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(WFRF:(Temmingh H.)) pers:(Andreassen OA) pers:(Pomarol Clotet E)
 

Sökning: (WFRF:(Temmingh H.)) pers:(Andreassen OA) pers:(Pomarol Clotet E) > Dipping and variabi...

Dipping and variability of blood pressure and heart rate at night are heritable traits.

Fava, Cristiano (författare)
Lund University,Lunds universitet,Genomik, diabetes och endokrinologi,Forskargrupper vid Lunds universitet,Genomics, Diabetes and Endocrinology,Lund University Research Groups
Burri, Philippe (författare)
Lund University,Lunds universitet,Institutionen för kliniska vetenskaper, Malmö,Medicinska fakulteten,Department of Clinical Sciences, Malmö,Faculty of Medicine
Almgren, Peter (författare)
Lund University,Lunds universitet,Genomik, diabetes och endokrinologi,Forskargrupper vid Lunds universitet,Genomics, Diabetes and Endocrinology,Lund University Research Groups
visa fler...
Arcaro, Guido (författare)
Groop, Leif (författare)
Lund University,Lunds universitet,Genomik, diabetes och endokrinologi,Forskargrupper vid Lunds universitet,Genomics, Diabetes and Endocrinology,Lund University Research Groups
Hulthén, Lennart (författare)
Lund University,Lunds universitet,Institutionen för kliniska vetenskaper, Malmö,Medicinska fakulteten,Department of Clinical Sciences, Malmö,Faculty of Medicine
Melander, Olle (författare)
Lund University,Lunds universitet,Institutionen för kliniska vetenskaper, Malmö,Medicinska fakulteten,Department of Clinical Sciences, Malmö,Faculty of Medicine
visa färre...
 (creator_code:org_t)
Oxford University Press (OUP), 2005
2005
Engelska.
Ingår i: American Journal of Hypertension. - : Oxford University Press (OUP). - 1941-7225 .- 0895-7061. ; 18:11, s. 1402-1407
  • Konferensbidrag (refereegranskat)
Abstract Ämnesord
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  • Background: Blunted nocturnal blood pressure dipping (NBPD) as well as high variability in blood pressure (BPV) and low variability in heart rate (HRV), are associated with increased cardiovascular morbidity and mortality. The aim of this study was to determine whether these traits are heritable. Methods: We studied 260 healthy siblings without antihypertensive drugs from 118 Swedish families. The BPV and HRV were defined as the standard deviation of BP and heart rate values recorded during 24 h, daytime (6 AM to 10 Pm), and night-time (10 Pm to 6 AM). The NBPD was defined as the ratio between night-time and daytime BP. Heritability was estimated with a maximal likelihood method implemented in the Solar software package with and without adjustment for significant covariates. Results: At night, significant heritability was found for systolic (33%, P <.05), diastolic (36%, P <.05), and mean (42%, P <.01) BPV. After covariate adjustment the corresponding heritability values were 23% (P =.08), 29% (P <.05), and 37% (P <.05). Daytime BPV was not heritable. The heritability of NBPD was 38% (P <.05) for systolic, 9% (P =.29) for diastolic, and 36% (P <.05) for mean BP, but after adjustment only systolic NBPD was significant (29%, P <.05). Heart rate was highly heritable both during daytime (57%, P <.001) and night-time (58%, P <.001), but the variability of heart rate, after adjustment, was only significant at night (37%, P <.05). Conclusions: Our data suggest that BPV and HRV are partially under genetic control and that genetic loci of importance for these traits could be mapped by linkage analysis. Am J Hypertens 2005;18:1402-1407 0 2005 American Journal of Hypertension, Ltd.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

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