; in contrast to those found in a larger population &#40;the PHYSA study&#41; on the mainland&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">6&#44;7</span></a> Regardless of the differences in sampling methods between these two studies&#44; the explanation for the association of this variant with hypertension on this Portuguese island&#44; which is not observed on the mainland&#44; probably lies in the fact that the Madeira population is a genetic isolate in which the effect of stratification of these genes is likely to be maximized&#44; despite its common ethnic origins with mainland populations&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">8</span></a></p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of interest</span><p id="par0025" class="elsevierStylePara elsevierViewall">The author has no conflicts of interest to declare&#46;</p></span></span>"
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Editorial comment
Genetic predisposition for essential hypertension, based on studies of genetic polymorphisms in modern global human populations: The perspective of evolutionary biology
Perspetivas de biologia evolutiva da predisposição genética para hipertensão arterial essencial, estudada com base em polimorfismos genéticos nas atuais populações humanas globais
Manuel Bicho
Laboratório de Genética e Instituto de Saúde Ambiental (ISAMB) da Faculdade de Medicina da Universidade de Lisboa, Lisboa, Portugal
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as described in an important article by Young et al&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">2</span></a> The factors acting at that time were temperature and humidity&#44; inversely related to latitude in Africa&#44; which activated compensatory adaptive hypertensive mechanisms secondary to decreased volume-dependent blood pressure associated with severe loss of sodium chloride by sweating&#46; Young et al&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">2</span></a> identified several polymorphic variants of five genes encoding proteins involved in these compensatory mechanisms of volume change and vascular reactivity secondary to salt loss&#46; The genetic variant most strongly associated with current global variation in susceptibility to hypertension is the C825T polymorphism of the <span class="elsevierStyleItalic">GNB3</span> gene&#46; The frequency distribution of genetic variants associated with adaptive mechanisms&#44; especially the one analyzed by Sousa et al&#46;&#44; is independent of the continent where they occur&#44; as shown by the similarity of their distribution in Native Americans of the equatorial zones to that of modern African populations&#46; We performed a study<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">3</span></a> of the Hp1 polymorphic variant &#40;only found in humans&#41; of haptoglobin&#44; an acute phase protein that for more than 30 years has been associated with higher blood pressure sensitivity to sodium&#46; In this work we found very similar allelic frequencies of the <span class="elsevierStyleItalic">HP</span> gene in Honduras &#40;Central America&#41; and in Mozambique &#40;Africa&#41;&#46; These countries are at similar latitudes&#44; although in the case of Native American populations the adaptations occurred over the course of less than 20<span class="elsevierStyleHsp" style=""></span>000 years&#46; This is the result of movements in Eurasia&#44; in the opposite direction &#40;north to south&#41; to the initial movement subsequent to the departure from Africa of the original populations in which these gene variants were initially fixed&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">With regard to the same Hp allele&#44; we published a paper in the <span class="elsevierStyleItalic">Journal</span> in 2000&#44;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">4</span></a> the results of which showed a different nocturnal blood pressure response in salt-sensitive hypertensive individuals&#44; compared to normotensive and non-sensitive individuals&#44; after a change of diet from low to high sodium&#46; The Hp1-1 allele was found in 100&#37; of both normotensive and hypertensive salt-sensitive subjects&#46; In this study we also showed that in urban settings in modern African populations&#44; these individuals have increased cardiovascular risk&#44; even compared to those in the current African diaspora&#44; which confirms the epidemiological transition of these populations with respect to the original ones 50 years ago&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">As further evidence of the effect of these ancestral gene variants&#44; the work by Sousa et al&#46; shows that the risk for obesity conferred by the 825T allele of the <span class="elsevierStyleItalic">GNB3</span> gene in Madeira&#44; also demonstrated in other populations&#44; is associated with a higher risk of essential hypertension&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">5</span></a> The frequency of this morbid allele is higher in hypertensive patients than in controls in the population of the Madeira archipelago&#44; in contrast to those found in a larger population &#40;the PHYSA study&#41; on the mainland&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">6&#44;7</span></a> Regardless of the differences in sampling methods between these two studies&#44; the explanation for the association of this variant with hypertension on this Portuguese island&#44; which is not observed on the mainland&#44; probably lies in the fact that the Madeira population is a genetic isolate in which the effect of stratification of these genes is likely to be maximized&#44; despite its common ethnic origins with mainland populations&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">8</span></a></p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of interest</span><p id="par0025" class="elsevierStylePara elsevierViewall">The author has no conflicts of interest to declare&#46;</p></span></span>"
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Informação do artigo
ISSN: 08702551
Idioma original: Inglês
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2024 Outubro 43 34 77
2024 Setembro 62 31 93
2024 Agosto 48 34 82
2024 Julho 40 26 66
2024 Junho 39 18 57
2024 Maio 44 27 71
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2021 Novembro 31 40 71
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2021 Setembro 32 25 57
2021 Agosto 32 28 60
2021 Julho 30 22 52
2021 Junho 22 23 45
2021 Maio 32 43 75
2021 Abril 49 13 62
2021 Maro 71 27 98
2021 Fevereiro 72 22 94
2021 Janeiro 36 24 60
2020 Dezembro 42 14 56
2020 Novembro 41 17 58
2020 Outubro 17 24 41
2020 Setembro 73 20 93
2020 Agosto 19 11 30
2020 Julho 51 16 67
2020 Junho 28 12 40
2020 Maio 37 8 45
2020 Abril 40 21 61
2020 Maro 37 7 44
2020 Fevereiro 67 30 97
2020 Janeiro 25 6 31
2019 Dezembro 36 11 47
2019 Novembro 23 13 36
2019 Outubro 33 10 43
2019 Setembro 14 15 29
2019 Agosto 33 10 43
2019 Julho 40 8 48
2019 Junho 28 11 39
2019 Maio 37 15 52
2019 Abril 21 19 40
2019 Maro 72 15 87
2019 Fevereiro 58 12 70
2019 Janeiro 81 7 88
2018 Dezembro 66 10 76
2018 Novembro 46 11 57
2018 Outubro 92 17 109
2018 Setembro 42 16 58
2018 Agosto 34 16 50
2018 Julho 52 25 77
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