Abstract
Objective
We suggested association of family history of type 2 diabetes (FHD) with microvascular dysfunction, which may cause blood pressure (BP) elevations. We test whether FHD may be associated with higher BP.
Research design and methods
Resting BP, heart rates (in beats per minute: bpm), body composition and fasting concentrations of glucose, insulin, leptin and adiponectin were measured in 332 Japanese women aged 18–24 years. They were grouped according to BP category defined by the 2017 American College of Cardiology/American Heart Association Blood Pressure Guideline.
Results
BMI averaged < 22 kg/m2 and did not differ cross-sectionally between 73 with (FHD+) and 259 without FHD (FHD−). FHD+ had higher mean (81 ± 9 vs. 77 ± 7 mmHg, p < 0.001), systolic (111 ± 13 vs. 106 ± 10 mmHg, p = 0.003) and diastolic BP (65 ± 8 vs. 60 ± 7 mmHg, p < 0.001). Prevalence of elevated BP (11.0 vs. 6.2%), hypertension stage 1 (4.1 vs. 0.8%) and stage 2 (2.7 vs. 0.4%) was higher as well (p = 0.01). Endurance training in FHD+ abolished the differences in BP readings and BP prevalence. However, the mean resting heart rate in FHD+ athletes (61.2 bpm) was close to those in FHD+ (64.7 bpm) and FHD− nonathletes (64.6 bpm) and was higher than in FHD− athletes (56.5 bpm). Fat mass and distribution evaluated by dual-energy X-ray absorptiometry, markers of insulin resistance, and serum adipokines studied did not differ between the two groups.
Conclusions
FHD was associated with higher BP and higher prevalence of elevated BP and hypertension, suggesting contribution of microvascular dysfunction in BP elevations in normal weight young Japanese women. FHD may be associated with reduced heart rate response to endurance training as well.
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References
DeFronzo RA. Banting lecture. From the triumvirate to the ominous octet: a new paradigm for the treatment of type 2 diabetes mellitus. Diabetes. 2009;58:773–95.
Tsimihodimos V, Gonzalez-Villalpando C, Meigs JB, et al. Hypertension and diabetes mellitus: coprediction and time trajectories. Hypertension. 2018;71:422–8.
Serné EH, de Jongh RT, Eringa EC, et al. Microvascular dysfunction: a potential pathophysiological role in the metabolic syndrome. Hypertension. 2007;50:204–11.
Levy BI, Ambrosio G, Pries AR, et al. Microcirculation in hypertension: a new target for treatment? Circulation. 2001;104:736–41.
De Boer MP, Meijer RI, Wijnstok NJ, et al. Microvascular dysfunction: a potential mechanism in the pathogenesis of obesity-associated insulin resistance and hypertension. Microcirculation. 2012;19:5–18.
Middlebrooke AR, Armstrong N, Welsman JR, et al. Does aerobic fitness influence microvascular function in healthy adults at risk of developing Type 2 diabetes? Diabet Med. 2005;22:483–9.
Caballero AE, Arora S, Saouaf R, et al. Microvascular and macrovascular reactivity is reduced in subjects at risk for type 2 diabetes. Diabetes. 1999;48:1856–62.
Jaap AJ, Hammersley MS, Shore AC, et al. Reduced microvascular hyperaemia in subjects at risk of developing type 2 (non-insulin-dependent) diabetes mellitus. Diabetologia. 1994;37:214–6.
Lee BC, Shore AC, Humphreys JM, et al. Skin microvascular vasodilatory capacity in offspring of two parents with type 2 diabetes. Diabet Med. 2001;18:541–5.
Kähönen E, Lyytikäinen LP, Aatola H, et al. Systemic vascular resistance predicts the development of hypertension: the cardiovascular risk in young Finns’ study. Blood Press. 2020;29:1–8.
Westerhof N, Westerhof BE. A review of methods to determine the functional arterial parameters stiffness and resistance. J Hypertens. 2013;31:1769–75.
Julius S, Krause L, Schork NJ, et al. Hyperkinetic borderline hypertension in Tecumseh. Michigan J Hypertens. 1991;9:77–84.
Park C, Fraser A, Howe LD, et al. Elevated blood pressure in adolescence is attributable to a combination of elevated cardiac output and total peripheral resistance. Hypertension. 2018;72:1103–8.
Nardin C, Maki-Petaja KM, Miles KL, et al. Cardiovascular phenotype of elevated blood pressure differs markedly between young males and females: the enigma study. Hypertension. 2018;72:1277–84.
Takeuchi M, Wu B, Honda M, et al. Decreased arterial distensibility and postmeal hyperinsulinemia in young Japanese women with family history of diabetes. BMJ Open Diabetes Res Care. 2020;8(1):e001244.
Kitaoka K, Takeuchi M, Tsuboi A, et al. Increased adipose and muscle insulin sensitivity without changes in serum adiponectin in young female collegiate athletes. Metab Syndr Relat Disord. 2017;15:246–51.
Tanaka S, Wu B, Honda M, et al. Associations of lower-body fat mass with favorable profile of lipoproteins and adipokines in healthy, slim women in early adulthood. J Atheroscler Thromb. 2011;18:365–72.
Whelton PK, Carey RM, Aronow WS, et al. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA Guideline for the prevention, detection, evaluation, and management of high blood pressure in adults: executive summary: a report of the American college of cardiology/American heart association task force on clinical practice guidelines. Circulation. 2018;138(17):e426–83.
Matthews DR, Hosker JP, Rudenski AS, et al. Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985;28:412–9.
Lim U, Turner SD, Franke AA, et al. Predicting total, abdominal, visceral and hepatic adiposity with circulating biomarkers in Caucasian and Japanese American women. PLoS ONE. 2012;7:e43502.
Honda M, Tsuboi A, Minato-Inokawa S, et al. Reduced birth weight, decreased early-phase insulin secretion and increased glucose concentrations after oral glucose tolerance test in Japanese women aged 20 years with family history of type 2 diabetes. J Diabetes Res. 2020. https://doi.org/10.1155/2020/8822135.
Bonnet F, Roussel R, Natali A, et al. Parental history of type 2 diabetes, TCF7L2 variant and lower insulin secretion are associated with incident hypertension. Data from the DESIR and RISC cohorts. Diabetologia. 2013;56:2414–23.
Richards OC, Raines SM, Attie AD. The role of blood vessels, endothelial cells, and vascular pericytes in insulin secretion and peripheral insulin action. Endocr Rev. 2010;31:343–63.
Stehouwer CDA. Microvascular dysfunction and hyperglycemia: a vicious cycle with widespread consequences. Diabetes. 2018;67:1729–41.
Srinivasan SR, Frontini MG, Berenson GS, et al. Longitudinal changes in risk variables of insulin resistance syndrome from childhood to young adulthood in offspring of parents with type 2 diabetes: the Bogalusa heart study. Metabolism. 2003;52:443–50.
Ahn CW, Song YD, Nam JH, et al. Insulin sensitivity in physically fit and unfit children of parents with type 2 diabetes. Diabet Med. 2004;21:59–63.
Barwell ND, Malkova D, Moran CN, et al. Exercise training has greater effects on insulin sensitivity in daughters of patients with type 2 diabetes than in women with no family history of diabetes. Diabetologia. 2008;51:1912–9.
Søgaard D, Østergård T, Blachnio-Zabielska AU, et al. Training does not alter muscle ceramide and diacylglycerol in offsprings of type 2 diabetic patients despite improved insulin sensitivity. J Diabetes Res. 2016;2016:1–12.
Sjøberg KA, Frøsig C, Kjøbsted R, et al. Exercise increases human skeletal muscle insulin sensitivity via coordinated increases in microvascular perfusion and molecular signaling. Diabetes. 2017;66:1501–10.
Prior SJ, Goldberg AP, Ortmeyer HK, et al. Increased skeletal muscle capillarization independently enhances insulin sensitivity in older adults after exercise training and detraining. Diabetes. 2015;64:3386–95.
Bahrainy S, Levy WC, Busey JM, et al. Exercise training bradycardia is largely explained by reduced intrinsic heart rate. Int J Cardiol. 2016;222:213–6.
Gourine AV, Ackland GL. Cardiac vagus and exercise. Physiology (Bethesda). 2019;34:71–80.
van de Vegte YJ, Tegegne BS, Verweij N, et al. Genetics and the heart rate response to exercise. Cell Mol Life Sci. 2019;76:2391–409.
Arslanian SA, Bacha F, Saad R, et al. Family history of type 2 diabetes is associated with decreased insulin sensitivity and an impaired balance between insulin sensitivity and insulin secretion in white youth. Diabetes Care. 2005;28:115–9.
Doi K, Taniguchi A, Nakai Y, et al. Decreased glucose effectiveness but not insulin resistance in glucose-tolerant offspring of Japanese non-insulin-dependent diabetic patients: a minimal-model analysis. Metabolism. 1997;46:880–3.
Matsumoto K, Sakamaki H, Izumino K, et al. Increased insulin sensitivity and decreased insulin secretion in offspring of insulin-sensitive type 2 diabetic patients. Metabolism. 2000;49:1219–23.
Tanaka M, Yoshida T, Bin W, et al. FTO, abdominal adiposity, fasting hyperglycemia associated with elevated HbA1c in Japanese middle-aged women. J Atheroscler Thromb. 2012;19:633–42.
Igarashi R, Fujihara K, Heianza Y, et al. Impact of individual components and their combinations within a family history of hypertension on the incidence of hypertension: Toranomon hospital health management center study 22. Medicine (Baltimore). 2016;95(38):e4564.
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We thank all participants for their dedicated and conscientious collaboration.
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Honda, M., Tsuboi, A., Minato-Inokawa, S. et al. Association of family history of type 2 diabetes with blood pressure and resting heart rate in young normal weight Japanese women. Diabetol Int 13, 220–225 (2022). https://doi.org/10.1007/s13340-021-00525-2
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DOI: https://doi.org/10.1007/s13340-021-00525-2