Geriatric Research and Education Clinical Center, Palo Alto VA Health Care System, Palo Alto, California
Division of Nephrology, Stanford University School of Medicine, Palo Alto, California.
J Am Soc Nephrol. 2020 Sep;31(9):2122-2132. doi: 10.1681/ASN.2020010038. Epub 2020 Jun 26.
Intensively treating hypertension may benefit cardiovascular disease and cognitive function, but at the short-term expense of reduced kidney function.
We investigated markers of kidney function and the effect of intensive hypertension treatment on incidence of dementia and mild cognitive impairment (MCI) in 9361 participants in the randomized Systolic Blood Pressure Intervention Trial, which compared intensive versus standard systolic BP lowering (targeting <120 mm Hg versus <140 mm Hg, respectively). We categorized participants according to baseline and longitudinal changes in eGFR and urinary albumin-to-creatinine ratio. Primary outcomes were occurrence of adjudicated probable dementia and MCI.
Among 8563 participants who completed at least one cognitive assessment during follow-up (median 5.1 years), probable dementia occurred in 325 (3.8%) and MCI in 640 (7.6%) participants. In multivariable adjusted analyses, there was no significant association between baseline eGFR <60 ml/min per 1.73 m and risk for dementia or MCI. In time-varying analyses, eGFR decline ≥30% was associated with a higher risk for probable dementia. Incident eGFR <60 ml/min per 1.73 m was associated with a higher risk for MCI and a composite of dementia or MCI. Although these kidney events occurred more frequently in the intensive treatment group, there was no evidence that they modified or attenuated the effect of intensive treatment on dementia and MCI incidence. Baseline and incident urinary ACR ≥30 mg/g were not associated with probable dementia or MCI, nor did the urinary ACR modify the effect of intensive treatment on cognitive outcomes.
Among hypertensive adults, declining kidney function measured by eGFR is associated with increased risk for probable dementia and MCI, independent of the intensity of hypertension treatment.
强化高血压治疗可能有益于心血管疾病和认知功能,但会在短期内导致肾功能下降。
我们研究了肾功能标志物以及强化高血压治疗对随机收缩压干预试验 9361 名参与者中痴呆症和轻度认知障碍(MCI)发病率的影响,该试验比较了强化与标准收缩压降低(目标分别为<120mmHg 与<140mmHg)。我们根据基线和 eGFR 及尿白蛋白/肌酐比值的纵向变化对参与者进行分类。主要结局为经裁决的可能痴呆和 MCI 的发生。
在至少完成一次认知评估的 8563 名参与者中(中位随访时间 5.1 年),325 名(3.8%)发生可能痴呆,640 名(7.6%)发生 MCI。在多变量调整分析中,基线 eGFR<60ml/min/1.73m 与痴呆或 MCI 风险之间无显著关联。在时变分析中,eGFR 下降≥30%与更高的可能痴呆风险相关。新发 eGFR<60ml/min/1.73m 与 MCI 以及痴呆或 MCI 的复合终点风险升高相关。虽然这些肾脏事件在强化治疗组中更为常见,但没有证据表明它们改变或减弱了强化治疗对痴呆和 MCI 发生率的影响。基线和新发尿 ACR≥30mg/g 与可能痴呆或 MCI 无关,尿 ACR 也未改变强化治疗对认知结局的影响。
在高血压成年人中,eGFR 下降提示肾功能下降与更高的可能痴呆和 MCI 风险相关,与高血压治疗的强度无关。