TY - JOUR
T1 - Hypertension in High School Students
T2 - Genetic and Environmental Factors: The HYGEF Study
AU - Bigazzi, Roberto
AU - Zagato, Laura
AU - Lanzani, Chiara
AU - Fontana, Simone
AU - Messaggio, Elisabetta
AU - Delli Carpini, Simona
AU - Citterio, Lorena
AU - Simonini, Marco
AU - Brioni, Elena
AU - Magnaghi, Cristiano
AU - Colombo, Gualtiero Ivanoe
AU - Santini, Giada
AU - Nistri, Francesca
AU - Cellai, Filippo
AU - Lenti, Salvatore
AU - Bianchi, Stefano
AU - Pertosa, Giovanni Battista
AU - Rocchetti, Maria Teresa
AU - Papale, Massimo
AU - Mezzolla, Valeria
AU - Gesualdo, Loreto
AU - Pina Concas, Maria
AU - Campese, Vito
AU - Manunta, Paolo
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Hypertension and obesity in the young population are major risk factors for renal and cardiovascular events, which could arise in adulthood. A candidate-gene approach was applied in a cohort observational study, in which we collected data from 2638 high school adolescent students. Participants underwent anthropometric and blood pressure (BP) measurements, as well as saliva and urine sample collection for genomic DNA extraction and renal function evaluation, respectively. We tested whether candidate genes previously implicated in salt-sensitive hypertension in adults impact BP also among adolescents. Since inflammatory mechanisms may be involved in pathophysiology of hypertension and in endothelial dysfunction and atherosclerosis through reactive oxygen species, the baseline urinary excretion of inflammatory and oxidative stress markers in a subgroup of adolescents stratified according to ADD1(alpha adducin) rs4961 genotypes was assessed. Regression analysis of BP values with genetic polymorphisms, highlighted an association with a missense variant of LSS (lanosterol synthase, rs2254524), a gene coding for an enzyme involved in endogenous ouabain synthesis. Higher diastolic and systolic BP were associated with LSS A allele (P=0.011 and P=0.023, respectively). BP resulted associated with 5 more SNPs. The KL (klotho) rs9536314 missense variant was associated with 24 hour urinary Na+ excretion (P=0.0083). Urinary protein tests showed a greater excretion of IL1β (interleukin 1β) and interleukin 10 (P<0.0001) in carriers of the ADD1 rs4961 T allele. In conclusion, 3 missense gene variants already implicated in adult hypertension impact BP or Na+ excretion among adolescents, and, together with activated pro-inflammatory pathways, might predispose to early cardiovascular damage.
AB - Hypertension and obesity in the young population are major risk factors for renal and cardiovascular events, which could arise in adulthood. A candidate-gene approach was applied in a cohort observational study, in which we collected data from 2638 high school adolescent students. Participants underwent anthropometric and blood pressure (BP) measurements, as well as saliva and urine sample collection for genomic DNA extraction and renal function evaluation, respectively. We tested whether candidate genes previously implicated in salt-sensitive hypertension in adults impact BP also among adolescents. Since inflammatory mechanisms may be involved in pathophysiology of hypertension and in endothelial dysfunction and atherosclerosis through reactive oxygen species, the baseline urinary excretion of inflammatory and oxidative stress markers in a subgroup of adolescents stratified according to ADD1(alpha adducin) rs4961 genotypes was assessed. Regression analysis of BP values with genetic polymorphisms, highlighted an association with a missense variant of LSS (lanosterol synthase, rs2254524), a gene coding for an enzyme involved in endogenous ouabain synthesis. Higher diastolic and systolic BP were associated with LSS A allele (P=0.011 and P=0.023, respectively). BP resulted associated with 5 more SNPs. The KL (klotho) rs9536314 missense variant was associated with 24 hour urinary Na+ excretion (P=0.0083). Urinary protein tests showed a greater excretion of IL1β (interleukin 1β) and interleukin 10 (P<0.0001) in carriers of the ADD1 rs4961 T allele. In conclusion, 3 missense gene variants already implicated in adult hypertension impact BP or Na+ excretion among adolescents, and, together with activated pro-inflammatory pathways, might predispose to early cardiovascular damage.
KW - adolescents
KW - blood pressure
KW - human
KW - hypertension
KW - sodiuria
UR - http://www.scopus.com/inward/record.url?scp=85076450335&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85076450335&partnerID=8YFLogxK
U2 - 10.1161/HYPERTENSIONAHA.119.13818
DO - 10.1161/HYPERTENSIONAHA.119.13818
M3 - Article
C2 - 31760884
VL - 75
SP - 71
EP - 78
JO - Hypertension
JF - Hypertension
SN - 0194-911X
IS - 1
ER -